Variant #0000893623 (NC_000017.10:g.41215926C>G, NM_007294.3:c.5117G>C (BRCA1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41215926C>G |
DNA change (hg38) |
- |
Published as |
BRCA1(NM_007294.3):c.5117G>C (p.G1706A, p.(Gly1706Ala)), BRCA1(NM_007294.4):c.5117G>C (p.G1706A), BRCA1(NM_007300.4):c.5180G>C (p.G1727A) |
ISCN |
- |
DB-ID |
BRCA1_000391 See all 39 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2022-11-01 13:41:49 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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