Variant #0008354923 (NC_000012.11:g.123444557G>C, NM_019625.3:c.226C>G (ABCB9))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.123444557G>C
DB-ID -
dbSNP ID rs762377904
gnomAD frequency 1/244954
gnomAD homozygote count 0/122476
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     
ABCB9 NM_001243013.1 ./. c.226C>G r.(?) p.(Pro76Ala)
ABCB9 NM_001243014.1 ./. c.226C>G r.(?) p.(Pro76Ala)
ABCB9 NM_019624.3 ./. c.226C>G r.(?) p.(Pro76Ala)
ABCB9 NM_019625.3 ./. c.226C>G r.(?) p.(Pro76Ala)
ABCB9 NM_203444.3 ./. c.226C>G r.(?) p.(Pro76Ala)