LINC01226

long intergenic non-protein coding RNA 1226, the group of Long intergenic non-protein coding RNAs

Basic information

Region (hg38): 1:31506209-31583306

Links

ENSG00000284543NCBI:284551HGNC:49678GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the LINC01226 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the LINC01226 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 LINC01226

This is a list of pathogenic ClinVar variants found in the LINC01226 region.

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

Position Type Phenotype Significance ClinVar
1-31577156-G-A not specified Uncertain significance (Nov 08, 2024)3456674
1-31577204-C-T not specified Uncertain significance (Jun 27, 2022)2408637
1-31577215-C-G not specified Uncertain significance (Feb 12, 2024)3177604
1-31577231-G-A not specified Uncertain significance (Jun 05, 2023)2524213
1-31577232-C-T Likely benign (Jul 10, 2018)749342
1-31577270-G-A not specified Uncertain significance (Sep 30, 2021)2366975
1-31577276-C-T not specified Uncertain significance (Sep 01, 2021)2386335
1-31577281-G-A not specified Uncertain significance (Sep 22, 2022)2250089
1-31577284-C-T not specified Uncertain significance (Apr 18, 2023)2538446
1-31577285-G-A not specified Uncertain significance (Jan 09, 2024)3177599
1-31577326-G-A not specified Uncertain significance (Sep 10, 2024)3456672
1-31577329-G-T not specified Uncertain significance (Oct 06, 2021)2253394
1-31577339-T-G not specified Uncertain significance (Jul 25, 2024)2215544
1-31577437-C-T not specified Uncertain significance (Aug 12, 2021)2342601
1-31579222-G-A not specified Uncertain significance (Dec 17, 2023)3177601
1-31579228-A-C not specified Uncertain significance (Oct 26, 2024)2387576
1-31579228-A-T not specified Uncertain significance (Apr 18, 2024)3326201
1-31579249-G-T not specified Uncertain significance (May 26, 2024)3326204
1-31583162-A-G not specified Uncertain significance (Mar 14, 2023)2469071
1-31583228-C-G not specified Uncertain significance (Oct 03, 2022)3177602

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP