NM_182902.4(KIF9):c.1721C>T (p.Pro574Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004414323.1
Allele description [Variation Report for NM_182902.4(KIF9):c.1721C>T (p.Pro574Leu)]
NM_182902.4(KIF9):c.1721C>T (p.Pro574Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
GREB1-like protein isoform X15 [Homo sapiens]
GREB1-like protein isoform X15 [Homo sapiens]gi|2462561530|ref|XP_054175119.1|Protein
-
PREDICTED: Homo sapiens GREB1 like retinoic acid receptor coactivator (GREB1L), ...
PREDICTED: Homo sapiens GREB1 like retinoic acid receptor coactivator (GREB1L), transcript variant X26, mRNAgi|2217317711|ref|XM_047437827.1|Nucleotide
-
M.musculus mRNA for ribosomal protein L7
M.musculus mRNA for ribosomal protein L7gi|53911|emb|X57960.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024