Variant #0000053241 (NC_000013.10:g.32900405C>A, NM_000059.3:c.502C>A (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.32900405C>A |
DNA change (hg38) |
g.32326268C>A |
Published as |
P168T |
ISCN |
- |
DB-ID |
BRCA2_000033 See all 13 reported entries |
Variant remarks |
Multifactorial likelihood-ratio model; predicted neutral |
Reference |
PubMed: Easton 2007 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-5 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 14:54:15 +02:00 (CEST) |

Variant on transcripts
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