Full data view for gene MUTYH


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

11 entries on 1 page. Showing entries 1 - 11.
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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     

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     
+/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Unknown - pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
+?/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Unknown - likely pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - PubMed: Bouguen 2007 - - Unknown - - - - - DNA SEQ - - cancer, colon - PubMed: Bouguen 2007 APC negative patients M - France white - - - - 1 Astrid Out
+/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Unknown - pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - 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.1012C>T r.(1012c>u) p.(Gln338X) - Parent #1 - pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - PubMed: Sampson 2003 - - Unknown - - - - - DNA SEQ - - ? - PubMed: Sampson 2003 - - - United Kingdom (Great Britain) - - - - - 1 Astrid Out
+/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Parent #1 - pathogenic g.45797507G>A g.45331835G>A 969C>T (Gln324X) - MUTYH_000062 - MGZ, Munchen, DE - - Unknown - - - - - DNA SEQ - - ? - MGZ, Munchen, Germany - - - (Germany) - - - - - 1 Elke Holinski-Feder
+/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Parent #1 - pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - PubMed: Cattaneo 2008 - - Germline - - - - - DNA SEQ leukocyte screen MUTYH gene (index) cancer, colon - PubMed: Cattaneo 2008 recessive inheritance (see paper) M - Greece - - - - - 1 Carli Tops
+?/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Unknown - likely pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - Molecular Diagnostics, NSCR Demokritos, Athens, GR - - Germline - - - - - DNA SEQ leukocyte screen MUTYH gene (index) CRC - Molecular Diagnostics, NSCR Demokritos, Athens, GR - M - Greece - - - - - 1 Florentia Fostira
+/. 12 c.1012C>T r.(1012c>u) p.(Gln338X) - Unknown - pathogenic g.45797507G>A g.45331835G>A 970C>T (Gln324X) - MUTYH_000062 - PubMed: Aretz 2006; PubMed: Vogt 2009 - - Germline - 1/658 - - - DNA SEQ leukocyte screen MUTYH gene (index) ? - PubMed: Aretz 2006, PubMed: Vogt 2009 - M - (Germany) - - - - - 1 Stefan Aretz
+/. 12 c.1012C>T r.(?) p.Gln338* - Unknown - NA g.45797507G>A g.45331835G>A 20848659_ Q310X - MUTYH_000062 in vitro test of the DNA glycosylase activity on adenine mispaired with 8-hydroxyguanine; extremely severely defective PubMed: Goto 2010 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1012C>T r.(?) p.(Gln338*) - Unknown - pathogenic g.45797507G>A g.45331835G>A - - MUTYH_000062 - - - - Germline - - - - - DNA SEQ-NG - - cancer, colon contributed by Dept. of Dr Vaccaro - - - - Argentina - - - - - 1 Carlos Vaccaro
?/. - c.1012C>T r.(?) p.(Gln338*) - Parent #1 - NA g.45797507G>A - chr1_45797507_G_A - MUTYH_000062 not in 53461 controls; 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 - 2/60466 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 - 2 BRIDGES consortium
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