Variant #0013105178 (NC_000024.9:g.2655471A>C, NM_003140.2:c.174T>G (SRY))

Chromosome Y
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.2655471A>C
DB-ID -
dbSNP ID rs773764555
gnomAD frequency 29/67262
gnomAD homozygote count unknown
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     
SRY NM_003140.2 ./. c.174T>G r.(?) p.(Asp58Glu)