Variant #0000570401 (NC_000020.10:g.744167A>T, NM_033409.3:c.1048T>A (SLC52A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.744167A>T
DNA change (hg38) g.763523A>T
Published as SLC52A3(NM_001370086.1):c.1048T>A (p.L350M), SLC52A3(NM_033409.3):c.1048T>A (p.(Leu350Met)), SLC52A3(NM_033409.4):c.1048T>A (p.L350M)
ISCN -
DB-ID SLC52A3_000010 See all 5 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) 0.00384 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC52A3 NM_033409.3 -/. - c.1048T>A r.(?) p.(Leu350Met)


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