Variant #0000015101 (NC_000019.9:-, TNNI3(NM_000363.4):c.433C>T)

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID TNNI3_00007 See all 2 reported entries
Frequency -
Variant remarks Their offspring were not carriers of the mutation,

while remaining relatives were unwilling to participate in

the study at present.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNI3 NM_000363.4 ./. 07 c.433C>T - p.Arg145Trp