Variant ID | 22833 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |