Variant #0000720945 (NC_000006.11:g.42975043A>C, NM_006245.3:c.632A>C (PPP2R5D))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42975043A>C
DNA change (hg38) -
Published as PPP2R5D(NM_001270476.2):c.179A>C (p.Q60P)
ISCN -
DB-ID PPP2R5D_000005 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R5D NM_006245.3 +?/. - c.632A>C r.(?) p.(Gln211Pro)
MEA1 NM_014623.2 +?/. - c.*5165T>G r.(=) p.(=)
KLHDC3 NM_057161.3 +?/. - c.-7103A>C r.(?) p.(=)


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