NM_000360.4(TH):c.241G>A (p.Val81Met) AND not specified
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Dec 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000241867.8
Allele description [Variation Report for NM_000360.4(TH):c.241G>A (p.Val81Met)]
NM_000360.4(TH):c.241G>A (p.Val81Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024