DUBR
Basic information
Region (hg38): 3:107220744-107462923
Previous symbols: [ "LINC00883" ]
Links
Phenotypes
GenCC
Source:
ClinVar
This is a list of variants' phenotypes submitted to
Variants pathogenicity by type
Statistics on ClinVar variants can assist in determining whether a specific variant type in the DUBR 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 DUBR
This is a list of pathogenic ClinVar variants found in the DUBR region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
3-107377612-G-T | not specified | Uncertain significance (Dec 17, 2021) | ||
3-107377645-A-G | not specified | Uncertain significance (Sep 17, 2021) | ||
3-107377674-A-C | not specified | Uncertain significance (Apr 06, 2022) | ||
3-107377699-C-T | not specified | Uncertain significance (Apr 22, 2022) | ||
3-107377825-C-T | not specified | Uncertain significance (Oct 29, 2021) | ||
3-107377856-T-G | not specified | Uncertain significance (Jun 09, 2022) | ||
3-107377871-A-G | not specified | Uncertain significance (Jan 23, 2024) | ||
3-107377921-A-C | not specified | Uncertain significance (May 27, 2022) | ||
3-107377945-T-C | not specified | Uncertain significance (Sep 17, 2021) | ||
3-107377982-A-C | not specified | Uncertain significance (Dec 12, 2023) | ||
3-107378000-A-G | not specified | Uncertain significance (Jan 04, 2022) | ||
3-107378039-C-T | not specified | Uncertain significance (Apr 19, 2024) | ||
3-107378072-G-T | not specified | Uncertain significance (Aug 30, 2022) | ||
3-107378095-C-T | not specified | Uncertain significance (Oct 27, 2022) | ||
3-107378123-T-C | not specified | Uncertain significance (Sep 09, 2021) | ||
3-107378254-C-T | not specified | Uncertain significance (Jul 12, 2023) | ||
3-107378280-C-G | not specified | Uncertain significance (Jan 31, 2024) | ||
3-107378290-G-A | not specified | Uncertain significance (Oct 13, 2021) | ||
3-107378345-T-C | not specified | Uncertain significance (Jun 29, 2022) | ||
3-107378503-A-T | not specified | Uncertain significance (Feb 06, 2024) | ||
3-107378533-G-A | not specified | Uncertain significance (Jul 14, 2022) | ||
3-107378537-T-G | not specified | Uncertain significance (Jun 23, 2023) | ||
3-107378560-G-A | not specified | Uncertain significance (Jan 04, 2022) |
GnomAD
Source:
dbNSFP
Source:
Mouse Genome Informatics
- Gene name
- Dubr
- Phenotype