Variant #0000000161 (NC_000019.9:g.54313570C>G, NM_144687.3:c.1343G>C (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.54313570C>G
Reference -
DB-ID NLRP12_000003
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-27 09:03:38 +00:00 (UTC)
Date last edited 2023-06-27 09:04:41 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NLRP12 NM_144687.3 ?/? - c.1343G>C r.(?) p.(Gly448Ala)