Variant #0001033346 (NC_000002.11:g.44541068A>G, NM_000341.3:c.1595A>G (SLC3A1))

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.44541068A>G
DNA change (hg38) -
Published as SLC3A1(NM_000341.4):c.1595A>G (p.(Asp532Gly))
ISCN -
DB-ID SLC3A1_000094
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 ?/. - c.1595A>G r.(?) p.(Asp532Gly)
PREPL NM_006036.4 ?/. - c.*7427T>C r.(=) p.(=)


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