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

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
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