Variant #0000016720 (NC_000014.8:g.23243298A>G, NM_001126105.2:c.1273T>C (SLC7A7))

Chromosome 14
Allele Maternal (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.23243298A>G
DNA change (hg38) g.22774089A>G
Published as c.1273T>C: p.C425R
ISCN -
DB-ID SLC7A7_000043 See all 2 reported entries
Variant remarks 1 Spanish 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 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 +?/+? 10 c.1273T>C r.(1273u>c) p.(Cys425Arg)


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