Variant #0010852800 (NC_000017.10:g.74464914G>A, NM_024599.5:c.*2801C>T (RHBDF2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74464914G>A
DB-ID -
dbSNP ID rs141006262
gnomAD frequency 75/245160
gnomAD homozygote count 0/122503
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RHBDF2 NM_001005498.3 ./. c.*2801C>T r.(=) p.(=)
AANAT NM_001088.2 ./. c.86delGinsA r.(?) p.(Arg29His)
AANAT NM_001166579.1 ./. c.221delGinsA r.(?) p.(Arg74His)
RHBDF2 NM_024599.5 ./. c.*2801C>T r.(=) p.(=)