"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRIM28"[g - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2650595	NM_005762.3(TRIM28):c.114C>T (p.Ala38=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder +1 more	GBenign/Likely benign
Select item 2849324	NM_005762.3(TRIM28):c.189G>A (p.Glu63=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2836729	NM_005762.3(TRIM28):c.192C>T (p.His64=)	LOC130065239, TRIM28	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3036617	NM_005762.3(TRIM28):c.723G>A (p.Gln241=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder	GLikely benign
Select item 3049346	NM_005762.3(TRIM28):c.840-6C>T	TRIM28	Single nucleotide variant (intron variant)	TRIM28-related disorder	GBenign
Select item 2715450	NM_005762.3(TRIM28):c.1020G>A (p.Lys340=)	TRIM28	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1262310	NM_005762.3(TRIM28):c.1170G>A (p.Lys390=)	TRIM28	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3051340	NM_005762.3(TRIM28):c.1323+5G>A	TRIM28	Single nucleotide variant (intron variant)	TRIM28-related disorder	GLikely benign
Select item 2629798	NM_005762.3(TRIM28):c.1361G>A (p.Gly454Glu)	TRIM28 (G454E)	Single nucleotide variant (missense variant)	TRIM28-related disorder	GUncertain significance
Select item 2650597	NM_005762.3(TRIM28):c.1392T>C (p.His464=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder +1 more	GLikely benign
Select item 1879457	NM_005762.3(TRIM28):c.1581C>T (p.Ala527=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder +1 more	GBenign/Likely benign
Select item 2650599	NM_005762.3(TRIM28):c.1611G>A (p.Ala537=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder +1 more	GBenign/Likely benign
Select item 2253151	NM_005762.3(TRIM28):c.1639C>A (p.Leu547Met)	TRIM28 (L547M)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2712323	NM_005762.3(TRIM28):c.1699A>G (p.Thr567Ala)	TRIM28 (T567A)	Single nucleotide variant (missense variant)	TRIM28-related disorder +1 more	GBenign
Select item 3049245	NM_005762.3(TRIM28):c.1950C>T (p.Asp650=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder	GLikely benign
Select item 2735660	NM_005762.3(TRIM28):c.1983-5C>G	TRIM28	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2789323	NM_005762.3(TRIM28):c.2148C>T (p.Pro716=)	TRIM28	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2754468	NM_005762.3(TRIM28):c.2183C>T (p.Thr728Ile)	TRIM28 (T728I)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3051944	NM_005762.3(TRIM28):c.2184C>T (p.Thr728=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder	GLikely benign
Select item 3036483	NM_005762.3(TRIM28):c.2385C>T (p.Arg795=)	TRIM28	Single nucleotide variant (synonymous variant)	TRIM28-related disorder	GLikely benign

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Items: 20