Variant #0000002231 (NC_000022.11:g.43928847C>G, NM_025225.2:c.444C>G (PNPLA3))

Individual ID 00000466
Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43928847C>G
Published as -
Reference Shamsul Mohd Zain et al.(2012)
DB-ID PNPLA3_000001
dbSNP ID rs738409
Frequency -
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
Date created 2021-03-01 17:11:04 +08:00 (CST)
Date last edited 2021-08-01 13:09:55 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
PNPLA3 NM_025225.2 +/. - c.444C>G - r.(?) p.(Ile148Met) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000512 DNA TaqMan PNPLA3 1 Nur Aisyah Athirah