Variant #0000528893 (NC_000006.11:g.42980713_42980715del, NM_006245.3:c.*1689_*1691del (PPP2R5D))

Chromosome 6
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.42980713_42980715del
DNA change (hg38) g.43012975_43012977del
Published as MEA1(NM_001318942.1):c.320_322del (p.(Glu107del))
ISCN -
DB-ID KLHDC3_000005
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.*1689_*1691del r.(=) p.(=)
MEA1 NM_014623.2 -?/. - c.359_361del r.(?) p.(Glu120del)
KLHDC3 NM_057161.3 -?/. - c.-1433_-1431del r.(?) p.(=)


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