SEPTIN4-AS1

SEPTIN4 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 17:58514723-58583963

Previous symbols: [ "SEPT4-AS1" ]

Links

ENSG00000264672 ∙ NCBI:101927688 ∙ ∙ HGNC:51345 ∙ ∙ ∙ 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 SEPTIN4-AS1 gene.

• Inborn genetic diseases (16 variants)
• not provided (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the SEPTIN4-AS1 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			14	3	1	18
Total	0	0	14	3	1

Variants in SEPTIN4-AS1

This is a list of pathogenic ClinVar variants found in the SEPTIN4-AS1 region.

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

Position	Type	Phenotype	Significance	ClinVar
17-58520449-T-C		not specified	Uncertain significance (Aug 16, 2021)
17-58520472-T-A		not specified	Uncertain significance (Jun 24, 2022)
17-58520475-A-G		not specified	Uncertain significance (Oct 25, 2022)
17-58520745-C-T			Benign (Apr 26, 2018)
17-58520759-C-T		not specified	Uncertain significance (Aug 04, 2023)
17-58520832-G-A		not specified	Uncertain significance (Jan 23, 2024)
17-58520839-T-G		not specified	Uncertain significance (Sep 14, 2022)
17-58521025-C-T		not specified	Uncertain significance (Dec 21, 2023)
17-58521053-G-A		not specified	Uncertain significance (Apr 13, 2022)
17-58521067-T-C		not specified	Uncertain significance (Mar 24, 2023)
17-58521143-A-G		not specified	Uncertain significance (Feb 27, 2023)
17-58521149-C-A		not specified	Uncertain significance (Jul 05, 2023)
17-58521328-A-G		not specified	Uncertain significance (Feb 17, 2024)
17-58521616-T-C		not specified	Uncertain significance (Feb 14, 2023)
17-58521633-A-G		not specified	Uncertain significance (Apr 13, 2022)
17-58522051-C-T		not specified	Uncertain significance (May 06, 2024)
17-58522088-C-T		not specified	Uncertain significance (Feb 28, 2023)
17-58525121-C-A		not specified	Uncertain significance (May 24, 2023)
17-58525133-G-A		not specified	Uncertain significance (Jul 13, 2022)
17-58525162-A-G		not specified	Uncertain significance (Apr 08, 2023)
17-58525714-C-T			Likely benign (Apr 17, 2018)
17-58525722-G-A		not specified	Uncertain significance (Aug 04, 2023)
17-58525752-C-T		not specified	Uncertain significance (Aug 12, 2021)
17-58526304-C-G		not specified	Uncertain significance (May 09, 2023)
17-58526791-C-G		not specified	Uncertain significance (Oct 27, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP