DDIT4-AS1

DDIT4 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 10:72271272-72298146

Links

ENSG00000289506HGNC:52379GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the DDIT4-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the DDIT4-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
0
Total 0 0 0 0 0

Variants in DDIT4-AS1

This is a list of pathogenic ClinVar variants found in the DDIT4-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
10-72274223-A-G not specified Uncertain significance (Feb 28, 2024)3080770
10-72274226-C-T not specified Uncertain significance (Jan 22, 2024)3080765
10-72274227-T-C not specified Uncertain significance (Jun 14, 2023)2560229
10-72274292-C-T not specified Uncertain significance (Jun 16, 2023)2600336
10-72274298-C-T not specified Uncertain significance (Apr 19, 2023)2516932
10-72274359-G-T not specified Uncertain significance (Apr 19, 2024)3271203
10-72274371-C-T not specified Uncertain significance (Mar 30, 2024)3271202
10-72274707-T-C not specified Uncertain significance (Oct 24, 2024)3500291
10-72274733-G-C not specified Uncertain significance (May 18, 2022)3080766
10-72274765-G-C not specified Uncertain significance (Mar 19, 2024)3271204
10-72274773-A-G not specified Uncertain significance (Jul 26, 2021)2399785
10-72274812-G-A not specified Uncertain significance (May 08, 2024)3271201
10-72274827-G-T not specified Uncertain significance (Jul 09, 2021)2235667
10-72274846-G-T not specified Uncertain significance (Oct 21, 2024)3500290
10-72274886-C-T not specified Uncertain significance (Aug 02, 2021)2240568
10-72274902-A-G not specified Uncertain significance (Jan 04, 2024)3080768
10-72274931-G-A not specified Uncertain significance (Jan 30, 2025)3838754
10-72274935-T-C not specified Uncertain significance (Nov 13, 2024)2284055
10-72274949-G-A not specified Uncertain significance (Jul 14, 2022)2401869
10-72274955-A-G not specified Uncertain significance (Dec 08, 2023)3080769
10-72274966-C-G not specified Uncertain significance (Jul 20, 2021)2238649
10-72275070-G-T not specified Uncertain significance (Aug 15, 2023)2618548
10-72275183-T-C not specified Uncertain significance (Jan 23, 2023)2469677

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP