NUDT19-DT

NUDT19 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 19:32686680-32700147

Links

ENSG00000267475 ∙ ∙ ∙ HGNC:55296 ∙ ∙ ∙ 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 NUDT19-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the NUDT19-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 NUDT19-DT

This is a list of pathogenic ClinVar variants found in the NUDT19-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
19-32691968-G-A		not specified	Uncertain significance (Feb 07, 2023)
19-32691976-C-A			Likely benign (Jun 01, 2022)
19-32691976-C-T		not specified	Uncertain significance (Aug 26, 2022)
19-32692022-C-A		not specified	Uncertain significance (Sep 26, 2022)
19-32692024-G-C		not specified	Uncertain significance (Aug 16, 2021)
19-32692028-G-A		not specified	Uncertain significance (Nov 07, 2022)
19-32692057-C-G		not specified	Uncertain significance (Mar 30, 2024)
19-32692061-C-G		not specified	Uncertain significance (Sep 24, 2024)
19-32692091-T-A		not specified	Uncertain significance (Jan 04, 2022)
19-32692100-T-G		not specified	Uncertain significance (Jan 04, 2022)
19-32692105-C-T		not specified	Uncertain significance (Jan 30, 2024)
19-32692109-C-T		not specified	Uncertain significance (Sep 02, 2024)
19-32692127-T-C		not specified	Uncertain significance (Jul 02, 2024)
19-32692129-C-T		not specified	Uncertain significance (Jul 05, 2024)
19-32692156-G-A		not specified	Uncertain significance (Nov 25, 2024)
19-32692171-G-A		not specified	Uncertain significance (Feb 16, 2023)
19-32692175-G-C		not specified	Uncertain significance (May 26, 2023)
19-32692196-T-G		not specified	Uncertain significance (Jan 26, 2022)
19-32692201-G-A		not specified	Uncertain significance (Oct 26, 2022)
19-32692202-C-A		not specified	Uncertain significance (Oct 26, 2022)
19-32692211-A-T		not specified	Uncertain significance (Sep 04, 2024)
19-32692213-G-A		not specified	Uncertain significance (Mar 25, 2024)
19-32692223-G-C		not specified	Uncertain significance (May 01, 2022)
19-32692228-G-A		not specified	Uncertain significance (Sep 17, 2021)
19-32692252-C-T		not specified	Uncertain significance (Jun 18, 2024)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP