NM_000132.4(F8):c.5042T>C (p.Ile1681Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002511290.1
Allele description [Variation Report for NM_000132.4(F8):c.5042T>C (p.Ile1681Thr)]
NM_000132.4(F8):c.5042T>C (p.Ile1681Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Feb 7, 2023