Variant #0000371766 (NC_000002.11:g.47630263_47657080del, NC_000002.11(NM_000251.2):c.(?_-68)_(1276+1_1277-1)del (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.47630263_47657080del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_001645 See all 3 reported entries |
| Variant remarks |
Insight class: 5 Variant Error [EMISMATCH/EUNCERTAIN]: This transcript variant has an error. Please fix this entry and then remove this message. |
| 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-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2018-07-06 14:04:02 +02:00 (CEST) |
| Date last edited |
2025-06-07 02:01:27 +02:00 (CEST) |

Variant on transcripts
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