Related gene-specific medical variations for Gene (Select 23678) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3317934	NM_001033578.3(SGK3):c.544A>G (p.Lys182Glu)	C8orf44-SGK3, SGK3 (K182E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317933	NM_001033578.3(SGK3):c.491T>G (p.Phe164Cys)	C8orf44-SGK3, SGK3 (F164C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161031	NM_001033578.3(SGK3):c.790A>G (p.Arg264Gly)	C8orf44-SGK3, SGK3 (R264G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161030	NM_001033578.3(SGK3):c.542G>A (p.Arg181Gln)	C8orf44-SGK3, SGK3 (R181Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161029	NM_001033578.3(SGK3):c.331C>A (p.Pro111Thr)	C8orf44-SGK3, SGK3 (P111T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161028	NM_001033578.3(SGK3):c.202A>G (p.Met68Val)	C8orf44-SGK3, SGK3 (M68V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161027	NM_001033578.3(SGK3):c.155C>A (p.Ala52Glu)	C8orf44-SGK3, SGK3 (A52E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161026	NM_001033578.3(SGK3):c.1096G>C (p.Val366Leu)	C8orf44-SGK3, SGK3 (V334L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603823	NM_001033578.3(SGK3):c.1115A>G (p.Asn372Ser)	C8orf44-SGK3, SGK3 (N372S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558813	NM_001033578.3(SGK3):c.1301C>A (p.Pro434Gln)	C8orf44-SGK3, SGK3 (P434Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494738	NM_001033578.3(SGK3):c.1340G>A (p.Arg447Lys)	C8orf44-SGK3, SGK3 (R447K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492708	NM_001033578.3(SGK3):c.1038C>G (p.Cys346Trp)	C8orf44-SGK3, SGK3 (C346W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469019	NM_001033578.3(SGK3):c.832C>A (p.His278Asn)	C8orf44-SGK3, SGK3 (H278N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459915	NM_001033578.3(SGK3):c.1408A>G (p.Ile470Val)	C8orf44-SGK3, SGK3 (I470V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2443738	NM_001033578.3(SGK3):c.979-96T>A	C8orf44-SGK3, SGK3	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2356270	NM_001033578.3(SGK3):c.286G>A (p.Glu96Lys)	C8orf44-SGK3, SGK3 (E96K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267536	NM_001033578.3(SGK3):c.611A>G (p.Gln204Arg)	C8orf44-SGK3, SGK3 (Q204R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263750	NM_001033578.3(SGK3):c.799G>A (p.Ala267Thr)	C8orf44-SGK3, SGK3 (A267T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 161501	NM_001033578.3(SGK3):c.782A>G (p.His261Arg)	SGK3, C8orf44-SGK3 (H261R)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance