NM_006147.4(IRF6):c.1179+292CA[14] AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001688255.1
Allele description [Variation Report for NM_006147.4(IRF6):c.1179+292CA[14]]
NM_006147.4(IRF6):c.1179+292CA[14]
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens solute carrier family 6 member 2 (SLC6A2), transcript variant 3, mR...
Homo sapiens solute carrier family 6 member 2 (SLC6A2), transcript variant 3, mRNAgi|289191349|ref|NM_001043.3|Nucleotide
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Last Updated: Dec 24, 2023