IFIT1P1

interferon induced protein with tetratricopeptide repeats 1 pseudogene 1

Basic information

Region (hg38): 13:32384660-32386108

Previous symbols: [ "G13P1", "IFI56P", "IFIT1P" ]

Links

ENSG00000215515NCBI:8373HGNC:5408GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the IFIT1P1 gene.

  • Breast-ovarian cancer, familial, susceptibility to, 2 (14 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the IFIT1P1 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)
1
clinvar
1
splice region
0
non coding
13
clinvar
13
Total 0 0 0 0 14

Variants in IFIT1P1

This is a list of pathogenic ClinVar variants found in the IFIT1P1 region.

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

Position Type Phenotype Significance ClinVar
13-32384686-G-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209865
13-32384750-G-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209866
13-32384860-G-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209867
13-32385062-C-T Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209952
13-32385099-C-T Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209868
13-32385103-C-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209869
13-32385327-C-T Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Sep 28, 2016)264930
13-32385397-A-G Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209870
13-32385401-G-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209871
13-32385652-T-C Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209872
13-32385702-A-C Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209953
13-32385743-A-G Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Sep 28, 2016)264969
13-32385907-T-C Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Jan 12, 2015)209873
13-32386106-C-A Breast-ovarian cancer, familial, susceptibility to, 2 Benign (Sep 28, 2016)264945

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP