"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRIM8"[ge - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1596826	NM_030912.3(TRIM8):c.42C>G (p.Ile14Met)	TRIM8 (I14M)	Single nucleotide variant (missense variant +1 more)	TRIM8-related disorder +2 more	GLikely benign
Select item 2067843	NM_030912.3(TRIM8):c.333G>A (p.Glu111=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 2966658	NM_030912.3(TRIM8):c.357G>A (p.Val119=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	TRIM8-related disorder +1 more	GLikely benign
Select item 1577110	NM_030912.3(TRIM8):c.412G>A (p.Asp138Asn)	TRIM8 (D138N)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 2630745	NM_030912.3(TRIM8):c.878C>A (p.Thr293Lys)	TRIM8 (T261K +1 more)	Single nucleotide variant (missense variant +1 more)	TRIM8-related disorder	GUncertain significance
Select item 2063512	NM_030912.3(TRIM8):c.984G>A (p.Leu328=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1906011	NM_030912.3(TRIM8):c.1034G>A (p.Arg345Gln)	TRIM8 (R345Q +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2052866	NM_030912.3(TRIM8):c.1192G>A (p.Gly398Ser)	TRIM8 (G366S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 2060182	NM_030912.3(TRIM8):c.1497G>C (p.Ser499=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	TRIM8-related disorder +1 more	GLikely benign
Select item 1575679	NM_030912.3(TRIM8):c.1551C>A (p.Pro517=)	TRIM8	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign