Variant #0000267879 (NC_000010.10:g.50723684G>A, NC_000010.10(NM_000124.2):c.1397+8395C>T (ERCC6))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.50723684G>A |
DNA change (hg38) |
g.49515638G>A |
Published as |
ERCC6(NM_000124.4):c.1397+8395C>T, PGBD3(NM_170753.3):c.1477C>T (p.L493=) |
ISCN |
- |
DB-ID |
ERCC6_000066 |
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) |
0.91336 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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