Variant #0000192959 (NC_000013.10:g.32930598T>C, NM_000059.3:c.7469T>C (BRCA2))
| Chromosome |
13 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Does not affect function |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32930598T>C |
| DNA change (hg38) |
g.32356461T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
BRCA2_000195 See all 180 reported entries |
| Variant remarks |
Class 1 not pathogenic based on frequency >1% in an outbred sampleset. Frequency 0.1066 (Admixed American/Latino), derived from 1000 genomes (2013-05-02). |
| Reference |
ENIGMA classification criteria |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01926 View details |
| Owner |
ENIGMA consortium |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
ENIGMA consortium |
| Date created |
2016-09-28 12:00:00 +02:00 (CEST) |
| Date last edited |
2025-03-15 22:29:50 +01:00 (CET) |

Variant on transcripts
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