MTNAP1

Basic information

Region (hg38): 17:73232233-73248959

Links

ENSG00000141219 ∙ ∙ ∙ HGNC:29601 ∙ ∙ ∙ 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 MTNAP1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MTNAP1 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						0
Total	0	0	0	0	0

Variants in MTNAP1

This is a list of pathogenic ClinVar variants found in the MTNAP1 region.

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

Position	Type	Phenotype	Significance	ClinVar
17-73232245-G-A		not specified	Uncertain significance (Oct 06, 2021)
17-73232258-T-G		not specified	Uncertain significance (Dec 06, 2022)
17-73232261-G-A		not specified	Uncertain significance (Oct 29, 2021)
17-73232296-C-G		not specified	Uncertain significance (Mar 22, 2022)
17-73236149-G-A		not specified	Uncertain significance (Jun 23, 2021)
17-73236243-G-A		not specified	Uncertain significance (Jun 22, 2021)
17-73236455-C-T		Malignant tumor of prostate	Uncertain significance (-)
17-73236717-C-T		not specified	Uncertain significance (Jun 23, 2021)
17-73236797-A-G		not specified	Likely benign (Nov 09, 2021)
17-73242937-G-A		not specified	Uncertain significance (Oct 12, 2021)
17-73247312-G-A		not specified	Uncertain significance (Jul 06, 2021)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP