Variant #0000016701 (NC_000014.8:g.23248046C>T, NM_001126105.2:c.726G>A (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.23248046C>T
DNA change (hg38) g.22778837C>T
Published as 967G>A: W242X; 1012G>A: W242X
ISCN -
DB-ID SLC7A7_000024 See all 3 reported entries
Variant remarks 2 Italian, 1 North African and 3 Moroccan LPI families (all hom)
Reference PubMed: Sperandeo et al. 2000, PubMed: Mykkanen et al. 2000
ClinVar ID -
dbSNP ID rs121908679
Origin SUMMARY record
Segregation yes
Frequency -
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A7 NM_001126105.2 +/+ 05 c.726G>A r.(726g>a) p.(Trp242*)


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