Variant #0000419256 (NC_000001.10:g.45800156C>T, NM_001128425.1:c.64G>A (MUTYH))
| Chromosome |
1 |
| 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.45800156C>T |
| DNA change (hg38) |
g.45334484C>T |
| Published as |
(Val22Met) |
| ISCN |
- |
| DB-ID |
MUTYH_000005 See all 79 reported entries |
| Variant remarks |
- |
| Reference |
Molecular Diagnostics, NSCR Demokritos, Athens, GR |
| ClinVar ID |
- |
| dbSNP ID |
rs3219484 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.04874 View details |
| Owner |
Florentia Fostira |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Carli Tops |
| Date created |
2010-04-05 12:13:05 +02:00 (CEST) |
| Date last edited |
2020-08-07 13:25:51 +02:00 (CEST) |

Variant on transcripts
Screenings
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