NM_020661.4(AICDA):c.*235C>G AND Hyper-IgM syndrome type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000318639.5
Allele description [Variation Report for NM_020661.4(AICDA):c.*235C>G]
NM_020661.4(AICDA):c.*235C>G
Condition(s)
-
hypothetical protein Np111112_045 [Synechococcus phage S-RIM2]
hypothetical protein Np111112_045 [Synechococcus phage S-RIM2]gi|1063200026|gb|AOO01200.1|Protein
-
chromosome 14 open reading frame 93, isoform CRA_a [Homo sapiens]
chromosome 14 open reading frame 93, isoform CRA_a [Homo sapiens]gi|119586607|gb|EAW66203.1||gnl|WGS |hCP1919525Protein
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023