Variant #0001033354 (NC_000002.11:g.44586795T>G, NM_000341.3:c.*39017T>G (SLC3A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44586795T>G
DNA change (hg38) -
Published as PREPL(NM_001042385.2):c.60A>C (p.(Gly20=))
ISCN -
DB-ID SLC3A1_000102
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) 3.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC3A1 NM_000341.3 -?/. - c.*39017T>G r.(=) p.(=)
PREPL NM_001171613.2 -?/. - c.-49+1724A>C r.(=) p.(=)
PREPL NM_006036.4 -?/. - c.60A>C r.(?) p.(Gly20=)
CAMKMT NM_024766.4 -?/. - c.-2352T>G r.(?) p.(=)


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