Variant #0001015595 (NC_000017.10:g.59938863A>G, NM_032043.2:c.38T>C (BRIP1))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.59938863A>G
DNA change (hg38) -
Published as BRIP1(NM_032043.3):c.38T>C (p.V13A)
ISCN -
DB-ID BRIP1_000871
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
INTS2 NM_020748.2 ?/. - c.*6055T>C r.(=) p.(=) -
BRIP1 NM_032043.2 ?/. - c.38T>C r.(?) p.(Val13Ala) -


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