Variant #0000863427 (NC_000014.8:g.102348613C>T, NC_000014.8(NM_001352913.1):c.570+5C>T (PPP2R5C))

Chromosome 14
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.102348613C>T
DNA change (hg38) g.101882276C>T
Published as PPP2R5C(NM_001161725.1):c.498+5C>T (p.?)
ISCN -
DB-ID PPP2R5C_000007
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) 0.00545 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-03-01 09:57:36 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP2R5C NM_001352913.1 -?/. - c.570+5C>T r.spl? p.?


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