Variant #0000547919 (NC_000012.11:g.32994058A>C, NM_004572.3:c.1592T>G (PKP2))

Chromosome 12
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.32994058A>C
DNA change (hg38) g.32841124A>C
Published as PKP2(NM_001005242.2):c.1460T>G (p.(Ile487Ser)), PKP2(NM_004572.3):c.1592T>G (p.I531S), PKP2(NM_004572.4):c.1592T>G (p.I531S)
ISCN -
DB-ID PKP2_000056 See all 13 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) 0.00493 View details
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 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
PKP2 NM_001005242.2 ?/. - c.1460T>G r.(?) p.(Ile487Ser) -
PKP2 NM_004572.3 ?/. - c.1592T>G r.(?) p.(Ile531Ser) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.