NM_000222.3(KIT):c.200C>G (p.Thr67Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000503289.7
Allele description [Variation Report for NM_000222.3(KIT):c.200C>G (p.Thr67Ser)]
NM_000222.3(KIT):c.200C>G (p.Thr67Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024