Related gene-specific medical variations for Gene (Select 23456) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289949	NM_012089.3(ABCB10):c.184G>T (p.Val62Phe)	ABCB10, LOC129932735 (V62F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289898	NM_012089.3(ABCB10):c.148C>G (p.Arg50Gly)	ABCB10, LOC129932735 (R50G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289721	NM_012089.3(ABCB10):c.29G>C (p.Arg10Pro)	ABCB10, LOC129932735 (R10P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289440	NM_012089.3(ABCB10):c.425G>A (p.Gly142Glu)	ABCB10, LOC129932734 (G142E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119710	NM_012089.3(ABCB10):c.61G>A (p.Gly21Ser)	ABCB10, LOC129932735 (G21S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119473	NM_012089.3(ABCB10):c.29G>T (p.Arg10Leu)	ABCB10, LOC129932735 (R10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551078	NM_012089.3(ABCB10):c.303G>C (p.Arg101Ser)	ABCB10, LOC129932734 (R101S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542039	NM_012089.3(ABCB10):c.152T>G (p.Leu51Arg)	ABCB10, LOC129932735 (L51R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494000	NM_012089.3(ABCB10):c.361G>A (p.Gly121Ser)	ABCB10, LOC129932734 (G121S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391917	NM_012089.3(ABCB10):c.424G>C (p.Gly142Arg)	ABCB10, LOC129932734 (G142R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361236	NM_012089.3(ABCB10):c.204G>C (p.Trp68Cys)	ABCB10, LOC129932735 (W68C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344548	NM_012089.3(ABCB10):c.110C>G (p.Pro37Arg)	ABCB10, LOC129932735 (P37R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292784	NM_012089.3(ABCB10):c.407G>A (p.Gly136Glu)	ABCB10, LOC129932734 (G136E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262091	NM_012089.3(ABCB10):c.328G>C (p.Ala110Pro)	ABCB10, LOC129932734 (A110P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226264	NM_012089.3(ABCB10):c.41C>G (p.Pro14Arg)	ABCB10, LOC129932735 (P14R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215038	NM_012089.3(ABCB10):c.433G>A (p.Gly145Arg)	ABCB10, LOC129932734 (G145R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance