Variant #0000002672 (NC_000003.12:g.8113G>A, GHRL(NM_016362.5):c.152G>A)

Individual ID 00000603
Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.8113G>A
Published as -
Reference Sher Wyn Lui et al.(2012)(10.5923/j.diabetes.20120103.03
DB-ID GHRL_000001 See all 3 reported entries
dbSNP ID rs34911341
Frequency 52/184
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
GHRL NM_016362.5 -/. - c.152G>A - r.(?) p.(Arg51Gln) Risk-Factor



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000669 DNA PCR;SEQ GHRL 1 Nur Aisyah Athirah