Variant ID | 27029 |
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Entrez Gene ID | 56243 |
Gene | KIAA1217 (GeneCards) |
Location | hg19 10:24026455-24026455
hg38 10:23737526-23737526 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000010.10:g.24026455 G>T (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 | 135534747 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.273 |
CADD Raw score (version 1.3) | -0.382377 (Deleterious) |
FATHMM raw prediction score | 0.09445 (Tolerated) |
Deleterious probability by DeFine | 0.2279 (Neutral) |
Entrez Gene ID | 56243 (NCBI Gene) |
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Official Gene Symbol | KIAA1217 (GeneCards) |
Number of variants in KIAA1217 in this database | 9 (view all the variants) |
Full name | KIAA1217 |
Band | 10p12.2-p12.1 |
Other IDs | Vega: OTTHUMG00000017824 OMIM: 617367 HGNC: HGNC:25428 Ensembl: ENSG00000120549 |
Other names | SKT, ETL4 |
Summary | None |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |