Variant #0000309361 (NC_000011.9:g.1956104T>C, TNNT3(NM_006757.3):c.636T>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1956104T>C
DNA change (hg38) g.1934874T>C
Published as TNNT3(NM_001297646.2):c.612T>C (p.I204=)
ISCN -
DB-ID TNNT3_000007 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.04176 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT3 NM_006757.3 -/. - c.636T>C r.(?) p.(Ile212=)