Variant #0000054207 (NC_000017.10:g.41267784G>C, BRCA1(NM_007294.3):c.93C>G)
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41267784G>C |
DNA change (hg38) |
g.43115767G>C |
Published as |
I31M |
ISCN |
- |
DB-ID |
BRCA1_000025 See all 9 reported entries |
Variant remarks |
protein binding ability BARD1; normal binding |
Reference |
PubMed: Ransburgh 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 View details |
Owner |
Maaike Vreeswijk |
Database submission license |
No license selected |
Created by |
Maaike Vreeswijk |

Variant on transcripts
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