Variant #0010852787 (NC_000017.10:g.74464880C>G, NM_024599.5:c.*2835G>C (RHBDF2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74464880C>G
DB-ID -
dbSNP ID rs761686519
gnomAD frequency 1/244988
gnomAD homozygote count 0/122493
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.*2835G>C r.(=) p.(=)
AANAT NM_001088.2 ./. c.52C>G r.(?) p.(Pro18Ala)
AANAT NM_001166579.1 ./. c.187C>G r.(?) p.(Pro63Ala)
RHBDF2 NM_024599.5 ./. c.*2835G>C r.(=) p.(=)