Variant #0000420103 (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 |
19953527_1437_1439_MEF |
| ISCN |
- |
| DB-ID |
MUTYH_000086 See all 65 reported entries |
| Variant remarks |
In vivo complementation assay; Mutant MUTYH expression and function in MUTYH null mouse embryonic fibroblasts; Lower protein expression compared to wild-type and much less 8-oxodG repair; in nucleus of proliferating cells (like WT); Expression from transfected plasmid with site-directed mutated human MutYgamma3 cDNA (RefSeq: NM_001048173.1) |
| Reference |
PubMed: Molatore 2009 |
| 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 |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Astrid Out |
| Date created |
2009-12-28 17:30:00 +01:00 (CET) |
| Date last edited |
2020-07-14 21:56:45 +02:00 (CEST) |

Variant on transcripts
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