Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Effect: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Exon: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.
DNA change (cDNA): Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.
RNA change: Description of variant at RNA level (following HGVS recommendations).
- r.123c>u
- r.? = unknown
- r.(?) = RNA not analysed but probably transcribed copy of DNA variant
- r.spl? = RNA not analysed but variant probably affects splicing
- r.(spl?) = RNA not analysed but variant may affect splicing
- r.0? = change expected to abolish transcription
Protein: Description of variant at protein level (following HGVS recommendations).
- p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
- p.Arg345Pro = change derived from RNA analysis
- p.? = unknown effect
- p.0? = probably no protein produced
Allele: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
Type: Type of variant at DNA level; note that the variant type can also be derived from the variant description (for all levels).
All options:
- Substitution
- Deletion
- Duplication
- Insertion
- Inversion
- Insertion/Deletion
- Translocation
- Other/Complex
DNA change (genomic) (hg19): Description of variant at DNA level, based on the genomic DNA reference sequence (following HGVS recommendations).
- g.12345678C>T
- g.12345678_12345890del
- g.12345678_12345890dup
Reference: Reference to publication describing the variant, including links to OMIM (when available), PubMed or or other source, e.g. "den Dunnen ASHG2003 P2346".
DB-ID: Database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro.
Frequency: Frequency in which the variant was found; e.g 5/760 chromosomes (in 5 of 760 chromosomes tested), 1/33 patients (in 1 of 33 patients analysed in study), 0.05 controls (in 5% of control cases tested).
Variant remarks: Remarks regarding the variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
ClassClinical: ClassClinical
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Operator |
Column type |
Example |
Matches |
|
Text |
Arg |
all entries containing 'Arg' |
space |
Text |
Arg Ser |
all entries containing 'Arg' and 'Ser' |
| |
Text |
Arg|Ser |
all entries containing 'Arg' or 'Ser' |
! |
Text |
!fs |
all entries not containing 'fs' |
^ |
Text |
^p.(Arg |
all entries beginning with 'p.(Arg' |
$ |
Text |
Ser)$ |
all entries ending with 'Ser)' |
="" |
Text |
="" |
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="" |
Text |
="p.0" |
all entries exactly matching 'p.0' |
!="" |
Text |
!="" |
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!="" |
Text |
!="p.0" |
all entries not exactly matching 'p.0?' |
combination |
Text |
*|Ter !fs |
all entries containing '*' or 'Ter' but not containing 'fs' |
|
Date |
2020 |
all entries matching the year 2020 |
| |
Date |
2020-03|2020-04 |
all entries matching March or April, 2020 |
! |
Date |
!2020-03 |
all entries not matching March, 2020 |
< |
Date |
<2020 |
all entries before the year 2020 |
<= |
Date |
<=2020-06 |
all entries in or before June, 2020 |
> |
Date |
>2020-06 |
all entries after June, 2020 |
>= |
Date |
>=2020-06-15 |
all entries on or after June 15th, 2020 |
