Variant #0000367945 (NC_000001.10:g.45796895_45796897del, NM_001128425.1:c.1437_1439del (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.45796895_45796897del |
DNA change (hg38) |
g.45331223_45331225del |
Published as |
1437_1439del, 1434_1436del (Glu466del) |
ISCN |
- |
DB-ID |
MUTYH_000086 See all 65 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 13:19:57 +02:00 (CEST) |

Variant on transcripts
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