Variant #0000516201 (NC_000002.11:g.47698179A>G, NM_000251.2:c.1737A>G (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47698179A>G |
| DNA change (hg38) |
g.47471040A>G |
| Published as |
MSH2(NM_000251.2):c.1737A>G (p.K579=, p.(Lys579=), p.Lys579=, p.=), MSH2(NM_000251.3):c.1737A>G (p.K579=) |
| ISCN |
- |
| DB-ID |
MSH2_000218 See all 35 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00214 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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