Variant #0000420135 (NC_000001.10:g.45799121G>T, NM_001128425.1:c.312C>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.45799121G>T |
DNA change (hg38) |
g.45333449G>T |
Published as |
18534194_glycosylase_Y90X |
ISCN |
- |
DB-ID |
MUTYH_000032 See all 27 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) |
0.00012 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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