"Ambry Genetics"[submitter] AND "LOC101928034"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3157399	NM_002960.2(S100A3):c.289C>T (p.Pro97Ser)	LOC101928034, S100A3 (P97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157398	NM_002960.2(S100A3):c.278G>T (p.Cys93Phe)	LOC101928034, S100A3 (C93F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299152	NM_002960.2(S100A3):c.270C>G (p.Phe90Leu)	LOC101928034, S100A3 (F90L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157396	NM_002960.2(S100A3):c.167A>G (p.Asn56Ser)	LOC101928034, S100A3 (N56S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157395	NM_002960.2(S100A3):c.155A>G (p.Glu52Gly)	LOC101928034, S100A3 (E52G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271715	NM_002960.2(S100A3):c.143C>G (p.Thr48Ser)	LOC101928034, S100A3 (T48S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315936	NM_002960.2(S100A3):c.82A>G (p.Lys28Glu)	LOC101928034, S100A3 (K28E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157400	NM_002960.2(S100A3):c.58G>A (p.Ala20Thr)	LOC101928034, S100A3 (A20T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2341106	NM_002960.2(S100A3):c.37G>T (p.Val13Leu)	LOC101928034, S100A3 (V13L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3157397	NM_002960.2(S100A3):c.23C>T (p.Ala8Val)	LOC101928034, S100A3 (A8V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance