Variant #0000923649 (NC_000002.11:g.228563656_228563657del, NM_025243.3:c.776_777del (SLC19A3))

Chromosome 2
Allele Unknown
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.228563656_228563657del
DNA change (hg38) -
Published as SLC19A3(NM_001371414.1):c.764_765delTG (p.V255Gfs*34), SLC19A3(NM_025243.4):c.776_777delTG (p.V259Gfs*34)
ISCN -
DB-ID SLC19A3_000061 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC19A3 NM_025243.3 +/. - c.776_777del r.(?) p.(Val259Glyfs*34)


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