Overview

Variant ID 22833
Entrez Gene ID 347689
Gene SOX2-OT (GeneCards)
Location hg19 3:181462435-181462435
hg38 3:181744647-181744647
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000003.11:g.181462435 G>A (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 198022430

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.034
CADD Raw score (version 1.3) -0.123561 (Deleterious)
FATHMM raw prediction score 0.15123 (Tolerated)
Deleterious probability by DeFine 0.2685 (Neutral)
Entrez Gene ID 347689 (NCBI Gene)
Official Gene Symbol SOX2-OT (GeneCards)
Number of variants in SOX2-OT in this database 8 (view all the variants)
Full name SOX2 overlapping transcript
Band 3q26.33
Other IDs OMIM: 616338
HGNC: HGNC:20209
Other names SOX2OT, NCRNA00043
Summary This gene produces alternatively spliced long non-coding RNAs. These RNAs were observed to be upregulated in tumor cells and positively correlated to expression of the SRY-box 2 gene. Overexpression of these transcripts may promote cell proliferation. [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;