Variant #0000669115 (NC_000011.9:g.1956104T>C, TNNT3(NM_006757.3):c.636T>C)

Individual ID 00304298
Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
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 7 homozygous; Clinindb (India)
Reference Faruq 2020, submtted
ClinVar ID -
dbSNP ID rs16927166
Origin Germline
Segregation -
Frequency 7/2795 individuals
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.04176 View details
Owner Mohammed Faruq
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000305427 DNA arraySNP - Infinium Global Screening Array v1.0 - 1 Mohammed Faruq