Variant ID | 26347 |
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Entrez Gene ID | 401337 |
Gene | LINC01446 (GeneCards) |
Location | hg19 7:53845186-53845186
hg38 7:53777493-53777493 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000007.13:g.53845186 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 | 159138663 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.3289 |
CADD Raw score (version 1.3) | 0.051019 (Deleterious) |
FATHMM raw prediction score | 0.05965 (Tolerated) |
Deleterious probability by DeFine | 0.2332 (Neutral) |
Entrez Gene ID | 401337 (NCBI Gene) |
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Official Gene Symbol | LINC01446 (GeneCards) |
Number of variants in LINC01446 in this database | 7 (view all the variants) |
Full name | long intergenic non-protein coding RNA 1446 |
Band | 7p12.1 |
Other IDs | HGNC: HGNC:50773 Ensembl: ENSG00000205628 |
Other names | GS1-179L18.1 |
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 |