NM_020184.4(CNNM4):c.445G>T (p.Ala149Ser) AND Jalili syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001136913.4
Allele description [Variation Report for NM_020184.4(CNNM4):c.445G>T (p.Ala149Ser)]
NM_020184.4(CNNM4):c.445G>T (p.Ala149Ser)
Condition(s)
-
Homo sapiens mortality factor 4 like 2 (MORF4L2), transcript variant 2, mRNA
Homo sapiens mortality factor 4 like 2 (MORF4L2), transcript variant 2, mRNAgi|1519312242|ref|NM_012286.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 9, 2023