All variants in the PCNT gene

Information The variants shown are described using the NM_006031.5 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
-?/. - c.644G>A r.(?) p.(Cys215Tyr) - likely benign g.47766046G>A g.46346132G>A PCNT(NM_006031.5):c.644G>A (p.C215Y) - PCNT_000397 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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