CHMP3-AS1

CHMP3 and RNF103 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 2:86562070-86618766

Links

ENSG00000228363NCBI:105374845HGNC:55795GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the CHMP3-AS1 gene.

  • Inborn genetic diseases (22 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the CHMP3-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
22
clinvar
22
Total 0 0 22 0 0

Variants in CHMP3-AS1

This is a list of pathogenic ClinVar variants found in the CHMP3-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
2-86563309-C-T not specified Uncertain significance (Jul 14, 2023)2612097
2-86603934-C-T not specified Uncertain significance (Jan 26, 2023)2455594
2-86604086-T-G not specified Uncertain significance (Sep 27, 2021)2252550
2-86604087-T-C not specified Uncertain significance (May 24, 2023)2551548
2-86604177-G-A not specified Uncertain significance (Aug 15, 2023)2619263
2-86604285-G-C not specified Uncertain significance (Mar 16, 2022)2360386
2-86604312-T-G not specified Uncertain significance (Oct 26, 2021)2257118
2-86604317-C-T not specified Uncertain significance (Dec 09, 2023)3154914
2-86604354-C-T not specified Uncertain significance (Dec 07, 2021)2266206
2-86604421-C-T not specified Uncertain significance (Mar 16, 2022)2278538
2-86604558-T-C not specified Uncertain significance (Aug 02, 2021)2359513
2-86604563-T-A not specified Uncertain significance (May 08, 2024)3314662
2-86604582-C-T not specified Uncertain significance (Nov 10, 2022)2203780
2-86604590-C-A not specified Uncertain significance (Apr 20, 2024)3314658
2-86604595-T-C not specified Uncertain significance (Dec 06, 2022)2333712
2-86604736-A-T not specified Uncertain significance (May 20, 2024)3314663
2-86604920-A-C not specified Uncertain significance (Apr 08, 2024)3314660
2-86605080-T-C not specified Uncertain significance (Apr 08, 2024)3314659
2-86605082-G-C not specified Uncertain significance (Jun 21, 2021)3154918
2-86605091-A-T not specified Uncertain significance (Jun 22, 2023)2602226
2-86605140-C-G not specified Uncertain significance (Sep 27, 2021)2252496
2-86605189-A-G not specified Uncertain significance (Oct 14, 2023)3154917
2-86605209-T-C not specified Uncertain significance (Mar 16, 2022)2358585
2-86605217-A-T not specified Uncertain significance (Jul 06, 2021)2368437
2-86605317-C-T not specified Uncertain significance (Jun 12, 2023)2518370

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP