Variant #0000420267 (NC_000001.10:g.45796895_45796897del, NM_001128425.1:c.1437_1439del (MUTYH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45796895_45796897del |
DNA change (hg38) |
g.45331223_45331225del |
Published as |
20418187_c1437_1439_binding |
ISCN |
- |
DB-ID |
MUTYH_000086 See all 65 reported entries |
Variant remarks |
In vitro DNA binding assay; Expression human proteins, bacteria, glycosylase assay 8-oxoG:A; Surface plasmon resonance (SPR) real-time recording association/dissociation; severe reduction in the binding affinity |
Reference |
PubMed: D Agostino 2010 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Astrid Out |
Database submission license |
No license selected |
Created by |
Astrid Out |
Date created |
2010-04-29 22:05:02 +02:00 (CEST) |
Date last edited |
2020-07-14 21:56:45 +02:00 (CEST) |

Variant on transcripts
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