MINDY2-DT

MINDY2 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 15:58760350-58772120

Links

ENSG00000245975 ∙ NCBI:101928725 ∙ ∙ HGNC:55889 ∙ ∙ ∙ 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 MINDY2-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MINDY2-DT 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 MINDY2-DT

This is a list of pathogenic ClinVar variants found in the MINDY2-DT region.

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

Position	Type	Phenotype	Significance	ClinVar
15-58771495-A-T		not specified	Uncertain significance (Oct 12, 2021)
15-58771504-G-C		not specified	Uncertain significance (Mar 04, 2024)
15-58771522-G-A		not specified	Uncertain significance (Apr 18, 2023)
15-58771525-T-A		not specified	Uncertain significance (Dec 03, 2021)
15-58771610-C-G		not specified	Uncertain significance (Mar 20, 2023)
15-58771627-C-T		not specified	Uncertain significance (Mar 01, 2024)
15-58771645-G-T		not specified	Uncertain significance (Jan 23, 2024)
15-58771703-G-A		not specified	Uncertain significance (Apr 18, 2023)
15-58771706-G-A		not specified	Uncertain significance (Sep 16, 2021)
15-58771724-C-T		not specified	Uncertain significance (Aug 12, 2021)
15-58771736-C-T		not specified	Uncertain significance (Jan 23, 2024)
15-58771751-T-C		not specified	Likely benign (Dec 20, 2023)
15-58771835-G-T		not specified	Uncertain significance (Mar 28, 2024)
15-58771870-A-G		not specified	Uncertain significance (May 23, 2023)
15-58771946-C-A		not specified	Uncertain significance (Jan 10, 2022)
15-58771958-G-T		not specified	Uncertain significance (Sep 16, 2021)
15-58771993-A-G		not specified	Uncertain significance (Dec 13, 2023)
15-58772050-A-C		not specified	Uncertain significance (Mar 07, 2024)
15-58772055-G-C		not specified	Uncertain significance (Dec 01, 2022)
15-58772062-G-C		not specified	Uncertain significance (Aug 09, 2021)
15-58772071-A-G		not specified	Likely benign (Jul 08, 2022)
15-58772093-C-T		not specified	Uncertain significance (Oct 12, 2021)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP