NM_001048174.2(MUTYH):c.1131G>A (p.Pro377=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000475312.11
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1131G>A (p.Pro377=)]
NM_001048174.2(MUTYH):c.1131G>A (p.Pro377=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024