Variant #0000016713 (NC_000014.8:g.23244735C>T, NM_001126105.2:c.1013G>A (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.23244735C>T
DNA change (hg38) g.22775526C>T
Published as 1299G→A (exon 8): G338D
ISCN -
DB-ID SLC7A7_000036
Variant remarks 1 Swedish LPI family (hom)
Reference PubMed: Mykkanen et al. 2000
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
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 +?/+? 09 c.1013G>A r.1013g>a p.(Gly338Asp)


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