Variant #0012377045 (NC_000021.8:g.10906922C>T, NM_199261.2:c.1639G>A (TPTE))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.10906922C>T
DB-ID -
dbSNP ID rs144163164
gnomAD frequency 31/245966
gnomAD homozygote count 0/122952
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     
TPTE NM_199259.2 ./. c.1585G>A r.(?) p.(Val529Ile)
TPTE NM_199260.2 ./. c.1525G>A r.(?) p.(Val509Ile)
TPTE NM_199261.2 ./. c.1639G>A r.(?) p.(Val547Ile)