TRIM40[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 714621	NM_001286633.2(TRIM40):c.3G>A (p.Met1Ile)	TRIM40 (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3182439	NM_001286633.2(TRIM40):c.32A>C (p.Glu11Ala)	TRIM40 (E11A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182440	NM_001286633.2(TRIM40):c.37G>A (p.Val13Ile)	TRIM40 (V13I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3182437	NM_001286633.2(TRIM40):c.104G>A (p.Arg35Gln)	TRIM40 (R35Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335603	NM_001286633.2(TRIM40):c.190G>C (p.Val64Leu)	TRIM40 (V64L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377850	NM_001286633.2(TRIM40):c.247G>A (p.Glu83Lys)	TRIM40 (E83K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182438	NM_001286633.2(TRIM40):c.274G>A (p.Glu92Lys)	TRIM40 (E92K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366949	NM_001286633.2(TRIM40):c.290C>T (p.Pro97Leu)	TRIM40 (P97L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328728	NM_001286633.2(TRIM40):c.359G>A (p.Arg120His)	TRIM40 (R120H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381075	NM_001286633.2(TRIM40):c.361C>T (p.Arg121Trp)	TRIM40 (R121W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268944	NM_001286633.2(TRIM40):c.398A>G (p.Gln133Arg)	TRIM40 (Q133R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182441	NM_001286633.2(TRIM40):c.422A>C (p.Lys141Thr)	TRIM40 (K141T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362025	NM_001286633.2(TRIM40):c.539G>A (p.Gly180Asp)	TRIM40 (G151D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3328729	NM_001286633.2(TRIM40):c.617T>A (p.Val206Asp)	TRIM40 (V206D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366769	NM_001286633.2(TRIM40):c.640A>G (p.Lys214Glu)	TRIM40 (K185E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403537	NM_001286633.2(TRIM40):c.656A>G (p.Asn219Ser)	TRIM40 (N190S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 774645	NM_001286633.2(TRIM40):c.689+1G>T	TRIM40	Single nucleotide variant (splice donor variant)	not provided	GBenign