Variant #0000420202 (NC_000001.10:g.45796892C>A, NM_001128425.1:c.1438G>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.45796892C>A |
DNA change (hg38) |
g.45331220C>A |
Published as |
18534194_protein_Q466X |
ISCN |
- |
DB-ID |
MUTYH_000088 See all 17 reported entries |
Variant remarks |
Protein expression assay; GST-tagged 535 amino acid human MUTYH expressed from vector in E.Coli; Sodium dodecyl sulfateƱPAGE analysis for protein weight; Western blot; Molecular weight similar to the number of codons exprected to be expressed |
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) |
6.0E-5 View details |
Owner |
Astrid Out |
Database submission license |
No license selected |
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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