Variant #0000371356 (NC_000002.11:g.47630331A>C, NM_000251.2:c.1A>C (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47630331A>C |
| DNA change (hg38) |
g.47403192A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_001065 See all 6 reported entries |
| Variant remarks |
Insight class: 3 |
| Reference |
InSiGHT |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2018-07-06 14:04:02 +02:00 (CEST) |
| Date last edited |
2020-06-08 15:12:16 +02:00 (CEST) |

Variant on transcripts
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