Variant #0000693114 (NC_000022.10:g.21172810G>C, NM_058004.3:c.817C>G (PI4KA))

Chromosome 22
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.21172810G>C
DNA change (hg38) -
Published as PI4KA(NM_058004.3):c.817C>G (p.P273A)
ISCN -
DB-ID PI4KA_000050
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) 2.0E-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 2020-09-15 15:50:26 +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     
SERPIND1 NM_000185.3 -?/. - c.*31456G>C r.(=) p.(=)
PI4KA NM_058004.3 -?/. - c.817C>G r.(?) p.(Pro273Ala)


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