Variant #0000271989 (NC_000013.10:g.32914814C>T, NM_000059.3:c.6322C>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.32914814C>T |
DNA change (hg38) |
g.32340677C>T |
Published as |
BRCA2(NM_000059.3):c.6322C>T (p.R2108C, p.(Arg2108Cys)), BRCA2(NM_000059.4):c.6322C>T (p.R2108C) |
ISCN |
- |
DB-ID |
BRCA2_000508 See all 41 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) |
0.00059 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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