Variant #0000053530 (NC_000013.10:g.32929387C>T, NM_000059.3:c.7397C>T (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.32929387C>T |
| DNA change (hg38) |
g.32355250C>T |
| Published as |
A2466V |
| ISCN |
- |
| DB-ID |
BRCA2_000186 See all 56 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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