"Ambry Genetics"[submitter] AND "LOC129995496"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2351326	NM_203293.3(TRIM7):c.481C>G (p.His161Asp)	LOC129995496, TRIM7 (H161D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481459	NM_203293.3(TRIM7):c.460C>A (p.Arg154Ser)	LOC129995496, TRIM7 (R154S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205449	NM_203293.3(TRIM7):c.388T>A (p.Cys130Ser)	LOC129995496, TRIM7 (C130S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205448	NM_203293.3(TRIM7):c.376G>T (p.Ala126Ser)	LOC129995496, TRIM7 (A126S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328929	NM_203293.3(TRIM7):c.345G>T (p.Glu115Asp)	LOC129995496, TRIM7 (E115D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328921	NM_203293.3(TRIM7):c.325C>A (p.Pro109Thr)	LOC129995496, TRIM7 (P109T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402529	NM_203293.3(TRIM7):c.302C>G (p.Thr101Arg)	LOC129995496, TRIM7 (T101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328927	NM_203293.3(TRIM7):c.301A>C (p.Thr101Pro)	LOC129995496, TRIM7 (T101P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464179	NM_203293.3(TRIM7):c.278A>C (p.Asn93Thr)	LOC129995496, TRIM7 (N93T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328930	NM_203293.3(TRIM7):c.260C>T (p.Pro87Leu)	LOC129995496, TRIM7 (P87L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294698	NM_203293.3(TRIM7):c.244C>T (p.Arg82Cys)	LOC129995496, TRIM7 (R82C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182781	NM_203293.3(TRIM7):c.236C>A (p.Pro79Gln)	LOC129995496, TRIM7 (P79Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517593	NM_203293.3(TRIM7):c.218C>G (p.Pro73Arg)	LOC129995496, TRIM7 (P73R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance