NM_002474.3(MYH11):c.5160C>T (p.Ser1720=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jul 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000126958.20
Allele description [Variation Report for NM_002474.3(MYH11):c.5160C>T (p.Ser1720=)]
NM_002474.3(MYH11):c.5160C>T (p.Ser1720=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 26, 2024