RSL1D1-DT

RSL1D1 divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 16:11851613-11907490

Links

ENSG00000263307 ∙ NCBI:105371084 ∙ ∙ HGNC:55337 ∙ ∙ ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the RSL1D1-DT gene.

• Inborn genetic diseases (17 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the RSL1D1-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			17			17
Total	0	0	17	0	0

Variants in RSL1D1-DT

This is a list of pathogenic ClinVar variants found in the RSL1D1-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
16-11873133-G-A		not specified	Uncertain significance (Dec 20, 2023)
16-11875857-G-C		not specified	Uncertain significance (Aug 20, 2023)
16-11876132-T-C		not specified	Uncertain significance (Sep 07, 2022)
16-11877414-T-C		not specified	Uncertain significance (Nov 21, 2022)
16-11883080-C-T		not specified	Uncertain significance (May 27, 2022)
16-11886558-T-C		not specified	Uncertain significance (Mar 31, 2024)
16-11886782-A-T		not specified	Uncertain significance (May 25, 2022)
16-11887682-C-T		not specified	Uncertain significance (Apr 25, 2023)
16-11891110-G-A		not specified	Uncertain significance (Sep 28, 2022)
16-11891126-T-C		not specified	Uncertain significance (Mar 07, 2024)
16-11896591-C-G		not specified	Uncertain significance (Dec 15, 2023)
16-11896611-G-A		not specified	Uncertain significance (Jan 16, 2024)
16-11896620-A-G		not specified	Uncertain significance (Jan 04, 2022)
16-11896639-T-C		not specified	Uncertain significance (May 08, 2024)
16-11896676-C-G		not specified	Uncertain significance (May 28, 2024)
16-11896677-T-C		not specified	Uncertain significance (May 25, 2022)
16-11896699-A-T		not specified	Uncertain significance (Oct 25, 2022)
16-11896705-C-G		not specified	Uncertain significance (Jul 06, 2022)
16-11896708-C-A		not specified	Uncertain significance (Feb 15, 2023)
16-11896759-G-T		not specified	Uncertain significance (Apr 06, 2023)
16-11897876-T-C		not specified	Uncertain significance (Aug 04, 2023)
16-11898032-G-C		not specified	Uncertain significance (Jan 23, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP