Full data view for gene MUTYH


Information The variants shown are described using the NM_001128425.1 transcript reference sequence.

6 entries on 1 page. Showing entries 1 - 6.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 11 c.940C>T r.(940c>u) p.(Gln314X) - Unknown - pathogenic g.45797752G>A g.45332080G>A 898C>T (Gln300X) - MUTYH_000119 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
+?/. 11 c.940C>T r.(940c>u) p.(Gln314X) - Unknown - likely pathogenic g.45797752G>A g.45332080G>A 898C>T (Gln300X) - MUTYH_000119 - PubMed: Eliason 2005 - - Unknown - 1/219 APC neg FAP patients; 0/306 MLH1 and MSH2 neg HNPCC patients - - - DNA SEQ - - cancer, colon - PubMed: Eliason 2005 - - - United States - - - - - 1 Astrid Out
+/. 11 c.940C>T r.(940c>u) p.(Gln314X) - Unknown - pathogenic g.45797752G>A g.45332080G>A 898C>T (Gln300X) - MUTYH_000119 - PubMed: Olschwang 2007 - - Unknown - - - - - DNA SEQ - - CRC - PubMed: Olschwang 2007 No info 2nd allele; Among 406 patients with >5 polyps and/or CRC in France - - - - - - - - 1 Astrid Out
+/. - c.940C>T r.(?) p.(Gln314*) - Unknown - pathogenic g.45797752G>A g.45332080G>A - - MUTYH_000119 - PubMed: Baert-Desurmont 2018 - - Germline - - - - - DNA ? - - CRC - PubMed: Baert-Desurmont 2018 - - - France - - - - - 1 Stephanie Baert-Desurmont
?/. - c.940C>T r.(?) p.(Gln314*) - Parent #1 - NA g.45797752G>A - chr1_45797752_G_A - MUTYH_000119 the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 1/60466 cases - - - DNA SEQ-NG - 34-gene panel cancer, breast - PubMed: Dorling 2021, Journal: Dorling 2021 analysis 60466 cases (BRIDGES) - - - - - - bcac.ccge.medschl.cam.ac.uk/contact - 1 BRIDGES consortium
?/. - c.940C>T r.(?) p.(Gln314*) - Parent #1 - NA g.45797752G>A - chr1_45797752_G_A - MUTYH_000119 the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 2/53461 controls - - - DNA SEQ-NG - 34-gene panel Healthy/Control - PubMed: Dorling 2021, Journal: Dorling 2021 analysis 53461 controls (BRIDGES) - - - - - - bcac.ccge.medschl.cam.ac.uk/contact - 2 BRIDGES consortium
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.