FAM151B-DT

FAM151B divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 5:80411231-80488101

Links

ENSG00000249042 ∙ ∙ ∙ HGNC:55578 ∙ ∙ ∙ 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 FAM151B-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the FAM151B-DT 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	84	9	4	98
Total	0	1	84	9	4

Variants in FAM151B-DT

This is a list of pathogenic ClinVar variants found in the FAM151B-DT region.

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

Position	Type	Phenotype	Significance	ClinVar
5-80434209-A-G		not specified	Uncertain significance (May 15, 2024)
5-80436812-G-A			Benign (Jun 10, 2018)
5-80436840-G-A		not specified	Uncertain significance (Nov 07, 2023)
5-80436845-T-C		not specified	Uncertain significance (Sep 04, 2024)
5-80436872-G-A		not specified	Likely benign (Apr 27, 2022)
5-80436882-G-T		not specified	Uncertain significance (Nov 17, 2022)
5-80436903-A-G		not specified	Likely benign (May 05, 2023)
5-80436935-A-G		not specified	Uncertain significance (Jun 23, 2023)
5-80437014-C-A		not specified	Uncertain significance (Nov 25, 2024)
5-80437047-G-A		not specified	Uncertain significance (Nov 17, 2023)
5-80437140-A-G		not specified	Uncertain significance (Dec 28, 2022)
5-80437163-T-G		not specified	Uncertain significance (Aug 07, 2024)
5-80437187-T-C		not specified	Uncertain significance (Aug 09, 2021)
5-80437341-A-G		not specified	Likely benign (Sep 19, 2023)
5-80437434-G-A			Benign (Jun 10, 2018)
5-80437449-T-C		not specified	Uncertain significance (Jul 19, 2022)
5-80437491-G-A		not specified	Uncertain significance (Feb 27, 2024)
5-80437543-C-T			Likely benign (Jun 01, 2023)
5-80437553-G-A		not specified	Likely benign (Nov 22, 2022)
5-80437574-G-A		not specified	Uncertain significance (Jan 04, 2024)
5-80437605-C-T		not specified	Uncertain significance (Jul 21, 2021)
5-80437607-A-G		not specified	Uncertain significance (Jul 21, 2021)
5-80437617-A-T		not specified	Uncertain significance (Mar 28, 2024)
5-80437657-C-A		not specified	Uncertain significance (Dec 03, 2021)
5-80437718-G-T		not specified	Uncertain significance (Jan 12, 2024)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP