MAP3K14-AS1

MAP3K14 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 17:45247905-45269836

Links

ENSG00000267278 ∙ NCBI:100133991 ∙ ∙ HGNC:44359 ∙ ∙ ∙ 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 MAP3K14-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MAP3K14-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				1	1	2
non coding			108	69	5	182
Total	0	0	108	69	5

Variants in MAP3K14-AS1

This is a list of pathogenic ClinVar variants found in the MAP3K14-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
17-45254488-C-T		not specified	Uncertain significance (Sep 10, 2024)
17-45255208-C-T		not specified	Uncertain significance (Dec 10, 2024)
17-45255213-G-T		not specified	Uncertain significance (Jul 12, 2022)
17-45255322-C-T		not specified	Likely benign (Nov 21, 2024)
17-45255338-T-C		not specified	Uncertain significance (Feb 12, 2024)
17-45255347-G-A		not specified	Uncertain significance (Feb 16, 2023)
17-45255350-C-G		not specified	Uncertain significance (Aug 20, 2024)
17-45255374-G-C		not specified	Uncertain significance (Aug 02, 2022)
17-45255392-T-A		not specified	Uncertain significance (Sep 11, 2024)
17-45255406-G-A		not specified	Uncertain significance (Jun 29, 2023)
17-45255409-A-G		not specified	Uncertain significance (Sep 11, 2024)
17-45255430-G-A		not specified	Uncertain significance (May 09, 2024)
17-45255542-A-T		not specified	Uncertain significance (Aug 12, 2021)
17-45255572-C-T		not specified	Likely benign (Dec 15, 2022)
17-45255599-C-G		not specified	Uncertain significance (Nov 20, 2024)
17-45255623-G-C		not specified	Uncertain significance (Mar 28, 2023)
17-45255662-C-T		not specified	Uncertain significance (Aug 26, 2024)
17-45255704-C-A		not specified	Uncertain significance (Nov 13, 2023)
17-45255716-G-A		not specified	Uncertain significance (Nov 20, 2023)
17-45255772-G-A		not specified	Uncertain significance (Dec 03, 2024)
17-45255779-T-G		not specified	Uncertain significance (Jan 24, 2024)
17-45255781-C-T		not specified	Uncertain significance (Dec 06, 2021)
17-45255805-G-T		not specified	Likely benign (Aug 22, 2023)
17-45255848-C-T		not specified	Uncertain significance (Jun 16, 2023)
17-45255888-G-C		not specified	Uncertain significance (Sep 01, 2021)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP