Variant #0010852765 (NC_000017.10:g.74464789T>G, NM_024599.5:c.*2926A>C (RHBDF2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74464789T>G
DB-ID -
dbSNP ID rs776403673
gnomAD frequency 1/198988
gnomAD homozygote count 0/99493
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.*2926A>C r.(=) p.(=)
AANAT NM_001088.2 ./. c.-40T>G r.(=) p.(=)
AANAT NM_001166579.1 ./. c.96T>G r.(?) p.(Leu32=)
RHBDF2 NM_024599.5 ./. c.*2926A>C r.(=) p.(=)