Overview

Variant ID 29844
Entrez Gene ID 390168
Gene OR5M1 (GeneCards)
Location hg19 11:56380550-56380550
hg38 11:56613074-56613074
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500
Mutation(HGVS format) NC_000011.9:g.56380550 A>C (Genome Assembly: hg19)

Other information

Exon or Intron Exon
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 135006516

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -1.2705
CADD Raw score (version 1.3) 1.486819 (Deleterious)
FATHMM raw prediction score 0.01493 (Tolerated)
SIFT score 0.192 (Tolerated)
LRT score 0.755 (Tolerated)
MutationTaster score 1 (Tolerated)
MutatioinAssessor score 0.28 (Tolerated)
PROVEAN score -3.16 (Deleterious)
MetaSVM score -1.091 (Tolerated)
MetaLR score 0 (Tolerated)
MCAP score 0.007 (Tolerated)
FitCons score 0.487 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score -0.226
PhyloP score based on multiple alignment of 100 vertebrates -3.683
PhastCons score based on multiple alignment of 100 vertebrates 0
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 4.356
Deleterious probability by iFish2 0.0132 (Neutral)
Deleterious probability by DeFine 0.7461 (Deleterious)
Entrez Gene ID 390168 (NCBI Gene)
Official Gene Symbol OR5M1 (GeneCards)
Number of variants in OR5M1 in this database 1 (view all the variants)
Full name olfactory receptor family 5 subfamily M member 1
Band 11q12.1
Other IDs Vega: OTTHUMG00000166863
HGNC: HGNC:8352
Ensembl: ENSG00000255012
Other names OST050, OR11-208
Summary Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 28867142.12 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Female Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;