Variant #0000000113 (NC_000018.9:g.2940603G>A, NM_014646.2:c.698C>T (LPIN2))

Chromosome 18
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.2940603G>A
Reference -
DB-ID LPIN2_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 9.0E-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 2021-02-05 11:34:13 +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     
LPIN2 NM_014646.2 ./. 5 c.698C>T r.(?) p.(Thr233Ile)