Variant #0000368117 (NC_000001.10:g.45796852G>A, NC_000001.10(NM_001128425.1):c.1476+2C>T (MUTYH))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45796852G>A
DNA change (hg38) g.45331180G>A
Published as 1434+2C>T (Val429_Val479del)
ISCN -
DB-ID MUTYH_000281 See all 4 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) 0.00012 View details
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 2019-02-22 12:09:43 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MUTYH NM_001128425.1 ?/. 15i c.1476+2C>T r.(1324_1476del) p.(Val443_Val493del) -


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