Variant #0000809496 (NC_000022.10:g.21159269G>A, NM_058004.3:c.1353C>T (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.21159269G>A
DNA change (hg38) -
Published as PI4KA(NM_058004.3):c.1353C>T (p.D451=)
ISCN -
DB-ID PI4KA_000055
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 2021-09-17 14:40:49 +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.*17915G>A r.(=) p.(=)
PI4KA NM_058004.3 -?/. - c.1353C>T r.(?) p.(Asp451=)


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