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.2308A>G r.(?) p.(Met770Val) - likely benign g.47783548A>G g.46363633A>G PCNT(NM_006031.5):c.2308A>G (p.M770V, p.(Met770Val)) - PCNT_000222 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.2308A>G r.(?) p.(Met770Val) - likely benign g.47783548A>G g.46363633A>G PCNT(NM_006031.5):c.2308A>G (p.M770V, p.(Met770Val)) - PCNT_000222 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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