FAM174A-DT

FAM174A divergent transcript, the group of Divergent transcripts

Basic information

Region (hg38): 5:100223281-100535947

Links

ENSG00000247877HGNC:55584GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the FAM174A-DT gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the FAM174A-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 FAM174A-DT

This is a list of pathogenic ClinVar variants found in the FAM174A-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
5-100535537-G-C not specified Uncertain significance (May 09, 2024)3277269
5-100535554-C-G not specified Uncertain significance (Jul 05, 2024)3511869
5-100535556-G-C not specified Uncertain significance (Jan 24, 2024)3092055
5-100535567-C-G not specified Uncertain significance (Aug 13, 2021)2284086
5-100535601-C-T not specified Uncertain significance (Jan 26, 2023)2456718
5-100535606-C-A not specified Uncertain significance (Sep 30, 2024)3511871
5-100535640-C-G not specified Uncertain significance (Jun 25, 2024)3511867
5-100535690-C-T not specified Uncertain significance (Jul 12, 2023)2611097
5-100535733-G-A not specified Uncertain significance (Jan 16, 2024)3092053
5-100535741-G-C not specified Uncertain significance (Oct 16, 2023)3092054
5-100535766-C-A not specified Uncertain significance (Aug 02, 2021)2237152
5-100535775-G-A not specified Uncertain significance (Aug 14, 2023)2618253
5-100535818-C-A not specified Uncertain significance (May 27, 2022)2291760
5-100535834-G-A not specified Uncertain significance (Jul 23, 2024)3511870
5-100535874-C-G not specified Uncertain significance (Dec 12, 2023)3092056
5-100535895-A-G not specified Uncertain significance (Sep 16, 2021)2348076
5-100535928-G-T not specified Uncertain significance (May 05, 2023)2544723

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP