Variant #0001498857 (NC_000002.11:g.44055158G>C, NM_022436.2:c.598delCinsG (ABCG5))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44055158G>C
DB-ID -
dbSNP ID rs764189303
gnomAD frequency 15/246026
gnomAD homozygote count 0/122996
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
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     
ABCG5 NM_022436.2 ./. c.598delCinsG r.(?) p.(Arg200Gly)
DYNC2LI1 XM_005264364.1 ./. c.*649G>C r.(=) p.(=)
DYNC2LI1 XM_005264365.1 ./. c.*649G>C r.(=) p.(=)