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) |
0.02074 View details |
Owner |
VKGL-NL_AMC |

Variant on transcripts
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