NM_198271.5(LMOD3):c.1123T>C (p.Tyr375His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004035369.1
Allele description [Variation Report for NM_198271.5(LMOD3):c.1123T>C (p.Tyr375His)]
NM_198271.5(LMOD3):c.1123T>C (p.Tyr375His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
membrane glycoprotein E3 CR1-alpha [Human mastadenovirus F]
membrane glycoprotein E3 CR1-alpha [Human mastadenovirus F]gi|9626579|ref|NP_040869.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 13, 2024