Variant #0000015295 (NC_000001.10:-, TNNT2(NM_001001430.1):c.690)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type novel; The mutation occurred within a not highly conserved location and was therefore considered a v
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID TNNT2_00078
Frequency -
Variant remarks Substitution
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT2 NM_001001430.1 ./. 14 c.690 - -