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Gene entry

MUTYH

mutY DNA glycosylase

Chromosome
1
Cytoband
1p34.1
Variants (rsID)
96

MUTYH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p34.1). Its official name is “mutY DNA glycosylase”. The reference table lists 96 variants (rsID) for this gene.

Clinically classified variants

89 reference-table entries with clinical significance.

  • rs139977567Benignsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Carcinoma of colon
  • rs3219484Benignsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Breast carcinoma|Carcinoma of colon
  • rs3219485Benignsingle nucleotide variant
  • rs3219496Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Carcinoma of colon|Familial adenomatous polyposis 2
  • rs1057517765Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Carcinoma of colon
  • rs1060504205Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2
  • rs138089183Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs140288388Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs144616312Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs149866955Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs150792276Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon
  • rs200165598Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs201412035Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs201678305Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs35352891Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs367908623Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs372673338Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs376600220Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs558173961Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587780742Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs587781864Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs730881838Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs750592289Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Familial cancer of breast|Breast carcinoma
  • rs751875215Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs75321043Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon
  • rs766553845Conflicting interpretationsDeletionFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs77542170Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Gastric cancer|Carcinoma of colon
  • rs786202141Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs786203213Conflicting interpretationsDeletionHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs79777494Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon
  • rs864622450Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs879254257Conflicting interpretationssingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs767717597Likely benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs1057517459Likely pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs1057520660Likely pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs1060501333Likely pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs1064793198Likely pathogenicsingle nucleotide variant
  • rs1383826978Likely pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs587781337Likely pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs786203161Likely pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs864621967Likely pathogenicDeletionHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs876659420Likely pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs876660837Likely pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome
  • rs1057517457PathogenicDeletionFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs1060501321Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs1060501324Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs1060501335Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs1060501336PathogenicDeletionFamilial adenomatous polyposis 2
  • rs1064795480PathogenicDeletionFamilial adenomatous polyposis 2
  • rs1064795596Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs121908381Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Carcinoma of colon
  • rs121908383Pathogenicsingle nucleotide variantGastric cancer
  • rs1338038953Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs140342925Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Pilomatrixoma|Neoplasm of stomach|Familial adenomatous polyposis 2|Breast carcinoma|Carcinoma of colon
  • rs143353451Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs200495564Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Familial colorectal cancer
  • rs34126013Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs34612342Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Endometrial carcinoma|Hereditary cancer-predisposing syndrome|Carcinoma of colon|Pilomatrixoma|Familial adenomatous polyposis 2|Neoplasm of stomach|Gastric cancer|See cases
  • rs36053993Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Endometrial cancer|Hereditary cancer-predisposing syndrome|Carcinoma of colon|Familial adenomatous polyposis 2|Neoplasm of stomach|Small intestine carcinoid|Colorectal adenomatous polyposis, autosomal recessive, with pilomatricomas|Pilomatrixoma|Familial adenomatous polyposis 2|Neoplasm of stomach|Ovarian carcinoma|Breast carcinoma|Colon cancer|Familial colorectal cancer|See cases
  • rs370124822Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs372267274Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs374950566Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon|Breast carcinoma
  • rs376561094Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587778541PathogenicMicrosatelliteHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Breast carcinoma|Colorectal polyposis
  • rs587780078PathogenicDuplicationHereditary cancer-predisposing syndrome|Carcinoma of colon|Familial adenomatous polyposis 2
  • rs587780088Pathogenicsingle nucleotide variantCarcinoma of colon|Familial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Pilomatrixoma|Neoplasm of stomach
  • rs587781295Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587781338Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587782730Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587783057Pathogenicsingle nucleotide variantCarcinoma of colon|Familial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Breast carcinoma|Familial colorectal cancer
  • rs745921592Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs762307622Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon
  • rs766420907Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs781222233PathogenicDeletionFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome|Colonic neoplasm
  • rs863224452Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2
  • rs863224502Pathogenicsingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs876659625Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome
  • rs876659676Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Carcinoma of colon
  • rs876660190PathogenicDuplicationHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs876660774Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs876660787Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs878854189PathogenicDuplicationFamilial adenomatous polyposis 2
  • rs886039606PathogenicDeletionFamilial adenomatous polyposis 2
  • rs121908382Uncertain significancesingle nucleotide variantGastric cancer|Familial adenomatous polyposis 2
  • rs1331273811Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome
  • rs147923905Uncertain significancesingle nucleotide variantFamilial adenomatous polyposis 2|Hereditary cancer-predisposing syndrome
  • rs200229669Uncertain significancesingle nucleotide variantCarcinoma of colon|Hereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2|Pilomatrixoma|Neoplasm of stomach|Familial adenomatous polyposis 2
  • rs376790729Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2
  • rs587782263Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome|Familial adenomatous polyposis 2

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.