CHMP1B-AS1

CHMP1B antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 18:11851414-11852751

Links

ENSG00000267165 ∙ ∙ ∙ HGNC:52778 ∙ ∙ ∙ 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 CHMP1B-AS1 gene.

• Inborn genetic diseases (9 variants)
• not provided (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the CHMP1B-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			9	1	1	11
Total	0	0	9	1	1

Variants in CHMP1B-AS1

This is a list of pathogenic ClinVar variants found in the CHMP1B-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
18-11851532-C-G		not specified	Uncertain significance (Jun 24, 2022)
18-11851600-A-G		not specified	Uncertain significance (Mar 06, 2023)
18-11851602-G-C		not specified	Uncertain significance (Nov 14, 2023)
18-11851638-G-A		not specified	Uncertain significance (May 31, 2023)
18-11851642-A-G		not specified	Uncertain significance (Oct 29, 2024)
18-11851654-C-G		not specified	Uncertain significance (Oct 22, 2021)
18-11851672-A-G		not specified	Uncertain significance (May 20, 2024)
18-11851681-G-C		not specified	Uncertain significance (Sep 21, 2023)
18-11851686-A-G		not specified	Uncertain significance (Jul 12, 2023)
18-11851696-C-A		not specified	Uncertain significance (Dec 20, 2023)
18-11851728-G-T		not specified	Uncertain significance (Apr 11, 2023)
18-11851780-A-C		not specified	Uncertain significance (Oct 04, 2022)
18-11851814-G-A			Benign (Jun 15, 2018)
18-11851816-C-T		not specified	Uncertain significance (Dec 22, 2023)
18-11851827-A-G		not specified	Uncertain significance (Jan 30, 2024)
18-11851857-G-T		not specified	Uncertain significance (Jun 10, 2024)
18-11851907-G-A		not specified	Uncertain significance (Dec 18, 2023)
18-11851956-G-A		not specified	Uncertain significance (Jun 13, 2023)
18-11851976-A-C		not specified	Uncertain significance (Apr 29, 2024)
18-11852017-C-T		not specified	Uncertain significance (Jun 05, 2024)
18-11852051-G-T			Likely benign (Dec 01, 2020)
18-11852056-C-T		not specified	Uncertain significance (Oct 19, 2024)
18-11852106-G-A		not specified	Uncertain significance (Mar 22, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP