Variant #0000879787 (NC_000002.11:g.47639552G>C, NC_000002.11(NM_000251.2):c.646-1G>C (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47639552G>C |
| DNA change (hg38) |
g.47412413G>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MSH2_001845 See all 6 reported entries |
| Variant remarks |
data from in-vitro expression mini-gene splicing assay |
| Reference |
PubMed: Meulemans 2022 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-09-29 09:45:35 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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