Variant #0000855035 (NC_000017.10:g.59938833G>A, NM_032043.2:c.68C>T (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.59938833G>A
DNA change (hg38) -
Published as BRIP1(NM_032043.2):c.68C>T (p.P23L)
ISCN -
DB-ID BRIP1_000778 See all 2 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) 1.0E-5 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
INTS2 NM_020748.2 ?/. - c.*6085C>T r.(=) p.(=) -
BRIP1 NM_032043.2 ?/. - c.68C>T r.(?) p.(Pro23Leu) -


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