NM_000360.4(TH):c.977+8C>G AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- May 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000250457.11
Allele description [Variation Report for NM_000360.4(TH):c.977+8C>G]
NM_000360.4(TH):c.977+8C>G
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024