Variant #0011147466 (NC_000019.9:g.110783C>A, NM_001005240.1:c.105delCinsA (OR4F17))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.110783C>A
DB-ID -
dbSNP ID rs148836883
gnomAD frequency 179/237340
gnomAD homozygote count 0/118491
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     
OR4F17 NM_001005240.1 ./. c.105delCinsA r.(?) p.(Asn35Lys)