Variant #0000567698 (NC_000019.9:g.45855507G>C, NM_000400.3:c.2150C>G (ERCC2))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45855507G>C |
| DNA change (hg38) |
g.45352249G>C |
| Published as |
ERCC2(NM_000400.3):c.2150C>G (p.A717G), ERCC2(NM_000400.4):c.2150C>G (p.(Ala717Gly), p.A717G) |
| ISCN |
- |
| DB-ID |
ERCC2_000050 See all 7 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) |
0.00032 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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