Variant #0000016229 (NC_000002.11:g.219525942A>G, NM_004328.4:c.232A>G (BCS1L))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.219525942A>G
DNA change (hg38) g.218661219A>G
Published as -
ISCN -
DB-ID BCS1L_000003 See all 2 reported entries
Variant remarks functional studies, variant causes functional defect in BCS1L protein; Finnish Major GRACILE mutation: 11 Finnish GRACILE families (hom) and 3 Finnish GRACILE patients (hom), also 1 British GRACILE patient (com-het)
Reference PubMed: Visapää et al. 2002, PubMed: Fellman et al. 2008
ClinVar ID -
dbSNP ID rs28937590
Origin SUMMARY record
Segregation -
Frequency 1/494 FIN (het)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0005 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-13 12:27:28 +01:00 (CET)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCS1L NM_004328.4 +/+ 03 c.232A>G r.232a>g p.Ser78Gly


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