NFATC2IP-AS1
Basic information
Region (hg38): 16:28952816-28966883
Links
Phenotypes
GenCC
Source:
ClinVar
This is a list of variants' phenotypes submitted to
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 | |||||
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) | ||
16-28954607-C-T | not specified | Uncertain significance (Jul 27, 2024) | ||
16-28956031-C-T | not specified | Uncertain significance (Jul 20, 2021) | ||
16-28956039-C-T | not specified | Uncertain significance (Jun 01, 2023) | ||
16-28956275-C-T | not specified | Uncertain significance (May 25, 2022) | ||
16-28956299-C-T | not specified | Uncertain significance (Nov 13, 2023) | ||
16-28956306-G-A | not specified | Uncertain significance (Sep 17, 2021) | ||
16-28958779-G-C | not specified | Uncertain significance (Nov 25, 2024) | ||
16-28958801-A-T | not specified | Uncertain significance (Jul 07, 2024) | ||
16-28958843-G-A | not specified | Uncertain significance (Dec 28, 2022) | ||
16-28963727-T-G | not specified | Uncertain significance (Dec 28, 2022) |
GnomAD
Source:
dbNSFP
Source: