Variant #0000355087 (NC_000011.9:g.1955609G>A, TNNT3(NM_006757.3):c.414G>A)

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.1955609G>A
DNA change (hg38) g.1934379G>A
Published as -
ISCN -
DB-ID TNNT3_000006
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2292470
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00054 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 ?/. 12 c.414G>A r.(?) p.(Glu138=)