Variant #0000053427 (NC_000013.10:g.32913055G>A, NM_000059.3:c.4563G>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.32913055G>A |
DNA change (hg38) |
g.32338918G>A |
Published as |
4791G/A (L1521L) |
ISCN |
- |
DB-ID |
BRCA2_000123 See all 35 reported entries |
Variant remarks |
Prevalence in normal controls; predicted neutral Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message. |
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) |
Retrieve |
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 |
2019-02-25 21:51:16 +01:00 (CET) |

Variant on transcripts
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