Related gene-specific medical variations for Gene (Select 55366) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3118551	NM_018490.5(LGR4):c.124G>C (p.Asp42His)	LGR4, LGR4-AS1 (D42H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621177	NM_018490.5(LGR4):c.182C>T (p.Ala61Val)	LGR4, LGR4-AS1 (A61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534237	NM_018490.5(LGR4):c.88G>T (p.Ala30Ser)	LGR4, LGR4-AS1 +1 more (A30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534236	NM_018490.5(LGR4):c.79C>T (p.Pro27Ser)	LGR4, LGR4-AS1 +1 more (P27S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534235	NM_018490.5(LGR4):c.49G>T (p.Gly17Cys)	LGR4, LGR4-AS1 +1 more (G17C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534234	NM_018490.5(LGR4):c.47T>G (p.Leu16Arg)	LGR4, LGR4-AS1 +1 more (L16R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2532247	NM_018490.5(LGR4):c.155C>T (p.Pro52Leu)	LGR4, LGR4-AS1 (P52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522407	NM_018490.5(LGR4):c.59G>A (p.Gly20Glu)	LGR4, LGR4-AS1 +1 more (G20E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302882	NM_018490.5(LGR4):c.53C>T (p.Ser18Leu)	LGR4, LGR4-AS1 +1 more (S18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance