Variant #0000009466 (NC_000002.11:-, MSH2(NM_000251.1):c.(?_-68)_1076+?del)
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Type |
del ex1_6 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
| Reference |
GenBank |
| DB-ID |
MSH2_00128 See all 2 reported entries |
| Frequency |
0.0238 |
| Variant remarks |
Exon |
| 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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