NM_002658.6(PLAU):c.1234G>C (p.Val412Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004511677.1
Allele description [Variation Report for NM_002658.6(PLAU):c.1234G>C (p.Val412Leu)]
NM_002658.6(PLAU):c.1234G>C (p.Val412Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ33832 fis, clone CTONG2004115
Homo sapiens cDNA FLJ33832 fis, clone CTONG2004115gi|21749453|dbj|AK091151.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024