Variant #0001236363 (NC_000001.10:g.229694149A>G, NM_012089.2:c.251T>C (ABCB10))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.229694149A>G
DB-ID -
dbSNP ID rs138947511
gnomAD frequency 151/13740
gnomAD homozygote count 3/6722
Average frequency (gnomAD v.2.1.1) 0.01099 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.251T>C r.(?) p.(Leu84Pro)