APC R2673G
Gene Variant Detail

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Gene APC
Variant R2673G
Impact List missense
Protein Effect unknown
Gene Variant Descriptions APC R2673G lies within a region of the APC protein necessary for interaction with DLG1 (UniProt.org). R2673G has been identified in sequencing studies (PMID: 36896836, PMID: 38925616), but has not been biochemically characterized and therefore, its effect on Apc protein function is unknown (PubMed, Apr 2026).
Associated Drug Resistance
Category Variants Paths

APC mutant APC R2673G

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Transcript NM_000038.6
gDNA chr5:g.112843611A>G
cDNA c.8017A>G
Protein p.R2673G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354900.2 chr5:g.112843734C>G c.8017C>G p.R2673G RefSeq GRCh38/hg38
NM_001127510 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_000038 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_000038.6 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001354905.2 chr5:g.112844091C>G c.8017C>G p.R2673G RefSeq GRCh38/hg38
NM_000038.5 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001354895.1 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001127510.2 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001354905.1 chr5:g.112844091C>G c.8017C>G p.R2673G RefSeq GRCh38/hg38
NM_001407450.1 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001127510.3 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001354895.2 chr5:g.112843611A>G c.8017A>G p.R2673G RefSeq GRCh38/hg38
NM_001354900.1 chr5:g.112843734C>G c.8017C>G p.R2673G RefSeq GRCh38/hg38

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References