Variant #0000371753 (NC_000002.11:g.47554933_47699909del, NC_000002.11(NM_000251.2):c.-75398_1759+1708del (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.47554933_47699909del |
| DNA change (hg38) |
g.47327794_47472770del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_001624 See all 3 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 |
2018-11-09 17:29:21 +01:00 (CET) |

Variant on transcripts
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