Variant #0009873466 (NC_000016.9:g.48286206T>G, NM_031490.2:c.398T>G (LONP2))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48286206T>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/246088
gnomAD homozygote count 0/123043
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
LONP2 NM_031490.2 ./. c.398T>G r.(?) p.(Phe133Cys)
ABCC11 XM_005256209.1 ./. c.-5000A>C r.(=) p.(=)