Variant #0001236377 (NC_000001.10:g.229694387G>C, NM_012089.2:c.13C>G (ABCB10))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.229694387G>C
DB-ID -
dbSNP ID rs769361678
gnomAD frequency 1/31686
gnomAD homozygote count 0/15842
Average frequency (gnomAD v.2.1.1) 3.0E-5 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.13C>G r.(?) p.(Pro5Ala)