Variant ID | 27746 |
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Entrez Gene ID | 104355293 |
Gene | LINC00376 (GeneCards) |
Location | hg19 13:64133596-64133596
hg38 13:63559463-63559463 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000013.10:g.64133596 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 | 115169878 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1376 |
CADD Raw score (version 1.3) | 0.006154 (Deleterious) |
FATHMM raw prediction score | 0.0983 (Tolerated) |
Deleterious probability by DeFine | 0.2966 (Neutral) |
Entrez Gene ID | 104355293 (NCBI Gene) |
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Official Gene Symbol | LINC00376 (GeneCards) |
Number of variants in LINC00376 in this database | 7 (view all the variants) |
Full name | long intergenic non-protein coding RNA 376 |
Band | 13q21.31 |
Other IDs | HGNC: HGNC:42701 Ensembl: ENSG00000227564 |
Other names | None |
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 |