Variant #0000292218 (NC_000001.10:g.45797228C>T, NM_001128425.1:c.1187G>A (MUTYH))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45797228C>T |
| DNA change (hg38) |
g.45331556C>T |
| Published as |
MUTYH(NM_001048171.1):c.1145G>A (p.(Gly382Asp)), MUTYH(NM_001128425.1):c.1187G>A (p.G396D, p.Gly396Asp), MUTYH(NM_001128425.2):c.1187G>A (p.G396D) |
| ISCN |
- |
| DB-ID |
MUTYH_000075 See all 593 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) |
0.00296 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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