Variant #0000568311 (NC_000019.9:g.52716214G>A, NM_014225.5:c.658G>A (PPP2R1A))

Chromosome 19
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.52716214G>A
DNA change (hg38) g.52212961G>A
Published as PPP2R1A(NM_001363656.1):c.121G>A (p.V41M)
ISCN -
DB-ID PPP2R1A_000009 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R1A NM_014225.5 ?/. - c.658G>A r.(?) p.(Val220Met)


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