Variant #0000514986 (NC_000002.11:g.228552992G>A, NM_025243.3:c.1204C>T (SLC19A3))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.228552992G>A
DNA change (hg38) g.227688276G>A
Published as SLC19A3(NM_025243.3):c.1204C>T (p.R402C), SLC19A3(NM_025243.4):c.1204C>T (p.(Arg402Cys))
ISCN -
DB-ID SLC19A3_000039 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00015 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC19A3 NM_025243.3 ?/. - c.1204C>T r.(?) p.(Arg402Cys)


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