Variant #0000053385 (NC_000013.10:g.32912299T>C, NM_000059.3:c.3807T>C (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32912299T>C |
DNA change (hg38) |
g.32338162T>C |
Published as |
4035T/C (V1269V) |
ISCN |
- |
DB-ID |
BRCA2_000096 See all 886 reported entries |
Variant remarks |
Prevalence in normal controls; predicted neutral |
Reference |
PubMed: Wagner 1999 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.17469 View details |
Owner |
Peter Devilee |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2009-10-03 17:15:53 +02:00 (CEST) |
Date last edited |
2020-07-03 15:21:45 +02:00 (CEST) |

Variant on transcripts
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