Variant #0000420149 (NC_000001.10:g.45800167G>A, NM_001128425.1:c.53C>T (MUTYH))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45800167G>A |
| DNA change (hg38) |
g.45334495G>A |
| Published as |
18811933_test_53 |
| ISCN |
- |
| DB-ID |
MUTYH_000024 See all 19 reported entries |
| Variant remarks |
In vivo localization assay; Immunofluorescense; cDNAs with c.53C>T+c.74G>A, c.53C>T, c.74G>A or WT (Flag-tagged + polyclonal anti-Flag); transfection cos-7 cells; subcellular localizations; c.53C>T+c.74G>A: nucleus+mitochondria; c.53C>T only: mitochondria; c.74G>A only: mitochondria; wild-type: mitochondria |
| Reference |
PubMed: Chen 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00104 View details |
| Owner |
Astrid Out |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Astrid Out |
| Date created |
2010-02-04 13:35:40 +01:00 (CET) |
| Date last edited |
2020-07-14 21:54:44 +02:00 (CEST) |

Variant on transcripts
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