Variant ID | 24055 |
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Entrez Gene ID | 55614 |
Gene | KIF16B (GeneCards) |
Location | hg19 20:16611768-16611768
hg38 20:16631123-16631123 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000020.10:g.16611768 G>C (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 | 63025520 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.0379 |
CADD Raw score (version 1.3) | -0.086953 (Deleterious) |
FATHMM raw prediction score | 0.1058 (Tolerated) |
Deleterious probability by DeFine | 0.6145 (Deleterious) |
Entrez Gene ID | 55614 (NCBI Gene) |
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Official Gene Symbol | KIF16B (GeneCards) |
Number of variants in KIF16B in this database | 7 (view all the variants) |
Full name | kinesin family member 16B |
Band | 20p12.1 |
Other IDs | Vega: OTTHUMG00000031927 HGNC: HGNC:15869 Ensembl: ENSG00000089177 |
Other names | SNX23, C20orf23, KISC20ORF |
Summary | The protein encoded by this gene is a kinesin-like protein that may be involved in intracellular trafficking. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010] |
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; |