combination |
Date |
2019|2020 <2020-03 |
all entries in 2019 or 2020, and before March, 2020 |
|
Numeric |
23 |
all entries exactly matching 23 |
| |
Numeric |
23|24 |
all entries exactly matching 23 or 24 |
! |
Numeric |
!23 |
all entries not exactly matching 23 |
< |
Numeric |
<23 |
all entries lower than 23 |
<= |
Numeric |
<=23 |
all entries lower than, or equal to, 23 |
> |
Numeric |
>23 |
all entries higher than 23 |
>= |
Numeric |
>=23 |
all entries higher than, or equal to, 23 |
combination |
Numeric |
>=20 <30 !23 |
all entries with values from 20 to 29, but not equal to 23 |
Some more advanced examples:
Example |
Matches |
Asian |
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc. |
Asian !Caucasian |
all entries containing 'Asian' but not containing 'Caucasian' |
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all entries containing 'Asian' or 'African', but not containing 'Caucasian' |
"South Asian" |
all entries containing 'South Asian', but not containing 'South East Asian' |
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|
Legend |
How to query |
« First |
Prev |
|
1 |
2 |
|
Next |
Last » |
Effect
|
Exon
|
DNA change (cDNA)
|
RNA change
|
Protein
|
Type
|
DNA change (genomic) (hg19)
|
Reference
|
DB-ID
|
Frequency
|
Variant remarks
|
ClassClinical
|
Owner
|
./. |
01 |
c.3G>C |
- |
P.Met1Ile |
This change alters the translation
initiation codon ATG to ATC (3G.C) and leads to a substi-
tut |
- |
GenBank |
DSG2_00021 |
- |
3G>C |
- |
Qi Ming |
./. |
01 |
c.44T>A |
- |
p.Leu15Gln |
- |
- |
GenBank |
DSG2_00028 |
- |
- |
- |
Qi Ming |
./. |
02 |
c.81+86G>A |
- |
- |
- |
- |
GenBank |
DSG2_00049 |
- |
c.124 + 86G > A |
- |
Qi Ming |
./. |
03 |
c.136C>T |
- |
p.Arg46Trp |
- |
- |
GenBank |
DSG2_00052 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.137G>A |
- |
P.Arg46Gln |
abolish furin cleavage of pro-desmoglein-2, thereby disrupting production ofmature, functional prote |
- |
GenBank |
DSG2_00015 |
- |
134G>A |
- |
Qi Ming |
./. |
03 |
c.137G>A |
- |
p.Arg46Gln |
- |
- |
GenBank |
DSG2_00015 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.137G>A |
- |
p.Arg46Gln |
- |
- |
GenBank |
DSG2_00015 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.137G>A |
- |
p.Arg46Gln |
- |
- |
GenBank |
DSG2_00015 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.146G>A |
- |
P.Arg49His |
abolish furin cleavage of pro-desmoglein-2, thereby disrupting production ofmature, functional prote |
- |
GenBank |
DSG2_00016 |
- |
c.143G>A |
- |
Qi Ming |
./. |
03 |
c.146G>A |
- |
p.Arg49His |
- |
- |
GenBank |
DSG2_00016 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.146G>A |
- |
p.Arg49His |
- |
- |
GenBank |
DSG2_00016 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.146G>A |
- |
p.Arg49His |
- |
- |
GenBank |
DSG2_00016 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.166G>A |
- |
p.Val56Met |
- |
- |
GenBank |
DSG2_00022 |
- |
165G>A |
- |
Qi Ming |
./. |
03 |
c.166G>A |
- |
p.Val56Met |
- |
- |
GenBank |
DSG2_00022 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.166G>A |
- |
p.Val56Met |
- |
- |
GenBank |
DSG2_00022 |
- |
- |
- |
Qi Ming |
./. |
