NM_000391.4(TPP1):c.1253G>A (p.Arg418Gln) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Dec 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000125591.10
Allele description [Variation Report for NM_000391.4(TPP1):c.1253G>A (p.Arg418Gln)]
NM_000391.4(TPP1):c.1253G>A (p.Arg418Gln)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024