Variant #0001078320 (NC_000003.11:g.3182499G>T, NC_000003.11(NM_182916.2):c.481+167G>T (TRNT1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.3182499G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TRNT1_000038
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs951612896
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-05-29 18:36:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRNT1 NM_182916.2 ?/. - c.481+167G>T r.(?) p.(?)


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