Variant #0000001543 (NC_000001.11:g.230710048A>G, NM_000029.3:c.803T>C (AGT))

Individual ID 00000327
Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.230710048A>G
Published as M235T
Reference Yee-How Say et al. (2005), dbSNP, (OMIM 0001), ClinVar
DB-ID AGT_000001 See all 14 reported entries
dbSNP ID rs699
Frequency 26/97
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 13:35:17 +08:00 (CST)
Date last edited 2021-09-01 11:57:15 +08:00 (CST)
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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     
0000000342 DNA PCR AGT 2 Nuur Athirah Binti Mohd Daud