Variant #0000000130 (NC_000011.9:g.5294135delT)
Individual ID |
00000001, 00000007, 00000008, 00000012, 00000013, 00000014, 00000015, 00000022, 00000028, 00000029, 00000030, 00000034, 00000038, 00000039, 00000040, 00000041, 00000043, 00000046, 00000047, 00000051, 00000052, 00000053, 00000055, 00000058, 00000059, 00000060, 00000061, 00000062, 00000065, 00000067, 00000068, 00000070, 00000071, 00000075, 00000076, 00000078, 00000081, 00000083, 00000084, 00000085, 00000087, 00000089, 00000091, 00000092, 00000093, 00000094, 00000096, 00000097, 00000102, 00000103, 00000105, 00000107, 00000108, 00000113, 00000116, 00000117, 00000118, 00000126, 00000127, 00000128, 00000129, 00000131, 00000133, 00000134, 00000135, 00000138, 00000141, 00000144, 00000145, 00000148, 00000149, 00000150, 00000152, 00000153, 00000156, 00000157, 00000158, 00000159, 00000160, 00000161, 00000165, 00000166, 00000167, 00000171, 00000172 |
Chromosome |
11 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5294135delT |
Reference |
GenBank |
DB-ID |
HBE1_000008 See all 2 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
uncertain significance |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
Screenings
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