Variant #0000891235 (NC_000013.10:g.32914174C>G, NM_000059.3:c.5682C>G (BRCA2))
| Chromosome |
13 |
| 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.32914174C>G |
| DNA change (hg38) |
- |
| Published as |
BRCA2(NM_000059.3):c.5682C>G (p.Y1894*, p.(Tyr1894Ter)), BRCA2(NM_000059.4):c.5682C>G (p.Y1894*) |
| ISCN |
- |
| DB-ID |
BRCA2_001092 See all 67 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 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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