TRIM8[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1275111	NM_030912.3(TRIM8):c.-40A>T	TRIM8	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 1318796	NM_030912.3(TRIM8):c.1A>G (p.Met1Val)	TRIM8 (M1V)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2414579	NM_030912.3(TRIM8):c.23G>T (p.Cys8Phe)	TRIM8 (C8F)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2859125	NM_030912.3(TRIM8):c.32A>T (p.Glu11Val)	TRIM8 (E11V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1331611	NM_030912.3(TRIM8):c.35A>C (p.Glu12Ala)	TRIM8 (E12A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2739457	NM_030912.3(TRIM8):c.36G>C (p.Glu12Asp)	TRIM8 (E12D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1596826	NM_030912.3(TRIM8):c.42C>G (p.Ile14Met)	TRIM8 (I14M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GLikely benign
Select item 1627263	NM_030912.3(TRIM8):c.45C>T (p.Cys15=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2992535	NM_030912.3(TRIM8):c.54C>T (p.Cys18=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1899368	NM_030912.3(TRIM8):c.60C>A (p.His20Gln)	TRIM8 (H20Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2007154	NM_030912.3(TRIM8):c.69G>T (p.Val23=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2007000	NM_030912.3(TRIM8):c.74C>T (p.Pro25Leu)	TRIM8 (P25L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2776337	NM_030912.3(TRIM8):c.90C>T (p.Cys30=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1933748	NM_030912.3(TRIM8):c.94C>G (p.His32Asp)	TRIM8 (H32D)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1914217	NM_030912.3(TRIM8):c.110G>T (p.Gly37Val)	TRIM8 (G37V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1969181	NM_030912.3(TRIM8):c.243G>C (p.Leu81=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1949559	NM_030912.3(TRIM8):c.244C>T (p.His82Tyr)	TRIM8 (H82Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2796831	NM_030912.3(TRIM8):c.246C>T (p.His82=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2082563	NM_030912.3(TRIM8):c.246C>G (p.His82Gln)	TRIM8 (H82Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2071212	NM_030912.3(TRIM8):c.256C>G (p.Pro86Ala)	TRIM8 (P86A)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2045536	NM_030912.3(TRIM8):c.257C>T (p.Pro86Leu)	TRIM8 (P86L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1905327	NM_030912.3(TRIM8):c.260C>T (p.Pro87Leu)	TRIM8 (P87L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1592123	NM_030912.3(TRIM8):c.267G>A (p.Ala89=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1969344	NM_030912.3(TRIM8):c.269T>C (p.Leu90Pro)	TRIM8 (L90P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1328030	NM_030912.3(TRIM8):c.270G>A (p.Leu90=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 1316048	NM_030912.3(TRIM8):c.299dup (p.Leu101fs)	TRIM8 (L101fs)	Duplication (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2829247	NM_030912.3(TRIM8):c.295C>T (p.Pro99Ser)	TRIM8 (P99S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2442782	NM_030912.3(TRIM8):c.313_315del (p.Lys105del)	TRIM8 (K105del)	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 2702478	NM_030912.3(TRIM8):c.312G>T (p.Gln104His)	TRIM8 (Q104H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2500505	NM_030912.3(TRIM8):c.315G>T (p.Lys105Asn)	TRIM8 (K105N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3343820	NM_030912.3(TRIM8):c.320G>A (p.Cys107Tyr)	TRIM8 (C107Y)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2067843	NM_030912.3(TRIM8):c.333G>A (p.Glu111=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2012513	NM_030912.3(TRIM8):c.335C>G (p.Ala112Gly)	TRIM8 (A112G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2413587	NM_030912.3(TRIM8):c.339C>G (p.Pro113=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2831773	NM_030912.3(TRIM8):c.346C>T (p.Gln116Ter)	TRIM8 (Q116*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2066069	NM_030912.3(TRIM8):c.350C>T (p.Ser117Phe)	TRIM8 (S117F)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2499192	NM_030912.3(TRIM8):c.353A>T (p.His118Leu)	TRIM8 (H118L)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999814	NM_030912.3(TRIM8):c.354C>T (p.His118=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2114747	NM_030912.3(TRIM8):c.354C>A (p.His118Gln)	TRIM8 (H118Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2966658	NM_030912.3(TRIM8):c.357G>A (p.Val119=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2078239	NM_030912.3(TRIM8):c.369G>A (p.Leu123=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2027229	NM_030912.3(TRIM8):c.379T>G (p.Ser127Ala)	TRIM8 (S127A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1983029	NM_030912.3(TRIM8):c.386C>T (p.Ala129Val)	TRIM8 (A129V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2973687	NM_030912.3(TRIM8):c.400C>A (p.Leu134Met)	TRIM8 (L134M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1927788	NM_030912.3(TRIM8):c.409G>A (p.Ala137Thr)	TRIM8 (A137T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1577110	NM_030912.3(TRIM8):c.412G>A (p.Asp138Asn)	TRIM8 (D138N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2895075	NM_030912.3(TRIM8):c.415G>A (p.Asp139Asn)	TRIM8 (D139N)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2903237	NM_030912.3(TRIM8):c.417C>T (p.Asp139=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2766442	NM_030912.3(TRIM8):c.422G>C (p.Arg141Pro)	TRIM8 (R141P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2974305	NM_030912.3(TRIM8):c.426C>T (p.Ala142=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1917724	NM_030912.3(TRIM8):c.435C>T (p.Cys145=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2868681	NM_030912.3(TRIM8):c.448G>T (p.Ala150Ser)	TRIM8 (A150S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2776968	NM_030912.3(TRIM8):c.450C>T (p.Ala150=)	TRIM8	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2413588	NM_030912.3(TRIM8):c.459C>G (p.Leu153=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1922947	NM_030912.3(TRIM8):c.468C>T (p.Cys156=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2765980	NM_030912.3(TRIM8):c.471_472delinsTA (p.Glu157_Ala158delinsAspThr)	TRIM8	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 1946279	NM_030912.3(TRIM8):c.471G>A (p.Glu157=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2082739	NM_030912.3(TRIM8):c.478C>T (p.Gln160Ter)	TRIM8 (Q160*)	Single nucleotide variant (nonsense +1 more)	not provided	GUncertain significance
Select item 2062117	NM_030912.3(TRIM8):c.484G>A (p.Ala162Thr)	TRIM8 (A162T)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2864800	NM_030912.3(TRIM8):c.486C>A (p.Ala162=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1723502	NM_030912.3(TRIM8):c.487G>A (p.Val163Met)	TRIM8 (V163M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2025258	NM_030912.3(TRIM8):c.500GCT[1] (p.Cys168del)	TRIM8 (C168del)	Microsatellite (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 2903238	NM_030912.3(TRIM8):c.519G>C (p.Ala173=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2846656	NM_030912.3(TRIM8):c.527G>T (p.Gly176Val)	TRIM8 (G176V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2996831	NM_030912.3(TRIM8):c.528A>T (p.Gly176=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2893773	NM_030912.3(TRIM8):c.531C>T (p.His177=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2841861	NM_030912.3(TRIM8):c.544G>C (p.Val182Leu)	TRIM8 (V182L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2991058	NM_030912.3(TRIM8):c.546G>A (p.Val182=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2806350	NM_030912.3(TRIM8):c.547G>C (p.Glu183Gln)	TRIM8 (E183Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1803749	NM_030912.3(TRIM8):c.553C>T (p.Arg185Ter)	TRIM8 (R185*)	Single nucleotide variant (nonsense +1 more)	Focal segmental glomerulosclerosis and neurodevelopmental syndrome	GUncertain significance
Select item 3022159	NM_030912.3(TRIM8):c.565A>T (p.Ile189Phe)	TRIM8 (I189F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2748562	NM_030912.3(TRIM8):c.570+7A>G	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1672361	NM_030912.3(TRIM8):c.570+13CG[7]	TRIM8	Microsatellite (intron variant)	not provided	GBenign
Select item 1563636	NM_030912.3(TRIM8):c.570+13CG[8]	TRIM8	Microsatellite (intron variant)	not provided	GBenign
Select item 1945512	NM_030912.3(TRIM8):c.570+17C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1902145	NM_030912.3(TRIM8):c.570+20G>A	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2177292	NM_030912.3(TRIM8):c.595C>T (p.Arg199Trp)	TRIM8 (R199W)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2078107	NM_030912.3(TRIM8):c.596G>A (p.Arg199Gln)	TRIM8 (R199Q)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2790998	NM_030912.3(TRIM8):c.603G>A (p.Glu201=)	TRIM8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2785628	NM_030912.3(TRIM8):c.608G>A (p.Arg203Gln)	TRIM8 (R203Q)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 1485270	NM_030912.3(TRIM8):c.631C>A (p.Leu211Met)	TRIM8 (L211M)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 1929735	NM_030912.3(TRIM8):c.642C>T (p.Leu214=)	TRIM8	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2815448	NM_030912.3(TRIM8):c.643G>A (p.Glu215Lys)	TRIM8 (E215K)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2978379	NM_030912.3(TRIM8):c.655C>T (p.Arg219Cys)	TRIM8 (R219C)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2026198	NM_030912.3(TRIM8):c.656G>T (p.Arg219Leu)	TRIM8 (R219L)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1923641	NM_030912.3(TRIM8):c.666+12C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1965003	NM_030912.3(TRIM8):c.666+18C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1942069	NM_030912.3(TRIM8):c.667-19C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3013901	NM_030912.3(TRIM8):c.667-7C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2640795	NM_030912.3(TRIM8):c.667-5C>T	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2870250	NM_030912.3(TRIM8):c.667-4G>A	TRIM8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2696131	NM_030912.3(TRIM8):c.674T>A (p.Val225Glu)	TRIM8 (V193E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2098534	NM_030912.3(TRIM8):c.677A>G (p.Asn226Ser)	TRIM8 (N194S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1951729	NM_030912.3(TRIM8):c.680A>G (p.Gln227Arg)	TRIM8 (Q195R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2020619	NM_030912.3(TRIM8):c.685A>C (p.Lys229Gln)	TRIM8 (K197Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2871192	NM_030912.3(TRIM8):c.691G>A (p.Glu231Lys)	TRIM8 (E199K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1723865	NM_030912.3(TRIM8):c.697C>T (p.Arg233Trp)	TRIM8 (R201W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2071917	NM_030912.3(TRIM8):c.708C>T (p.Tyr236=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1967928	NM_030912.3(TRIM8):c.727C>G (p.Leu243Val)	TRIM8 (L243V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2083644	NM_030912.3(TRIM8):c.732C>T (p.Asp244=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

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