Related gene-specific medical variations for Gene (Select 10155) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182338	NM_005762.3(TRIM28):c.323C>T (p.Ala108Val)	LOC130065239, TRIM28 (A108V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182335	NM_005762.3(TRIM28):c.155C>G (p.Ala52Gly)	LOC130065239, TRIM28 (A52G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2849324	NM_005762.3(TRIM28):c.189G>A (p.Glu63=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2836729	NM_005762.3(TRIM28):c.192C>T (p.His64=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2650595	NM_005762.3(TRIM28):c.114C>T (p.Ala38=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2650594	NM_005762.3(TRIM28):c.84C>T (p.Gly28=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650593	NM_005762.3(TRIM28):c.51T>G (p.Ser17=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2650592	NM_005762.3(TRIM28):c.12C>T (p.Ser4=)	LOC130065238, TRIM28	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2540623	NM_005762.3(TRIM28):c.140C>T (p.Ala47Val)	LOC130065239, TRIM28 (A47V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535218	NM_005762.3(TRIM28):c.287C>T (p.Ala96Val)	LOC130065239, TRIM28 (A96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2444895	NM_005762.3(TRIM28):c.161G>T (p.Gly54Val)	LOC130065239, TRIM28 (G54V)	Single nucleotide variant (missense variant)	Wilms tumor 1	GUncertain significance
Select item 2444882	NM_005762.3(TRIM28):c.83G>T (p.Gly28Val)	LOC130065239, TRIM28 (G28V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2373521	NM_005762.3(TRIM28):c.95G>T (p.Arg32Leu)	LOC130065239, TRIM28 (R32L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347242	NM_005762.3(TRIM28):c.130G>C (p.Ala44Pro)	LOC130065239, TRIM28 (A44P)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2329138	NM_005762.3(TRIM28):c.137C>T (p.Ala46Val)	LOC130065239, TRIM28 (A46V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294606	NM_005762.3(TRIM28):c.119C>G (p.Ala40Gly)	LOC130065239, TRIM28 (A40G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 973190	NM_005762.3(TRIM28):c.2101C>T (p.Gln701Ter)	TRIM28 (Q701*)	Single nucleotide variant (nonsense)	Nephroblastoma	GPathogenic
Select item 161641	NM_005762.3(TRIM28):c.2193+3G>T	TRIM28	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 91860	NM_005762.3(TRIM28):c.1216+23C>T	TRIM28	Single nucleotide variant (intron variant)	Familial colorectal cancer	Gnot provided