Variant #0001236364 (NC_000001.10:g.229694152A>C, NM_012089.2:c.248T>G (ABCB10))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.229694152A>C
DB-ID -
dbSNP ID rs779088507
gnomAD frequency 24/11652
gnomAD homozygote count 0/5802
Average frequency (gnomAD v.2.1.1) 0.00206 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB10 NM_012089.2 ./. c.248T>G r.(?) p.(Val83Gly)