Overview

Variant ID 8197
Entrez Gene ID 375449
Gene MAST4 (GeneCards)
Location hg19 5:66199748-66199748
hg38 5:66903920-66903920
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000005.9:g.66199748 C>G (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 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3967
CADD Raw score (version 1.3) -0.251303 (Deleterious)
FATHMM raw prediction score 0.11796 (Tolerated)
Deleterious probability by DeFine 0.4559 (Neutral)
Entrez Gene ID 375449 (NCBI Gene)
Official Gene Symbol MAST4 (GeneCards)
Number of variants in MAST4 in this database 7 (view all the variants)
Full name microtubule associated serine/threonine kinase family member 4
Band 5q12.3
Other IDs Vega: OTTHUMG00000152471
OMIM: 618002
HGNC: HGNC:19037
Ensembl: ENSG00000069020
Other names None
Summary This gene encodes a member of the microtubule-associated serine/threonine protein kinases. The proteins in this family contain a domain that gives the kinase the ability to determine its own scaffold to control the effects of their kinase activities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

Individual #1

Individual ID 29217584.12 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
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;