Variant #0000426138 (NC_000002.11:g.47637246A>G, NM_000251.2:c.380A>G (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47637246A>G |
| DNA change (hg38) |
g.47410107A>G |
| Published as |
N127S |
| ISCN |
- |
| DB-ID |
MSH2_000031 See all 49 reported entries |
| Variant remarks |
{GR:148} |
| Reference |
PubMed: Auclair 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00548 View details |
| 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 22:00:36 +02:00 (CEST) |

Variant on transcripts
|