THBS1-AS1

THBS1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 15:39588357-39588882

Links

ENSG00000278621

∙ ∙ ∙ HGNC:55224 ∙ ∙ ∙ 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 THBS1-AS1 gene.

not specified (2 variants)
Inborn genetic diseases (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the THBS1-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			1 clinvar		2 clinvar	3
Total	0	0	1	0	2

Variants in THBS1-AS1

This is a list of pathogenic ClinVar variants found in the THBS1-AS1 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position	Phenotype	Significance	ClinVar
15-39588598-G-A	not specified	Uncertain significance (May 08, 2023)	2545061
15-39588604-G-A	not specified	Uncertain significance (Aug 06, 2021)	3176949
15-39588617-C-T	not specified • THBS1-related disorder	Benign (Mar 28, 2016)	403536
15-39588621-A-G	not specified • THBS1-related disorder	Benign (Mar 28, 2016)	403537

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP