NM_001003937.3(TSPYL6):c.142G>C (p.Val48Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004354396.1
Allele description [Variation Report for NM_001003937.3(TSPYL6):c.142G>C (p.Val48Leu)]
NM_001003937.3(TSPYL6):c.142G>C (p.Val48Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens leucine rich repeat and Ig domain containing 2 (LINGO2),...
PREDICTED: Homo sapiens leucine rich repeat and Ig domain containing 2 (LINGO2), transcript variant X9, mRNAgi|2217375609|ref|XM_047422817.1|Nucleotide
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Last Updated: Oct 13, 2024