NM_012134.3(LMOD1):c.828C>T (p.Pro276=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000924106.3
Allele description [Variation Report for NM_012134.3(LMOD1):c.828C>T (p.Pro276=)]
NM_012134.3(LMOD1):c.828C>T (p.Pro276=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
PREDICTED: Homo sapiens ring finger protein 32 (RNF32), transcript variant X7, m...
PREDICTED: Homo sapiens ring finger protein 32 (RNF32), transcript variant X7, mRNAgi|2462612404|ref|XM_054357274.1|Nucleotide
-
PREDICTED: Homo sapiens opioid growth factor receptor like 1 (OGFRL1), transcrip...
PREDICTED: Homo sapiens opioid growth factor receptor like 1 (OGFRL1), transcript variant X1, mRNAgi|2462610586|ref|XM_054356431.1|Nucleotide
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Last Updated: Aug 23, 2022