LINC01564

long intergenic non-protein coding RNA 1564, the group of Long intergenic non-protein coding RNAs

Basic information

Region (hg38): 6:53614863-53707024

Links

ENSG00000235899NCBI:101927171HGNC:51361GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the LINC01564 gene.

  • Inborn genetic diseases (19 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the LINC01564 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
19
clinvar
19
Total 0 0 19 0 0

Variants in LINC01564

This is a list of pathogenic ClinVar variants found in the LINC01564 region.

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

Position Type Phenotype Significance ClinVar
6-53651681-A-G not specified Uncertain significance (Nov 22, 2022)2214068
6-53651708-C-T not specified Uncertain significance (Nov 14, 2023)3115664
6-53651794-A-G not specified Uncertain significance (Apr 24, 2024)3288986
6-53651807-G-A not specified Uncertain significance (Oct 10, 2023)3115663
6-53651878-G-T not specified Uncertain significance (Jul 06, 2021)2235141
6-53651920-T-C not specified Uncertain significance (Sep 29, 2023)3115662
6-53652043-T-A not specified Uncertain significance (Jan 16, 2024)3115660
6-53652071-C-A not specified Uncertain significance (Nov 30, 2022)2358193
6-53652083-A-G not specified Uncertain significance (Oct 12, 2021)2255143
6-53652118-G-A not specified Uncertain significance (Apr 23, 2024)3288989
6-53652181-G-C not specified Uncertain significance (Mar 16, 2022)2278529
6-53652221-T-C not specified Uncertain significance (Aug 02, 2022)2313282
6-53652258-G-T not specified Uncertain significance (Aug 28, 2023)2589895
6-53654162-C-T not specified Uncertain significance (Apr 28, 2023)2509919
6-53654303-G-A not specified Uncertain significance (Aug 09, 2021)2301918
6-53654318-C-T not specified Uncertain significance (Jun 10, 2024)3288987
6-53654329-C-G not specified Uncertain significance (Aug 16, 2021)2325242
6-53654350-C-T not specified Uncertain significance (Nov 22, 2022)2411465
6-53654399-T-C not specified Uncertain significance (Jan 30, 2024)3115670
6-53654402-C-T not specified Uncertain significance (Aug 04, 2023)2616526
6-53654408-C-T not specified Uncertain significance (May 14, 2024)3288990
6-53654545-A-C not specified Uncertain significance (Aug 02, 2021)3115669
6-53654573-A-G not specified Uncertain significance (Oct 20, 2023)3115668
6-53654607-A-C not specified Uncertain significance (Sep 01, 2021)2248159
6-53654762-T-C not specified Uncertain significance (Mar 25, 2024)3288988

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP