Variant #0002135765 (NC_000002.11:g.220088513G>A, NM_005689.2:c.-5118C>T (ABCB6))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.220088513G>A
DB-ID -
dbSNP ID rs777522002
gnomAD frequency 1/244780
gnomAD homozygote count 0/122389
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     
ATG9A NM_001077198.1 ./. c.1420-27C>T r.(=) p.(=)
ABCB6 NM_005689.2 ./. c.-5118C>T r.(=) p.(=)
ATG9A NM_024085.3 ./. c.1420-27C>T r.(=) p.(=)