FARSA-AS1

FARSA antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 19:12930522-12933296

Links

ENSG00000266975HGNC:50479GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

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

  • Inborn genetic diseases (1 variants)

Variants pathogenicity by type

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

Variants in FARSA-AS1

This is a list of pathogenic ClinVar variants found in the FARSA-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
19-12930653-G-A Rajab interstitial lung disease with brain calcifications 2 Uncertain significance (Jun 02, 2022)3068613
19-12930683-G-A not specified Uncertain significance (Dec 15, 2023)3092913
19-12930727-G-A not specified Uncertain significance (Oct 02, 2023)3092912
19-12930737-C-T not specified Uncertain significance (Apr 12, 2023)2536414
19-12930743-C-T not specified Uncertain significance (Oct 01, 2024)3513090

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP