Variant #0002112895 (NC_000002.11:g.219137271G>A, NM_001087.3:c.-2462C>T (AAMP))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.219137271G>A
DB-ID -
dbSNP ID rs370894207
gnomAD frequency 2/246152
gnomAD homozygote count 0/123074
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PNKD NM_001077399.2 ./. c.237-22G>A r.(=) p.(=)
AAMP NM_001087.3 ./. c.-2462C>T r.(=) p.(=)
TMBIM1 NM_022152.4 ./. c.*2927C>T r.(=) p.(=)