KCNC4-DT

KCNC4 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 1:110208424-110212592

Previous symbols: [ "KCNC4-AS1", "LINC02586" ]

Links

ENSG00000224965 ∙ NCBI:100873974 ∙ ∙ HGNC:39958 ∙ ∙ ∙ 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 KCNC4-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KCNC4-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 KCNC4-DT

This is a list of pathogenic ClinVar variants found in the KCNC4-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
1-110211605-G-A		not specified	Uncertain significance (Nov 26, 2024)
1-110211633-C-T		not specified	Uncertain significance (Mar 11, 2024)
1-110211704-G-T		not specified	Uncertain significance (Dec 28, 2023)
1-110211725-A-T		not specified	Likely benign (Apr 07, 2023)
1-110211741-T-C		not specified	Likely benign (Apr 07, 2023)
1-110211801-G-A		not specified	Uncertain significance (May 18, 2022)
1-110211995-G-C		not specified	Uncertain significance (Dec 16, 2023)
1-110212004-A-G		not specified	Likely benign (Apr 07, 2023)
1-110212006-C-G		not specified	Uncertain significance (Apr 07, 2023)
1-110212008-G-C		not specified	Uncertain significance (Apr 07, 2023)
1-110212019-A-G		not specified	Likely benign (Aug 12, 2021)
1-110212028-G-A		not specified	Uncertain significance (Jun 29, 2023)
1-110212046-G-A		not specified	Uncertain significance (Apr 15, 2024)
1-110212066-G-C			Likely benign (Mar 01, 2024)
1-110212076-G-C		not specified	Uncertain significance (Jan 11, 2023)
1-110212085-G-C		not specified	Uncertain significance (Mar 31, 2022)
1-110212097-G-T		not specified	Uncertain significance (May 23, 2024)
1-110212098-C-T		not specified	Uncertain significance (Feb 16, 2023)
1-110212104-C-T		not specified	Uncertain significance (Jan 03, 2022)
1-110212142-C-T		not specified	Uncertain significance (May 20, 2024)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP