NUTM2A-AS1

NUTM2A antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 10:87189002-87342612

Previous symbols: [ "FAM22A-AS1" ]

Links

ENSG00000223482 ∙ NCBI:728190 ∙ ∙ HGNC:45161 ∙ ∙ ∙ 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 NUTM2A-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the NUTM2A-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			5			5
Total	0	0	5	0	0

Variants in NUTM2A-AS1

This is a list of pathogenic ClinVar variants found in the NUTM2A-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
10-87190531-C-T		not specified	Uncertain significance (Jul 14, 2023)
10-87190535-C-G		not specified	Uncertain significance (Jan 29, 2024)
10-87190552-G-A		not specified	Uncertain significance (May 23, 2023)
10-87190645-C-T		not specified	Uncertain significance (Aug 05, 2024)
10-87190661-A-T		not specified	Uncertain significance (Nov 27, 2023)
10-87228286-G-A		not specified	Uncertain significance (Jun 24, 2022)
10-87228308-C-T		not specified	Uncertain significance (Nov 07, 2022)
10-87228331-C-T		not specified	Uncertain significance (May 20, 2024)
10-87228352-G-A		not specified	Uncertain significance (Jul 13, 2021)
10-87228388-G-T		not specified	Uncertain significance (May 23, 2023)
10-87228389-C-T		not specified	Likely benign (Jul 20, 2021)
10-87228478-G-T		not specified	Uncertain significance (Sep 08, 2024)
10-87228482-C-G		not specified	Uncertain significance (Mar 19, 2024)
10-87228501-G-A		not specified	Uncertain significance (Apr 17, 2023)
10-87228511-G-T		not specified	Uncertain significance (Jul 06, 2022)
10-87228529-G-A		not specified	Uncertain significance (Dec 05, 2022)
10-87228559-G-A		not specified	Uncertain significance (Sep 20, 2024)
10-87228560-C-G		not specified	Uncertain significance (Apr 17, 2024)
10-87228565-C-A		not specified	Uncertain significance (Feb 17, 2022)
10-87228568-G-A		not specified	Uncertain significance (Dec 02, 2024)
10-87228599-G-C		not specified	Uncertain significance (May 31, 2023)
10-87228613-C-T		not specified	Uncertain significance (Mar 26, 2024)
10-87228628-G-C		not specified	Uncertain significance (May 27, 2022)
10-87228734-C-T		not specified	Uncertain significance (Dec 10, 2024)
10-87228757-G-T		not specified	Uncertain significance (Oct 22, 2021)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP