Variant #0000001537 (NC_000001.11:g.230710048A>G, NM_000029.3:c.803T>C (AGT))

Individual ID 00000324
Chromosome 1
Allele Both (homozygous)
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.230710048A>G
Published as M235T
Reference Dzuzaini M Ghazali et al. (2008), dbSNP, (OMIM 0001), ClinVar
DB-ID AGT_000001 See all 14 reported entries
dbSNP ID rs699
Frequency 127/200
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-06 11:40:59 +08:00 (CST)
Date last edited 2021-09-01 11:48:59 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
AGT NM_000029.3 -/. - c.803T>C - r.(?) p.(Met268Thr) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000339 DNA SEQ AGT 2 Nuur Athirah Binti Mohd Daud