THRB-AS1

THRB antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 3:24493985-24681711

Links

ENSG00000228791NCBI:644990HGNC:44515GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

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

  • Thyroid hormone resistance, generalized, autosomal dominant (5 variants)
  • Thyroid hormone resistance syndrome (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the THRB-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
6
clinvar
6
Total 0 0 6 0 0

Variants in THRB-AS1

This is a list of pathogenic ClinVar variants found in the THRB-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
3-24494647-C-G Thyroid hormone resistance, generalized, autosomal dominant Uncertain significance (Jan 13, 2018)344643
3-24494665-C-A Thyroid hormone resistance, generalized, autosomal dominant Uncertain significance (Jan 13, 2018)901328
3-24494758-C-T Thyroid hormone resistance, generalized, autosomal dominant Uncertain significance (Jan 13, 2018)901329
3-24494772-GTC-G Thyroid hormone resistance syndrome Uncertain significance (Jun 14, 2016)344644
3-24494784-A-G Thyroid hormone resistance, generalized, autosomal dominant Uncertain significance (Jan 12, 2018)344645
3-24494795-A-G Thyroid hormone resistance, generalized, autosomal dominant Uncertain significance (Jan 13, 2018)901330

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP