Variant #0000930777 (NC_000017.10:g.41245071G>T, NM_007294.3:c.2477C>A (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.41245071G>T
DNA change (hg38) -
Published as BRCA1(NM_007294.3):c.2477C>A (p.(Thr826Lys), p.T826K), BRCA1(NM_007294.4):c.2477C>A (p.T826K), BRCA1(NM_007300.4):c.2477C>A (p.T826K)
ISCN -
DB-ID BRCA1_000206 See all 27 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) 0.00019 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
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 -?/. - c.2477C>A r.(?) p.(Thr826Lys) -


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