Variant #0000547906 (NC_000012.11:g.32977026C>T, NM_004572.3:c.1759G>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.32977026C>T
DNA change (hg38) g.32824092C>T
Published as PKP2(NM_001005242.3):c.1627G>A (p.(Val543Ile)), PKP2(NM_004572.3):c.1759G>A (p.V587I), PKP2(NM_004572.4):c.1759G>A (p.V587I)
ISCN -
DB-ID PKP2_000068 See all 10 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) 0.00244 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 2024-04-19 20:27:30 +02:00 (CEST)
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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.1627G>A r.(?) p.(Val543Ile) -
PKP2 NM_004572.3 -?/. - c.1759G>A r.(?) p.(Val587Ile) -


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