MAGEA8-AS1

MAGEA8 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): X:149876186-149897038

Links

ENSG00000230899 ∙ NCBI:101410537 ∙ ∙ HGNC:45093 ∙ ∙ ∙ 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 MAGEA8-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MAGEA8-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						0
Total	0	0	0	0	0

Variants in MAGEA8-AS1

This is a list of pathogenic ClinVar variants found in the MAGEA8-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
X-149884285-C-G		not specified	Uncertain significance (Oct 12, 2022)
X-149884300-T-C		not specified	Uncertain significance (Apr 20, 2023)
X-149884309-G-A		not specified	Uncertain significance (Sep 29, 2023)
X-149884391-C-A		not specified	Uncertain significance (Apr 26, 2023)
X-149884400-C-G		not specified	Uncertain significance (Aug 08, 2023)
X-149884410-C-G		not specified	Uncertain significance (Mar 07, 2023)
X-149884429-G-C		not specified	Uncertain significance (Nov 15, 2021)
X-149884472-G-A		not specified	Uncertain significance (Aug 28, 2023)
X-149884475-C-T		not specified	Uncertain significance (Jul 08, 2021)
X-149884586-A-G		not specified	Uncertain significance (Nov 19, 2022)
X-149884595-T-G		not specified	Uncertain significance (Apr 23, 2024)
X-149884598-G-A		not specified	Uncertain significance (Dec 12, 2023)
X-149884684-A-G		not specified	Uncertain significance (Jan 07, 2022)
X-149884858-G-A		not specified	Uncertain significance (Apr 23, 2024)
X-149884865-G-A		not specified	Uncertain significance (Feb 17, 2024)
X-149884871-C-T		not specified	Uncertain significance (Dec 09, 2023)
X-149884891-A-G			Likely benign (-)
X-149884922-G-A		not specified	Uncertain significance (Oct 12, 2022)
X-149884998-T-C			Likely benign (May 01, 2022)
X-149885036-A-G		not specified	Uncertain significance (Mar 07, 2024)
X-149885066-C-T		not specified	Uncertain significance (Oct 02, 2023)
X-149885084-G-A		not specified	Uncertain significance (Jan 04, 2022)
X-149885089-G-A		not specified	Uncertain significance (May 08, 2024)
X-149885143-G-C		not specified	Uncertain significance (Sep 14, 2022)
X-149885183-A-G		not specified	Uncertain significance (Apr 22, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP