Variant #0000325527 (NC_000017.10:g.58740581A>G, NM_003620.3:c.1486A>G (PPM1D))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.58740581A>G
DNA change (hg38) g.60663220A>G
Published as PPM1D(NM_003620.3):c.1486A>G (p.(Ile496Val)), PPM1D(NM_003620.4):c.1486A>G (p.I496V)
ISCN -
DB-ID PPM1D_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) 0.00081 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
PPM1D NM_003620.3 -?/. - c.1486A>G r.(?) p.(Ile496Val)


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