Variant #0000355514 (NC_000011.9:g.1955200C>T, TNNT3(NM_006757.3):c.328C>T)

Individual ID 00154879
Chromosome 11
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1955200C>T
DNA change (hg38) g.1933970C>T
Published as -
ISCN -
DB-ID TNNT3_000009
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00015 View details
Owner Tom Winder
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT3 NM_006757.3 ?/. 11 c.328C>T r.(?) p.(Arg110Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000155737 DNA PCR;SEQ - - TNNT3 1 Tom Winder