Variant #0000253239 (NC_000022.10:g.21213416A>G, NM_058004.3:c.-403T>C (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.21213416A>G
DNA change (hg38) g.20859128A>G
Published as SNAP29(NM_004782.3):c.18A>G (p.K6=), SNAP29(NM_004782.4):c.18A>G (p.K6=)
ISCN -
DB-ID SNAP29_000004 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) 0.51626 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 2021-09-17 14:40:49 +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.*72062A>G r.(=) p.(=)
SNAP29 NM_004782.3 -/. - c.18A>G r.(?) p.(Lys6=)
PI4KA NM_058004.3 -/. - c.-403T>C r.(?) p.(=)


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