NM_003673.4(TCAP):c.378G>C (p.Gln126His) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001223485.8
Allele description [Variation Report for NM_003673.4(TCAP):c.378G>C (p.Gln126His)]
NM_003673.4(TCAP):c.378G>C (p.Gln126His)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024