ZNF790-AS1

ZNF790 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 19:36776080-36831596

Links

ENSG00000267254NCBI:284408HGNC:27617GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the ZNF790-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF790-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 ZNF790-AS1

This is a list of pathogenic ClinVar variants found in the ZNF790-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
19-36818449-A-C not specified Uncertain significance (Nov 14, 2024)3478498
19-36818459-T-C not specified Uncertain significance (Aug 17, 2022)2406806
19-36818492-C-T not specified Uncertain significance (Jun 22, 2024)3259572
19-36818506-A-G not specified Uncertain significance (Mar 20, 2023)2527100
19-36818515-A-C not specified Uncertain significance (Feb 14, 2024)3198428
19-36818563-T-G not specified Uncertain significance (Aug 30, 2021)2339799
19-36818570-T-C not specified Uncertain significance (Mar 15, 2024)3259573
19-36818741-C-T not specified Uncertain significance (Oct 25, 2024)2403994
19-36818767-C-A not specified Uncertain significance (Sep 10, 2024)3478497
19-36818792-C-G not specified Uncertain significance (Jan 10, 2022)2271526
19-36818815-T-C not specified Uncertain significance (Nov 18, 2022)2365034
19-36818821-C-T not specified Uncertain significance (Feb 21, 2024)3198427
19-36818856-G-C not specified Uncertain significance (May 08, 2023)2516592
19-36818909-C-T not specified Uncertain significance (Jun 02, 2023)2555768
19-36818923-C-G not specified Uncertain significance (Jul 14, 2023)2612169
19-36818942-G-A not specified Uncertain significance (Feb 05, 2024)2378130
19-36818951-A-G not specified Uncertain significance (Sep 22, 2022)2367764
19-36818953-T-C not specified Uncertain significance (Jan 06, 2023)2457818
19-36818959-C-T not specified Uncertain significance (Mar 18, 2024)3259574
19-36819004-C-T not specified Uncertain significance (Dec 02, 2024)3478496
19-36819020-T-C not specified Uncertain significance (Mar 31, 2024)2310916
19-36819045-C-G not specified Uncertain significance (Jun 23, 2021)2406629
19-36819077-C-G not specified Uncertain significance (Dec 31, 2023)3198425
19-36819214-C-T not specified Uncertain significance (Aug 26, 2022)2350619
19-36819230-C-T not specified Uncertain significance (May 20, 2024)3259575

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP