NM_001063.4(TF):c.2012G>A (p.Gly671Glu) AND Transferrin variant B2
- Germline classification:
- no classifications from unflagged records (1 submission)
- Last evaluated:
- Dec 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000013450.25
Allele description [Variation Report for NM_001063.4(TF):c.2012G>A (p.Gly671Glu)]
NM_001063.4(TF):c.2012G>A (p.Gly671Glu)
Condition(s)
- Name:
- Transferrin variant B2
- Identifiers:
Assertion and evidence details
Flagged submissions
Submission Accession | Submitter | Review Status (Assertion method) | Clinical Significance (Last evaluated) | Origin | Method | Citations |
---|---|---|---|---|---|---|
SCV000033697 | OMIM | flagged submission Reason: Outlier claim with insufficient supporting evidence Notes: None | Pathogenic (May 1, 1984) | germline | literature only |
Last Updated: Apr 15, 2024