Variant #0000615431 (NC_000015.9:g.63978726G>A, NM_003922.3:c.6057C>T (HERC1))
Chromosome |
15 |
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.63978726G>A |
DNA change (hg38) |
g.63686527G>A |
Published as |
HERC1(NM_003922.3):c.6057C>T (p.G2019=) |
ISCN |
- |
DB-ID |
HERC1_000048 |
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) |
0.00031 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-07-06 15:19:49 +02:00 (CEST) |

Variant on transcripts
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