MFSD4B-DT

MFSD4B divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 6:111187110-111259320

Links

ENSG00000231046 ∙ NCBI:107986521 ∙ ∙ HGNC:55773 ∙ ∙ ∙ 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 MFSD4B-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the MFSD4B-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						0
Total	0	0	0	0	0

Variants in MFSD4B-DT

This is a list of pathogenic ClinVar variants found in the MFSD4B-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
6-111206605-A-G		not specified	Uncertain significance (Feb 16, 2023)
6-111206692-G-A		not specified	Uncertain significance (Mar 28, 2022)
6-111206715-G-A		not specified	Uncertain significance (Jun 17, 2024)
6-111218829-T-G		not specified	Uncertain significance (Aug 16, 2021)
6-111218838-C-T			Likely benign (Jul 17, 2018)
6-111218841-A-C		not specified	Uncertain significance (Jul 14, 2021)
6-111218884-T-C		not specified	Uncertain significance (Jan 30, 2024)
6-111218901-A-C		not specified	Uncertain significance (Dec 18, 2023)
6-111218974-T-A		not specified	Uncertain significance (Nov 16, 2022)
6-111218986-T-C		not specified	Uncertain significance (Nov 22, 2023)
6-111222096-C-T		not specified	Uncertain significance (Apr 07, 2022)
6-111222141-G-C		not specified	Uncertain significance (Aug 02, 2023)
6-111222162-T-C		not specified	Uncertain significance (May 13, 2024)
6-111222178-C-G		not specified	Uncertain significance (Nov 21, 2022)
6-111222182-C-G		not specified	Uncertain significance (Feb 12, 2024)

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP