Variant #0012377031 (NC_000021.8:g.10906894G>A, NM_199261.2:c.*11C>T (TPTE))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.10906894G>A
DB-ID -
dbSNP ID rs200860223
gnomAD frequency 790/243390
gnomAD homozygote count 0/120902
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     
TPTE NM_199259.2 ./. c.*11C>T r.(=) p.(=)
TPTE NM_199260.2 ./. c.*11C>T r.(=) p.(=)
TPTE NM_199261.2 ./. c.*11C>T r.(=) p.(=)