Variant #0000849784 (NC_000002.11:g.228564048T>C, NM_025243.3:c.383A>G (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.228564048T>C
DNA change (hg38) -
Published as SLC19A3(NM_025243.3):c.383A>G (p.Y128C), SLC19A3(NM_025243.4):c.383A>G (p.(Tyr128Cys), p.Y128C)
ISCN -
DB-ID SLC19A3_000048 See all 3 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) 0.00013 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC19A3 NM_025243.3 ?/. - c.383A>G r.(?) p.(Tyr128Cys)


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