GeneBe

CFLAR-AS1

CFLAR antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 2:201140278-201157823

Previous symbols: [ "ALS2CR10" ]

Links

ENSG00000226312 ∙ NCBI:65072 ∙ ∙ HGNC:14437 ∙ ∙ ∙ 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 CFLAR-AS1 gene.

  • Inborn genetic diseases (3 variants)
  • not provided (1 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the CFLAR-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
2
clinvar
1
clinvar
1
clinvar
 4
Total 0 0 2 1 1

Variants in CFLAR-AS1

This is a list of pathogenic ClinVar variants found in the CFLAR-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
2-201140403-C-G not specified Uncertain significance (Dec 06, 2022)2214824
2-201140405-A-C not specified Likely benign (Aug 19, 2023)2619452
2-201145378-C-A Benign (Feb 16, 2018)783347
2-201145426-G-A not specified Likely benign (Mar 16, 2024)3266617
2-201145430-A-T not specified Uncertain significance (Aug 30, 2022)2309532

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP