Overview

Variant ID 23164
Entrez Gene ID 387066
Gene SNHG5 (GeneCards)
Location hg19 6:87384052-87384052
hg38 6:86674334-86674334
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.87384052 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
EIGEN score -0.2572
CADD Raw score (version 1.3) -0.154733 (Deleterious)
FATHMM raw prediction score 0.0515 (Tolerated)
Deleterious probability by DeFine 0.0677 (Neutral)
Entrez Gene ID 387066 (NCBI Gene)
Official Gene Symbol SNHG5 (GeneCards)
Number of variants in SNHG5 in this database 11 (view all the variants)
Full name small nucleolar RNA host gene 5
Band 6q14.3
Other IDs OMIM: 613263
HGNC: HGNC:21026
Ensembl: ENSG00000203875
Other names U50HG, C6orf160, LINC00044, NCRNA00044
Summary This gene represent a snoRNA host gene and produces a long non-coding RNA. This RNA may regulate gene expression by acting as a sponge for microRNAs. This transcript may also stabilize mRNAs by blocking degradation by staufen double-stranded RNA binding protein 1. [provided by RefSeq, Dec 2017]

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;