Variant #0000000355 (NC_000019.9:g.54313859G>A, NM_144687.3:c.1054C>T (NLRP12))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.54313859G>A
Reference -
DB-ID NLRP12_000005
Frequency -
Average frequency (gnomAD v.2.1.1) 0.00041 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-07-17 13:49:35 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP12 NM_144687.3 ?/? - c.1054C>T r.(?) p.(Arg352Cys)