Variant #0000348596 (NC_000011.9:g.62469980G>A, NM_001122955.3:c.446C>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.62469980G>A
DNA change (hg38) g.62702508G>A
Published as -
ISCN -
DB-ID BSCL2_000074
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 17:13:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPUL2 NM_001079559.2 ?/. - c.*12791C>T r.(=) p.(=)
BSCL2 NM_001122955.3 ?/. - c.446C>T r.(?) p.(Pro149Leu)
GNG3 NM_012202.4 ?/. - c.-5409G>A r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 ?/. - n.2966C>T r.(?) -


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