Variant #0001498197 (NC_000002.11:g.44040320T>A, NM_022436.2:c.1891delAinsT (ABCG5))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44040320T>A
DB-ID -
dbSNP ID rs769429015
gnomAD frequency 5/245420
gnomAD homozygote count 0/122700
Average frequency (gnomAD v.2.1.1) 2.0E-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     
DYNC2LI1 NM_001193464.1 ./. c.*3414T>A r.(=) p.(=)
DYNC2LI1 NM_016008.3 ./. c.*3414T>A r.(=) p.(=)
ABCG5 NM_022436.2 ./. c.1891delAinsT r.(?) p.(Ile631Phe)