GPR84-AS1

GPR84, ZNF385A, ITGA5 and GTSF1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 12:54352429-54497688

Links

ENSG00000258086NCBI:102724050HGNC:56187GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the GPR84-AS1 gene.

  • Inborn genetic diseases (62 variants)
  • not provided (14 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the GPR84-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
58
clinvar
4
clinvar
14
clinvar
76
Total 0 0 58 4 14

Variants in GPR84-AS1

This is a list of pathogenic ClinVar variants found in the GPR84-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
12-54362807-G-A not specified Uncertain significance (Oct 20, 2021)2256145
12-54362810-G-A not specified Uncertain significance (Apr 27, 2022)2286378
12-54362842-A-G not specified Uncertain significance (Jan 29, 2024)3101877
12-54362896-C-T not specified Likely benign (Sep 03, 2024)3522164
12-54362906-T-C not specified Uncertain significance (Sep 04, 2024)3522162
12-54362908-C-T not specified Uncertain significance (Mar 25, 2024)3282457
12-54362938-C-G not specified Uncertain significance (Jun 29, 2023)2607919
12-54362942-C-T not specified Uncertain significance (Nov 12, 2024)3522166
12-54363091-A-G not specified Uncertain significance (Nov 19, 2022)2376358
12-54363128-C-G not specified Uncertain significance (Jun 03, 2024)3282458
12-54363143-G-A not specified Uncertain significance (Nov 06, 2023)3101883
12-54363194-C-T not specified Uncertain significance (Dec 03, 2024)3522167
12-54363199-C-T not specified Uncertain significance (Jul 14, 2024)2345836
12-54363206-T-G not specified Uncertain significance (Mar 02, 2023)2493775
12-54363229-G-A not specified Uncertain significance (Dec 18, 2023)3101881
12-54363232-C-T not specified Uncertain significance (Jul 27, 2024)3522160
12-54363244-C-T not specified Uncertain significance (May 18, 2023)2525561
12-54363245-G-A not specified Uncertain significance (Sep 30, 2024)3522161
12-54363284-C-G not specified Uncertain significance (Nov 30, 2022)2231543
12-54363326-G-A not specified Uncertain significance (Feb 05, 2024)3101880
12-54363338-G-A not specified Uncertain significance (Mar 31, 2024)3282455
12-54363356-A-G not specified Uncertain significance (Feb 21, 2024)3101879
12-54363362-C-T not specified Uncertain significance (Jan 26, 2022)2222483
12-54363664-G-T not specified Uncertain significance (Jul 23, 2024)3522163
12-54363668-G-A not specified Uncertain significance (Nov 10, 2024)3522165

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP