NM_018401.3(STK32B):c.503C>T (p.Ala168Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004093762.1
Allele description [Variation Report for NM_018401.3(STK32B):c.503C>T (p.Ala168Val)]
NM_018401.3(STK32B):c.503C>T (p.Ala168Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens similar to speedy homolog A, transcript variant 7 (LOC44...
PREDICTED: Homo sapiens similar to speedy homolog A, transcript variant 7 (LOC442609), mRNAgi|239508993|ref|XM_935540.4|Nucleotide
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Last Updated: Oct 8, 2024