Variant #0000039756 (NC_000006.11:g.74351439A>G, NM_012434.4:c.500T>C (SLC17A5))

Chromosome 6
Allele Unknown
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.74351439A>G
DNA change (hg38) g.73641716A>G
Published as -
ISCN -
DB-ID SLC17A5_000015
Variant remarks 1 Spanish patient (com-het) with SD
Reference PubMed: Couce et al. 2014
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 2014-07-26 17:45:37 +02:00 (CEST)
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 +?/+? 3 c.500T>C r.(?) p.(Leu167Pro)


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