ANKRD34C-AS1

ANKRD34C antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 15:79123546-79283967

Links

ENSG00000259234 ∙ NCBI:729911 ∙ ∙ HGNC:48618 ∙ ∙ ∙ 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 ANKRD34C-AS1 gene.

• not provided (6 variants)
• EDICT syndrome (1 variants)
• Developmental cataract (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ANKRD34C-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	1		1	1	5	8
Total	1	0	1	1	5

Variants in ANKRD34C-AS1

This is a list of pathogenic ClinVar variants found in the ANKRD34C-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
15-79209525-T-G			Benign (Jul 09, 2018)
15-79209754-G-C			Benign (Jul 09, 2018)
15-79209778-T-C			Likely benign (Feb 14, 2019)
15-79209826-G-T			Benign (Jan 18, 2024)
15-79209839-T-C		Developmental cataract • MIR184-related disorder	Uncertain significance (Feb 13, 2024)
15-79209842-G-A			Likely benign (Nov 28, 2023)
15-79209844-C-T		EDICT syndrome	Pathogenic (Jan 25, 2012)
15-79209980-T-C			Benign (Jul 14, 2018)
15-79210027-G-C			Benign (Jul 09, 2018)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP