NM_000455.5(STK11):c.116G>T (p.Arg39Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000780767.1
Allele description [Variation Report for NM_000455.5(STK11):c.116G>T (p.Arg39Leu)]
NM_000455.5(STK11):c.116G>T (p.Arg39Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
RPN2 [Neogale vison]
RPN2 [Neogale vison]Gene ID:122916093Gene
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024