Variant #0000616586 (NC_000017.10:g.41243509T>C, NM_007294.3:c.4039A>G (BRCA1))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41243509T>C |
DNA change (hg38) |
g.43091492T>C |
Published as |
BRCA1(NM_007294.2):c.4039A>G, BRCA1(NM_007294.3):c.4039A>G (p.R1347G, p.(Arg1347Gly)), BRCA1(NM_007294.4):c.4039A>G (p.R1347G), BRCA1(NM_007300.4):... |
ISCN |
- |
DB-ID |
BRCA1_000285 See all 54 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) |
0.00383 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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