Variant #0000693112 (NC_000022.10:g.21119465G>C, NM_058004.3:c.2497C>G (PI4KA))

Chromosome 22
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.21119465G>C
DNA change (hg38) -
Published as PI4KA(NM_058004.3):c.2497C>G (p.L833V)
ISCN -
DB-ID PI4KA_000048
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPIND1 NM_000185.3 ?/. - c.-8985G>C r.(?) p.(=)
PI4KA NM_058004.3 ?/. - c.2497C>G r.(?) p.(Leu833Val)


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