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     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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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     

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Panel size     

Owner     
-?/. - c.1000C>G r.(?) p.(Pro334Ala) - Unknown - likely benign g.45797519G>C g.45331847G>C MUTYH(NM_001048171.1):c.958C>G (p.(Pro320Ala)), MUTYH(NM_001128425.1):c.1000C>G (p.P334A) - MUTYH_000327 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. 12 c.1000C>G r.(?) p.Pro334Ala - Unknown - VUS g.45797519G>C g.45331847G>C - - MUTYH_000327 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
?/. 12 c.1000C>G r.(?) p.Pro334Ala - Unknown - VUS g.45797519G>C g.45331847G>C - - MUTYH_000327 - Clinical Genetics, ErasmusMC, Rotterdam, NL - - Unknown - - - - - DNA SEQ - - ? - Clinical Genetics, ErasmusMC, Rotterdam, NL - - - - - - - - - 1 Ans M.W. van den Ouweland
?/. - c.1000C>G r.(?) p.(Pro334Ala) - Parent #1 - NA g.45797519G>C - chr1_45797519_G_C - MUTYH_000327 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 - 5/60466 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 - 5 BRIDGES consortium
?/. - c.1000C>G r.(?) p.(Pro334Ala) - Parent #1 - NA g.45797519G>C - chr1_45797519_G_C - MUTYH_000327 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 - 5/53461 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 - 5 BRIDGES consortium
?/. - c.1000C>G r.(?) p.(Pro334Ala) - Unknown - VUS g.45797519G>C - MUTYH(NM_001048171.1):c.958C>G (p.(Pro320Ala)), MUTYH(NM_001128425.1):c.1000C>G (p.P334A) - MUTYH_000327 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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