Variant #0000367947 (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 |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45796892C>A |
DNA change (hg38) |
g.45331220C>A |
Published as |
Glu466*; E466* |
ISCN |
- |
DB-ID |
MUTYH_000088 See all 17 reported entries |
Variant remarks |
- |
Reference |
DUPLICATE – to be removed |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
6.0E-5 View details |
Owner |
InSiGHT - John-Paul Plazzer |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-04-06 17:05:13 +02:00 (CEST) |
Date last edited |
2020-06-04 13:20:16 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|