Variant #0000999971 (NC_000012.11:g.33049495C>T, NM_004572.3:c.171G>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.33049495C>T
DNA change (hg38) -
Published as PKP2(NM_004572.4):c.171G>A (p.Q57=)
ISCN -
DB-ID PKP2_000587
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
PKP2 NM_001005242.2 -?/. - c.171G>A r.(?) p.(=) -
PKP2 NM_004572.3 -?/. - c.171G>A r.(?) p.(=) -


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