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 | ROS1 |
Variant | A887V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ROS1 A887V lies within the extracellular domain of the Ros1 protein (UniProt.org). A887V has been identified in the scientific literature (PMID: 29642553), but has not been biochemically characterized and therefore, its effect on Ros1 protein function is unknown (PubMed, Mar 2024). |
Associated Drug Resistance | |
Category Variants Paths |
ROS1 mutant ROS1 A887V |
Transcript | NM_002944.3 |
gDNA | chr6:g.117366228G>A |
cDNA | c.2660C>T |
Protein | p.A887V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011536049 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536056.2 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536057.4 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
NM_002944 | chr6:g.117366228G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
NM_002944.3 | chr6:g.117366228G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536055.2 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536049.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536055.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536058.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536058 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536055 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536057 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536054.2 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
NM_002944.2 | chr6:g.117366228G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536054.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536057.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536056.3 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536049.2 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536056 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536054 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
XM_011536058.2 | chr6:g.117366258G>A | c.2660C>T | p.A887V | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|