Variant #0000015081 (NC_000017.10:-, TCAP(NM_003673.3):c.316C>T)
| 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_00007 |
| Frequency |
- |
| Variant remarks |
however, only the two individuals who were double-heterozygous
for the p.Arg145Trp mutation as well as a TCAP mutation were
clinically affected. |
| 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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