Variant #0000975298 (NC_000002.11:g.44587179T>A, NM_000341.3:c.*39401T>A (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.44587179T>A
DNA change (hg38) -
Published as PREPL(NM_001171606.2):c.-323-2A>T
ISCN -
DB-ID SLC3A1_000084
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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 ?/. - c.*39401T>A r.(=) p.(=)
PREPL NM_001171613.2 ?/. - c.-49+1340A>T r.(=) p.(=)
PREPL NM_006036.4 ?/. - c.-325A>T r.(?) p.(=)
CAMKMT NM_024766.4 ?/. - c.-1968T>A r.(?) p.(=)


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