Variant #0000426536 (NC_000002.11:g.47703590G>T, NM_000251.2:c.2090G>T (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.47703590G>T |
| DNA change (hg38) |
g.47476451G>T |
| Published as |
C697F |
| ISCN |
- |
| DB-ID |
MSH2_001569 See all 42 reported entries |
| Variant remarks |
{GR:13} |
| Reference |
PubMed: Ollila 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rolf Sijmons |
| Database submission license |
No license selected |
| Created by |
Rolf Sijmons |
| Date created |
2009-02-06 12:00:00 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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