GeneBe

MIR6841

microRNA 6841, the group of MicroRNAs

Basic information

Region (hg38): 8:24953796-24953867

Links

ENSG00000283327 ∙ NCBI:102465506 ∙ ∙ HGNC:50070 ∙ ∙ ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MIR6841 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR6841 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
0
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 0 0 0

Variants in MIR6841

This is a list of pathogenic ClinVar variants found in the MIR6841 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position Type Phenotype Significance ClinVar
8-24953798-G-A Charcot-Marie-Tooth disease type 2E Uncertain significance (Feb 02, 2021)1368810
8-24953808-A-G not specified • Charcot-Marie-Tooth disease, type I • Charcot-Marie-Tooth disease • Charcot-Marie-Tooth disease type 2E Benign/Likely benign (Feb 01, 2024)138510
8-24953814-G-A Charcot-Marie-Tooth disease type 2E • Charcot-Marie-Tooth disease Likely benign (Feb 17, 2024)916904

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP