Variant #0000367920 (NC_000001.10:g.45798812del, NM_001128425.1:c.421del (MUTYH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45798812del |
DNA change (hg38) |
g.45333140del |
Published as |
379delC (Gln127ArgfsX5) |
ISCN |
- |
DB-ID |
MUTYH_000061 See all 5 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) |
Retrieve |
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 13:40:15 +02:00 (CEST) |

Variant on transcripts
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