Full data view for gene MUTYH


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

5 entries on 1 page. Showing entries 1 - 5.
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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     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 12 c.1163T>C r.(1163u>c) p.(Leu388Pro) - Unknown - likely pathogenic g.45797356A>G g.45331684A>G 1121T>C (Leu374Pro) - MUTYH_000071 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
?/. 12 c.1163T>C r.(1163u>c) p.(Leu388Pro) - Unknown - VUS g.45797356A>G g.45331684A>G 1121T>C (Leu374Pro) - MUTYH_000071 - PubMed: Aceto 2005 - - Unknown - 1/29 (3.4%) APC mutation negative (A)FAP patients; 0/79 controls - - - DNA DHPLC, SEQ - - cancer, colon - PubMed: Aceto 2005 - - - Italy - - - - - 1 Astrid Out
?/. 12 c.1163T>C r.(1163u>c) p.(Leu388Pro) - Unknown - VUS g.45797356A>G g.45331684A>G 1121T>C (Leu374Pro) - MUTYH_000071 - 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
+?/. 12 c.1163T>C r.(1163u>c) p.(Leu388Pro) - Unknown - likely pathogenic g.45797356A>G g.45331684A>G 1121T>C (Leu374Pro) - MUTYH_000071 Significance remains to be proved; highly conserved domain; catalytic core (Guan , 1998; Yang , 2001); Polyphen: damaging; not in 50 controls PubMed: Lejeune 2006 - - Unknown - - - - - DNA SEQ - SEQ (ex1-16), screen MUTYH gene (index) ? 16941501_Li-19 PubMed: Lejeune 2006 Among 33 unrelated patients with multiple adenomas or CRC without evidence of APC or MMR defect; one monoallelic (3.3%) and 7 biallelic (21%) detected M - France - - - - - 1 Carli Tops
+?/. 12 c.1163T>C r.(?) p.Leu388Pro - Unknown - NA g.45797356A>G g.45331684A>G 20848659_L360P - MUTYH_000071 in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; extremely severely defective PubMed: Goto 2010 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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