NM_003673.4(TCAP):c.423C>T (p.Pro141=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000544689.6
Allele description [Variation Report for NM_003673.4(TCAP):c.423C>T (p.Pro141=)]
NM_003673.4(TCAP):c.423C>T (p.Pro141=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024