FAM170B-AS1

FAM170B antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 10:49121834-49151555

Links

ENSG00000234736 ∙ NCBI:100506733 ∙ ∙ HGNC:45006 ∙ ∙ ∙ 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 FAM170B-AS1 gene.

• Inborn genetic diseases (21 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the FAM170B-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			18	3		21
Total	0	0	18	3	0

Variants in FAM170B-AS1

This is a list of pathogenic ClinVar variants found in the FAM170B-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
10-49131624-C-T		not specified	Likely benign (May 14, 2024)
10-49131646-C-G		not specified	Uncertain significance (Sep 01, 2021)
10-49131647-T-G		not specified	Uncertain significance (Jul 15, 2024)
10-49131648-C-T		not specified	Likely benign (Mar 23, 2022)
10-49131662-G-A		not specified	Uncertain significance (Apr 25, 2022)
10-49131665-C-T		not specified	Uncertain significance (May 15, 2024)
10-49131671-C-T		not specified	Uncertain significance (Mar 07, 2023)
10-49131684-G-T		not specified	Uncertain significance (Dec 05, 2022)
10-49131716-G-A		not specified	Uncertain significance (Sep 06, 2022)
10-49131731-C-T		not specified	Uncertain significance (Aug 10, 2021)
10-49131786-T-A		not specified	Uncertain significance (Dec 19, 2022)
10-49131846-C-T		not specified	Uncertain significance (Feb 06, 2023)
10-49131878-C-G		not specified	Uncertain significance (Apr 01, 2024)
10-49131896-A-G		not specified	Uncertain significance (Apr 01, 2024)
10-49131905-A-C		not specified	Uncertain significance (Jun 23, 2023)
10-49131909-A-G		not specified	Uncertain significance (Feb 14, 2023)
10-49131944-C-T		not specified	Uncertain significance (Jan 30, 2024)
10-49131949-G-C		not specified	Uncertain significance (Aug 28, 2023)
10-49131966-C-T		not specified	Uncertain significance (Sep 16, 2021)
10-49132031-T-A		not specified	Uncertain significance (Feb 10, 2022)
10-49132073-G-A		not specified	Uncertain significance (Sep 22, 2023)
10-49132128-C-T		not specified	Uncertain significance (Aug 08, 2023)
10-49132133-G-A		not specified	Uncertain significance (Jun 26, 2024)
10-49132142-G-A		not specified	Uncertain significance (Aug 16, 2021)
10-49132176-C-T		not specified	Uncertain significance (Feb 10, 2023)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP