Variant #0000016230 (NC_000002.11:g.219526031G>T, NC_000002.11(NM_004328.4):c.320+1G>T (BCS1L))

Chromosome 2
Allele Unknown
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.219526031G>T
DNA change (hg38) g.218661308G>T
Published as intron 2, donor 321G>T
ISCN -
DB-ID BCS1L_000004
Variant remarks 1 British patient (com-het) with GRACILE syndrome; splice site, polypeptide truncation
Reference PubMed: Visapää et al. 2002
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation ?
Frequency 0/140 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 2020-06-11 15:29:05 +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 +?/+? 3i c.320+1G>T r.spl p.?


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