Variant #0000266258 (NC_000013.10:g.32929059_32929060del, NM_000059.3:c.7069_7070del (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.32929059_32929060del |
DNA change (hg38) |
g.32354922_32354923del |
Published as |
BRCA2(NM_000059.3):c.7069_7070del (p.(Leu2357ValfsTer2)), BRCA2(NM_000059.3):c.7069_7070delCT (p.L2357Vfs*2), BRCA2(NM_000059.4):c.7069_7070delCT ... |
ISCN |
- |
DB-ID |
BRCA2_001277 See all 47 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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