Variant #0002135751 (NC_000002.11:g.220088444G>A, NM_005689.2:c.-5049C>T (ABCB6))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.220088444G>A
DB-ID -
dbSNP ID rs761747353
gnomAD frequency 10/245588
gnomAD homozygote count 0/122784
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ATG9A NM_001077198.1 ./. c.1462C>T r.(?) p.(Leu488Phe)
ABCB6 NM_005689.2 ./. c.-5049C>T r.(=) p.(=)
ATG9A NM_024085.3 ./. c.1462C>T r.(?) p.(Leu488Phe)