Variant #0000355093 (NC_000011.9:g.1944636A>T, TNNT3(NM_006757.3):c.32-149A>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.1944636A>T
DNA change (hg38) g.1923406A>T
Published as -
ISCN -
DB-ID TNNT3_000005
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2734500
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT3 NM_006757.3 ?/. 3i c.32-149A>T r.(?) p.(=)