Related gene-specific medical variations for Gene (Select 126863064) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059051	NM_198437.3(AURKA):c.169A>G (p.Ile57Val)	AURKA, LOC126863064 (I57V +1 more)	Single nucleotide variant (synonymous variant +1 more)	AURKA-related condition	GBenign
Select item 3033554	NM_198437.3(AURKA):c.311C>T (p.Ser104Leu)	AURKA, LOC126863064 (S104L +1 more)	Single nucleotide variant (missense variant)	AURKA-related condition	GLikely benign
Select item 2620010	NM_198437.3(AURKA):c.314C>T (p.Ala105Val)	AURKA, LOC126863064 (A105V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610055	NM_198437.3(AURKA):c.209C>T (p.Pro70Leu)	AURKA, LOC126863064 (P104L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2601244	NM_198437.3(AURKA):c.189G>C (p.Lys63Asn)	AURKA, LOC126863064 (K63N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471489	NM_198437.3(AURKA):c.222G>C (p.Gln74His)	AURKA, LOC126863064 (Q74H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 6642	NM_198437.3(AURKA):c.91T>A (p.Phe31Ile)	AURKA, LOC126863064 (F31I)	Single nucleotide variant (missense variant)	AURKA-related condition +1 more	GBenign

ClinVar