Variant #0000418530 (NC_000001.10:g.45799121G>T, NM_001128425.1:c.312C>A (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.45799121G>T
DNA change (hg38) g.45333449G>T
Published as 270C>A (Tyr90X); Tyr90X
ISCN -
DB-ID MUTYH_000032 See all 27 reported entries
Variant remarks Review
Reference PubMed: Pineda 2009 reviewed: PubMed: Sampson 2003
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner Astrid Out
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Astrid Out
Date created 2009-12-29 15:39:29 +01:00 (CET)
Date last edited 2020-08-07 13:26:41 +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 +/. 3 c.312C>A r.(312c>a) p.(Tyr104X) -



Screenings

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