Variant #0000550699 (NC_000013.10:g.32972744_32972745insGAATTATAT, NM_000059.3:c.10094_10095insGAATTATAT (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32972744_32972745insGAATTATAT |
DNA change (hg38) |
g.32398607_32398608insGAATTATAT |
Published as |
BRCA2(NM_000059.3):c.10094_10095insGAATTATAT (p.(Val3365_Ser3366insAsnTyrIle)), BRCA2(NM_000059.4):c.10094_10095insGAATTATAT (p.V3365_S3366insNYI) |
ISCN |
- |
DB-ID |
BRCA2_006065 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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