Variant #0012377055 (NC_000021.8:g.10906947G>A, NM_199261.2:c.1614C>T (TPTE))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.10906947G>A
DB-ID -
dbSNP ID rs148444026
gnomAD frequency 646/243708
gnomAD homozygote count 0/121204
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.1560C>T r.(?) p.(Gly520=)
TPTE NM_199260.2 ./. c.1500C>T r.(?) p.(Gly500=)
TPTE NM_199261.2 ./. c.1614C>T r.(?) p.(Gly538=)