PAXBP1-AS1

PAXBP1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 21:32728079-32747065

Previous symbols: [ "GCFC1-AS1" ]

Links

ENSG00000238197NCBI:100506215HGNC:39603GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the PAXBP1-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the PAXBP1-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
6
clinvar
2
clinvar
1
clinvar
9
Total 0 0 6 2 1

Variants in PAXBP1-AS1

This is a list of pathogenic ClinVar variants found in the PAXBP1-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
21-32728196-C-T Likely benign (Feb 13, 2020)1202487
21-32734996-C-T not specified Uncertain significance (May 06, 2022)2287864
21-32737332-C-G not specified Uncertain significance (Nov 09, 2023)3209001
21-32738186-T-C not specified Uncertain significance (Sep 16, 2021)2250886
21-32743263-A-C not specified Uncertain significance (Aug 04, 2023)2615965
21-32743320-T-TA Likely benign (Sep 01, 2022)2652603
21-32743731-C-G not specified Uncertain significance (Feb 28, 2024)3208999
21-32744811-G-T not specified Uncertain significance (Dec 23, 2024)3886005
21-32744819-T-G Benign (Sep 19, 2018)777615
21-32745640-T-G not specified Uncertain significance (Dec 12, 2024)3886001
21-32745713-T-G not specified Uncertain significance (May 17, 2023)2546933

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP