Variant #0000008983 (NC_000012.11:-, MMAB(NM_052845.3):c.?)
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
SNP |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MMAB_00041 See all 2 reported entries |
Frequency |
N.D |
Variant remarks |
Substitution |
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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