Variant #0000016708 (NC_000014.8:g.23245147T>C, NC_000014.8(NM_001126105.2):c.895-2A>G (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.23245147T>C
DNA change (hg38) g.22775938T>C
Published as A-to-G transition in a splice acceptor sequence 6 (IVS6-2A G)
ISCN -
DB-ID SLC7A7_000031
Variant remarks 1 Lithuanian LPI patient (hom)
Reference PubMed: Cimbalistiene et al. 2007
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 15:16:59 +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 +?/+? i06 c.895-2A>G r.spl? p.?


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