Variant #0000624709 (NC_000023.10:g.71425175C>T, NM_006223.3:c.*7799C>T (PIN4))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71425175C>T |
| DNA change (hg38) |
g.72205325C>T |
| Published as |
ERCC6L(NM_001009954.2):c.3073G>A (p.G1025R), ERCC6L(NM_017669.2):c.3442G>A (p.(Gly1148Arg)) |
| ISCN |
- |
| DB-ID |
ERCC6L_000001 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) |
0.00061 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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