NM_005726.6(TSFM):c.88C>T (p.Pro30Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 9, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002569610.1
Allele description [Variation Report for NM_005726.6(TSFM):c.88C>T (p.Pro30Ser)]
NM_005726.6(TSFM):c.88C>T (p.Pro30Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 13, 2023