RPL9P16

ribosomal protein L9 pseudogene 16

Basic information

Region (hg38): 4:168755816-168756382

Links

ENSG00000214676NCBI:727835HGNC:36851GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the RPL9P16 gene.

  • Pancreatic adenocarcinoma (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the RPL9P16 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
clinvar
1
clinvar
2
Total 0 0 1 0 1

Variants in RPL9P16

This is a list of pathogenic ClinVar variants found in the RPL9P16 region.

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

Position Type Phenotype Significance ClinVar
4-168756240-CA-TG Pancreatic adenocarcinoma Uncertain significance (Dec 16, 2023)998866
4-168756241-A-G Pancreatic adenocarcinoma Benign (Jan 29, 2024)1164338

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP