SLFNL1-AS1

SLFNL1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 1:41014590-41043890

Links

ENSG00000281207NCBI:100507178HGNC:44126GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the SLFNL1-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the SLFNL1-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
1
1
non coding
65
clinvar
5
clinvar
70
Total 0 0 65 5 0

Variants in SLFNL1-AS1

This is a list of pathogenic ClinVar variants found in the SLFNL1-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
1-41016132-C-T not specified Likely benign (Mar 25, 2024)3320480
1-41016168-C-G not specified Uncertain significance (Aug 04, 2024)3445562
1-41016171-T-C not specified Uncertain significance (Aug 04, 2024)3445558
1-41016185-G-A not specified Likely benign (Aug 13, 2021)2376249
1-41016196-C-A not specified Uncertain significance (Dec 07, 2024)3445567
1-41017288-G-T not specified Uncertain significance (Aug 02, 2022)2382692
1-41017290-C-T not specified Uncertain significance (Nov 28, 2024)2361901
1-41017292-C-T not specified Uncertain significance (May 15, 2024)3320479
1-41017295-C-T not specified Uncertain significance (Mar 02, 2023)2493554
1-41017326-A-G not specified Uncertain significance (Jun 07, 2023)2559203
1-41017370-C-T not specified Uncertain significance (Jun 17, 2024)3320474
1-41017647-G-T not specified Uncertain significance (May 17, 2023)2546843
1-41017691-A-G not specified Uncertain significance (Jul 14, 2024)3445563
1-41017736-C-A not specified Uncertain significance (Apr 07, 2022)2394437
1-41017754-G-A not specified Uncertain significance (Jun 30, 2023)2591103
1-41017784-C-T not specified Uncertain significance (Feb 03, 2022)2275402
1-41017802-C-T not specified Uncertain significance (Mar 04, 2024)3165998
1-41017805-C-T not specified Uncertain significance (Jul 09, 2024)3445560
1-41017814-C-T not specified Uncertain significance (Nov 03, 2023)3165997
1-41017829-C-T not specified Uncertain significance (Jan 19, 2024)2349606
1-41017846-G-A not specified Uncertain significance (May 14, 2024)3320475
1-41017853-C-T not specified Uncertain significance (Oct 20, 2023)3165996
1-41017859-G-A not specified Uncertain significance (Oct 05, 2021)2401020
1-41017895-C-T not specified Uncertain significance (Dec 14, 2023)3165995
1-41017898-C-T not specified Uncertain significance (Mar 14, 2023)2459977

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP