"GeneDx"[submitter] AND "TRIM63"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1283076	NM_032588.4(TRIM63):c.1041G>A (p.Gly347=)	TRIM63	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1269179	NM_032588.4(TRIM63):c.980-274_980-273insA	LOC122056803, TRIM63	Insertion (intron variant)	not provided	GBenign
Select item 1237163	NM_032588.4(TRIM63):c.979+76G>C	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275187	NM_032588.4(TRIM63):c.979+42_979+48del	TRIM63	Deletion (intron variant)	not provided	GBenign
Select item 1314830	NM_032588.4(TRIM63):c.888del (p.Lys297fs)	TRIM63 (K297fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1267089	NM_032588.4(TRIM63):c.855-57T>C	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287450	NM_032588.4(TRIM63):c.854+106T>C	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226300	NM_032588.4(TRIM63):c.831+191A>C	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1240550	NM_032588.4(TRIM63):c.709A>G (p.Lys237Glu)	TRIM63 (K237E)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 1228184	NM_032588.4(TRIM63):c.598-36C>G	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182874	NM_032588.4(TRIM63):c.598-192C>A	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1180375	NM_032588.4(TRIM63):c.501+234C>T	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272333	NM_032588.4(TRIM63):c.501+32T>G	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279875	NM_032588.4(TRIM63):c.333-144A>T	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256725	NM_032588.4(TRIM63):c.332+224G>A	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258664	NM_032588.4(TRIM63):c.332+96T>A	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264681	NM_032588.4(TRIM63):c.267G>T (p.Val89=)	TRIM63	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 373560	NM_032588.4(TRIM63):c.206C>T (p.Ser69Phe)	TRIM63 (S69F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1280531	NM_032588.4(TRIM63):c.160-40T>G	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283114	NM_032588.4(TRIM63):c.160-43A>G	TRIM63	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1298266	NM_032588.4(TRIM63):c.12G>A (p.Lys4=)	TRIM63	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1246258	NC_000001.11:g.26067710C>T	TRIM63	Single nucleotide variant	not provided	GBenign
Select item 1271566	NC_000001.11:g.26067810G>T	TRIM63	Single nucleotide variant	not provided	GBenign

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Items: 23