Variant #0000002955 (NC_000019.10:g.4536T>C, NM_000660.7:c.-1347T>C (TGFB1))

Individual ID 00000724
Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.4536T>C
Published as -
Reference Azadeh Emami et al.(2012)
DB-ID TGFB1_000002
dbSNP ID rs1800469
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-06-28 12:33:10 +08:00 (CST)
Date last edited 2021-08-01 13:14:27 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
TGFB1 NM_000660.7 +/. - c.-1347T>C -509T>C r.(=) p.(=) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000817 DNA PCR TGFB1 2 Nur Aisyah Athirah