LINC01847

long intergenic non-protein coding RNA 1847, the group of Long intergenic non-protein coding RNAs

Basic information

Region (hg38): 5:159698584-159937766

Links

ENSG00000253311 ∙ NCBI:101927766 ∙ ∙ HGNC:52662 ∙ ∙ ∙ 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 LINC01847 gene.

• Inborn genetic diseases (6 variants)
• not provided (2 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the LINC01847 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			6	2		8
Total	0	0	6	2	0

Variants in LINC01847

This is a list of pathogenic ClinVar variants found in the LINC01847 region.

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

Position	Type	Phenotype	Significance	ClinVar
5-159916930-C-T		not specified	Uncertain significance (May 10, 2022)
5-159916960-G-C		not specified	Uncertain significance (Oct 25, 2023)
5-159916976-A-C		not specified	Uncertain significance (Nov 10, 2022)
5-159916983-T-C			Likely benign (Feb 01, 2023)
5-159917042-T-C		not specified	Uncertain significance (Jun 16, 2024)
5-159917083-A-G		not specified	Uncertain significance (Apr 24, 2023)
5-159917327-T-C		not specified	Uncertain significance (Mar 20, 2023)
5-159917380-C-G		not specified	Uncertain significance (Nov 18, 2022)
5-159917449-C-A		not specified	Uncertain significance (Apr 20, 2023)
5-159917462-A-G		not specified	Uncertain significance (Dec 09, 2023)
5-159917734-A-C		not specified	Uncertain significance (Dec 12, 2023)
5-159917805-C-G			Likely benign (Feb 01, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP