Related gene-specific medical variations for Gene (Select 10403) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298948	NM_006101.3(NDC80):c.934G>A (p.Ala312Thr)	LOC126862679, NDC80 (A312T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185704	NM_006101.3(NDC80):c.778G>A (p.Val260Met)	LOC126862679, NDC80 (V260M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185638	NM_006101.3(NDC80):c.1012G>C (p.Val338Leu)	LOC126862679, NDC80 (V338L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538963	NM_006101.3(NDC80):c.940A>G (p.Met314Val)	LOC126862679, NDC80 (M314V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276742	NM_006101.3(NDC80):c.958C>T (p.His320Tyr)	LOC126862679, NDC80 (H320Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269696	NM_006101.3(NDC80):c.929A>G (p.Tyr310Cys)	LOC126862679, NDC80 (Y310C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230930	NM_006101.3(NDC80):c.899A>C (p.Lys300Thr)	LOC126862679, NDC80 (K300T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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