Variant #0000371545 (NC_000002.11:g.47641402_47642007del, NC_000002.11(NM_000251.2):c.793-6_942+450del (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47641402_47642007del |
| DNA change (hg38) |
g.47414263_47414868del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_001280 See all 7 reported entries |
| Variant remarks |
Insight class: 5 |
| Reference |
InSiGHT |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| 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 15:23:44 +02:00 (CEST) |

Variant on transcripts
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