MIR3661

microRNA 3661, the group of MicroRNAs

Basic information

Region (hg38): 5:134225757-134225852

Links

ENSG00000266751 ∙ NCBI:100500905 ∙ ∙ HGNC:38892 ∙ ∙ ∙ 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 MIR3661 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR3661 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 MIR3661

This is a list of pathogenic ClinVar variants found in the MIR3661 region.

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

Position	Type	Phenotype	Significance	ClinVar
5-134225759-C-T			Likely pathogenic (Jun 17, 2022)
5-134225759-CCTT-C			Uncertain significance (May 19, 2021)
5-134225772-G-A			Likely benign (Jan 05, 2025)
5-134225777-T-C			Uncertain significance (Oct 28, 2024)
5-134225781-C-T			Likely benign (Aug 23, 2021)
5-134225784-G-A			Likely benign (Aug 04, 2023)
5-134225784-G-C			Likely benign (May 15, 2024)
5-134225785-G-A			Uncertain significance (May 30, 2022)
5-134225785-G-C			Uncertain significance (Nov 01, 2024)
5-134225785-GAC-G			Pathogenic (Aug 23, 2021)
5-134225788-T-A			Uncertain significance (Jan 29, 2020)
5-134225790-G-A			Likely benign (Oct 22, 2024)
5-134225790-G-C			Likely benign (Aug 11, 2024)
5-134225791-G-A			Uncertain significance (Mar 24, 2024)
5-134225795-G-A			Likely benign (Apr 25, 2024)
5-134225800-T-C			Likely benign (Mar 01, 2025)
5-134225801-T-C			Uncertain significance (Jun 13, 2022)
5-134225805-C-T			Likely benign (Aug 23, 2022)
5-134225806-T-TCGTTC			Pathogenic (Sep 17, 2021)
5-134225814-CT-G			Uncertain significance (Aug 05, 2024)
5-134225816-G-A		Houge-Janssens syndrome 3	Likely pathogenic (-)
5-134225819-C-T		Inborn genetic diseases	Uncertain significance (Jan 08, 2024)
5-134225820-G-A			Likely benign (Dec 07, 2022)
5-134225821-A-G			Uncertain significance (May 01, 2023)
5-134225824-C-T			Pathogenic (Mar 14, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP