Related gene-specific medical variations for Gene (Select 10081) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3210598	NM_005707.2(PDCD7):c.592G>A (p.Ala198Thr)	LOC130057312, PDCD7 (A198T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622590	NM_005707.2(PDCD7):c.181G>A (p.Ala61Thr)	LOC130057313, PDCD7 (A61T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614387	NM_005707.2(PDCD7):c.374C>T (p.Ala125Val)	LOC130057312, PDCD7 (A125V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611179	NM_005707.2(PDCD7):c.727C>T (p.Arg243Trp)	LOC130057312, PDCD7 (R243W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599321	NM_005707.2(PDCD7):c.400G>T (p.Gly134Trp)	LOC130057312, PDCD7 (G134W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598299	NM_005707.2(PDCD7):c.358C>T (p.Pro120Ser)	LOC130057312, PDCD7 (P120S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2555912	NM_005707.2(PDCD7):c.692A>G (p.Tyr231Cys)	LOC130057312, PDCD7 (Y231C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548799	NM_005707.2(PDCD7):c.722G>C (p.Arg241Thr)	LOC130057312, PDCD7 (R241T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547320	NM_005707.2(PDCD7):c.160C>G (p.Pro54Ala)	LOC130057313, PDCD7 (P54A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370805	NM_005707.2(PDCD7):c.467G>A (p.Arg156Gln)	LOC130057312, PDCD7 (R156Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365467	NM_005707.2(PDCD7):c.193C>G (p.Arg65Gly)	LOC130057313, PDCD7 (R65G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342874	NM_005707.2(PDCD7):c.241T>C (p.Tyr81His)	LOC130057313, PDCD7 (Y81H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270527	NM_005707.2(PDCD7):c.176C>T (p.Pro59Leu)	LOC130057313, PDCD7 (P59L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2256464	NM_005707.2(PDCD7):c.539G>A (p.Arg180Gln)	LOC130057312, PDCD7 (R180Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213422	NM_005707.2(PDCD7):c.713G>A (p.Arg238Lys)	LOC130057312, PDCD7 (R238K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance