Variant #0000528890 (NC_000006.11:g.42975224G>A, NM_006245.3:c.706G>A (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.42975224G>A
DNA change (hg38) g.43007486G>A
Published as PPP2R5D(NM_001270476.2):c.253G>A (p.D85N)
ISCN -
DB-ID KLHDC3_000002
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.706G>A r.(?) p.(Asp236Asn)
MEA1 NM_014623.2 ?/. - c.*4984C>T r.(=) p.(=)
KLHDC3 NM_057161.3 ?/. - c.-6922G>A r.(?) p.(=)


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