Overview

Variant ID 27037
Entrez Gene ID 102465944
Gene MIR6072 (GeneCards)
Location hg19 10:2298548-2298548
hg38 10:2256354-2256354
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000010.10:g.2298548 T>C (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
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

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2414
CADD Raw score (version 1.3) -0.138051 (Deleterious)
FATHMM raw prediction score 0.07821 (Tolerated)
Deleterious probability by DeFine 0.6516 (Deleterious)
Entrez Gene ID 102465944 (NCBI Gene)
Official Gene Symbol MIR6072 (GeneCards)
Number of variants in MIR6072 in this database 7 (view all the variants)
Full name microRNA 6072
Band 10p15.3
Other IDs miRBase: MI0020349
HGNC: HGNC:50144
Ensembl: ENSG00000278069
Other names hsa-mir-6072
Summary microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID