Variant #0009873381 (NC_000016.9:g.48278291G>C, NM_031490.2:c.-9G>C (LONP2))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48278291G>C
DB-ID -
dbSNP ID rs150981618
gnomAD frequency 1/183230
gnomAD homozygote count 0/89772
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.-9G>C r.(=) p.(=)
ABCC11 XM_005256208.1 ./. c.-236C>G r.(=) p.(=)
ABCC11 XM_005256209.1 ./. c.-19+2934C>G r.(=) p.(=)
ABCC11 XM_005256210.1 ./. c.-236C>G r.(=) p.(=)