Variant #0000305568 (NC_000022.10:g.21088806C>T, NM_058004.3:c.3777G>A (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.21088806C>T
DNA change (hg38) g.20734518C>T
Published as PI4KA(NM_058004.3):c.3777G>A (p.T1259=)
ISCN -
DB-ID PI4KA_000005
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) 0.00024 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-17 11:05:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPIND1 NM_000185.3 -?/. - c.-39644C>T r.(?) p.(=)
PI4KA NM_058004.3 -?/. - c.3777G>A r.(?) p.(Thr1259=)


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