Variant #0000015102 (NC_000019.9:-, TNNI3(NM_000363.4):c.511G>A)

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_00008 See all 2 reported entries
Frequency -
Variant remarks He was an

only child, and no clinical data or DNA was available on

his deceased parents. Subsequent mutation analysis of

his children did not reveal further carriers.
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.511G>A - p.Ala171Thr