Overview

Variant ID 27127
Entrez Gene ID 9886
Gene RHOBTB1 (GeneCards)
Location hg19 10:62660143-62660143
hg38 10:60900385-60900385
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000010.10:g.62660143 G>C (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
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 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0612
CADD Raw score (version 1.3) -0.405918 (Deleterious)
FATHMM raw prediction score 0.1628 (Tolerated)
Deleterious probability by DeFine 0.595 (Deleterious)
Entrez Gene ID 9886 (NCBI Gene)
Official Gene Symbol RHOBTB1 (GeneCards)
Number of variants in RHOBTB1 in this database 2 (view all the variants)
Full name Rho related BTB domain containing 1
Band 10q21.2
Other IDs Vega: OTTHUMG00000018292
OMIM: 607351
HGNC: HGNC:18738
Ensembl: ENSG00000072422
Other names None
Summary The protein encoded by this gene belongs to the Rho family of the small GTPase superfamily. It contains a GTPase domain, a proline-rich region, a tandem of 2 BTB (broad complex, tramtrack, and bric-a-brac) domains, and a conserved C-terminal region. The protein plays a role in small GTPase-mediated signal transduction and the organization of the actin filament system. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID