All variants in the DSG2 gene

Information The variants shown are described using the NM_001943.3 transcript reference sequence.

105 entries on 2 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA 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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