Variant #0000009503 (NC_000002.11:-, MSH2(NM_000251.1):c.1168C>T)
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
1168,C>T;390,Arg-Phe |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
MSH2_00015 See all 7 reported entries |
Frequency |
0.0238 |
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
|
|