Variant #0000016718 (NC_000014.8:g.23243580G>A, NM_001126105.2:c.1228C>T (SLC7A7))

Chromosome 14
Allele Both (homozygous)
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.23243580G>A
DNA change (hg38) g.22774371G>A
Published as CGA>TGA: R410X
ISCN -
DB-ID SLC7A7_000041 See all 2 reported entries
Variant remarks 12 Japanese LPI families (7 hom and 5 com-het) and 1 Moroccan LPI family (hom)
Reference PubMed: Noguchi et al.v2000, PubMed: Shoji et al. 2002, PubMed: Font-Llitjos et al. 2009
ClinVar ID -
dbSNP ID rs121908678
Origin SUMMARY record
Segregation yes
Frequency 0/50 JAP CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 16:25:21 +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     
SLC7A7 NM_001126105.2 +/+ 09 c.1228C>T r.1228c>u p.(Arg410*)


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