LMCD1-AS1

LMCD1 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 3:7951263-8611961

Links

ENSG00000227110NCBI:100288428HGNC:44477GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the LMCD1-AS1 gene.

  • Inborn genetic diseases (22 variants)
  • not provided (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the LMCD1-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
0
non coding
22
clinvar
1
clinvar
23
Total 0 0 22 1 0

Variants in LMCD1-AS1

This is a list of pathogenic ClinVar variants found in the LMCD1-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
3-8532757-G-T not specified Uncertain significance (Oct 25, 2024)3119256
3-8532765-G-C not specified Uncertain significance (Sep 09, 2021)3119257
3-8532792-G-A not specified Uncertain significance (Jun 05, 2024)3290910
3-8532794-A-G not specified Uncertain significance (Jul 09, 2021)2235689
3-8532809-G-A not specified Uncertain significance (Nov 14, 2024)3538646
3-8537252-C-T not specified Uncertain significance (Sep 27, 2021)2385566
3-8537262-G-C not specified Uncertain significance (Aug 02, 2021)2213071
3-8537265-G-A not specified Uncertain significance (Aug 05, 2024)3538642
3-8537303-C-G not specified Uncertain significance (Sep 08, 2024)3538647
3-8537303-C-T not specified Uncertain significance (Feb 13, 2024)3119252
3-8537321-G-A not specified Uncertain significance (Dec 03, 2024)3538641
3-8537327-C-T not specified Uncertain significance (Apr 20, 2023)2535630
3-8537345-C-T not specified Uncertain significance (Apr 17, 2023)2537185
3-8537407-C-T Likely benign (Jan 01, 2023)2653466
3-8548572-T-C not specified Uncertain significance (Jun 29, 2023)2608428
3-8548606-G-T not specified Uncertain significance (Dec 06, 2024)2225774
3-8548619-A-C not specified Uncertain significance (Dec 05, 2022)2332787
3-8548620-C-T not specified Uncertain significance (Nov 07, 2023)3119253
3-8548638-G-A not specified Uncertain significance (Jun 28, 2024)3538643
3-8548640-C-T not specified Uncertain significance (Dec 12, 2023)3119254
3-8548665-C-T not specified Uncertain significance (Jul 09, 2024)3538644
3-8548694-C-T not specified Uncertain significance (Apr 27, 2023)2541396
3-8548695-G-A not specified Uncertain significance (May 09, 2023)2511189
3-8548695-G-C not specified Uncertain significance (May 24, 2023)2551045
3-8548722-T-A not specified Uncertain significance (Jan 23, 2023)2477341

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP