Variant #0000003903 (NC_000001.10:-, FH(NM_000143.3):c.-?_132+?del)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
This mutation is novel, not a frequent cause of HLRCC syndrome. The mitochondrial signal peptide of |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
FH_00144 |
| Frequency |
- |
| Variant remarks |
blood samples or cultured lymphocytes |
| ClassClinical |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Qi Ming |
| Database submission license |
No license selected |
| Created by |
Qi Ming |
Variant on transcripts
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