Related gene-specific medical variations for Gene (Select 27141) - ClinVar

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Items: 58

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3292200	NM_019839.5(LTB4R2):c.454C>T (p.Leu152Phe)	CIDEB, LTB4R2 (L152F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292199	NM_019839.5(LTB4R2):c.121G>C (p.Val41Leu)	CIDEB, LTB4R2 (V41L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292198	NM_019839.5(LTB4R2):c.385G>T (p.Ala129Ser)	CIDEB, LOC130055420 +1 more (A129S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292197	NM_019839.5(LTB4R2):c.155G>C (p.Arg52Pro)	CIDEB, LTB4R2 (R52P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292196	NM_019839.5(LTB4R2):c.208G>A (p.Ala70Thr)	CIDEB, LTB4R2 (A70T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292195	NM_019839.5(LTB4R2):c.467C>T (p.Ala156Val)	CIDEB, LTB4R2 (A156V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292193	NM_019839.5(LTB4R2):c.646G>C (p.Gly216Arg)	CIDEB, LOC130055421 +1 more (G216R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3292192	NM_019839.5(LTB4R2):c.170C>T (p.Ala57Val)	CIDEB, LTB4R2 (A57V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3267351	NM_001393339.1(CIDEB):c.293G>A (p.Cys98Tyr)	CIDEB, NOP9 (C98Y)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3267350	NM_001393339.1(CIDEB):c.73C>T (p.Arg25Trp)	CIDEB, NOP9 (R25W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3267349	NM_001393339.1(CIDEB):c.247G>A (p.Ala83Thr)	CIDEB, NOP9 (A83T)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3144985	NM_001393339.1(CIDEB):c.74G>A (p.Arg25Gln)	CIDEB, NOP9 (R25Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144984	NM_001393339.1(CIDEB):c.68T>C (p.Phe23Ser)	CIDEB, NOP9 (F23S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144983	NM_001393339.1(CIDEB):c.431G>A (p.Arg144Gln)	CIDEB, NOP9 (R144Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144982	NM_001393339.1(CIDEB):c.172G>A (p.Glu58Lys)	CIDEB, NOP9 (E58K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144981	NM_001393339.1(CIDEB):c.109C>A (p.Pro37Thr)	CIDEB, NOP9 (P37T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121395	NM_019839.5(LTB4R2):c.737T>C (p.Leu246Pro)	CIDEB, LOC130055421 +1 more (L246P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121394	NM_019839.5(LTB4R2):c.542A>T (p.His181Leu)	CIDEB, LTB4R2 (H181L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121393	NM_019839.5(LTB4R2):c.464C>T (p.Pro155Leu)	CIDEB, LTB4R2 (P155L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121392	NM_019839.5(LTB4R2):c.437G>C (p.Trp146Ser)	CIDEB, LTB4R2 (W146S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121391	NM_019839.5(LTB4R2):c.392G>A (p.Arg131Gln)	CIDEB, LOC130055420 +1 more (R131Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121390	NM_019839.5(LTB4R2):c.391C>T (p.Arg131Trp)	CIDEB, LOC130055420 +1 more (R131W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3121388	NM_019839.5(LTB4R2):c.176C>A (p.Thr59Lys)	CIDEB, LTB4R2 (T59K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2609929	NM_019839.5(LTB4R2):c.566C>T (p.Ala189Val)	CIDEB, LTB4R2 (A189V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2609356	NM_019839.5(LTB4R2):c.155G>A (p.Arg52Gln)	CIDEB, LTB4R2 (R52Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2588034	NM_001393339.1(CIDEB):c.188C>A (p.Ala63Glu)	CIDEB, NOP9 (A63E)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2547126	NM_019839.5(LTB4R2):c.707T>C (p.Leu236Pro)	CIDEB, LOC130055421 +1 more (L236P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534260	NM_019839.5(LTB4R2):c.338G>C (p.Gly113Ala)	CIDEB, LOC130055420 +1 more (G113A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534259	NM_019839.5(LTB4R2):c.337G>T (p.Gly113Cys)	CIDEB, LOC130055420 +1 more (G113C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2534258	NM_019839.5(LTB4R2):c.304G>A (p.Ala102Thr)	CIDEB, LTB4R2 (A102T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2515819	NM_019839.5(LTB4R2):c.107C>T (p.Pro36Leu)	CIDEB, LTB4R2 (P36L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2496122	NM_019839.5(LTB4R2):c.733C>T (p.Leu245Phe)	CIDEB, LOC130055421 +1 more (L245F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2494502	NM_019839.5(LTB4R2):c.248C>T (p.Thr83Ile)	CIDEB, LTB4R2 (T83I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2488406	NM_019839.5(LTB4R2):c.470C>T (p.Ala157Val)	CIDEB, LTB4R2 (A157V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2485996	NM_019839.5(LTB4R2):c.209C>T (p.Ala70Val)	CIDEB, LTB4R2 (A70V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2468141	NM_019839.5(LTB4R2):c.650G>A (p.Arg217Gln)	CIDEB, LOC130055421 +1 more (R217Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2396315	NM_019839.5(LTB4R2):c.460G>C (p.Val154Leu)	CIDEB, LTB4R2 (V154L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2362214	NM_001393339.1(CIDEB):c.622G>A (p.Glu208Lys)	CIDEB, NOP9 (E208K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2356853	NM_019839.5(LTB4R2):c.376C>T (p.Pro126Ser)	CIDEB, LOC130055420 +1 more (P126S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2339611	NM_019839.5(LTB4R2):c.125T>C (p.Val42Ala)	CIDEB, LTB4R2 (V42A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2327453	NM_019839.5(LTB4R2):c.48G>C (p.Trp16Cys)	CIDEB, LTB4R2 (W16C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2320251	NM_001393339.1(CIDEB):c.116G>A (p.Arg39His)	CIDEB, NOP9 (R39H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2316580	NM_019839.5(LTB4R2):c.760C>T (p.Pro254Ser)	CIDEB, LTB4R2 (P254S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2286863	NM_001393339.1(CIDEB):c.115C>T (p.Arg39Cys)	CIDEB, NOP9 (R39C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2280230	NM_001393339.1(CIDEB):c.521T>C (p.Val174Ala)	CIDEB, NOP9 (V124A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2266286	NM_019839.5(LTB4R2):c.65C>T (p.Thr22Ile)	CIDEB, LTB4R2 (T22I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2246438	NM_019839.5(LTB4R2):c.737T>A (p.Leu246Gln)	CIDEB, LOC130055421 +1 more (L246Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2245332	NM_019839.5(LTB4R2):c.553G>C (p.Glu185Gln)	CIDEB, LTB4R2 (E185Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2244197	NM_001393339.1(CIDEB):c.143G>A (p.Arg48Gln)	CIDEB, NOP9 (R48Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2239430	NM_001393339.1(CIDEB):c.607G>C (p.Ala203Pro)	CIDEB, NOP9 (A153P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2232291	NM_019839.5(LTB4R2):c.266T>G (p.Leu89Arg)	CIDEB, LTB4R2 (L89R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2227097	NM_001393339.1(CIDEB):c.142C>T (p.Arg48Trp)	CIDEB, NOP9 (R48W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2223737	NM_019839.5(LTB4R2):c.194C>T (p.Ala65Val)	CIDEB, LTB4R2 (A65V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2214611	NM_001393339.1(CIDEB):c.173A>G (p.Glu58Gly)	CIDEB, NOP9 (E58G)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2213806	NM_019839.5(LTB4R2):c.557C>G (p.Thr186Ser)	CIDEB, LTB4R2 (T186S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 783684	NM_019839.5(LTB4R2):c.559_560del (p.Leu187fs)	CIDEB, LTB4R2 (L187fs)	Microsatellite (5 prime UTR variant +1 more)	not provided	GBenign
Select item 768643	NM_019839.5(LTB4R2):c.564C>T (p.Thr188=)	CIDEB, LTB4R2	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 712146	NM_019839.5(LTB4R2):c.388C>T (p.Pro130Ser)	CIDEB, LOC130055420 +1 more (P130S)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign

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Links from Gene

Items: 58