Variant ID | 27324 |
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Entrez Gene ID | 101929222 |
Gene | DISC1FP1 (GeneCards) |
Location | hg19 11:90270583-90270583
hg38 11:90537415-90537415 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000011.9:g.90270583 C>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 | 135006516 |
MAF in gnomAD genome (version 2.0.1) | 0.00009704 |
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EIGEN score | -0.2784 |
CADD Raw score (version 1.3) | -0.186513 (Deleterious) |
FATHMM raw prediction score | 0.08091 (Tolerated) |
Deleterious probability by DeFine | 0.4671 (Neutral) |
Entrez Gene ID | 101929222 (NCBI Gene) |
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Official Gene Symbol | DISC1FP1 (GeneCards) |
Number of variants in DISC1FP1 in this database | 40 (view all the variants) |
Full name | DISC1 fusion partner 1 |
Band | 11q14.3 |
Other IDs | HGNC: HGNC:33625 Ensembl: ENSG00000261645 |
Other names | Boymaw |
Summary | None |
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 |