03 |
c.166G>A |
- |
p.Val56Met |
Yet, in the present study only the DSG2-V55M variant showed segregation with DCM in a family
pedi |
- |
GenBank |
DSG2_00022 |
- |
c.209G>A |
- |
Qi Ming |
./. |
03 |
c.167T>A |
- |
p.Val56Glu |
A novel
mutation in DSG2, V56M, was detected in an individual
carrying the 2146-1GC mutation in |
- |
GenBank |
DSG2_00073 |
- |
- |
- |
Qi Ming |
./. |
04 |
c.260A>G |
- |
p.Tyr87Cys |
- |
- |
GenBank |
DSG2_00008 |
- |
- |
- |
Qi Ming |
./. |
04 |
c.266A>G |
- |
p.Tyr89Cys |
- |
- |
GenBank |
DSG2_00076 |
NA |
- |
- |
Qi Ming |
./. |
04 |
c.298G>C |
- |
P.Gly100Arg |
missense mutations |
- |
GenBank |
DSG2_00005 |
- |
- |
- |
Qi Ming |
./. |
04 |
c.298G>C |
- |
p.Gly100Arg |
- |
- |
GenBank |
DSG2_00005 |
- |
- |
- |
Qi Ming |
./. |
05 |
c.437G>T |
- |
p.Arg146Leu |
- |
- |
GenBank |
DSG2_00058 |
- |
- |
- |
Qi Ming |
./. |
05 |
c.437G>T |
- |
p.Arg146Leu |
- |
- |
GenBank |
DSG2_00058 |
NA |
- |
- |
Qi Ming |
./. |
05 |
c.445G>T |
- |
p.Val149Phe |
- |
- |
GenBank |
DSG2_00029 |
- |
- |
- |
Qi Ming |
./. |
05 |
c.462C>A |
- |
p.Asp154Glu |
In particular, a C!A transversion
in exon 5 resulting in the substitution of an aspartic acid
wi |
- |
GenBank |
DSG2_00023 |
- |
462C>A |
- |
Qi Ming |
./. |
05 |
c.473T>G |
- |
p.Val158Gly |
Families E and F had a
T>G change which replaces a valine with a glycine at
position 158 (V158G) |
- |
GenBank |
DSG2_00024 |
- |
473T>G |
- |
Qi Ming |
./. |
05 |
c.473T>G |
- |
p.Val158Gly |
- |
- |
GenBank |
DSG2_00024 |
- |
c.516T > G |
- |
Qi Ming |
./. |
05 |
c.523+2T>C |
- |
- |
- |
- |
GenBank |
DSG2_00053 |
- |
- |
- |
Qi Ming |
./. |
06 |
c.560A>G |
- |
p.Asp187Gly |
- |
- |
GenBank |
DSG2_00061 |
- |
- |
- |
Qi Ming |
./. |
06 |
c.614C>T |
- |
p.Pro205Leu |
- |
- |
GenBank |
DSG2_00030 |
- |
- |
- |
Qi Ming |
./. |
06 |
c.690+1G>A |
- |
p.= |
- |
- |
GenBank |
DSG2_00054 |
- |
- |
- |
Qi Ming |
./. |
07 |
c.792T>A |
- |
p.Asp264Glu |
- |
- |
GenBank |
DSG2_00059 |
- |
- |
- |
Qi Ming |
./. |
07 |
c.797A>G |
- |
p.Asn266Ser |
MISSENSE MUTATION |
- |
GenBank |
DSG2_00009 |
- |
- |
- |
Qi Ming |
./. |
07 |
c.806T>C |
- |
p.Ile269Thr |
- |
- |
GenBank |
DSG2_00060 |
- |
- |
- |
Qi Ming |
./. |
07 |
c.828+16C>A |
- |
- |
- |
- |
GenBank |
DSG2_00044 |
- |
c.871 + 16C > A |
- |
Qi Ming |
./. |
08 |
c.829_836del |
- |
p.Leu277AspfsX3 |
- |
- |
GenBank |
DSG2_00051 |
- |
c.829-1_835del |
- |
Qi Ming |
./. |
08 |
c.829_840delCTTGAAGGGATG |
- |
p.Leu277_Met280del |
- |
- |
GenBank |
DSG2_00025 |
- |
829_840delCTTGAAGGGATG |
- |
Qi Ming |
./. |
08 |
c.861C>T |
- |
p.Asn287Asn |
- |
- |
GenBank |
DSG2_00046 |
- |
c.904C > T |
- |
Qi Ming |
./. |
08 |
c.861C>T |
- |
p.Asn287Asn |
- |
- |
GenBank |
DSG2_00046 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.877A>G |
- |
p.Ile293Val |
- |
- |
GenBank |
DSG2_00045 |
- |
c.920A > G |
- |
Qi Ming |
./. |
08 |
c.877A>G |
- |
p.Ile293Val |
- |
- |
GenBank |
DSG2_00045 |
G=0.043/54 |
- |
- |
Qi Ming |
./. |
08 |
c.880A>G |
- |
p.Lys294Glu |
MISSENSE MUTATION |
- |
GenBank |
DSG2_00010 |
- |
.877A>G |
- |
Qi Ming |
./. |
08 |
c.882dupA |
- |
p.Val295SerfsX6 |
- |
- |
GenBank |
DSG2_00072 |
- |
c.882_883insA |
- |
Qi Ming |
./. |
08 |
c.889G>A |
- |
p.Asp297Asn |
- |
- |
GenBank |
DSG2_00031 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.918G>A |
- |
p.Trp306X |
- |
- |
GenBank |
DSG2_00017 |
- |
915G>A |
- |
Qi Ming |
./. |
08 |
c.918G>A |
- |
p.Trp306X |
- |
- |
GenBank |
DSG2_00017 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.961T>A |
- |
p.Phe321Ile |
- |
- |
GenBank |
DSG2_00062 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.977A>T |
- |
p.Asp326Val |
- |
- |
GenBank |
DSG2_00056 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.988A>G |
- |
p.Asn330Asp |
- |
- |
GenBank |
DSG2_00063 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.991G>A |
- |
p.Glu331Lys |
- |
- |
GenBank |
DSG2_00020 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.1003A>G |
- |
p.Thr335Ala |
one missense mutation
(DSG2 p.T335A, family J) affecting a highly conserved residue |
- |
GenBank |
DSG2_00034 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.1003A>G |
- |
p.Thr335Ala |
- |
- |
GenBank |
DSG2_00034 |
- |
- |
- |
Qi Ming |
./. |
08 |
c.1003A>G |
- |
p.Thr335Ala |
- |
- |
GenBank |
DSG2_00034 |
- |
- |
- |
Qi Ming |
./. |
09 |
c.1051A>G |
- |
p.Ser351Gly |
- |
- |
GenBank |
DSG2_00077 |
NA |
- |
- |
Qi Ming |
./. |
09 |
c.1174G>A |
- |
p.Val392Ile |
- |
- |
GenBank |
DSG2_00001 |
- |
1174G>A |
- |
Qi Ming |
./. |
09 |
c.1174G>A |
- |
p.Val392Ile |
- |
- |
GenBank |
DSG2_00001 |
- |
- |
- |
Qi Ming |
./. |
09 |
c.1252_1253insATGA |
- |
p.Glu418AspfsX18 |
The 4-bp insertion in exon 9 (1253_1257insATGA)causes the addition of an amino acid residue before a |
- |
GenBank |
DSG2_00006 |
- |
1253_1257insATGA |
- |
Qi Ming |
./. |
10 |
c.1423+1G>T |
- |
- |
Mutation 1423+1G>T affected the splice donor
site of intron 10, which may cause inclusion of
int |
- |
GenBank |
DSG2_00064 |
- |
- |
- |
Qi Ming |
./. |
11 |
c.1520G>A |
- |
p.Cys507Try |
- |
- |
GenBank |
DSG2_00018 |
- |
1517G-A |
- |
Qi Ming |
./. |
11 |
c.1520G>A |
- |
p.Cys507Tyr |
- |
- |
GenBank |
DSG2_00018 |
- |
- |
- |
Qi Ming |
./. |
11 |
c.1520G>A |
- |
p.Cys507Tyr |
- |
- |
GenBank |
DSG2_00018 |
- |
- |
- |
Qi Ming |
./. |
11 |
c.1543G>A |
- |
p.Val515Ile |
- |
- |
GenBank |
DSG2_00078 |
A=0.020/15 |
- |
- |
Qi Ming |
./. |
11 |
c.1592T>G |
- |
p.Phe531Cys |
- |
- |
GenBank |
DSG2_00065 |
- |
- |
- |
Qi Ming |
./. |
12 |
c.1669C>T |
- |
p.Gln557X |
- |
- |
GenBank |
DSG2_00074 |
- |
- |
- |
Qi Ming |
./. |
12 |
c.1672C>T |
- |
p.Gln558X |
NONSENSE MUTATION |
- |
GenBank |
DSG2_00011 |
- |
- |
- |
Qi Ming |
./. |
12 |
c.1773_1774del |
- |
p.Cys591X |
- |
- |
GenBank |
DSG2_00026 |
- |
1773_1774delTG |
- |
Qi Ming |
./. |
13 |
c.1919_1932del |
- |
p.Gly640AspfsX15 |
- |
- |
GenBank |
DSG2_00057 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2036delG |
- |
p.Gly679AlafsX3 |
The single base pair deletion in exon 14 (2036delG)
results in a frameshift mutation that would le |
- |
GenBank |
DSG2_00007 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2110A>G |
- |
p.Ile704Val |
- |
- |
GenBank |
DSG2_00079 |
NA |
- |
- |
Qi Ming |
./. |
14 |
c.2137G>A |
- |
P.Glu713Lys |
we
found the presence of this variant in 4 out of 86 blood donors.
