Variant #0000300925 (NC_000012.11:g.32949101G>T, NM_004572.3:c.2431C>A (PKP2))

Chromosome 12
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.32949101G>T
DNA change (hg38) g.32796167G>T
Published as PKP2(NM_001005242.2):c.2299C>A (p.(Arg767Ser)), PKP2(NM_004572.3):c.2431C>A (p.R811S), PKP2(NM_004572.4):c.2431C>A (p.R811S)
ISCN -
DB-ID PKP2_000271 See all 9 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) 0.0009 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
PKP2 NM_001005242.2 -?/. - c.2299C>A r.(?) p.(Arg767Ser) -
PKP2 NM_004572.3 -?/. - c.2431C>A r.(?) p.(Arg811Ser) -


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