ZNF225-AS1

ZNF225 and ZNF224 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 19:44103007-44113320

Links

ENSG00000186019 ∙ NCBI:100379224 ∙ ∙ HGNC:55916 ∙ ∙ ∙ 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 ZNF225-AS1 gene.

• Inborn genetic diseases (25 variants)
• not provided (7 variants)
• Malignant tumor of prostate (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF225-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			24	2	7	33
Total	0	0	24	2	7

Variants in ZNF225-AS1

This is a list of pathogenic ClinVar variants found in the ZNF225-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
19-44106470-T-C		not specified	Uncertain significance (Apr 18, 2023)
19-44106480-T-C		not specified	Uncertain significance (Nov 20, 2023)
19-44106539-G-A		not specified	Uncertain significance (Jul 19, 2023)
19-44106559-G-T		not specified	Uncertain significance (Mar 21, 2023)
19-44106635-G-A		not specified	Uncertain significance (May 04, 2022)
19-44106687-A-G		not specified	Uncertain significance (May 27, 2022)
19-44106771-A-G		not specified	Uncertain significance (Feb 15, 2023)
19-44106801-G-A			Benign (Jul 23, 2018)
19-44106817-G-T			Benign (Aug 16, 2018)
19-44106822-C-T		not specified	Uncertain significance (Nov 27, 2023)
19-44106852-C-T		not specified	Uncertain significance (Sep 27, 2021)
19-44106956-G-A		not specified	Uncertain significance (Sep 09, 2021)
19-44106969-T-G		not specified	Uncertain significance (Jan 10, 2022)
19-44107008-C-T		not specified	Uncertain significance (May 13, 2024)
19-44107013-G-A		not specified	Uncertain significance (Oct 05, 2023)
19-44107092-C-T		not specified	Uncertain significance (Jul 27, 2022)
19-44107220-A-G		not specified	Uncertain significance (Dec 13, 2021)
19-44107224-G-A		not specified	Uncertain significance (Apr 10, 2023)
19-44107242-C-T		not specified	Uncertain significance (Sep 20, 2023)
19-44107286-G-C			Benign (Jul 23, 2018)
19-44107335-G-A		not specified	Uncertain significance (Oct 29, 2021)
19-44107374-G-A		not specified	Uncertain significance (May 24, 2023)
19-44107380-A-G		not specified	Uncertain significance (Jul 09, 2021)
19-44107404-G-A		not specified	Uncertain significance (Jun 24, 2022)
19-44107431-G-A		not specified	Uncertain significance (Jun 22, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP