GeneBe

PRR7-AS1

PRR7 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 5:177433655-177455513

Links

ENSG00000246334 ∙ NCBI:340037 ∙ ∙ HGNC:27961 ∙ ∙ ∙ 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 PRR7-AS1 gene.

  • Inborn genetic diseases (6 variants)
  • not provided (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the PRR7-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
4
clinvar
3
clinvar
 7
Total 0 0 4 3 0

Variants in PRR7-AS1

This is a list of pathogenic ClinVar variants found in the PRR7-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
5-177434040-G-A not specified Uncertain significance (Feb 21, 2024)3102623
5-177435092-A-G not specified Uncertain significance (Dec 12, 2023)3102618
5-177436090-A-G not specified Uncertain significance (May 09, 2024)3282849
5-177436109-G-C not specified Uncertain significance (Feb 22, 2025)2360560
5-177436211-G-A not specified Uncertain significance (Jan 21, 2025)3855897
5-177436246-C-T not specified Uncertain significance (Sep 04, 2024)3522829
5-177436251-T-G not specified Uncertain significance (Dec 31, 2024)3855898
5-177436407-C-A not specified Uncertain significance (Nov 11, 2024)3522834
5-177436429-C-T not specified Uncertain significance (Nov 09, 2024)3522830
5-177436513-C-T not specified Uncertain significance (Nov 24, 2024)3522836
5-177440749-C-T not specified Uncertain significance (Nov 24, 2024)3522835
5-177440764-A-T not specified Uncertain significance (Apr 07, 2022)2206787
5-177440830-A-G not specified Uncertain significance (Jan 18, 2022)2272053
5-177440931-G-A not specified Uncertain significance (Nov 08, 2024)3522833
5-177440973-G-C not specified Uncertain significance (Dec 15, 2023)3102619
5-177441049-G-A not specified Uncertain significance (May 23, 2023)2549815
5-177441053-A-G Likely benign (May 01, 2022)2656121
5-177441758-G-A not specified Likely benign (Aug 20, 2024)3522831
5-177441763-C-T not specified Likely benign (Dec 21, 2022)2338283
5-177441764-G-A not specified Likely benign (Jun 22, 2023)2600793
5-177441778-C-T not specified Uncertain significance (Oct 10, 2023)3102621
5-177441823-G-A not specified Uncertain significance (Jul 28, 2021)2379018
5-177455140-G-C not specified Uncertain significance (Jan 03, 2024)3219559
5-177455185-C-T not specified Uncertain significance (Mar 16, 2022)2278537
5-177455266-G-A not specified Uncertain significance (Jan 03, 2024)3219555

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP