Variant #0000999204 (NC_000011.9:g.62457868G>A, NM_001122955.3:c.1360C>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.62457868G>A
DNA change (hg38) -
Published as BSCL2(NM_001122955.3):c.1360C>T (p.(Arg454*))
ISCN -
DB-ID GNG3_000020
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*24903C>T r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.1360C>T r.(?) p.(Arg454*)
GNG3 NM_012202.4 ?/. - c.-17521G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.3880C>T r.(?) -


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