Variant #0000001156 (NC_000001.11:g.99880679C>T, NM_000642.2:c.1783C>T (AGL))

Individual ID 00000233
Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.99880679C>T
Published as -
Reference Ili Syazwana Abdullah et al. (2019)dbSNP
DB-ID AGL_000009
dbSNP ID rs150866831
Frequency 2
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 2020-12-07 16:57:31 +08:00 (CST)
Date last edited 2021-09-08 11:20:24 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
AGL NM_000642.2 -?/. 15 c.1783C>T - r.(?) p.(Arg595*) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000248 DNA PCRdig;TaqMan AGL 1 Nuur Athirah Binti Mohd Daud