Variant #0001236359 (NC_000001.10:g.229694051G>C, NM_012089.2:c.349C>G (ABCB10))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.229694051G>C
DB-ID -
dbSNP ID -
gnomAD frequency 2/13356
gnomAD homozygote count 0/6676
Average frequency (gnomAD v.2.1.1) 0.00015 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB10 NM_012089.2 ./. c.349C>G r.(?) p.(Arg117Gly)