MIR3195

microRNA 3195, the group of MicroRNAs

Basic information

Region (hg38): 20:62064802-62064885

Links

ENSG00000265306 ∙ NCBI:100422838 ∙ ∙ HGNC:38250 ∙ ∙ ∙ 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 MIR3195 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR3195 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 MIR3195

This is a list of pathogenic ClinVar variants found in the MIR3195 region.

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

Position	Type	Phenotype	Significance	ClinVar
20-62064804-G-A		Inborn genetic diseases	Uncertain significance (May 09, 2022)
20-62064808-CC-TT		not specified	Uncertain significance (Mar 03, 2025)
20-62064810-G-A		Inborn genetic diseases	Uncertain significance (Dec 01, 2022)
20-62064831-C-A		Inborn genetic diseases	Uncertain significance (Jan 21, 2025)
20-62064831-C-T		Inborn genetic diseases	Uncertain significance (Apr 05, 2023)
20-62064838-C-A		Inborn genetic diseases	Uncertain significance (Mar 03, 2022)
20-62064842-C-A			Benign (Oct 02, 2019)
20-62064846-G-A		Inborn genetic diseases	Uncertain significance (Apr 08, 2024)
20-62064847-G-A		Inborn genetic diseases	Uncertain significance (May 13, 2024)
20-62064848-GC-G		Intellectual developmental disorder, autosomal dominant 73	Likely pathogenic (Apr 10, 2024)
20-62064849-C-T		Inborn genetic diseases	Uncertain significance (Apr 23, 2024)
20-62064867-G-C		Inborn genetic diseases	Uncertain significance (Jul 12, 2023)
20-62064871-C-G		Inborn genetic diseases	Uncertain significance (Jan 10, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP