Variant #0000516396 (NC_000002.11:g.48132711_48132713dup, NM_000179.2:c.*98712_*98714dup (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.48132711_48132713dup |
| DNA change (hg38) |
g.47905572_47905574dup |
| Published as |
FBXO11(NM_001190274.1):c.167_169dup (p.(Gln56dup)), FBXO11(NM_001190274.2):c.167_169dupAGC (p.Q56dup) |
| ISCN |
- |
| DB-ID |
FBXO11_000041 See all 2 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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