Variant #0000647960 (NC_000010.10:g.73122283C>G, SLC29A3(NM_018344.5):c.1346C>G)

Individual ID 00290103
Chromosome 10
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73122283C>G
DNA change (hg38) g.71362526C>G
Published as -
ISCN -
DB-ID SLC29A3_000007 See all 3 reported entries
Variant remarks 2 heterozygous, no homozygous; Clinindb (India)
Reference PubMed: Narang 2020, Journal: Narang 2020
ClinVar ID -
dbSNP ID rs267607058
Origin Germline
Segregation -
Frequency 2/2788 individuals
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Mohammed Faruq
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC29A3 NM_018344.5 +/. - c.1346C>G r.(?) p.(Thr449Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000291271 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq