Variant #0000328903 (NC_000022.10:g.21212981_21212992dup, NM_058004.3:c.36_47dup (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.21212981_21212992dup
DNA change (hg38) g.20858693_20858704dup
Published as PI4KA(NM_058004.3):c.36_47dupAGGCGGAGGCGG (p.G15_G18dup), PI4KA(NM_058004.4):c.36_47dup (p.(Gly15_Gly18dup))
ISCN -
DB-ID PI4KA_000014 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.*71627_*71638dup r.(=) p.(=)
SNAP29 NM_004782.3 -?/. - c.-418_-407dup r.(?) p.(=)
PI4KA NM_058004.3 -?/. - c.36_47dup r.(?) p.(Gly15_Gly18dup)


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