NM_003673.4(TCAP):c.387C>T (p.Asp129=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001418100.6
Allele description [Variation Report for NM_003673.4(TCAP):c.387C>T (p.Asp129=)]
NM_003673.4(TCAP):c.387C>T (p.Asp129=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024