Variant #0000613501 (NC_000011.9:g.62491775G>C, NM_001122955.3:c.-17108C>G (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.62491775G>C
DNA change (hg38) g.62724303G>C
Published as HNRNPUL2(NM_001079559.2):c.662C>G (p.A221G)
ISCN -
DB-ID GNG3_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-30 17:14:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.662C>G r.(?) p.(Ala221Gly)
BSCL2 NM_001122955.3 ?/. - c.-17108C>G r.(?) p.(=)
GNG3 NM_012202.4 ?/. - c.*15497G>C r.(=) p.(=)
TTC9C NM_173810.3 ?/. - c.-4546G>C r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.890C>G r.(?) -


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