Variant #0000015082 (NC_000017.10:-, TCAP(NM_003673.3):c.53G>A)
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
blood |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
TCAP_00008 |
Frequency |
1/313 |
Variant remarks |
Three protein-altering variants were identified in TCAP, also known as titin-cap or
telethonin, a part of the titin complex.this proband was also known to carry a likely disease-causing lamin A/C mutation |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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