DERPC

DERPC proline and glycine rich nuclear protein

Basic information

Region (hg38): 16:69118010-69132588

Links

ENSG00000286140 ∙ NCBI:113455421 ∙ ∙ HGNC:54084 ∙ Uniprot:P0CG12 ∙ AlphaFold ∙ 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 DERPC gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the DERPC 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				1		1
missense				1		1
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding			9			9
Total	0	0	9	2	0

Variants in DERPC

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

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

Position	Type	Phenotype	Significance	ClinVar
16-69119240-T-G			Likely benign (Feb 01, 2023)
16-69119610-G-A			Likely benign (Apr 01, 2022)
16-69120466-G-A		not specified	Uncertain significance (Jun 09, 2022)
16-69120471-T-G		not specified	Uncertain significance (May 29, 2024)
16-69120514-G-A		not specified	Uncertain significance (Dec 02, 2022)
16-69120528-C-T		not specified	Uncertain significance (Dec 17, 2021)
16-69120529-G-T		not specified	Uncertain significance (Sep 01, 2021)
16-69120590-C-G		not specified	Uncertain significance (Nov 03, 2023)
16-69120613-A-G		not specified	Uncertain significance (Jan 20, 2023)
16-69121096-C-T		not specified	Uncertain significance (Jan 23, 2024)
16-69121109-G-A		not specified	Uncertain significance (Nov 30, 2022)
16-69121111-G-A		not specified	Uncertain significance (Nov 30, 2022)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP