NM_181783.4(TMTC3):c.441G>A (p.Leu147=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 14, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000928558.3
Allele description [Variation Report for NM_181783.4(TMTC3):c.441G>A (p.Leu147=)]
NM_181783.4(TMTC3):c.441G>A (p.Leu147=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022