Variant #0000420166 (NC_000001.10:g.45797201G>A, NM_001128425.1:c.1214C>T (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.45797201G>A |
| DNA change (hg38) |
g.45331529G>A |
| Published as |
20848659_ P377L |
| ISCN |
- |
| DB-ID |
MUTYH_000077 See all 51 reported entries |
| Variant remarks |
in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; extremely severely defective |
| Reference |
PubMed: Goto 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
| Owner |
Carli Tops |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Carli Tops |
| Date created |
2011-01-25 19:31:59 +01:00 (CET) |
| Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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