NM_001048174.2(MUTYH):c.1227G>A (p.Arg409=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000611753.1
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1227G>A (p.Arg409=)]
NM_001048174.2(MUTYH):c.1227G>A (p.Arg409=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
AGENCOURT_6563434 NIH_MGC_88 Homo sapiens cDNA clone IMAGE:5739983 5', mRNA sequ...
AGENCOURT_6563434 NIH_MGC_88 Homo sapiens cDNA clone IMAGE:5739983 5', mRNA sequencegi|18799725|gnl|dbEST|11130537|gb|B 07.1|Nucleotide
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Last Updated: May 7, 2024