Variant #0000016695 (NC_000014.8:g.23249197G>A, NM_001126105.2:c.563C>T (SLC7A7))

Chromosome 14
Allele Paternal (confirmed)
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.23249197G>A
DNA change (hg38) g.22779988G>A
Published as 849C>T: T188I; p.T188I (c.563C>T)
ISCN -
DB-ID SLC7A7_000018
Variant remarks 1 Greek LPI family (com-het); Functional studies confirmed disease-causative role
Reference PubMed: PalacĂ­n et al. 2001, PubMed: Sperandeo et al. 2005
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 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 +/+ 04 c.563C>T r.563c>u p.(Thr188Ile)


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