Variant #0000355088 (NC_000011.9:g.1956104T>C, TNNT3(NM_006757.3):c.636T>C)

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.1956104T>C
DNA change (hg38) g.1934874T>C
Published as -
ISCN -
DB-ID TNNT3_000007 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs16927166
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.04176 View details
Owner Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT3 NM_006757.3 ?/. 14 c.636T>C r.(?) p.(Ile212=)