Related gene-specific medical variations for Gene (Select 79799) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330854	NM_024743.4(UGT2A3):c.1193T>A (p.Leu398His)	LOC126807070, UGT2A3 (L398H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186153	NM_024743.4(UGT2A3):c.1515G>T (p.Leu505Phe)	LOC126807070, UGT2A3 (L505F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3186152	NM_024743.4(UGT2A3):c.1424G>C (p.Arg475Pro)	LOC126807070, UGT2A3 (R475P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624194	NM_024743.4(UGT2A3):c.1216G>A (p.Ala406Thr)	LOC126807070, UGT2A3 (A406T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588708	NM_024743.4(UGT2A3):c.1441C>T (p.Leu481Phe)	LOC126807070, UGT2A3 (L481F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473952	NM_024743.4(UGT2A3):c.1226C>A (p.Ala409Glu)	LOC126807070, UGT2A3 (A409E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469789	NM_024743.4(UGT2A3):c.1343A>G (p.His448Arg)	LOC126807070, UGT2A3 (H448R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411412	NM_024743.4(UGT2A3):c.1400G>A (p.Arg467His)	LOC126807070, UGT2A3 (R467H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330490	NM_024743.4(UGT2A3):c.1399C>T (p.Arg467Cys)	LOC126807070, UGT2A3 (R467C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270939	NM_024743.4(UGT2A3):c.1580A>G (p.Glu527Gly)	LOC126807070, UGT2A3 (E527G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250981	NM_024743.4(UGT2A3):c.1231G>A (p.Val411Ile)	LOC126807070, UGT2A3 (V411I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238294	NM_024743.4(UGT2A3):c.1538C>T (p.Ser513Phe)	LOC126807070, UGT2A3 (S513F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance