Related gene-specific medical variations for Gene (Select 8832) - ClinVar - NCBI

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Links from Gene

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140693	NM_003874.4(CD84):c.886A>G (p.Asn296Asp)	CD84, LOC105371468 (N296D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140692	NM_003874.4(CD84):c.782T>C (p.Ile261Thr)	CD84, LOC105371468 (I261T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140691	NM_003874.4(CD84):c.715A>G (p.Ile239Val)	CD84, LOC105371468 (I125V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140689	NM_003874.4(CD84):c.277A>T (p.Asn93Tyr)	CD84, LOC105371468 (N93Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140688	NM_003874.4(CD84):c.191C>A (p.Thr64Lys)	CD84, LOC105371468 (T64K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609990	NM_003874.4(CD84):c.904G>A (p.Val302Met)	CD84, LOC105371468 (V302M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598384	NM_003874.4(CD84):c.331A>T (p.Ile111Leu)	CD84, LOC105371468 (I111L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538874	NM_003874.4(CD84):c.935G>A (p.Ser312Asn)	CD84, LOC105371468 +1 more (S312N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470389	NM_003874.4(CD84):c.625C>T (p.Arg209Trp)	CD84, LOC105371468 (R209W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470239	NM_003874.4(CD84):c.244T>G (p.Tyr82Asp)	CD84, LOC105371468 (Y82D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467678	NM_003874.4(CD84):c.646G>A (p.Ala216Thr)	CD84, LOC105371468 (A102T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402348	NM_003874.4(CD84):c.685G>A (p.Val229Met)	CD84, LOC105371468 (V115M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399596	NM_003874.4(CD84):c.452T>G (p.Val151Gly)	CD84, LOC105371468 (V151G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363410	NM_003874.4(CD84):c.269C>T (p.Pro90Leu)	CD84, LOC105371468 (P90L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2360924	NM_003874.4(CD84):c.658C>T (p.Arg220Cys)	CD84, LOC105371468 (R106C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281540	NM_003874.4(CD84):c.620C>T (p.Ser207Phe)	CD84, LOC105371468 (S93F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242046	NM_003874.4(CD84):c.550C>G (p.Pro184Ala)	CD84, LOC105371468 (P184A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214446	NM_003874.4(CD84):c.215C>T (p.Pro72Leu)	CD84, LOC105371468 (P72L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1321326	NM_003874.4(CD84):c.319del (p.Tyr107fs)	CD84, LOC105371468 (Y107fs)	Deletion (frameshift variant +1 more)	Multisystem inflammatory syndrome in children	Grisk factor