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.136-19A>G likely benign r.(=) p.(=) - - - g.112102004A>G - APC(NM_001127511.1):c.136-19A>G - APC_001819 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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