Related gene-specific medical variations for Gene (Select 58476) - ClinVar

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Links from Gene

Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3328227	NM_021202.3(TP53INP2):c.365C>T (p.Pro122Leu)	LOC130065730, TP53INP2 (P122L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328226	NM_021202.3(TP53INP2):c.521G>A (p.Arg174Gln)	LOC130065732, TP53INP2 (R174Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328224	NM_021202.3(TP53INP2):c.213G>C (p.Trp71Cys)	LOC130065730, TP53INP2 (W71C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181452	NM_021202.3(TP53INP2):c.518A>G (p.Gln173Arg)	LOC130065732, TP53INP2 (Q173R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181450	NM_021202.3(TP53INP2):c.47C>T (p.Pro16Leu)	LOC125387262, TP53INP2 (P16L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181449	NM_021202.3(TP53INP2):c.436G>A (p.Glu146Lys)	LOC130065732, TP53INP2 (E146K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181448	NM_021202.3(TP53INP2):c.316A>T (p.Met106Leu)	LOC130065730, TP53INP2 (M106L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181447	NM_021202.3(TP53INP2):c.284C>G (p.Pro95Arg)	LOC130065730, TP53INP2 (P95R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181446	NM_021202.3(TP53INP2):c.202G>A (p.Asp68Asn)	LOC130065730, TP53INP2 (D68N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181445	NM_021202.3(TP53INP2):c.145A>G (p.Ser49Gly)	LOC130065730, TP53INP2 (S49G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541552	NM_021202.3(TP53INP2):c.440C>T (p.Pro147Leu)	LOC130065732, TP53INP2 (P147L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530745	NM_021202.3(TP53INP2):c.427G>A (p.Ala143Thr)	LOC130065732, TP53INP2 (A143T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368393	NM_021202.3(TP53INP2):c.146G>A (p.Ser49Asn)	LOC130065730, TP53INP2 (S49N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362012	NM_021202.3(TP53INP2):c.205G>C (p.Glu69Gln)	LOC130065730, TP53INP2 (E69Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354985	NM_021202.3(TP53INP2):c.433C>G (p.Arg145Gly)	LOC130065732, TP53INP2 (R145G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346124	NM_021202.3(TP53INP2):c.260G>C (p.Gly87Ala)	LOC130065730, TP53INP2 (G87A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342536	NM_021202.3(TP53INP2):c.466C>G (p.Leu156Val)	LOC130065732, TP53INP2 (L156V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330244	NM_021202.3(TP53INP2):c.49G>C (p.Glu17Gln)	LOC125387262, TP53INP2 (E17Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323708	NM_021202.3(TP53INP2):c.431G>A (p.Arg144His)	LOC130065732, TP53INP2 (R144H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301160	NM_021202.3(TP53INP2):c.76G>T (p.Val26Leu)	LOC125387262, TP53INP2 (V26L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 20