Variant #0001068885 (NC_000014.8:g.24731399G>A, NM_000359.2:c.160C>T (TGM1))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.24731399G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TGM1_000103 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs140000324
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-03-02 11:41:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGM1 NM_000359.2 +/. - c.160C>T r.(?) p.(Arg54Ter)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.