NM_001048174.2(MUTYH):c.1102+1G>A AND not provided
- Germline classification:
- Likely pathogenic (3 submissions)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001353653.4
Allele description [Variation Report for NM_001048174.2(MUTYH):c.1102+1G>A]
NM_001048174.2(MUTYH):c.1102+1G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024