Variant #0000016227 (NC_000002.11:g.219525123T>A, NC_000002.11(NM_004328.4):c.-50+155T>A (BCS1L))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.219525123T>A
DNA change (hg38) g.218660400T>A
Published as intron 1, -588T>A
ISCN -
DB-ID BCS1L_000001
Variant remarks 1 British patient (com-het) with GRACILE syndrome; pathogenicity not confirmed
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) Retrieve
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 15:28:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BCS1L NM_004328.4 ?/? 2i c.-50+155T>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.