Variant #0000657301 (NC_000013.10:g.32953549G>T, NM_000059.3:c.8850G>T (BRCA2))
Chromosome |
13 |
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.32953549G>T |
DNA change (hg38) |
g.32379412G>T |
Published as |
BRCA2(NM_000059.3):c.8850G>T (p.K2950N, p.(Lys2950Asn)), BRCA2(NM_000059.4):c.8850G>T (p.K2950N) |
ISCN |
- |
DB-ID |
BRCA2_000379 See all 34 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) |
0.00074 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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