Variant #0000002248 (NC_000013.10:-, BRCA2(NM_000059.3):c.681+56C>T)
Chromosome |
13 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
SNP, Allele frequency in Chinese population is less then 0.002 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
BRCA2_00016 |
Frequency |
0.002 |
Variant remarks |
Substitution |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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