Variant #0000345992 (NC_000002.11:g.47643457G>A, NM_000251.2:c.965G>A (MSH2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47643457G>A |
| DNA change (hg38) |
g.47416318G>A |
| Published as |
MSH2(NM_000251.2):c.965G>A (p.G322D, p.(Gly322Asp), p.Gly322Asp), MSH2(NM_000251.3):c.965G>A (p.G322D) |
| ISCN |
- |
| DB-ID |
MSH2_001563 See all 149 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) |
0.01364 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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