Variant ID | 27095 |
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Entrez Gene ID | 22982 |
Gene | DIP2C (GeneCards) |
Location | hg19 10:816430-816430
hg38 10:770490-770490 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000010.10:g.816430 A>G (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 | -0.7608 |
CADD Raw score (version 1.3) | -0.080284 (Deleterious) |
FATHMM raw prediction score | 0.04825 (Tolerated) |
Deleterious probability by DeFine | 0.4965 (Neutral) |
Entrez Gene ID | 22982 (NCBI Gene) |
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Official Gene Symbol | DIP2C (GeneCards) |
Number of variants in DIP2C in this database | 6 (view all the variants) |
Full name | disco interacting protein 2 homolog C |
Band | 10p15.3 |
Other IDs | Vega: OTTHUMG00000017532 OMIM: 611380 HGNC: HGNC:29150 Ensembl: ENSG00000151240 |
Other names | KIAA0934 |
Summary | This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008] |
Individual ID | 29217587.03 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |