NM_017882.3(CLN6):c.414C>T (p.Leu138=) AND Neuronal ceroid lipofuscinosis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001457224.7
Allele description [Variation Report for NM_017882.3(CLN6):c.414C>T (p.Leu138=)]
NM_017882.3(CLN6):c.414C>T (p.Leu138=)
Condition(s)
-
Homo sapiens synaptotagmin XII (SYT12), mRNA
Homo sapiens synaptotagmin XII (SYT12), mRNAgi|29366827|ref|NM_177963.1|Nucleotide
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Last Updated: Sep 29, 2024