TRABD-AS1

TRABD antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 22:50199049-50201596

Links

ENSG00000273253HGNC:56049GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

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

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the TRABD-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 TRABD-AS1

This is a list of pathogenic ClinVar variants found in the TRABD-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
22-50201041-C-T not specified Uncertain significance (Jul 22, 2022)3159591
22-50201058-C-G not specified Uncertain significance (Jul 20, 2022)3159576
22-50201061-G-C not specified Uncertain significance (Mar 12, 2024)3159577
22-50201062-G-A not specified Uncertain significance (Oct 03, 2022)3159578
22-50201121-C-T not specified Uncertain significance (Feb 28, 2024)3159599
22-50201141-C-G Likely benign (Mar 01, 2023)2653367
22-50201148-A-G not specified Uncertain significance (Jan 24, 2024)3159544
22-50201164-G-C not specified Uncertain significance (Aug 13, 2021)3159550
22-50201196-G-T not specified Uncertain significance (Sep 08, 2023)2620873
22-50201205-G-C not specified Uncertain significance (Apr 23, 2024)3317238
22-50201245-C-T not specified Uncertain significance (Jun 13, 2022)3159575
22-50201299-C-T not specified Uncertain significance (Jun 16, 2023)2590810
22-50201317-G-A not specified Uncertain significance (Aug 16, 2022)3159579
22-50201336-G-T not specified Uncertain significance (Oct 12, 2021)3159580
22-50201341-C-T not specified Uncertain significance (Sep 20, 2023)3159581
22-50201355-G-A not specified Uncertain significance (Aug 23, 2021)3159582
22-50201377-G-A not specified Uncertain significance (Apr 18, 2023)2537660
22-50201381-G-T not specified Uncertain significance (May 23, 2023)2568437
22-50201385-G-C not specified Uncertain significance (May 07, 2024)3317246
22-50201388-G-T not specified Uncertain significance (Mar 06, 2023)2459809
22-50201397-G-T not specified Uncertain significance (Jan 31, 2024)3159583
22-50201412-G-A not specified Uncertain significance (Nov 08, 2022)3159584
22-50201412-G-T not specified Uncertain significance (May 13, 2024)3317247
22-50201416-A-G not specified Uncertain significance (May 09, 2022)3159585
22-50201433-G-T not specified Uncertain significance (Apr 07, 2023)2534536

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP