"TRAF7-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045378	NM_032271.3(TRAF7):c.64_75del (p.Pro22_Thr25del)	TRAF7	Deletion (inframe deletion)	TRAF7-related condition	GLikely benign
Select item 736474	NM_032271.3(TRAF7):c.81+5_81+13del	TRAF7	Deletion (intron variant)	TRAF7-related condition +1 more	GBenign/Likely benign
Select item 2352785	NM_032271.3(TRAF7):c.200C>G (p.Ala67Gly)	TRAF7 (A67G)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 3048974	NM_032271.3(TRAF7):c.462C>T (p.Cys154=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GBenign
Select item 2646042	NM_032271.3(TRAF7):c.465C>T (p.Ala155=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition +1 more	GLikely benign
Select item 2629255	NM_032271.3(TRAF7):c.511G>C (p.Val171Leu)	TRAF7 (V171L)	Single nucleotide variant (missense variant)	TRAF7-related condition	GUncertain significance
Select item 2646044	NM_032271.3(TRAF7):c.546G>A (p.Gly182=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2498641	NM_032271.3(TRAF7):c.591C>T (p.Ser197=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition +1 more	GLikely benign
Select item 2630532	NM_032271.3(TRAF7):c.642C>G (p.Ile214Met)	TRAF7 (I214M)	Single nucleotide variant (missense variant)	TRAF7-related condition	GUncertain significance
Select item 3043714	NM_032271.3(TRAF7):c.723G>A (p.Pro241=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 3047155	NM_032271.3(TRAF7):c.727C>G (p.Leu243Val)	TRAF7 (L243V)	Single nucleotide variant (missense variant)	TRAF7-related condition	GLikely benign
Select item 774920	NM_032271.3(TRAF7):c.792C>T (p.Tyr264=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3042227	NM_032271.3(TRAF7):c.807C>T (p.Ile269=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 3046630	NM_032271.3(TRAF7):c.825C>T (p.Tyr275=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 2633150	NM_032271.3(TRAF7):c.897C>A (p.His299Gln)	TRAF7 (H299Q)	Single nucleotide variant (missense variant)	TRAF7-related condition	GUncertain significance
Select item 3057662	NM_032271.3(TRAF7):c.918C>G (p.Ala306=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 3033290	NM_032271.3(TRAF7):c.1089C>T (p.Asp363=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 2646048	NM_032271.3(TRAF7):c.1209C>T (p.Cys403=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3039686	NM_032271.3(TRAF7):c.1346+9_1346+33del	TRAF7	Deletion (intron variant)	TRAF7-related condition	GLikely benign
Select item 3030055	NM_032271.3(TRAF7):c.1365C>G (p.Gly455=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 3050387	NM_032271.3(TRAF7):c.1377C>T (p.Cys459=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3035376	NM_032271.3(TRAF7):c.1464A>C (p.Ser488=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 2646049	NM_032271.3(TRAF7):c.1605C>T (p.Ser535=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2631656	NM_032271.3(TRAF7):c.1639C>T (p.Arg547Ter)	TRAF7 (R547*)	Single nucleotide variant (nonsense)	TRAF7-related condition	GUncertain significance
Select item 3024827	NM_032271.3(TRAF7):c.1668G>A (p.Gln556=)	TRAF7	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3054586	NM_032271.3(TRAF7):c.1872C>T (p.Ser624=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GLikely benign
Select item 3040648	NM_032271.3(TRAF7):c.1941C>T (p.Thr647=)	TRAF7	Single nucleotide variant (synonymous variant)	TRAF7-related condition	GBenign
Select item 3045693	NM_032271.3(TRAF7):c.1999-4G>A	TRAF7	Single nucleotide variant (intron variant)	TRAF7-related condition	GBenign

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Items: 28