"Australian Red Cross Blood Service"[submitter] AND "KEL"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 870126	NM_000420.3(KEL):c.2065G>T (p.Asp689Tyr)	KEL (D689Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1185000	NM_000420.3(KEL):c.1934C>T (p.Ala645Val)	KEL (A645V)	Single nucleotide variant (missense variant)	Kell blood group system	GAffects
Select item 1184987	NM_000420.3(KEL):c.1720G>A (p.Ala574Thr)	KEL (A574T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1184732	NM_000420.3(KEL):c.586C>G (p.Leu196Val)	KEL (L196V)	Single nucleotide variant (missense variant)	Kell blood group system	GUncertain significance
Select item 1184986	NM_000420.3(KEL):c.575G>A (p.Arg192Gln)	KEL (R192Q)	Single nucleotide variant (missense variant)	Kell blood group system	GAffects
Select item 1184988	NM_000420.3(KEL):c.257G>A (p.Arg86Gln)	KEL (R86Q)	Single nucleotide variant (missense variant)	Kell blood group system	GAffects

ClinVar