Variant #0000355089 (NC_000011.9:g.1959707C>T, TNNT3(NM_006757.3):c.762C>T)

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.1959707C>T
DNA change (hg38) g.1938477C>T
Published as -
ISCN -
DB-ID TNNT3_000008 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs4727
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.11446 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 ?/. 16 c.762C>T r.(?) p.(Gly254=)