BRD10

Basic information

Region (hg38): 9:5881596-6008482

Links

ENSG00000183354HGNC:23378GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the BRD10 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the BRD10 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 BRD10

This is a list of pathogenic ClinVar variants found in the BRD10 region.

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

Position Type Phenotype Significance ClinVar
9-5892542-C-A not specified Uncertain significance (Nov 08, 2021)2259217
9-5892542-C-T not specified Uncertain significance (Nov 21, 2022)2400602
9-5897609-G-A not specified Uncertain significance (Oct 04, 2024)3396504
9-5897618-T-C not specified Uncertain significance (Aug 02, 2021)2406025
9-5906925-G-C not specified Uncertain significance (Jun 25, 2024)3396505
9-5906947-T-G not specified Likely benign (Jun 21, 2022)2295667
9-5906952-A-T not specified Uncertain significance (Sep 20, 2024)2244648
9-5908647-A-G not specified Uncertain significance (Mar 05, 2024)3192758
9-5919718-G-A not specified Uncertain significance (May 18, 2022)2401324
9-5919734-G-A not specified Uncertain significance (May 20, 2024)2204359
9-5919736-A-C not specified Uncertain significance (Dec 18, 2023)2378463
9-5919748-G-C not specified Uncertain significance (Feb 10, 2022)2404062
9-5919754-C-T not specified Uncertain significance (Oct 27, 2021)2351729
9-5919769-A-G not specified Uncertain significance (Mar 29, 2022)2280060
9-5919782-G-A not specified Uncertain significance (Oct 20, 2023)3235686
9-5919788-G-C not specified Uncertain significance (May 20, 2024)2205594
9-5919793-A-T not specified Uncertain significance (Jun 17, 2024)3261671
9-5919817-G-A not specified Uncertain significance (Nov 07, 2024)3482243
9-5919820-T-C not specified Uncertain significance (Feb 13, 2024)3235685
9-5919869-C-T not specified Uncertain significance (Nov 17, 2022)2259963
9-5919880-A-C not specified Uncertain significance (Nov 17, 2022)3235684
9-5919913-G-A not specified Uncertain significance (May 24, 2023)2551672
9-5919920-T-C not specified Uncertain significance (Aug 16, 2022)3235683
9-5919939-C-A not specified Uncertain significance (Mar 06, 2023)2494761
9-5919943-G-C not specified Uncertain significance (Jun 03, 2022)2347767

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP