Variant #0000016699 (NC_000014.8:g.23249134C>G, NC_000014.8(NM_001126105.2):c.625+1G>C (SLC7A7))

Chromosome 14
Allele Paternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.23249134C>G
DNA change (hg38) g.22779925C>G
Published as c.625+1G>C: p.C167_G209delinsX
ISCN -
DB-ID SLC7A7_000022
Variant remarks 1 English/Argentinean LPI family (com-het)
Reference PubMed: Font-Llitjos et al. 2009
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 0/50 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 2012-12-04 16:25:21 +01:00 (CET)
Date last edited 2020-07-04 15:17:16 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC7A7 NM_001126105.2 +?/+? i04 c.625+1G>C r.spl? p.?


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