Variant #0000016686 (NC_000014.8:g.23282395_23282398del, NM_001126105.2:c.215_218del (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.23282395_23282398del
DNA change (hg38) g.22813186_22813189del
Published as 455delCTCT: Frameshift after Leu71, termination at codon 167; c.211_214delCTCT p.S72WfsX97
ISCN -
DB-ID SLC7A7_000009
Variant remarks 1 Italian (Molise) LPI family (hom)
Reference PubMed: Sperandeo et al. 2000
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 15:17:28 +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 +/+ 03 c.215_218del r.(?) p.(Ser72Trpfs*97)


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