Variant #0000808178 (NC_000017.10:g.59938933A>G, NC_000017.10(NM_032043.2):c.-30-3T>C (BRIP1))

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.59938933A>G
DNA change (hg38) -
Published as BRIP1(NM_032043.2):c.-30-3T>C
ISCN -
DB-ID BRIP1_000092 See all 4 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) 0.00017 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 2021-09-17 14:40:49 +02:00 (CEST)
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.*5985T>C r.(=) p.(=) -
BRIP1 NM_032043.2 -?/. - c.-30-3T>C r.spl? p.? -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.