Variant ID | 25820 |
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Entrez Gene ID | 340107 |
Gene | LOC340107 (GeneCards) |
Location | hg19 5:25694751-25694751
hg38 5:25694642-25694642 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000005.9:g.25694751 T>C (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 | -0.0077 |
CADD Raw score (version 1.3) | -0.108541 (Deleterious) |
FATHMM raw prediction score | 0.1269 (Tolerated) |
Deleterious probability by DeFine | 0.2352 (Neutral) |
Entrez Gene ID | 340107 (NCBI Gene) |
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Official Gene Symbol | LOC340107 (GeneCards) |
Number of variants in LINC02239 in this database | 35 (view all the variants) |
Full name | long intergenic non-protein coding RNA 2239 |
Band | 5p14.1 |
Other IDs | HGNC: HGNC:27969 Ensembl: ENSG00000248908 |
Other names | None |
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 |