Variant #0000854003 (NC_000015.9:g.42446564C>T, NM_015289.2:c.*6388G>A (VPS39))

Chromosome 15
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.42446564C>T
DNA change (hg38) -
Published as PLA2G4F(NM_213600.3):c.277G>A (p.E93K)
ISCN -
DB-ID PLA2G4F_000002
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +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     
VPS39 NM_015289.2 -?/. - c.*6388G>A r.(=) p.(=)
PLA2G4F NM_213600.3 -?/. - c.277G>A r.(?) p.(Glu93Lys)


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