Variant #0001499015 (NC_000002.11:g.44059148A>G, NM_022436.2:c.340delTinsC (ABCG5))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44059148A>G
DB-ID -
dbSNP ID -
gnomAD frequency 0/166400
gnomAD homozygote count 0/83199
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     
ABCG5 NM_022436.2 ./. c.340delTinsC r.(?) p.(Tyr114His)
DYNC2LI1 XM_005264364.1 ./. c.*4639A>G r.(=) p.(=)
DYNC2LI1 XM_005264365.1 ./. c.*4639A>G r.(=) p.(=)