Variant #0000656111 (NC_000008.10:g.48882409A>T, NM_005914.3:c.1226A>T (MCM4))
| Chromosome |
8 |
| 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.48882409A>T |
| DNA change (hg38) |
g.47969849A>T |
| Published as |
MCM4(NM_005914.4):c.1226A>T (p.K409M) |
| ISCN |
- |
| DB-ID |
MCM4_000023 |
| 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) |
6.0E-5 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
|