Full data view for gene MUTYH


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

3 entries on 1 page. Showing entries 1 - 3.
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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     
?/. 10 c.836A>G r.(836a>g) p.(Asn279Ser) - Unknown - VUS g.45797935T>C g.45332263T>C 794A>G (Asn265Ser) - MUTYH_000133 - DUPLICATE – to be removed - - Germline - - - - - - - - - - - - - - - - - - - - - - -
?/. 10 c.836A>G r.(836a>g) p.(Asn279Ser) - Unknown - VUS g.45797935T>C g.45332263T>C 794A>G (Asn265Ser) - MUTYH_000133 - 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
+?/. 10 c.836A>G r.(836a>g) p.(Asn279Ser) - Unknown - likely pathogenic g.45797935T>C g.45332263T>C 794A>G (Asn265Ser) - MUTYH_000133 - Clinical Genetics, LUMC, Leiden, NL - - Germline - - - - - DNA SEQ leukocyte screen MUTYH gene (index) ? - Clinical Genetics, LUMC, Leiden, NL - M - Netherlands - - - - - 1 Carli Tops
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