GeneBe

MIR23AHG

miR-23a/27a/24-2 cluster host gene, the group of MicroRNA non-coding host genes

Basic information

Region (hg38): 19:13823880-13842928

Links

ENSG00000267519 ∙ NCBI:284454 ∙ ∙ HGNC:27620 ∙ ∙ ∙ 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 MIR23AHG gene.

  • Inborn genetic diseases (13 variants)
  • not provided (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MIR23AHG 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
13
clinvar
2
clinvar
 15
Total 0 0 13 2 0

Variants in MIR23AHG

This is a list of pathogenic ClinVar variants found in the MIR23AHG region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position Type Phenotype Significance ClinVar
19-13825636-G-A not specified Uncertain significance (Dec 07, 2021)3199533
19-13825661-G-A not specified Uncertain significance (Jun 17, 2024)3260134
19-13825692-C-G not specified Uncertain significance (May 15, 2024)3260126
19-13828649-T-C not specified Uncertain significance (Jul 31, 2024)3479491
19-13828679-G-A not specified Uncertain significance (Feb 07, 2023)2465289
19-13828682-G-A not specified Uncertain significance (Aug 17, 2022)2308364
19-13828697-G-A not specified Uncertain significance (Oct 13, 2021)2342268
19-13830253-G-A not specified Uncertain significance (May 29, 2024)3260132
19-13830261-C-T Likely benign (Jan 01, 2023)2649399
19-13830285-C-G not specified Uncertain significance (Feb 22, 2023)2457551
19-13830299-G-A not specified Uncertain significance (Jul 15, 2021)2237941
19-13830334-T-C not specified Uncertain significance (Sep 23, 2023)3199534
19-13830336-G-C not specified Uncertain significance (Oct 30, 2024)3479498
19-13830344-C-T not specified Uncertain significance (Nov 01, 2021)2258601
19-13830345-C-T Likely benign (Jan 01, 2023)2649400
19-13830374-A-C not specified Uncertain significance (Nov 18, 2022)2393382
19-13830400-G-T not specified Uncertain significance (Jun 07, 2023)2558646
19-13830533-C-G not specified Uncertain significance (Jun 16, 2023)2604003
19-13830539-G-A not specified Uncertain significance (Nov 13, 2024)3479490
19-13830635-C-G not specified Uncertain significance (Jun 03, 2022)2294089
19-13830746-C-T not specified Uncertain significance (Sep 03, 2024)3479492
19-13830782-C-T not specified Uncertain significance (Dec 13, 2022)2334194
19-13830812-C-T not specified Uncertain significance (Dec 17, 2021)2323314
19-13830868-C-T not specified Uncertain significance (Aug 15, 2023)2592769
19-13830875-C-T not specified Uncertain significance (Dec 19, 2023)3199537

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP