Variant #0000269084 (NC_000017.10:g.41222975C>T, NM_007294.3:c.4956G>A (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.41222975C>T
DNA change (hg38) g.43070958C>T
Published as BRCA1(NM_007294.3):c.4956G>A (p.M1652I, p.(Met1652Ile)), BRCA1(NM_007294.4):c.4956G>A (p.M1652I)
ISCN -
DB-ID BRCA1_000348 See all 152 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) 0.01825 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA1 NM_007294.3 -/. 16 c.4956G>A r.(?) p.(Met1652Ile) -


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