Variant #0000016693 (NC_000014.8:g.23241434_23253569del, NC_000014.8(NM_001126105.2):c.500-4294_1908+1028del (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.23241434_23253569del
DNA change (hg38) g.22772225_22784360del
Published as c.500-4294_1908+1028 del12136: p.L168_N511delfsX19
ISCN -
DB-ID SLC7A7_000016
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 2020-07-04 15:15:57 +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 +/+ i03- c.500-4294_1908+1028del r.? p.?


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