DPP3-DT

DPP3 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 11:66472958-66480301

Links

ENSG00000255517 ∙ NCBI:101928069 ∙ ∙ HGNC:55494 ∙ ∙ ∙ 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 DPP3-DT gene.

• Inborn genetic diseases (5 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the DPP3-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)			1			1
splice region						0
non coding			4			4
Total	0	0	5	0	0

Variants in DPP3-DT

This is a list of pathogenic ClinVar variants found in the DPP3-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
11-66473248-G-A		not specified	Uncertain significance (Jun 13, 2024)
11-66473287-C-T		not specified	Uncertain significance (Nov 19, 2022)
11-66473290-C-G		not specified	Uncertain significance (May 05, 2023)
11-66473307-G-A		not specified	Uncertain significance (Dec 05, 2024)
11-66473310-G-A		not specified	Uncertain significance (Nov 21, 2022)
11-66473371-G-A		not specified	Uncertain significance (Apr 27, 2023)
11-66473380-A-G		not specified	Uncertain significance (Jun 01, 2023)
11-66473383-C-G		not specified	Uncertain significance (Aug 28, 2024)
11-66473855-G-A		not specified	Uncertain significance (Apr 24, 2024)
11-66473870-G-T		not specified	Uncertain significance (Aug 31, 2022)
11-66473915-G-A		not specified	Uncertain significance (Jun 05, 2024)
11-66475667-C-T		not specified	Uncertain significance (Dec 30, 2023)
11-66475722-G-A		not specified	Uncertain significance (Jan 02, 2024)
11-66475799-C-T		not specified	Uncertain significance (Aug 02, 2024)
11-66475806-C-T		not specified	Uncertain significance (Mar 01, 2024)
11-66475815-A-T		not specified	Uncertain significance (Jun 11, 2021)
11-66475905-A-T		not specified	Uncertain significance (Jan 20, 2023)
11-66476153-G-C		not specified	Uncertain significance (Jun 28, 2023)
11-66476157-C-T		not specified	Uncertain significance (Aug 16, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP