Variant #0000014366 (NC_000005.9:-, SGCD(NM_000337.5):c.451T>G)
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
Substitution |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
SGCD_00018 See all 3 reported entries |
| Frequency |
- |
| Variant remarks |
a single nucleotide (T for G) resulting in an amino-acid change from serine to alanine at codon 151 |
| 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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