Variant #0001235842 (NC_000001.10:g.229662966C>G, NM_012089.2:c.1725+10delGinsC (ABCB10))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.229662966C>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/239984
gnomAD homozygote count 0/119989
Average frequency (gnomAD v.2.1.1) 0 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.1725+10delGinsC r.(=) p.(=)