Variant #0000036141 (NC_000002.11:g.219526006C>T, NM_004328.4:c.296C>T (BCS1L))

Chromosome 2
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.219526006C>T
DNA change (hg38) g.218661283C>T
Published as -
ISCN -
DB-ID BCS1L_000007
Variant remarks 1 patient (hom) with GRACILE syndrome
Reference PubMed: Kasapkara et al. 2014
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2014-04-03 16:29:23 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCS1L NM_004328.4 +?/+? 1 c.296C>T r.(296c>u) p.(Pro99Leu)


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