Variant #0000016711 (NC_000014.8:g.23244747A>C, NM_001126105.2:c.1001T>G (SLC7A7))

Chromosome 14
Allele Parent #1
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.23244747A>C
DNA change (hg38) g.22775538A>C
Published as c.1287T>G: L334R
ISCN -
DB-ID SLC7A7_000034
Variant remarks 1 Spanish LPI family (com-het) and 1 Chilean sibpair (hom) with LPI; Mutation nearly abolished (approximately 10% residual activity) sodium-independent L-arginine and sodium-dependent L-leucine transport activity
Reference PubMed: Torrens et al. 1999, PubMed: Font-Llitjos et al. 2009
ClinVar ID -
dbSNP ID rs72552272
Origin SUMMARY record
Segregation yes
Frequency 0/50 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 2012-12-04 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 +/+ 08 c.1001T>G r.1001u>g p.Leu334Arg


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