Variant #0000420131 (NC_000001.10:g.45798117C>T, NM_001128425.1:c.734G>A (MUTYH))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45798117C>T |
| DNA change (hg38) |
g.45332445C>T |
| Published as |
18534194_glycosylase_R231H |
| ISCN |
- |
| DB-ID |
MUTYH_000051 See all 37 reported entries |
| Variant remarks |
In vitro glycosylase assay; GST-tagged 535 amino acid human MUTYH; Adenine glycosylase assay for GO:A; absent glycosylase activity for GO:A |
| Reference |
PubMed: Ali 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
8.0E-5 View details |
| Owner |
Astrid Out |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Astrid Out |
| Date created |
2010-02-09 11:21:32 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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