NM_000360.4(TH):c.186G>A (p.Ser62=) AND not provided
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Jul 30, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000713849.7
Allele description [Variation Report for NM_000360.4(TH):c.186G>A (p.Ser62=)]
NM_000360.4(TH):c.186G>A (p.Ser62=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024