Variant #0000053454 (NC_000013.10:g.32914236C>T, NM_000059.3:c.5744C>T (BRCA2))
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32914236C>T |
DNA change (hg38) |
g.32340099C>T |
Published as |
p.Thr1915Met |
ISCN |
- |
DB-ID |
BRCA2_000145 See all 155 reported entries |
Variant remarks |
LOH analysis; partial loss of wild type allele |
Reference |
PubMed: Beristain 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.01767 View details |
Owner |
Maaike Vreeswijk |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Maaike Vreeswijk |
Date created |
2011-09-23 13:43:57 +02:00 (CEST) |
Date last edited |
2020-07-03 15:35:29 +02:00 (CEST) |

Variant on transcripts
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