Variant ID | 9903 |
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Entrez Gene ID | 6098 |
Gene | ROS1 (GeneCards) |
Location | hg19 6:117643390-117643390
hg38 6:117322227-117322227 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000006.11:g.117643390 C>T (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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Position in protein | NA |
Amino acid changes in protein | NA > NA |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.0676 |
CADD Raw score (version 1.3) | -0.092599 (Deleterious) |
FATHMM raw prediction score | 0.13535 (Tolerated) |
Deleterious probability by DeFine | 0.5323 (Deleterious) |
Entrez Gene ID | 6098 (NCBI Gene) |
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Official Gene Symbol | ROS1 (GeneCards) |
Number of variants in ROS1 in this database | 4 (view all the variants) |
Full name | ROS proto-oncogene 1, receptor tyrosine kinase |
Band | 6q22.1 |
Other IDs | Vega: OTTHUMG00000016188 OMIM: 165020 HGNC: HGNC:10261 Ensembl: ENSG00000047936 |
Other names | ROS, MCF3, c-ros-1 |
Summary | This proto-oncogene, highly-expressed in a variety of tumor cell lines, belongs to the sevenless subfamily of tyrosine kinase insulin receptor genes. The protein encoded by this gene is a type I integral membrane protein with tyrosine kinase activity. The protein may function as a growth or differentiation factor receptor. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.14 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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Title | Aging and neurodegeneration are associated with increased mutations in single human neurons. |
Journal | Science |
Publication date | 2018.02 |
Disease | Cockayne syndrome Xeroderma Pigmentosum |
Number of cases | Male cases: 3; Female cases: 6; cases of unknown sex: 15; |