NFATC2IP-AS1

NFATC2IP antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 16:28952816-28966883

Links

ENSG00000260853HGNC:56085GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the NFATC2IP-AS1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the NFATC2IP-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
7
clinvar
7
Total 0 0 7 0 0

Variants in NFATC2IP-AS1

This is a list of pathogenic ClinVar variants found in the NFATC2IP-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
16-28954583-C-T not specified Uncertain significance (Dec 14, 2023)3196666
16-28954607-C-T not specified Uncertain significance (Jul 27, 2024)3405120
16-28956031-C-T not specified Uncertain significance (Jul 20, 2021)2388277
16-28956039-C-T not specified Uncertain significance (Jun 01, 2023)2513826
16-28956275-C-T not specified Uncertain significance (May 25, 2022)2341303
16-28956299-C-T not specified Uncertain significance (Nov 13, 2023)3196677
16-28956306-G-A not specified Uncertain significance (Sep 17, 2021)2223747
16-28958779-G-C not specified Uncertain significance (Nov 25, 2024)3405125
16-28958801-A-T not specified Uncertain significance (Jul 07, 2024)3405121
16-28958843-G-A not specified Uncertain significance (Dec 28, 2022)2340183
16-28963727-T-G not specified Uncertain significance (Dec 28, 2022)2340814

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP