Variant #0000571453 (NC_000022.10:g.21213528T>C, NM_058004.3:c.-515A>G (PI4KA))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.21213528T>C
DNA change (hg38) g.20859240T>C
Published as SNAP29(NM_004782.3):c.130T>C (p.Y44H)
ISCN -
DB-ID PI4KA_000030
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) 0.00191 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPIND1 NM_000185.3 -/. - c.*72174T>C r.(=) p.(=)
SNAP29 NM_004782.3 -/. - c.130T>C r.(?) p.(Tyr44His)
PI4KA NM_058004.3 -/. - c.-515A>G r.(?) p.(=)


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