Variant #0000854223 (NC_000015.9:g.85411581C>T, NM_020778.4:c.5618C>T (ALPK3))

Chromosome 15
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.85411581C>T
DNA change (hg38) -
Published as ALPK3(NM_020778.4):c.5618C>T (p.A1873V), ALPK3(NM_020778.5):c.5012C>T (p.A1671V)
ISCN -
DB-ID ALPK3_000192 See all 5 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) 0.00355 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALPK3 NM_020778.4 -/. - c.5618C>T r.(?) p.(Ala1873Val)


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