"Ambry Genetics"[submitter] AND "TRAF6"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2509811	NM_004620.4(TRAF6):c.1258A>C (p.Ser420Arg)	TRAF6 (S420R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394580	NM_004620.4(TRAF6):c.1205G>A (p.Arg402His)	TRAF6 (R402H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328434	NM_004620.4(TRAF6):c.1086G>A (p.Met362Ile)	TRAF6 (M362I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328436	NM_004620.4(TRAF6):c.1084A>G (p.Met362Val)	TRAF6 (M362V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320742	NM_004620.4(TRAF6):c.1072G>A (p.Gly358Ser)	TRAF6 (G358S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217062	NM_004620.4(TRAF6):c.1033G>A (p.Glu345Lys)	TRAF6 (E345K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382318	NM_004620.4(TRAF6):c.856T>C (p.Ser286Pro)	TRAF6 (S286P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328435	NM_004620.4(TRAF6):c.848T>C (p.Ile283Thr)	TRAF6 (I283T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2206211	NM_004620.4(TRAF6):c.844G>A (p.Val282Ile)	TRAF6 (V282I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181796	NM_004620.4(TRAF6):c.809T>G (p.Met270Arg)	TRAF6 (M270R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328433	NM_004620.4(TRAF6):c.759G>A (p.Met253Ile)	TRAF6 (M253I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181795	NM_004620.4(TRAF6):c.608T>C (p.Ile203Thr)	TRAF6 (I203T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533836	NM_004620.4(TRAF6):c.586A>G (p.Met196Val)	TRAF6 (M196V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2275955	NM_004620.4(TRAF6):c.580G>A (p.Ala194Thr)	TRAF6 (A194T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181793	NM_004620.4(TRAF6):c.520A>G (p.Ile174Val)	TRAF6 (I174V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181792	NM_004620.4(TRAF6):c.481G>A (p.Asp161Asn)	TRAF6 (D161N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2292002	NM_004620.4(TRAF6):c.430G>A (p.Glu144Lys)	TRAF6 (E144K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181791	NM_004620.4(TRAF6):c.342A>C (p.Glu114Asp)	TRAF6 (E114D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3181790	NM_004620.4(TRAF6):c.233G>A (p.Arg78Gln)	LOC126861190, TRAF6 (R78Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243529	NM_004620.4(TRAF6):c.131A>G (p.Asn44Ser)	LOC126861190, TRAF6 (N44S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328431	NM_004620.4(TRAF6):c.88G>A (p.Val30Ile)	LOC126861190, TRAF6 (V30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549644	NM_004620.4(TRAF6):c.59G>A (p.Cys20Tyr)	LOC126861190, TRAF6 (C20Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22