ZNF337-AS1

ZNF337 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 20:25624017-25689032

Links

ENSG00000213742NCBI:102724826HGNC:40759GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the ZNF337-AS1 gene.

  • Inborn genetic diseases (41 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF337-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
40
clinvar
1
clinvar
41
Total 0 0 40 1 0

Variants in ZNF337-AS1

This is a list of pathogenic ClinVar variants found in the ZNF337-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
20-25675069-C-T not specified Uncertain significance (Aug 12, 2021)2410277
20-25675070-G-A not specified Uncertain significance (Aug 16, 2022)2380163
20-25675070-G-C not specified Uncertain significance (Jul 17, 2023)2612301
20-25675129-C-A not specified Uncertain significance (Apr 05, 2023)2533599
20-25675225-T-C not specified Uncertain significance (Jan 09, 2024)3195238
20-25675262-A-G not specified Uncertain significance (Jun 02, 2023)2555550
20-25675300-T-C not specified Uncertain significance (Apr 11, 2023)2517205
20-25675309-A-G not specified Uncertain significance (Dec 07, 2021)2265633
20-25675336-G-A not specified Uncertain significance (Apr 04, 2023)2532635
20-25675397-T-C not specified Uncertain significance (Jan 29, 2024)3195236
20-25675502-C-T not specified Uncertain significance (Feb 22, 2024)3195235
20-25675552-C-T not specified Uncertain significance (Apr 20, 2024)3335517
20-25675556-C-T not specified Uncertain significance (Apr 15, 2024)3335518
20-25675576-G-A not specified Uncertain significance (Mar 21, 2022)2279283
20-25675579-C-T not specified Uncertain significance (Jul 19, 2022)2302354
20-25675645-T-G not specified Uncertain significance (Dec 07, 2021)2265901
20-25675702-G-A not specified Uncertain significance (Mar 01, 2024)3195234
20-25675720-C-T not specified Uncertain significance (Sep 29, 2023)3195233
20-25675757-A-T not specified Uncertain significance (Mar 01, 2024)3195232
20-25675758-G-T not specified Uncertain significance (May 08, 2023)2515882
20-25675804-C-T not specified Uncertain significance (Mar 29, 2022)2382514
20-25675888-C-T not specified Uncertain significance (Dec 11, 2023)3195231
20-25675946-C-T not specified Uncertain significance (Jun 11, 2021)2352659
20-25675963-A-T not specified Uncertain significance (Jul 26, 2022)2345454
20-25676052-G-T not specified Uncertain significance (Aug 13, 2021)2244836

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP