Variant #0000995774 (NC_000006.11:g.42978901C>G, NM_006245.3:c.1686C>G (PPP2R5D))

Chromosome 6
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.42978901C>G
DNA change (hg38) -
Published as PPP2R5D(NM_006245.3):c.1686C>G (p.(Ile562Met))
ISCN -
DB-ID KLHDC3_000018
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R5D NM_006245.3 ?/. - c.1686C>G r.(?) p.(Ile562Met)
MEA1 NM_014623.2 ?/. - c.*1307G>C r.(=) p.(=)
KLHDC3 NM_057161.3 ?/. - c.-3245C>G r.(?) p.(=)


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