Variant #0000268927 (NC_000005.9:g.60194149T>C, NM_000082.3:c.797A>G (ERCC8))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.60194149T>C |
DNA change (hg38) |
g.60898322T>C |
Published as |
ERCC8(NM_000082.3):c.797A>G (p.D266G), ERCC8(NM_000082.4):c.797A>G (p.(Asp266Gly)), ERCC8(NM_001007233.3):c.623A>G (p.D208G) |
ISCN |
- |
DB-ID |
ERCC8_000015 See all 2 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) |
1.0E-5 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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