Variant #0010852766 (NC_000017.10:g.74464796C>G, NM_024599.5:c.*2919G>C (RHBDF2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74464796C>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/211478
gnomAD homozygote count 0/105738
Average frequency (gnomAD v.2.1.1) Retrieve
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     
RHBDF2 NM_001005498.3 ./. c.*2919G>C r.(=) p.(=)
AANAT NM_001088.2 ./. c.-33C>G r.(=) p.(=)
AANAT NM_001166579.1 ./. c.103C>G r.(?) p.(Leu35Val)
RHBDF2 NM_024599.5 ./. c.*2919G>C r.(=) p.(=)