Variant #0012377042 (NC_000021.8:g.10906906T>C, NM_199261.2:c.1655A>G (TPTE))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.10906906T>C
DB-ID -
dbSNP ID rs748371308
gnomAD frequency 1/246048
gnomAD homozygote count 0/123023
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.1601A>G r.(?) p.(Ter534=)
TPTE NM_199260.2 ./. c.1541A>G r.(?) p.(Ter514=)
TPTE NM_199261.2 ./. c.1655A>G r.(?) p.(Ter552=)