MYL6B-AS1

MYL6B antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 12:56150796-56158220

Links

ENSG00000257809HGNC:55472GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the MYL6B-AS1 gene.

  • Inborn genetic diseases (9 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MYL6B-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
9
clinvar
9
Total 0 0 9 0 0

Variants in MYL6B-AS1

This is a list of pathogenic ClinVar variants found in the MYL6B-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
12-56155061-A-G not specified Uncertain significance (Jun 03, 2022)2293962
12-56155091-G-A not specified Uncertain significance (Feb 07, 2023)2455951
12-56155117-T-C not specified Uncertain significance (Dec 18, 2023)3159513
12-56155119-T-G not specified Uncertain significance (Mar 16, 2022)2229823
12-56155129-A-G not specified Uncertain significance (Oct 03, 2022)2279235
12-56155159-G-A not specified Uncertain significance (May 09, 2022)2288174
12-56155169-T-C not specified Uncertain significance (Sep 17, 2021)2251371
12-56155186-C-T not specified Uncertain significance (Oct 06, 2021)2360406
12-56155460-A-T not specified Uncertain significance (May 27, 2022)2291643
12-56155523-C-T not specified Uncertain significance (Nov 09, 2023)3159542
12-56155547-G-A not specified Uncertain significance (Dec 17, 2023)3159553
12-56155547-G-C not specified Uncertain significance (Feb 01, 2023)3159561
12-56157480-C-G not specified Uncertain significance (Oct 22, 2021)2271689
12-56157721-G-A not specified Uncertain significance (Mar 31, 2024)3297577

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP