Related gene-specific medical variations for Gene (Select 1441) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2439595	NM_000760.4(CSF3R):c.1587dup (p.Ala530fs)	CSF3R (A530fs)	Duplication (frameshift variant)	not provided	GLikely pathogenic
Select item 1322165	NM_000760.4(CSF3R):c.189G>A (p.Trp63Ter)	CSF3R (W63*)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 376125	NM_000760.4(CSF3R):c.1843A>G (p.Thr615Ala)	CSF3R (T615A)	Single nucleotide variant (missense variant)	Chronic myelogenous leukemia, BCR-ABL1 positive	GLikely pathogenic

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