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 InternationalCreative Commons License
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 +/. 14 c.1437_1439del r.(1437_1439del) p.(Glu480del) -


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