Variant #0000000728 (NC_000019.9:g.54312838_54312839insAA, NC_000019.9(NM_144687.3):c.2072+2_2072+3insTT (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.54312838_54312839insAA
Reference -
DB-ID NLRP12_000012
Frequency -
Average frequency (gnomAD v.2.1.1) 8.0E-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 2025-12-09 12:29:33 +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     

Class     
NLRP12 NM_144687.3 ?/? - c.2072+2_2072+3insTT r.spl? p.? VUS