Variant #0000547985 (NC_000012.11:g.33031417G>A, NM_004572.3:c.397C>T (PKP2))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33031417G>A
DNA change (hg38) g.32878483G>A
Published as PKP2(NM_001005242.2):c.397C>T (p.(Gln133Ter)), PKP2(NM_004572.3):c.397C>T (p.Q133*), PKP2(NM_004572.4):c.397C>T (p.Q133*)
ISCN -
DB-ID PKP2_000017 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) Retrieve
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)
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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.397C>T r.(?) p.(Gln133Ter) -
PKP2 NM_004572.3 +/. - c.397C>T r.(?) p.(Gln133Ter) -


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