Variant ID | 25777 |
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Entrez Gene ID | 23379 |
Gene | ICE1 (GeneCards) |
Location | hg19 5:6265587-6265587
hg38 5:6265474-6265474 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000005.9:g.6265587 C>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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1901 |
CADD Raw score (version 1.3) | 0.188442 (Deleterious) |
FATHMM raw prediction score | 0.10955 (Tolerated) |
Deleterious probability by DeFine | 0.559 (Deleterious) |
Entrez Gene ID | 23379 (NCBI Gene) |
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Official Gene Symbol | ICE1 (GeneCards) |
Number of variants in ICE1 in this database | 14 (view all the variants) |
Full name | interactor of little elongation complex ELL subunit 1 |
Band | 5p15.32 |
Other IDs | Vega: OTTHUMG00000161639 OMIM: 617958 HGNC: HGNC:29154 Ensembl: ENSG00000164151 |
Other names | KIAA0947 |
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 |