PARD6G-AS1

PARD6G antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 18:80147907-80179839

Links

ENSG00000267270 ∙ NCBI:100130522 ∙ ∙ HGNC:44109 ∙ ∙ ∙ 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 PARD6G-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the PARD6G-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 PARD6G-AS1

This is a list of pathogenic ClinVar variants found in the PARD6G-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
18-80159782-C-A		not specified	Uncertain significance (May 05, 2023)
18-80159788-G-A		not specified	Uncertain significance (Jun 05, 2024)
18-80159824-G-C		not specified	Uncertain significance (Sep 28, 2022)
18-80159830-G-C		not specified	Uncertain significance (Feb 06, 2024)
18-80159875-C-G		not specified	Uncertain significance (Jan 29, 2024)
18-80159893-G-A		not specified	Uncertain significance (Mar 07, 2023)
18-80159922-T-C		not specified	Uncertain significance (Jul 12, 2023)
18-80159937-C-T		not specified	Uncertain significance (Sep 02, 2024)
18-80159976-G-C		not specified	Uncertain significance (Jan 17, 2023)
18-80159995-T-C		not specified	Uncertain significance (Apr 12, 2023)
18-80160037-G-A		not specified	Uncertain significance (Oct 11, 2024)
18-80160040-A-C		not specified	Uncertain significance (Aug 22, 2023)
18-80160057-G-T		not specified	Uncertain significance (Jul 05, 2024)
18-80160078-C-A		not specified	Uncertain significance (Jan 24, 2024)
18-80160082-C-T		not specified	Uncertain significance (Nov 21, 2023)
18-80160088-C-G		not specified	Uncertain significance (Apr 27, 2022)
18-80160089-G-C		not specified	Uncertain significance (Apr 08, 2022)
18-80160136-C-G		not specified	Uncertain significance (Jun 02, 2023)
18-80160171-A-G		not specified	Uncertain significance (Jun 10, 2024)
18-80160181-G-A		not specified	Uncertain significance (Oct 29, 2024)
18-80160358-C-T		not specified	Uncertain significance (May 21, 2024)
18-80160361-G-A		not specified	Uncertain significance (Nov 11, 2024)
18-80160409-C-T		not specified	Uncertain significance (Apr 04, 2024)
18-80160490-G-A		not specified	Uncertain significance (Oct 06, 2024)
18-80160528-C-A		not specified	Uncertain significance (Feb 10, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP