Variant #0000562981 (NC_000017.10:g.72916621T>C, NM_173477.2:c.310A>G (USH1G))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.72916621T>C |
DNA change (hg38) |
g.74920526T>C |
Published as |
USH1G(NM_001282489.2):c.1A>G (p.M1?), USH1G(NM_001282489.3):c.1A>G (p.M1?) |
ISCN |
- |
DB-ID |
USH1G_000030 See all 5 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00014 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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