Full data view for gene MUTYH


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

7 entries on 1 page. Showing entries 1 - 7.
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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     
?/. 14 c.1418C>A r.(1418c>a) p.(Ala473Asp) - Unknown - VUS g.45796912G>T g.45331240G>T 1376C>A (Ala459Asp) - MUTYH_000123 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
?/. 14 c.1418C>A r.(1418c>a) p.(Ala473Asp) - Parent #1 - VUS g.45796912G>T g.45331240G>T 1376C>A (Ala459Asp) - MUTYH_000123 - PubMed: Alhopuro 2005 - - Unknown - 1/24 individuals (22 families). FAP: 19, AFAP: 3; 0/85 controls - - - DNA SEQ - - cancer, colon - PubMed: Alhopuro 2005 - - - Finland - - - - - 1 Astrid Out
?/. 14 c.1418C>A r.(1418c>a) p.(Ala473Asp) - Unknown - VUS g.45796912G>T g.45331240G>T 1376C>A (Ala459Asp) - MUTYH_000123 - PubMed: Alhopuro 2005 - - Unknown - 1/24 individuals (22 families). FAP: 19, AFAP: 3; 0/85 controls - - - DNA SEQ - - cancer, colon - PubMed: Alhopuro 2005 - - - Finland - - - - - 1 Astrid Out
?/. 14 c.1418C>A r.(1418c>a) p.(Ala473Asp) - Parent #1 - VUS g.45796912G>T g.45331240G>T 1376C>A (Ala459Asp) - MUTYH_000123 - PubMed: Alhopuro 2005 - - Unknown - - - - - DNA DHPLC - - cancer, colon - PubMed: Alhopuro 2005 population-based series; 1 homozygote / 1,042 CRC patients (0/85 controls) - - Finland - - - - - 1 Astrid Out
+/. 14 c.1418C>A r.(1418c>a) p.(Ala473Asp) - Parent #1 - pathogenic g.45796912G>T g.45331240G>T 1376C>A (Ala459Asp) - MUTYH_000123 - MGZ, Munchen, DE - - Unknown - - - - - DNA SEQ - - ? - MGZ, Munchen, Germany - - - (Germany) - - - - - 1 Elke Holinski-Feder
+/. - c.1418C>A r.(?) p.(Ala473Asp) - Parent #1 - pathogenic g.45796912G>T g.45331240G>T - - MUTYH_000123 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs200844166 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
?/. - c.1418C>A r.(?) p.(Ala473Asp) - Parent #1 - NA g.45796912G>T - chr1_45796912_G_T - MUTYH_000123 not in 60466 cases; 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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