Related gene-specific medical variations for Gene (Select 56547) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3303121	NM_001005177.3(OR52R1):c.833T>C (p.Leu278Pro)	MMP26, OR52R1 (L278P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303120	NM_001005177.3(OR52R1):c.128T>C (p.Val43Ala)	MMP26, OR52R1 (V43A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303119	NM_001005177.3(OR52R1):c.513C>G (p.Phe171Leu)	MMP26, OR52R1 (F171L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303118	NM_001005177.3(OR52R1):c.595C>G (p.Arg199Gly)	MMP26, OR52R1 (R199G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303117	NM_001005177.3(OR52R1):c.110C>T (p.Thr37Met)	MMP26, OR52R1 (T37M)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3303116	NM_001005177.3(OR52R1):c.364G>T (p.Ala122Ser)	MMP26, OR52R1 (A122S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303044	NM_001004759.3(OR51T1):c.676A>G (p.Thr226Ala)	MMP26, OR51T1 (T226A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303043	NM_001004759.3(OR51T1):c.148G>C (p.Val50Leu)	MMP26, OR51T1 (V50L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303042	NM_001004758.1(OR51S1):c.49G>A (p.Ala17Thr)	MMP26, OR51S1 (A17T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303041	NM_001004758.1(OR51S1):c.97T>G (p.Ser33Ala)	MMP26, OR51S1 (S33A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303040	NM_001004758.1(OR51S1):c.775T>C (p.Tyr259His)	MMP26, OR51S1 (Y259H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303039	NM_001004758.1(OR51S1):c.885C>A (p.Asn295Lys)	MMP26, OR51S1 (N295K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303025	NM_001005238.2(OR51G2):c.578C>T (p.Ala193Val)	MMP26, OR51G2 (A193V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303024	NM_001005238.2(OR51G2):c.783T>G (p.Ile261Met)	MMP26, OR51G2 (I261M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303023	NM_001005238.2(OR51G2):c.247C>T (p.Leu83Phe)	MMP26, OR51G2 (L83F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303022	NM_001005238.2(OR51G2):c.191T>G (p.Met64Arg)	MMP26, OR51G2 (M64R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303021	NM_001005238.2(OR51G2):c.466C>T (p.Arg156Cys)	MMP26, OR51G2 (R156C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303020	NM_001005238.2(OR51G2):c.518A>G (p.Tyr173Cys)	MMP26, OR51G2 (Y173C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303019	NM_001005237.1(OR51G1):c.619T>G (p.Cys207Gly)	MMP26, OR51G1 (C207G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303018	NM_001005237.1(OR51G1):c.164C>T (p.Ala55Val)	MMP26, OR51G1 (A55V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3303017	NM_001005237.1(OR51G1):c.197G>T (p.Gly66Val)	MMP26, OR51G1 (G66V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303016	NM_001005237.1(OR51G1):c.158C>T (p.Thr53Ile)	MMP26, OR51G1 (T53I)	Single nucleotide variant (intron variant +1 more)	not specified	GUncertain significance
Select item 3303015	NM_001004753.2(OR51F2):c.313T>C (p.Phe105Leu)	MMP26, OR51F2 (F105L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303014	NM_001004753.2(OR51F2):c.875T>C (p.Ile292Thr)	MMP26, OR51F2 (I292T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303013	NM_001004753.2(OR51F2):c.199A>G (p.Met67Val)	MMP26, OR51F2 (M67V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303012	NM_001004753.2(OR51F2):c.610G>A (p.Ala204Thr)	MMP26, OR51F2 (A204T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303011	NM_001004753.2(OR51F2):c.284A>G (p.Asn95Ser)	MMP26, OR51F2 (N95S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3303010	NM_001004753.2(OR51F2):c.611C>T (p.Ala204Val)	MMP26, OR51F2 (A204V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303009	NM_001004753.2(OR51F2):c.710G>A (p.Arg237Gln)	MMP26, OR51F2 (R237Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3303008	NM_001004752.2(OR51F1):c.667A>G (p.Ile223Val)	MMP26, OR51F1 (I223V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303007	NM_001004752.2(OR51F1):c.194A>G (p.His65Arg)	MMP26, OR51F1 (H65R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303006	NM_001004752.2(OR51F1):c.155G>A (p.Ser52Asn)	MMP26, OR51F1 (S52N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3303005	NM_001004752.2(OR51F1):c.254C>G (p.Ser85Cys)	MMP26, OR51F1 (S85C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302985	NM_001004749.2(OR51A7):c.391A>G (p.Arg131Gly)	MMP26, OR51A7 (R131G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302984	NM_001005329.2(OR51A4):c.17C>T (p.Thr6Ile)	MMP26, OR51A4 (T6I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302983	NM_001005329.2(OR51A4):c.263T>C (p.Leu88Pro)	MMP26, OR51A4 (L88P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302982	NM_001004748.1(OR51A2):c.84G>C (p.Trp28Cys)	MMP26, OR51A2 (W28C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3302981	NM_001004748.1(OR51A2):c.557T>C (p.Val186Ala)	MMP26, OR51A2 (V186A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206033	NM_001005177.3(OR52R1):c.874C>T (p.Pro292Ser)	MMP26, OR52R1 (P292S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206032	NM_001005177.3(OR52R1):c.845T>C (p.Leu282Pro)	MMP26, OR52R1 (L282P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206031	NM_001005177.3(OR52R1):c.760C>T (p.Leu254Phe)	MMP26, OR52R1 (L254F)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3206030	NM_001005177.3(OR52R1):c.451G>A (p.Val151Met)	MMP26, OR52R1 (V151M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206029	NM_001005177.3(OR52R1):c.368T>C (p.Leu123Pro)	MMP26, OR52R1 (L123P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206027	NM_001005177.3(OR52R1):c.245C>T (p.Pro82Leu)	MMP26, OR52R1 (P82L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205878	NM_001004759.3(OR51T1):c.790C>A (p.His264Asn)	MMP26, OR51T1 (H264N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205877	NM_001004759.3(OR51T1):c.766C>T (p.Pro256Ser)	MMP26, OR51T1 (P256S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205876	NM_001004759.3(OR51T1):c.763G>A (p.Val255Met)	MMP26, OR51T1 (V255M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205873	NM_001004759.3(OR51T1):c.395T>G (p.Leu132Arg)	MMP26, OR51T1 (L132R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205872	NM_001004759.3(OR51T1):c.370C>T (p.Arg124Cys)	MMP26, OR51T1 (R124C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205871	NM_001004759.3(OR51T1):c.254G>C (p.Gly85Ala)	MMP26, OR51T1 (G85A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205869	NM_001004759.3(OR51T1):c.133A>C (p.Ser45Arg)	MMP26, OR51T1 (S45R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205868	NM_001004759.3(OR51T1):c.122T>G (p.Leu41Arg)	MMP26, OR51T1 (L41R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205867	NM_001004759.3(OR51T1):c.77A>T (p.His26Leu)	MMP26, OR51T1 (H26L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205866	NM_001004759.3(OR51T1):c.961G>A (p.Gly321Ser)	MMP26, OR51T1 (G321S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205864	NM_001004758.1(OR51S1):c.913G>A (p.Glu305Lys)	MMP26, OR51S1 (E305K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205863	NM_001004758.1(OR51S1):c.908T>C (p.Met303Thr)	MMP26, OR51S1 (M303T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205862	NM_001004758.1(OR51S1):c.722G>A (p.Arg241His)	MMP26, OR51S1 (R241H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205861	NM_001004758.1(OR51S1):c.710C>A (p.Ser237Tyr)	MMP26, OR51S1 (S237Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205859	NM_001004758.1(OR51S1):c.569C>T (p.Pro190Leu)	MMP26, OR51S1 (P190L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205858	NM_001004758.1(OR51S1):c.415C>T (p.His139Tyr)	MMP26, OR51S1 (H139Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205857	NM_001004758.1(OR51S1):c.37A>G (p.Ser13Gly)	MMP26, OR51S1 (S13G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205856	NM_001004758.1(OR51S1):c.193C>T (p.Arg65Cys)	MMP26, OR51S1 (R65C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205823	NM_001005238.2(OR51G2):c.802C>T (p.Arg268Cys)	MMP26, OR51G2 (R268C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205821	NM_001005238.2(OR51G2):c.725C>T (p.Ala242Val)	MMP26, OR51G2 (A242V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205820	NM_001005238.2(OR51G2):c.589A>C (p.Met197Leu)	MMP26, OR51G2 (M197L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205819	NM_001005238.2(OR51G2):c.467G>A (p.Arg156His)	MMP26, OR51G2 (R156H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205818	NM_001005238.2(OR51G2):c.170A>G (p.Glu57Gly)	MMP26, OR51G2 (E57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205817	NM_001005238.2(OR51G2):c.115A>C (p.Met39Leu)	MMP26, OR51G2 (M39L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205816	NM_001005237.1(OR51G1):c.832A>G (p.Met278Val)	MMP26, OR51G1 (M278V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205815	NM_001005237.1(OR51G1):c.661G>T (p.Ala221Ser)	MMP26, OR51G1 (A221S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205814	NM_001005237.1(OR51G1):c.581T>G (p.Ile194Ser)	MMP26, OR51G1 (I194S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205813	NM_001005237.1(OR51G1):c.502T>G (p.Phe168Val)	MMP26, OR51G1 (F168V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205812	NM_001005237.1(OR51G1):c.206C>T (p.Ala69Val)	MMP26, OR51G1 (A69V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205811	NM_001005237.1(OR51G1):c.196G>A (p.Gly66Ser)	MMP26, OR51G1 (G66S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205810	NM_001005237.1(OR51G1):c.113T>C (p.Leu38Pro)	MMP26, OR51G1 (L38P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205808	NM_001004753.2(OR51F2):c.794G>A (p.Arg265His)	MMP26, OR51F2 (R265H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3205807	NM_001004753.2(OR51F2):c.688A>T (p.Ile230Phe)	MMP26, OR51F2 (I230F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205806	NM_001004753.2(OR51F2):c.493G>T (p.Val165Phe)	MMP26, OR51F2 (V165F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205805	NM_001004753.2(OR51F2):c.-33A>G	MMP26, OR51F2	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3205804	NM_001004753.2(OR51F2):c.462T>G (p.Asn154Lys)	MMP26, OR51F2 (N154K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205803	NM_001004753.2(OR51F2):c.395T>G (p.Leu132Arg)	MMP26, OR51F2 (L132R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205802	NM_001004753.2(OR51F2):c.334A>G (p.Met112Val)	MMP26, OR51F2 (M112V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205801	NM_001004753.2(OR51F2):c.323G>T (p.Gly108Val)	MMP26, OR51F2 (G108V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205800	NM_001004753.2(OR51F2):c.183G>A (p.Met61Ile)	MMP26, OR51F2 (M61I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205799	NM_001004753.2(OR51F2):c.181A>G (p.Met61Val)	MMP26, OR51F2 (M61V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205798	NM_001004753.2(OR51F2):c.110A>G (p.Tyr37Cys)	MMP26, OR51F2 (Y37C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205797	NM_001004752.2(OR51F1):c.905G>A (p.Ser302Asn)	MMP26, OR51F1 (S302N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205796	NM_001004752.2(OR51F1):c.839T>G (p.Val280Gly)	MMP26, OR51F1 (V280G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205795	NM_001004752.2(OR51F1):c.497T>G (p.Leu166Trp)	MMP26, OR51F1 (L166W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205794	NM_001004752.2(OR51F1):c.379A>C (p.Thr127Pro)	MMP26, OR51F1 (T127P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205793	NM_001004752.2(OR51F1):c.31C>G (p.Leu11Val)	MMP26, OR51F1 (L11V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205750	NM_001004749.2(OR51A7):c.820C>T (p.Leu274Phe)	MMP26, OR51A7 (L274F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205749	NM_001004749.2(OR51A7):c.439A>C (p.Ile147Leu)	MMP26, OR51A7 (I147L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205748	NM_001004749.2(OR51A7):c.343C>T (p.Leu115Phe)	MMP26, OR51A7 (L115F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205747	NM_001004749.2(OR51A7):c.307T>G (p.Phe103Val)	MMP26, OR51A7 (F103V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205746	NM_001004749.2(OR51A7):c.249G>T (p.Arg83Ser)	MMP26, OR51A7 (R83S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205745	NM_001005329.2(OR51A4):c.871A>T (p.Ile291Phe)	MMP26, OR51A4 (I291F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205744	NM_001005329.2(OR51A4):c.637A>T (p.Ile213Phe)	MMP26, OR51A4 (I213F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205743	NM_001005329.2(OR51A4):c.463A>C (p.Met155Leu)	MMP26, OR51A4 (M155L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3205741	NM_001004748.1(OR51A2):c.585A>T (p.Arg195Ser)	MMP26, OR51A2 (R195S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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