Full data view for gene PKP2

Information The variants shown are described using the transcript reference sequence.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. 7 c.1577C>T r.(?) p.(Thr526Met) - Parent #1 - benign g.32994073G>A g.32841139G>A - - PKP2_000054 - PubMed: Allegue 2015, Journal: Allegue 2015 - rs146882581 Germline no - - - - DNA SEQ - - BRGDA - PubMed: Allegue 2015, Journal: Allegue 2015 - F - Belgium European >47y - - - 1 Anna Iglesias
-/. 7 c.1577C>T r.(?) p.(Thr526Met) - Parent #1 - benign g.32994073G>A g.32841139G>A - - PKP2_000054 - PubMed: Allegue 2015, Journal: Allegue 2015 - rs146882581 Germline no - - - - DNA SEQ-NG-S - - BRGDA - PubMed: Allegue 2015, Journal: Allegue 2015 - M - United States white >66y - - - 1 Anna Iglesias
-/. - c.1577C>T r.(?) p.(Thr526Met) - Unknown - benign g.32994073G>A g.32841139G>A PKP2(NM_004572.3):c.1577C>T (p.T526M), PKP2(NM_004572.4):c.1577C>T (p.T526M) - PKP2_000054 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1577C>T r.(?) p.(Thr526Met) - Unknown - likely benign g.32994073G>A g.32841139G>A PKP2(NM_004572.3):c.1577C>T (p.T526M), PKP2(NM_004572.4):c.1577C>T (p.T526M) - PKP2_000054 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1577C>T r.(?) p.(Thr526Met) - Unknown - likely benign g.32994073G>A g.32841139G>A PKP2(NM_004572.3):c.1577C>T (p.T526M), PKP2(NM_004572.4):c.1577C>T (p.T526M) - PKP2_000054 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. 7 c.1577C>T r.(?) p.(Thr526Met) - Unknown - likely benign g.32994073G>A g.32841139G>A - - PKP2_000054 - PubMed: Rasmussen 2013 - - Germline - - - - - DNA SEQ - - ARVC - PubMed: Rasmussen 2013 - - - - - - - - - - Torsten Bloch Rasmussen
-/- 7 c.1577C>T r.(?) p.(Thr526Met) - Unknown - benign g.32994073G>A g.32841139G>A - - PKP2_000054 - Journal: Albuisson 2007, ARVD/C database 7695 - - Germline - - - - - DNA SEQ - - BRGDA - Journal: Albuisson 2007 No familial segreation with Brugada syndrome - - - - - - - - 3 Paul van der Zwaag
-/. - c.1577C>T r.(?) p.(Thr526Met) - Unknown - benign g.32994073G>A g.32841139G>A PKP2(NM_004572.3):c.1577C>T (p.T526M), PKP2(NM_004572.4):c.1577C>T (p.T526M) - PKP2_000054 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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