Variant #0000015107 (NC_000019.9:-, TNNI3(NM_000363.4):c.422G>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_00011
Frequency -
Variant remarks In this cohort of 389 unrelated HCM patients from an

outpatient tertiary referral center, thin filament mutations

were uncommon (5%) and were not distinguishable from

non
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.422G>A - p.Arg141Gln