Variant #0000252570 (NC_000011.9:g.62469966A>G, NM_001122955.3:c.460T>C (BSCL2))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62469966A>G
DNA change (hg38) g.62702494A>G
Published as BSCL2(NM_001122955.3):c.460T>C (p.S154P)
ISCN -
DB-ID BSCL2_000073
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 17:13:29 +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.*12805T>C r.(=) p.(=)
BSCL2 NM_001122955.3 +/. - c.460T>C r.(?) p.(Ser154Pro)
GNG3 NM_012202.4 +/. - c.-5423A>G r.(?) p.(=)
HNRNPUL2-BSCL2 NR_037946.1 +/. - n.2980T>C r.(?) -


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