Variant #0000016712 (NC_000014.8:g.23244743_23244746del, NM_001126105.2:c.1005_1008del (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.23244743_23244746del
DNA change (hg38) g.22775534_22775537del
Published as 1291delCTTT: framesift
ISCN -
DB-ID SLC7A7_000035
Variant remarks 3 Spanish LPI families (1 hom and 2 com-het) and 1 Japanese LPI family (com-het)
Reference PubMed: Torrens et al. 1999, PubMed: Mykkanen et al. 2000, PubMed: Shoji et al. 2002
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 2020-07-04 15:16:51 +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 +/+ 08 c.1005_1008del r.1005_1008delcuuu p.Phe335Leufs*15


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