SLC30A4-AS1

SLC30A4 antisense RNA 1, the group of Antisense RNAs

Basic information

Region (hg38): 15:45448427-45519668

Links

ENSG00000259354NCBI:105376714HGNC:56661GenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the SLC30A4-AS1 gene.

  • Inborn genetic diseases (11 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the SLC30A4-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
10
clinvar
1
clinvar
11
Total 0 0 10 1 0

Variants in SLC30A4-AS1

This is a list of pathogenic ClinVar variants found in the SLC30A4-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
15-45485233-G-C not specified Uncertain significance (Aug 12, 2021)2244168
15-45485242-T-A not specified Uncertain significance (May 01, 2024)3319511
15-45485251-A-T not specified Uncertain significance (Jul 06, 2021)2341631
15-45485271-G-T not specified Likely benign (May 10, 2022)2288501
15-45487542-C-T not specified Uncertain significance (Jun 17, 2022)2393020
15-45488960-C-T not specified Uncertain significance (Mar 01, 2023)2491884
15-45488965-C-A not specified Uncertain significance (Jan 26, 2022)2272913
15-45488981-T-G not specified Uncertain significance (Feb 15, 2023)2484538
15-45489011-G-A not specified Uncertain significance (Mar 23, 2023)2523400
15-45489016-C-A not specified Uncertain significance (Sep 27, 2021)2219770
15-45490800-A-G not specified Uncertain significance (Apr 23, 2024)3319510
15-45490812-A-G not specified Uncertain significance (Apr 05, 2023)2525130
15-45490822-A-T not specified Uncertain significance (Aug 17, 2021)2246158

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP