Overview

Variant ID 24194
Entrez Gene ID 389906
Gene LOC389906 (GeneCards)
Location hg19 X:4270994-4270994
hg38 X:4352953-4352953
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000023.10:g.4270994 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 155270560

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.0003
CADD Raw score (version 1.3) -0.669501 (Deleterious)
FATHMM raw prediction score 0.03279 (Tolerated)
Deleterious probability by DeFine 0.0622 (Neutral)
Entrez Gene ID 389906 (NCBI Gene)
Official Gene Symbol LOC389906 (GeneCards)
Number of variants in LOC389906 in this database 5 (view all the variants)
Full name zinc finger protein 839 pseudogene
Band Xp22.33
Other IDs None:
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;