Variant #0000009435 (NC_000011.9:-, MRE11A(NM_005591.3):c.913C>T)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
novel heterozygous alterations,potentially disease-related, affected highly conserved amino acids an |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MRE11A_00005 |
Frequency |
- |
Variant remarks |
Substitution |
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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