Variant #0000016689 (NC_000014.8:g.23282108C>T, NC_000014.8(NM_001126105.2):c.499+1G>A (SLC7A7))

Chromosome 14
Allele Parent #1
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.23282108C>T
DNA change (hg38) g.22812899C>T
Published as IVS3 +1G>A in donor of intron 3; IVS3 +1G>A: exon 3 skipping
ISCN -
DB-ID SLC7A7_000012
Variant remarks 2 Japanese LPI families (com-het)
Reference PubMed: Sperandeo et al. 2000, PubMed: Kamada et al. 2001
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 15:17:19 +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 +/+ i03 c.499+1G>A r.-41_499del p.?


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