Variant #0000801766 (NC_000005.9:g.102523050A>G, NC_000005.9(NM_015216.2):c.3289+910A>G (PPIP5K2))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.102523050A>G
DNA change (hg38) -
Published as PPIP5K2(NM_001281471.2):c.3370A>G (p.I1124V)
ISCN -
DB-ID PPIP5K2_000005
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) 0.00083 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPIP5K2 NM_015216.2 ?/. - c.3289+910A>G r.(=) p.(=)


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