"Database of Curated Mutations (DoCM)"[submitter] AND "CSF1R"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 376269	NM_001288705.3(CSF1R):c.2907T>A (p.Tyr969Ter)	CSF1R (Y969* +1 more)	Single nucleotide variant (nonsense +1 more)	Neoplasm	GLikely pathogenic
Select item 376268	NM_001288705.3(CSF1R):c.2907T>G (p.Tyr969Ter)	CSF1R (Y969* +1 more)	Single nucleotide variant (nonsense +1 more)	Neoplasm	GLikely pathogenic
Select item 376271	NM_001288705.3(CSF1R):c.2906A>G (p.Tyr969Cys)	CSF1R (Y969C +1 more)	Single nucleotide variant (missense variant +1 more)	Neoplasm +1 more	GLikely pathogenic
Select item 376270	NM_001288705.3(CSF1R):c.2906A>T (p.Tyr969Phe)	CSF1R (Y969F +1 more)	Single nucleotide variant (missense variant +1 more)	Neoplasm +1 more	GLikely pathogenic
Select item 376272	NM_001288705.3(CSF1R):c.2905T>C (p.Tyr969His)	CSF1R (Y969H +1 more)	Single nucleotide variant (missense variant +1 more)	Neoplasm +1 more	GLikely pathogenic
Select item 376166	NM_001288705.3(CSF1R):c.1711T>G (p.Tyr571Asp)	CSF1R (Y571D +1 more)	Single nucleotide variant (missense variant +1 more)	Myeloproliferative disorder +1 more	GLikely pathogenic
Select item 376703	NM_001288705.3(CSF1R):c.903G>T (p.Leu301Phe)	CSF1R (L301F +1 more)	Single nucleotide variant (missense variant +1 more)	Hematologic neoplasm	GLikely pathogenic
Select item 376274	NM_001288705.3(CSF1R):c.902T>A (p.Leu301Ter)	CSF1R (L301* +1 more)	Single nucleotide variant (nonsense +1 more)	Neoplasm	GLikely pathogenic
Select item 376273	NM_001288705.3(CSF1R):c.902T>C (p.Leu301Ser)	CSF1R (L301S +1 more)	Single nucleotide variant (missense variant +1 more)	Neoplasm +1 more	GLikely pathogenic