"Ambry Genetics"[submitter] AND "RASSF9"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151979	NM_005447.4(RASSF9):c.1212T>G (p.Asn404Lys)	RASSF9 (N404K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300598	NM_005447.4(RASSF9):c.1145C>T (p.Ala382Val)	RASSF9 (A382V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3151978	NM_005447.4(RASSF9):c.1120G>A (p.Gly374Arg)	RASSF9 (G374R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151977	NM_005447.4(RASSF9):c.1047G>T (p.Leu349Phe)	RASSF9 (L349F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410485	NM_005447.4(RASSF9):c.974G>A (p.Ser325Asn)	RASSF9 (S325N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285608	NM_005447.4(RASSF9):c.961G>A (p.Asp321Asn)	RASSF9 (D321N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405774	NM_005447.4(RASSF9):c.953T>C (p.Val318Ala)	RASSF9 (V318A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331551	NM_005447.4(RASSF9):c.944T>C (p.Leu315Ser)	RASSF9 (L315S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343711	NM_005447.4(RASSF9):c.905C>T (p.Ala302Val)	RASSF9 (A302V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549959	NM_005447.4(RASSF9):c.803A>C (p.Gln268Pro)	RASSF9 (Q268P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468731	NM_005447.4(RASSF9):c.728T>G (p.Val243Gly)	RASSF9 (V243G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151985	NM_005447.4(RASSF9):c.686A>C (p.Asn229Thr)	RASSF9 (N229T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371212	NM_005447.4(RASSF9):c.658C>T (p.Leu220Phe)	RASSF9 (L220F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151984	NM_005447.4(RASSF9):c.615A>T (p.Lys205Asn)	RASSF9 (K205N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293782	NM_005447.4(RASSF9):c.615A>C (p.Lys205Asn)	RASSF9 (K205N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536442	NM_005447.4(RASSF9):c.606G>C (p.Lys202Asn)	RASSF9 (K202N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313001	NM_005447.4(RASSF9):c.541G>A (p.Asp181Asn)	RASSF9 (D181N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252447	NM_005447.4(RASSF9):c.490A>G (p.Thr164Ala)	RASSF9 (T164A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400488	NM_005447.4(RASSF9):c.463G>T (p.Asp155Tyr)	RASSF9 (D155Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151983	NM_005447.4(RASSF9):c.370C>T (p.Pro124Ser)	RASSF9 (P124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313003	NM_005447.4(RASSF9):c.352G>A (p.Asp118Asn)	RASSF9 (D118N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545572	NM_005447.4(RASSF9):c.329T>A (p.Met110Lys)	RASSF9 (M110K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315843	NM_005447.4(RASSF9):c.305C>T (p.Ala102Val)	RASSF9 (A102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151982	NM_005447.4(RASSF9):c.274C>T (p.Pro92Ser)	RASSF9 (P92S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313002	NM_005447.4(RASSF9):c.245A>T (p.Lys82Met)	RASSF9 (K82M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411357	NM_005447.4(RASSF9):c.203G>C (p.Arg68Pro)	RASSF9 (R68P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275399	NM_005447.4(RASSF9):c.188C>T (p.Thr63Met)	RASSF9 (T63M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151980	NM_005447.4(RASSF9):c.157A>G (p.Ile53Val)	RASSF9 (I53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305218	NM_005447.4(RASSF9):c.157A>T (p.Ile53Phe)	RASSF9 (I53F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371787	NM_005447.4(RASSF9):c.131C>T (p.Thr44Ile)	RASSF9 (T44I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339835	NM_005447.4(RASSF9):c.96G>C (p.Trp32Cys)	RASSF9 (W32C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317127	NM_005447.4(RASSF9):c.29A>G (p.Lys10Arg)	RASSF9 (K10R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32