Variant #0010852785 (NC_000017.10:g.74464871C>T, NM_024599.5:c.*2844G>A (RHBDF2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74464871C>T
DB-ID -
dbSNP ID rs34470791
gnomAD frequency 3/244596
gnomAD homozygote count 0/122295
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.*2844G>A r.(=) p.(=)
AANAT NM_001088.2 ./. c.43C>T r.(?) p.(Arg15Cys)
AANAT NM_001166579.1 ./. c.178C>T r.(?) p.(Arg60Cys)
RHBDF2 NM_024599.5 ./. c.*2844G>A r.(=) p.(=)