KRTAP5-AS1

KRTAP5-1/KRTAP5-2 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 11:1571353-1620791

Links

ENSG00000233930 ∙ NCBI:338651 ∙ ∙ HGNC:27877 ∙ ∙ ∙ 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 KRTAP5-AS1 gene.

• Inborn genetic diseases (27 variants)
• not provided (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the KRTAP5-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			27	1		28
Total	0	0	27	1	0

Variants in KRTAP5-AS1

This is a list of pathogenic ClinVar variants found in the KRTAP5-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
11-1584559-C-T		not specified	Uncertain significance (Jan 26, 2022)
11-1584579-G-A		not specified	Uncertain significance (Jul 28, 2021)
11-1584580-C-A		not specified	Uncertain significance (Oct 26, 2022)
11-1584580-C-T		not specified	Uncertain significance (Aug 17, 2022)
11-1584595-T-C		not specified	Uncertain significance (Dec 16, 2022)
11-1584631-C-T		not specified	Likely benign (Jan 10, 2022)
11-1584675-C-A		not specified	Uncertain significance (Apr 18, 2023)
11-1584688-C-T		not specified	Uncertain significance (Jan 31, 2023)
11-1584754-C-A		not specified	Uncertain significance (Nov 02, 2023)
11-1584781-A-G		not specified	Uncertain significance (May 03, 2023)
11-1584862-A-G		not specified	Uncertain significance (Jul 17, 2023)
11-1584886-C-T		not specified	Uncertain significance (Sep 29, 2022)
11-1584931-C-G		not specified	Uncertain significance (May 06, 2024)
11-1584987-C-T		not specified	Uncertain significance (Apr 07, 2022)
11-1585021-C-G		not specified	Uncertain significance (Aug 15, 2023)
11-1585044-C-T		not specified	Uncertain significance (Aug 13, 2021)
11-1585086-C-T		not specified	Uncertain significance (Aug 11, 2022)
11-1585095-A-C		not specified	Uncertain significance (Jul 25, 2023)
11-1585096-C-T		not specified	Uncertain significance (Jun 16, 2024)
11-1585114-C-T		not specified	Uncertain significance (Apr 12, 2022)
11-1585146-C-T		not specified	Uncertain significance (Mar 31, 2022)
11-1585151-AGAGCCACAGCCCCCACAGCCG-A			Likely benign (Feb 01, 2023)
11-1585183-C-T		not specified	Uncertain significance (Sep 17, 2021)
11-1585186-C-G		not specified	Uncertain significance (Aug 02, 2021)
11-1585203-C-G		not specified	Uncertain significance (Jun 02, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP