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Gene | MSH6 |
Variant | E1254del |
Impact List | deletion |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 E1254del results in the deletion of an amino acid in the ATPase domain of the Msh6 protein at amino acid 1254 (PMID: 17531815). E1254del has not been characterized in the scientific literature and therefore, its effect on Msh6 protein function is unknown (PubMed, Apr 2024). |
Associated Drug Resistance | |
Category Variants Paths |
MSH6 mutant MSH6 E1254del |
Transcript | NM_000179.3 |
gDNA | chr2:g.47806319_47806321delAGA |
cDNA | c.3762_3764delAGA |
Protein | p.E1254delE |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406797.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_000179.2 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_000179 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
XM_011532798 | chr2:g.47806593_47806595delAAG | c.3760_3762delAAG | p.K1254delK | RefSeq | GRCh38/hg38 |
NM_001406798.1 | chr2:g.47806584_47806586delGTT | c.3760_3762delGTT | p.V1254delV | RefSeq | GRCh38/hg38 |
NM_001406830.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406796.1 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406820.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406804.1 | chr2:g.47806488_47806490delCAG | c.3760_3762delCAG | p.Q1254delQ | RefSeq | GRCh38/hg38 |
XM_024452819.1 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406818.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406827.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
XM_011532799 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
XM_024452821.1 | chr2:g.47806614_47806616delGAA | c.3760_3762delGAA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406824.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406819.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406828.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406813.1 | chr2:g.47806311_47806313delTTA | c.3760_3762delTTA | p.L1254delL | RefSeq | GRCh38/hg38 |
NM_001406821.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406825.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406800.1 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
NM_001406802.1 | chr2:g.47806221_47806223delTTT | c.3760_3762delTTT | p.F1254delF | RefSeq | GRCh38/hg38 |
XM_024452820.1 | chr2:g.47806500_47806502delACG | c.3760_3762delACG | p.T1254delT | RefSeq | GRCh38/hg38 |
NM_001406805.1 | chr2:g.47806834_47806836delTTG | c.3760_3762delTTG | p.L1255delL | RefSeq | GRCh38/hg38 |
NM_001406795.1 | chr2:g.47806221_47806223delTTT | c.3760_3762delTTT | p.F1254delF | RefSeq | GRCh38/hg38 |
NM_001406826.1 | chr2:g.47806580_47806582delGGA | c.3762_3764delGGA | p.E1255delE | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47806319_47806321delAGA | c.3762_3764delAGA | p.E1254delE | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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