Related gene-specific medical variations for Gene (Select 100874100) - ClinVar

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Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3171162	NM_012449.3(STEAP1):c.550A>G (p.Met184Val)	STEAP1, STEAP2-AS1 (M184V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171160	NM_012449.3(STEAP1):c.406G>C (p.Ala136Pro)	STEAP1, STEAP2-AS1 (A136P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618663	NM_012449.3(STEAP1):c.508T>C (p.Phe170Leu)	STEAP1, STEAP2-AS1 (F170L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613710	NM_012449.3(STEAP1):c.410C>A (p.Ala137Glu)	STEAP1, STEAP2-AS1 (A137E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602582	NM_012449.3(STEAP1):c.965A>G (p.His322Arg)	STEAP1, STEAP2-AS1 (H322R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595526	NM_012449.3(STEAP1):c.107G>A (p.Ser36Asn)	STEAP1, STEAP2-AS1 (S36N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546222	NM_012449.3(STEAP1):c.166G>C (p.Asp56His)	STEAP1, STEAP2-AS1 (D56H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474171	NM_012449.3(STEAP1):c.772G>A (p.Gly258Arg)	STEAP1, STEAP2-AS1 (G258R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471507	NM_012449.3(STEAP1):c.908T>C (p.Ile303Thr)	STEAP1, STEAP2-AS1 (I303T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471451	NM_012449.3(STEAP1):c.823A>T (p.Asn275Tyr)	STEAP1, STEAP2-AS1 (N275Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464115	NM_012449.3(STEAP1):c.817G>A (p.Ala273Thr)	STEAP1, STEAP2-AS1 (A273T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455978	NM_012449.3(STEAP1):c.557G>A (p.Arg186Gln)	STEAP1, STEAP2-AS1 (R186Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366206	NM_012449.3(STEAP1):c.76G>A (p.Asp26Asn)	STEAP1, STEAP2-AS1 (D26N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361532	NM_012449.3(STEAP1):c.541T>A (p.Ser181Thr)	STEAP1, STEAP2-AS1 (S181T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357761	NM_012449.3(STEAP1):c.413T>C (p.Ile138Thr)	STEAP1, STEAP2-AS1 (I138T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330768	NM_012449.3(STEAP1):c.187C>G (p.His63Asp)	STEAP1, STEAP2-AS1 (H63D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306390	NM_012449.3(STEAP1):c.319T>C (p.Tyr107His)	STEAP1, STEAP2-AS1 (Y107H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252504	NM_012449.3(STEAP1):c.839T>C (p.Ile280Thr)	STEAP1, STEAP2-AS1 (I280T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206173	NM_012449.3(STEAP1):c.517G>A (p.Val173Ile)	STEAP1, STEAP2-AS1 (V173I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770940	NM_012449.3(STEAP1):c.804C>T (p.His268=)	STEAP1, STEAP2-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 144932	GRCh38/hg38 7q21.13(chr7:89941939-90066509)x1	STEAP2-AS1	Copy number loss	See cases	GBenign

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Links from Gene

Items: 21