Variant #0000003612 (NC_000017.10:-, ELAC2(NM_018127.6):c.650C>T)
Chromosome |
17 |
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 |
ELAC2_00001 See all 9 reported entries |
Frequency |
- |
Variant remarks |
The Leu217 homozygous
frequencies were similar in cases and controls,
indicating that this variant does not act in a recessive
manner as previously suggested |
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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