All variants in the PCNT gene

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

2 entries on 1 page. Showing entries 1 - 2.
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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.2556T>C r.(?) p.(Ala852=) - benign g.47783796T>C g.46363881T>C PCNT(NM_006031.5):c.2556T>C (p.A852=), PCNT(NM_006031.6):c.2556T>C (p.A852=) - PCNT_000226 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
-/. - c.2556T>C r.(?) p.(Ala852=) - benign g.47783796T>C g.46363881T>C PCNT(NM_006031.5):c.2556T>C (p.A852=), PCNT(NM_006031.6):c.2556T>C (p.A852=) - PCNT_000226 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
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