Variant #0000013658 (NC_000001.10:-, RNASEL(NM_021133.3):c.1385G>A)
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
G1385A,the single nucleotide polymorphism at nucleoide position 1385, which results in R462Q. |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
RNASEL_00005 See all 19 reported entries |
| Frequency |
11.6% |
| Variant remarks |
Exon |
| 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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