Variant #0000271422 (NC_000017.10:g.41244815T>C, NM_007294.3:c.2733A>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.41244815T>C
DNA change (hg38) g.43092798T>C
Published as BRCA1(NM_007294.3):c.2733A>G (p.G911=), BRCA1(NM_007294.4):c.2733A>G (p.G911=), BRCA1(NM_007300.4):c.2733A>G (p.G911=)
ISCN -
DB-ID BRCA1_001116 See all 33 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) 0.001 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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 -?/. 11 c.2733A>G r.(?) p.(Gly911=) -


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