Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | MSH6 |
Variant | G39W |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 G39W does not lie within any known functional domains of the Msh6 protein (UniProt.org). G39W 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 G39W |
Transcript | NM_000179.3 |
gDNA | chr2:g.47783348G>T |
cDNA | c.115G>T |
Protein | p.G39W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000179.2 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001281492.2 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_000179 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406800.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001281492.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406803.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
XM_024452819.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406802.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406798.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406813.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406796.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406795.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001406817.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001407362.1 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
NM_001281492 | chr2:g.47783348G>T | c.115G>T | p.G39W | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|