Variant #0012377029 (NC_000021.8:g.10906892G>C, NM_199261.2:c.*13C>G (TPTE))

Chromosome 21
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.10906892G>C
DB-ID -
dbSNP ID rs562924386
gnomAD frequency 0/245804
gnomAD homozygote count 0/122824
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.*13C>G r.(=) p.(=)
TPTE NM_199260.2 ./. c.*13C>G r.(=) p.(=)
TPTE NM_199261.2 ./. c.*13C>G r.(=) p.(=)