Variant #0000016431 (NC_000006.11:g.74354327C>G, NC_000006.11(NM_012434.4):c.95-1G>C (SLC17A5))

Chromosome 6
Allele Unknown
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.74354327C>G
DNA change (hg38) g.73644604C>G
Published as cDNA 95-1G>C: Removes splice site, deletion of exon 2 (95–291del)
ISCN -
DB-ID SLC17A5_000001
Variant remarks 1 Swedish SD patient (com-het)
Reference PubMed: Aula et al. 2000
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-15 14:02:15 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC17A5 NM_012434.4 +/+ 1i c.95-1G>C r.95_291del p.Ala32Glyfs*2


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