Overview

Variant ID 23163
Entrez Gene ID 101928601
Gene MEI4 (GeneCards)
Location hg19 6:78534945-78534945
hg38 6:77825228-77825228
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.78534945 G>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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003232
EIGEN score -0.1949
CADD Raw score (version 1.3) -0.429803 (Deleterious)
FATHMM raw prediction score 0.08646 (Tolerated)
Deleterious probability by DeFine 0.4952 (Neutral)
Entrez Gene ID 101928601 (NCBI Gene)
Official Gene Symbol MEI4 (GeneCards)
Number of variants in MEI4 in this database 17 (view all the variants)
Full name meiotic double-stranded break formation protein 4
Band 6q14.1
Other IDs Vega: OTTHUMG00000153472
HGNC: HGNC:43638
Ensembl: ENSG00000269964
Other names None
Summary None

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;