Variant #0000001074 (NC_000022.10:, SPECC1L(NM_015330.5):chr22:g.24718197A>C)
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
- |
| DB-ID |
SPECC1L_000001 |
| Frequency |
- |
| Variant remarks |
de novo |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
qingting114 |
| Database submission license |
No license selected |
| Created by |
qingting114 |
Variant on transcripts
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