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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), but has not been biochemically characterized and therefore, its effect on Apc protein function is unknown (PubMed, Aug 2024). |
Associated Drug Resistance | |
Category Variants Paths |
APC mutant APC R2673G |
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_001354905.2 | chr5:g.112844091C>G | c.8017C>G | p.R2673G | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.112843611A>G | c.8017A>G | p.R2673G | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.112843611A>G | c.8017A>G | p.R2673G | RefSeq | GRCh38/hg38 |
NM_001354900.2 | chr5:g.112843734C>G | c.8017C>G | p.R2673G | RefSeq | GRCh38/hg38 |
NM_001127510.2 | 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_001354905.1 | chr5:g.112844091C>G | c.8017C>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_001407450.1 | 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 |
NM_001354895.1 | chr5:g.112843611A>G | c.8017A>G | p.R2673G | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.112843611A>G | c.8017A>G | p.R2673G | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
APC R2673G | unknown |