Variant #0000308656 (NC_000022.10:g.21213394G>A, NM_058004.3:c.-381C>T (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.21213394G>A
DNA change (hg38) g.20859106G>A
Published as SNAP29(NM_004782.3):c.-5G>A
ISCN -
DB-ID SNAP29_000003
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) 0.00232 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 2020-03-23 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.*72040G>A r.(=) p.(=)
SNAP29 NM_004782.3 -/. - c.-5G>A r.(?) p.(=)
PI4KA NM_058004.3 -/. - c.-381C>T r.(?) p.(=)


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