All variants in the APC gene


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

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

Exon_old     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Predicted     

Predict/PolyPhenScore     

Type/DNA     

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.385G>C r.(?) p.(Glu129Gln) - - - - likely benign g.112103050G>C g.112767353G>C APC(NM_000038.5):c.385G>C (p.(Glu129Gln)), APC(NM_001127511.1):c.385G>C (p.E129Q) - APC_001822 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-?/. - - c.385G>C r.(?) p.(Glu129Gln) - - - - likely benign g.112103050G>C g.112767353G>C APC(NM_000038.5):c.385G>C (p.(Glu129Gln)), APC(NM_001127511.1):c.385G>C (p.E129Q) - APC_001822 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_AMC
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