Overview

Variant ID 23702
Entrez Gene ID 89795
Gene NAV3 (GeneCards)
Location hg19 12:79174747-79174747
hg38 12:78780967-78780967
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000012.11:g.79174747 C>T (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 133851895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0343
SNP ID (dbSNP ID version 137) rs116915418
EIGEN score -0.517
CADD Raw score (version 1.3) -0.493403 (Deleterious)
FATHMM raw prediction score 0.04068 (Tolerated)
Deleterious probability by DeFine 0.3035 (Neutral)
Entrez Gene ID 89795 (NCBI Gene)
Official Gene Symbol NAV3 (GeneCards)
Number of variants in NAV3 in this database 15 (view all the variants)
Full name neuron navigator 3
Band 12q21.2
Other IDs Vega: OTTHUMG00000170001
OMIM: 611629
HGNC: HGNC:15998
Ensembl: ENSG00000067798
Other names POMFIL1, nc53H3, STEERIN3
Summary This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;