Variant #0005355269 (NC_000007.13:g.150720934C>G, NM_007188.3:c.-4669C>G (ABCB8))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150720934C>G
DB-ID -
dbSNP ID rs78586299
gnomAD frequency 603/239696
gnomAD homozygote count 7/119251
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     
ABCB8 NM_007188.3 ./. c.-4669C>G r.(=) p.(=)
ATG9B NM_173681.5 ./. c.550+27G>C r.(=) p.(=)