We consider this variant ther |
- |
GenBank |
DSG2_00004 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2137G>A |
- |
p.Glu713Lys |
- |
- |
GenBank |
DSG2_00004 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2137G>A |
- |
p.Glu713Lys |
- |
- |
GenBank |
DSG2_00004 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2137G>A |
- |
p.Glu713Lys |
- |
- |
GenBank |
DSG2_00004 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2137G>A |
- |
p.Glu713Lys |
- |
- |
GenBank |
DSG2_00004 |
A=0.033/42 |
- |
- |
Qi Ming |
./. |
14 |
c.2318G>A |
- |
p.Arg773Lys |
- |
- |
GenBank |
DSG2_00040 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2318G>A |
- |
p.Arg773Lys |
- |
- |
GenBank |
DSG2_00040 |
- |
- |
- |
Qi Ming |
./. |
14 |
c.2318G>A |
- |
p.Arg773Lys |
- |
- |
GenBank |
DSG2_00040 |
A=0.266/334 |
- |
- |
Qi Ming |
./. |
15 |
c.2368C>T |
- |
p.His790Tyr |
- |
- |
GenBank |
DSG2_00080 |
T=0.011/4 |
- |
- |
Qi Ming |
./. |
15 |
c.2434G>T |
- |
p.Gly812Cys |
- |
- |
GenBank |
DSG2_00019 |
- |
2431G-T |
- |
Qi Ming |
./. |
15 |
c.2434G>T |
- |
p.Gly812Cys |
- |
- |
GenBank |
DSG2_00019 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.2505A>G |
- |
p.Thr835Thr |
- |
- |
GenBank |
DSG2_00041 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.2505A>G |
- |
p.Thr835Thr |
- |
- |
GenBank |
DSG2_00041 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.2587A>C |
- |
p.Met863Leu |
- |
- |
GenBank |
DSG2_00081 |
C=0.020/7 |
- |
- |
Qi Ming |
./. |
15 |
c.2647T>C |
- |
p.Ser883Pro |
- |
- |
GenBank |
DSG2_00082 |
C=0.006/5 |
- |
- |
Qi Ming |
./. |
15 |
c.2683C>A |
- |
p.Gln895Lys |
- |
- |
GenBank |
DSG2_00083 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.2708C>T |
- |
p.Thr903Ile |
- |
- |
GenBank |
DSG2_00084 |
T=0.014/5 |
- |
- |
Qi Ming |
./. |
15 |
c.2759T>G |
- |
p.Val920Gly |
- |
- |
GenBank |
DSG2_00027 |
- |
2759T>G |
- |
Qi Ming |
./. |
15 |
c.2759T>G |
- |
p.Val920Gly |
- |
- |
GenBank |
DSG2_00027 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.2759T>G |
- |
p.Val920Gly |
- |
- |
GenBank |
DSG2_00027 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.2780C>T |
- |
p.Pro927Leu |
- |
- |
GenBank |
DSG2_00085 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.2886T>G |
- |
p.Ile962Met |
- |
- |
GenBank |
DSG2_00086 |
G=0.003/4 |
- |
- |
Qi Ming |
./. |
15 |
c.2959G>T |
- |
p.Val987Phe |
- |
- |
GenBank |
DSG2_00087 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.3059_3062del |
- |
p.Glu1020AlafsX18 |
- |
- |
GenBank |
DSG2_00035 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.3082G>A |
- |
p.Gly1028Ser |
- |
- |
GenBank |
DSG2_00088 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.3175T>A |
- |
p.Ser1059Thr |
His relatives were
not available for evaluation, however, and a racial poly-
morphism cannot be |
- |
GenBank |
DSG2_00043 |
- |
3175T>A |
- |
Qi Ming |
./. |
15 |
c.3199A>G |
- |
p.Asn1067Asp |
- |
- |
GenBank |
DSG2_00032 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.3209C>T |
- |
p.Thr1070Met |
- |
- |
GenBank |
DSG2_00089 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.3247G>A |
- |
p.Gly1083Ser |
- |
- |
GenBank |
DSG2_00033 |
- |
- |
- |
Qi Ming |
./. |
15 |
c.3281G>T |
- |
p.Gly1094Val |
- |
- |
GenBank |
DSG2_00090 |
NA |
- |
- |
Qi Ming |
./. |
15 |
c.3283C>A |
- |
p.His1095Asn |
- |
- |
GenBank |
DSG2_00091 |
NA |
- |
- |
Qi Ming |
|
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