Related gene-specific medical variations for Gene (Select 2845) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282358	NM_005295.3(GPR22):c.67A>G (p.Ile23Val)	COG5, GPR22 (I23V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282357	NM_005295.3(GPR22):c.46A>G (p.Asn16Asp)	COG5, GPR22 (N16D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101686	NM_005295.3(GPR22):c.808G>A (p.Asp270Asn)	COG5, GPR22 (D270N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101685	NM_005295.3(GPR22):c.703C>A (p.Leu235Ile)	COG5, GPR22 (L235I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101684	NM_005295.3(GPR22):c.397G>A (p.Val133Ile)	COG5, GPR22 (V133I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457445	NM_005295.3(GPR22):c.1271A>G (p.Lys424Arg)	COG5, GPR22 (K424R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375448	NM_005295.3(GPR22):c.1295C>A (p.Thr432Lys)	COG5, GPR22 (T432K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353296	NM_005295.3(GPR22):c.1202T>C (p.Ile401Thr)	COG5, GPR22 (I401T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352795	NM_005295.3(GPR22):c.191T>C (p.Val64Ala)	COG5, GPR22 (V64A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336358	NM_005295.3(GPR22):c.1137A>C (p.Lys379Asn)	COG5, GPR22 (K379N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2332403	NM_005295.3(GPR22):c.1166T>C (p.Ile389Thr)	COG5, GPR22 (I389T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294279	NM_005295.3(GPR22):c.875T>C (p.Ile292Thr)	COG5, GPR22 (I292T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205259	NM_005295.3(GPR22):c.270A>G (p.Ile90Met)	COG5, GPR22 (I90M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance