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     
+/+ 6i 3i c.422+2T>A pathogenic r.spl p.? splicing affected - substitution g.112103089T>A g.112767392T>A 422+2T>A - APC_001521 - PubMed: Lagarde et al. 2010 - - Unknown ? - - 0 - Stefan Aretz
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