NM_004612.4(TGFBR1):c.1433A>G (p.Asn478Ser) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000199866.17
Allele description [Variation Report for NM_004612.4(TGFBR1):c.1433A>G (p.Asn478Ser)]
NM_004612.4(TGFBR1):c.1433A>G (p.Asn478Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024