GRCh37/hg19 14q23.1(chr14:61393999-61520353)x1 AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 9, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000846382.2
Allele description [Variation Report for GRCh37/hg19 14q23.1(chr14:61393999-61520353)x1]
GRCh37/hg19 14q23.1(chr14:61393999-61520353)x1
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
PREDICTED: Homo sapiens synaptojanin 1 (SYNJ1), transcript variant X1, mRNA
PREDICTED: Homo sapiens synaptojanin 1 (SYNJ1), transcript variant X1, mRNAgi|2217338337|ref|XM_017028495.3|Nucleotide
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Last Updated: Dec 11, 2022