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 | CHEK1 |
Variant | F93V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CHEK1 F93V lies within the protein kinase domain of the Chek1 protein (UniProt.org). F93V has not been characterized in the scientific literature and therefore, its effect on Chek1 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
CHEK1 mutant CHEK1 F93V |
Transcript | NM_001114121.2 |
gDNA | chr11:g.125627818T>G |
cDNA | c.277T>G |
Protein | p.F93V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024448337.1 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001244846.1 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
XM_047426311.1 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001274.5 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114121.2 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
XM_017017146.2 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
XM_024448337.2 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001244846.1 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114122 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001274 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001274.5 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
XM_017017146 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114121.2 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114122.3 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001244846 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114122.2 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
NM_001114121 | chr11:g.125627818T>G | c.277T>G | p.F93V | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|