SF1-DT

SF1 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 11:64778085-64779405

Links

ENSG00000269038HGNC:55278GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the SF1-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the SF1-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 SF1-DT

This is a list of pathogenic ClinVar variants found in the SF1-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
11-64778088-G-A not specified Uncertain significance (Sep 16, 2021)3160788
11-64778097-G-A not specified Uncertain significance (Jun 17, 2022)2410395
11-64778098-G-A not specified Uncertain significance (Apr 19, 2024)3317813
11-64778103-G-A not specified Uncertain significance (Aug 16, 2021)2245360
11-64778106-T-C not specified Uncertain significance (Sep 30, 2024)2397062
11-64778122-A-C not specified Uncertain significance (Mar 07, 2023)2495184
11-64778146-G-A not specified Uncertain significance (Nov 06, 2023)3160787
11-64778161-G-A not specified Uncertain significance (Nov 28, 2024)3440345
11-64778166-G-A not specified Uncertain significance (Apr 07, 2022)2281467
11-64778221-C-T not specified Uncertain significance (Aug 11, 2024)2382176
11-64778223-C-G not specified Uncertain significance (Dec 01, 2022)2331558
11-64778308-C-G not specified Uncertain significance (Aug 15, 2023)2601317
11-64778338-G-A not specified Uncertain significance (Dec 28, 2023)3160792
11-64778375-G-C not specified Uncertain significance (Aug 17, 2021)2246351
11-64778375-G-T not specified Uncertain significance (Feb 28, 2023)2457753

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP