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.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/. 12i c.1187-2A>G r.[(1187_1323del), (0)] p.[(Leu397CysfsX89, (0)] - Unknown - likely pathogenic g.45797230T>C g.45331558T>C 1145-2A>G (Leu383CysfsX89) - MUTYH_000022 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
+/. 12i c.1187-2A>G r.[(1187_1323del), (0)] p.[(Leu397CysfsX89, (0)] - Parent #2 - pathogenic g.45797230T>C g.45331558T>C 1145-2A>G - MUTYH_000022 only variants close to Tyr179Cys and Gly382Asp detected PubMed: Wang 2004 - - Unknown - - - - - DNA MCA, SEQ leukocyte genotyping, test known variant (group) ? PMID15236166_33 PubMed: Wang 2004 among 140 APC mutation negative polyposis patients. 16/140 (11.4%) biallelic (0/26 with 4-19 polyps, 3/22 (13,6%) with 20-49 polyps, 3/15 (20%) with 50-99 polyps, 4/20 (20%) with 50-100 polyps); 4/140 (2.9%) monoallelic M - United States - - - - - 1 Carli Tops
+/. 12i c.1187-2A>G r.[(1187_1323del, (0)] p.[(Leu397CysfsX89, (0)] - Parent #1 - pathogenic g.45797230T>C g.45331558T>C 1145-2A>G; nt 9639 a>g (AF527839) - MUTYH_000022 affects splicing, only transcript detected from other allele; Only c.1187G>A allele detectable; Compound heterozygous c.[1187-2A>G]+[1187G>A] PubMed: Farrington 2005 - - Germline - 1/4478 (0.02%) - - - DNA, RNA RT-PCR, SEQ leukocyte allelic discrimination, screen MUTYH gene (index) CRC 15931596_patient_c1187_c1187-2 PubMed: Farrington 2005 1 (0.04%) compound heterozygote c.[1187-2A>G]+[1187G>A] among 2,239 CRC patients; 0 compound heterozygotes among 1,845 controls; population-based association study - - Scotland - - - - - 1 Carli Tops
+?/. 12i c.1187-2A>G r.[(1187_1323del), (0)] p.[(Leu397CysfsX89, (0)] - Unknown - likely pathogenic g.45797230T>C g.45331558T>C 1145-2A>G (Leu383CysfsX89) - MUTYH_000022 only variants reported, not genotypes; in silico prediction by Alamut: splice acceptor site exon 13 dissapears, skip of exon 13 very likely Genetics, John Hunter Hospital, Newcastle, AU - - Germline - - - - - DNA SEQ - screen MUTYH gene ? - Genetics, John Hunter Hospital, Newcastle, AU - - - Australia - - - - - 1 Rodney Scott
?/. - c.1187-2A>G r.spl? p.? - Parent #1 - NA g.45797230T>C - chr1_45797230_T_C - MUTYH_000022 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 - 3/60466 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 - 3 BRIDGES consortium
?/. - c.1187-2A>G r.spl? p.? - Parent #1 - NA g.45797230T>C - chr1_45797230_T_C - MUTYH_000022 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 - 1/53461 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 - 1 BRIDGES consortium
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