Variant #0000247030 (NC_000011.9:g.1955546A>G, TNNT3(NM_006757.3):c.367-16A>G)

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.1955546A>G
DNA change (hg38) g.1934316A>G
Published as TNNT3(NM_001297646.2):c.343-16A>G
ISCN -
DB-ID TNNT3_000013
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) 0.03819 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.367-16A>G r.(=) p.(=)