Variant #0000890024 (NC_000011.9:g.62458289C>A, NM_001122955.3:c.1123G>T (BSCL2))

Chromosome 11
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.62458289C>A
DNA change (hg38) -
Published as BSCL2(NM_001122955.4):c.1123G>T (p.G375C)
ISCN -
DB-ID GNG3_000015
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*24482G>T r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.1123G>T r.(?) p.(Gly375Cys)
GNG3 NM_012202.4 ?/. - c.-17100C>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.3643G>T r.(?) -


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