Variant #0002112967 (NC_000002.11:g.219137470T>C, NM_001087.3:c.-2661A>G (AAMP))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.219137470T>C
DB-ID -
dbSNP ID rs764807276
gnomAD frequency 2/246232
gnomAD homozygote count 0/123114
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     
PNKD NM_001077399.2 ./. c.414T>C r.(?) p.(Ser138=)
AAMP NM_001087.3 ./. c.-2661A>G r.(=) p.(=)
TMBIM1 NM_022152.4 ./. c.*2728A>G r.(=) p.(=)