"Ambry Genetics"[submitter] AND "TRAF3IP3"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2320413	NM_025228.4(TRAF3IP3):c.8G>T (p.Ser3Ile)	TRAF3IP3 (S3I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392429	NM_025228.4(TRAF3IP3):c.16C>T (p.Pro6Ser)	TRAF3IP3 (P6S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181776	NM_025228.4(TRAF3IP3):c.17C>T (p.Pro6Leu)	TRAF3IP3 (P6L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545654	NM_025228.4(TRAF3IP3):c.28C>T (p.Pro10Ser)	TRAF3IP3 (P10S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366520	NM_025228.4(TRAF3IP3):c.41G>A (p.Arg14Gln)	TRAF3IP3 (R14Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385463	NM_025228.4(TRAF3IP3):c.107G>A (p.Arg36His)	TRAF3IP3 (R36H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253424	NM_025228.4(TRAF3IP3):c.113A>G (p.Asn38Ser)	TRAF3IP3 (N38S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374639	NM_025228.4(TRAF3IP3):c.128G>T (p.Arg43Leu)	TRAF3IP3 (R43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334119	NM_025228.4(TRAF3IP3):c.128G>A (p.Arg43His)	TRAF3IP3 (R43H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458161	NM_025228.4(TRAF3IP3):c.236C>T (p.Ala79Val)	TRAF3IP3 (A79V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181778	NM_025228.4(TRAF3IP3):c.250G>A (p.Ala84Thr)	TRAF3IP3 (A84T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511476	NM_025228.4(TRAF3IP3):c.265C>A (p.Pro89Thr)	TRAF3IP3 (P89T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559282	NM_025228.4(TRAF3IP3):c.415T>G (p.Ser139Ala)	TRAF3IP3 (S119A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2470548	NM_025228.4(TRAF3IP3):c.507G>C (p.Lys169Asn)	TRAF3IP3 (K149N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181779	NM_025228.4(TRAF3IP3):c.729G>C (p.Lys243Asn)	TRAF3IP3 (K223N +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2526840	NM_025228.4(TRAF3IP3):c.743C>G (p.Ser248Cys)	TRAF3IP3 (S248C +1 more)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2544348	NM_025228.4(TRAF3IP3):c.917G>A (p.Arg306Gln)	TRAF3IP3 (R286Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243061	NM_025228.4(TRAF3IP3):c.1020G>C (p.Glu340Asp)	TRAF3IP3 (E320D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181772	NM_025228.4(TRAF3IP3):c.1061A>G (p.Asp354Gly)	TRAF3IP3 (D334G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490174	NM_025228.4(TRAF3IP3):c.1186C>A (p.Gln396Lys)	TRAF3IP3 (Q376K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391716	NM_025228.4(TRAF3IP3):c.1327G>A (p.Val443Met)	C1orf74, TRAF3IP3 (V443M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2488885	NM_025228.4(TRAF3IP3):c.1370G>A (p.Gly457Asp)	C1orf74, TRAF3IP3 (G437D +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3181773	NM_025228.4(TRAF3IP3):c.1435G>A (p.Ala479Thr)	C1orf74, TRAF3IP3 (A459T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2224422	NM_025228.4(TRAF3IP3):c.1478A>G (p.Asn493Ser)	C1orf74, TRAF3IP3 (N493S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3181774	NM_025228.4(TRAF3IP3):c.1508G>A (p.Arg503His)	C1orf74, TRAF3IP3 (R503H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2313608	NM_025228.4(TRAF3IP3):c.1526G>A (p.Arg509Gln)	C1orf74, TRAF3IP3 (R489Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3181775	NM_025228.4(TRAF3IP3):c.1597G>A (p.Val533Met)	C1orf74, TRAF3IP3 (V533M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 27