Variant #0000927035 (NC_000020.10:g.5935825A>G, NM_032485.5:c.414A>G (MCM8))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5935825A>G |
| DNA change (hg38) |
- |
| Published as |
MCM8(NM_001281520.1):c.414A>G (p.(Ile138Met)), MCM8(NM_032485.5):c.414A>G (p.I138M) |
| ISCN |
- |
| DB-ID |
TRMT6_000004 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) |
0.00628 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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