ZSCAN16-AS1

ZSCAN16 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 6:28008599-28137319

Links

ENSG00000269293 ∙ NCBI:100129195 ∙ ∙ HGNC:48982 ∙ ∙ ∙ 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 ZSCAN16-AS1 gene.

• Inborn genetic diseases (26 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZSCAN16-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)				1		1
splice region						0
non coding			24	1		25
Total	0	0	24	2	0

Variants in ZSCAN16-AS1

This is a list of pathogenic ClinVar variants found in the ZSCAN16-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
6-28085559-G-A		not specified	Uncertain significance (Jan 23, 2024)
6-28085598-A-G		not specified	Uncertain significance (Sep 21, 2023)
6-28085616-G-A		not specified	Uncertain significance (Jun 13, 2024)
6-28085661-C-T		not specified	Uncertain significance (Nov 08, 2022)
6-28085670-C-G		not specified	Uncertain significance (Dec 15, 2023)
6-28085686-G-A		not specified	Uncertain significance (Aug 13, 2021)
6-28085770-T-C		not specified	Uncertain significance (Jun 30, 2022)
6-28086289-C-T		not specified	Uncertain significance (Oct 10, 2023)
6-28088751-C-T		not specified	Uncertain significance (May 30, 2024)
6-28088992-A-G		not specified	Uncertain significance (Sep 15, 2021)
6-28089000-A-G		not specified	Uncertain significance (Aug 22, 2023)
6-28089049-G-A		not specified	Uncertain significance (Apr 04, 2024)
6-28089057-T-A		not specified	Uncertain significance (Feb 06, 2023)
6-28089104-A-C		not specified	Uncertain significance (Apr 01, 2024)
6-28089163-G-A		not specified	Uncertain significance (Jun 03, 2022)
6-28089183-C-T		not specified	Uncertain significance (Dec 06, 2021)
6-28089187-G-A		not specified	Uncertain significance (Feb 16, 2023)
6-28089241-A-G		not specified	Likely benign (May 27, 2022)
6-28089346-G-A		not specified	Uncertain significance (Aug 04, 2023)
6-28089393-T-C		not specified	Uncertain significance (Dec 20, 2023)
6-28089423-C-G		not specified	Uncertain significance (Dec 31, 2023)
6-28125540-A-C		not specified	Uncertain significance (Sep 14, 2023)
6-28125628-T-G		not specified	Uncertain significance (Nov 09, 2021)
6-28125689-C-A		not specified	Uncertain significance (Feb 28, 2023)
6-28125705-C-A		not specified	Uncertain significance (Aug 19, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP

Haploinsufficiency Scores

• ghis: 0.394