Variant #0000528888 (NC_000006.11:g.42975013C>G, NM_006245.3:c.602C>G (PPP2R5D))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42975013C>G
DNA change (hg38) g.43007275C>G
Published as PPP2R5D(NM_001270476.1):c.149C>G (p.P50R)
ISCN -
DB-ID MEA1_000002 See all 3 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R5D NM_006245.3 +/. - c.602C>G r.(?) p.(Pro201Arg)
MEA1 NM_014623.2 +/. - c.*5195G>C r.(=) p.(=)
KLHDC3 NM_057161.3 +/. - c.-7133C>G r.(?) p.(=)


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