Variant #0000516387 (NC_000002.11:g.48033984_48033987dup, NM_000179.2:c.4068_4071dup (MSH6))
| 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.48033984_48033987dup |
| DNA change (hg38) |
g.47806845_47806848dup |
| Published as |
MSH6(NM_000179.2):c.4068_4071dup (p.(Lys1358Aspfs*2)), MSH6(NM_000179.2):c.4068_4071dupGATT (p.K1358Dfs*2), MSH6(NM_000179.3):c.4068_4071dupGATT ...) |
| ISCN |
- |
| DB-ID |
MSH6_000119 See all 17 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) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| 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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