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Gene | APC |
Variant | S130G |
Impact List | missense |
Protein Effect | no effect - predicted |
Gene Variant Descriptions | APC S130G lies within a coiled-coil domain of the Apc protein (UniProt.org). S130G does not result in increased Wnt signaling in cell culture (PMID: 15133491), and therefore, is predicted to have no effect on Apc protein function. |
Associated Drug Resistance | |
Category Variants Paths |
APC mutant APC S130G |
Transcript | NM_000038.6 |
gDNA | chr5:g.112767356A>G |
cDNA | c.388A>G |
Protein | p.S130G |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001407469.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407467.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354903.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407449.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407454.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407458.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407456.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354895.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407447.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407455.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354899.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407460.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407448.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354903.2 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407452.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354899.2 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407459.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354896.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001354896.2 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
NM_001407457.1 | chr5:g.112767356A>G | c.388A>G | p.S130G | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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