SOCS3-DT

SOCS3 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 17:78357451-78374619

Links

ENSG00000266970NCBI:101928674HGNC:52799GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the SOCS3-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the SOCS3-DT 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 SOCS3-DT

This is a list of pathogenic ClinVar variants found in the SOCS3-DT region.

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

Position Type Phenotype Significance ClinVar
17-78358464-G-A not specified Uncertain significance (Mar 11, 2024)3167400
17-78358474-T-A not specified Uncertain significance (May 15, 2023)2514300
17-78358485-T-C not specified Uncertain significance (Jun 26, 2023)2600153
17-78358507-C-T not specified Uncertain significance (Jan 21, 2025)3799765
17-78358654-G-A not specified Uncertain significance (Nov 09, 2023)3167399
17-78358665-G-A not specified Uncertain significance (May 03, 2023)2543364
17-78358675-T-C not specified Uncertain significance (Jan 31, 2023)2480120
17-78358688-G-T not specified Benign (May 04, 2022)1686332
17-78358758-G-A not specified Uncertain significance (Apr 08, 2024)3321395
17-78358773-G-A not specified Uncertain significance (Apr 09, 2024)3321398
17-78358833-G-C not specified Uncertain significance (Aug 20, 2024)3447100
17-78358948-C-T not specified Uncertain significance (Mar 30, 2024)3321396
17-78358968-T-C not specified Uncertain significance (Oct 03, 2022)2315483
17-78358971-T-C not specified Uncertain significance (Oct 06, 2021)2348931
17-78358987-C-T not specified Uncertain significance (Mar 30, 2024)3321397
17-78359019-C-T not specified Uncertain significance (May 13, 2024)2374348

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP