Variant #0000039755 (NC_000014.8:g.23243710dup, NM_001126105.2:c.1098dup (SLC7A7))

Chromosome 14
Allele Both (homozygous)
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.23243710dup
DNA change (hg38) g.22774501dup
Published as c.1099insT, p.Ile367TyrfsX16
ISCN -
DB-ID SLC7A7_000057
Variant remarks 2 Turkish patients (hom) with LPI
Reference PubMed: Güzel-Ozantürk et al. 2013
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 2014-07-26 16:59:19 +02:00 (CEST)
Date last edited 2020-07-04 15:16:49 +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 +?/+? 09 c.1098dup r.(?) p.(Ile367Tyrfs*17)


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