All transcript variants in gene APC


Information The variants shown are described using the NM_000038.5 transcript reference sequence.

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Effect     

Exon     

Exon_old     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

Predicted     

Predict/PolyPhenScore     

Type/DNA     

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.347del pathogenic r.(?) p.(Gly116Valfs*9) - - - g.112103012del - APC(NM_000038.4):c.347delG (p.G116Vfs*9) - APC_001757 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
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