ZNF433-AS1

ZNF433 and ZNF878 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 19:11987617-12046275

Links

ENSG00000219665NCBI:101928464HGNC:53776GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the ZNF433-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF433-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
61
clinvar
1
clinvar
62
Total 0 0 61 1 0

Variants in ZNF433-AS1

This is a list of pathogenic ClinVar variants found in the ZNF433-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
19-12014924-C-T not specified Uncertain significance (Dec 27, 2022)2306115
19-12014933-G-C not specified Uncertain significance (Dec 01, 2022)2405552
19-12014949-G-A not specified Uncertain significance (Mar 02, 2023)2493247
19-12014954-C-T not specified Uncertain significance (Jan 03, 2024)3195731
19-12014966-C-T not specified Uncertain significance (Feb 19, 2025)3820895
19-12014979-G-A not specified Uncertain significance (Aug 14, 2023)2599610
19-12015059-G-A not specified Uncertain significance (Apr 07, 2022)2368548
19-12015137-A-G not specified Uncertain significance (Mar 05, 2024)3195730
19-12015146-G-A not specified Uncertain significance (Feb 25, 2025)3820899
19-12015158-G-C not specified Uncertain significance (Oct 22, 2021)2256438
19-12015159-C-T not specified Uncertain significance (Aug 16, 2022)2307589
19-12015261-A-G not specified Uncertain significance (Mar 07, 2025)3820898
19-12015296-T-G not specified Uncertain significance (Apr 25, 2022)2374449
19-12015308-G-C not specified Uncertain significance (Oct 12, 2022)2387101
19-12015319-G-T not specified Uncertain significance (Dec 01, 2022)2330998
19-12015335-C-T not specified Uncertain significance (Jul 14, 2024)3475875
19-12015381-G-T not specified Uncertain significance (Mar 21, 2023)2527716
19-12015383-C-A not specified Uncertain significance (Oct 04, 2022)2374102
19-12015398-G-A not specified Uncertain significance (Feb 22, 2024)3195729
19-12015437-G-A not specified Uncertain significance (Jan 07, 2022)2222666
19-12015464-T-C not specified Uncertain significance (Nov 17, 2023)3195728
19-12015477-A-G not specified Uncertain significance (Nov 08, 2024)3475879
19-12015504-A-G not specified Uncertain significance (Dec 06, 2024)3475880
19-12015528-C-G not specified Uncertain significance (Aug 11, 2022)2384369
19-12015545-C-A not specified Uncertain significance (Jan 16, 2024)3195727

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP