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 |
PubMed: Narang 2020, Journal: Narang 2020 |
ClinVar ID |
- |
dbSNP ID |
rs16927166 |
Origin |
Germline |
Segregation |
- |
Frequency |
7/2795 individuals |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (large NGS studies) |
0.02088 View details |
Owner |
Mohammed Faruq |

Variant on transcripts
Screenings
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