Variant #0000000942 (NC_000019.10:g.12897788G>T, NM_000159.3:c.1168G>T (GCDH))

Individual ID 00000191
Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.12897788G>T
Published as -
Reference Siti Aishah Abdul Wahab et al. (2016)
DB-ID GCDH_000004
dbSNP ID rs876660106
Frequency 1/8
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 2020-11-26 10:08:59 +08:00 (CST)
Date last edited 2021-09-12 14:59:38 +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     
GCDH NM_000159.3 +/. - c.1168G>T - r.(?) p.(Gly390Trp) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000206 DNA PCR;SEQ GCDH 7 Nuur Athirah Binti Mohd Daud