Related gene-specific medical variations for Gene (Select 8683) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3322766	NM_003769.3(SRSF9):c.562A>G (p.Thr188Ala)	GATC, SRSF9 (T188A)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2570423	NM_003769.3(SRSF9):c.605G>A (p.Arg202His)	GATC, SRSF9 (R202H)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2556420	NM_003769.3(SRSF9):c.116G>C (p.Arg39Pro)	LOC130008941, SRSF9 (R39P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368718	NM_003769.3(SRSF9):c.644T>A (p.Phe215Tyr)	GATC, SRSF9 (F215Y)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2334149	NM_003769.3(SRSF9):c.172C>T (p.Arg58Cys)	LOC130008941, SRSF9 (R58C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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