Variant #0012040368 (NC_000019.9:g.58868892C>T, NM_001207009.1:c.110G>A (ZNF497))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.58868892C>T
DB-ID -
dbSNP ID rs370174117
gnomAD frequency 24/233292
gnomAD homozygote count 0/116622
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     
ZNF497 NM_001207009.1 ./. c.110G>A r.(?) p.(Gly37Asp)
A1BG NM_130786.3 ./. c.-4089G>A r.(=) p.(=)
ZNF497 NM_198458.2 ./. c.110G>A r.(?) p.(Gly37Asp)