RASSF9[gene] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	FERRY3, FGD4 +4837 more	Copy number gain	See cases	GPathogenic
Select item 155032	GRCh38/hg38 12q21.1-22(chr12:73485697-92795805)x1	ACSS3, ALX1 +287 more	Copy number loss	See cases	GPathogenic
Select item 153986	GRCh38/hg38 12q21.31(chr12:85578345-85815687)x1	LOC126861588, LOC126861589 +1 more	Copy number loss	See cases	GUncertain significance
Select item 155425	GRCh38/hg38 12q21.31-21.32(chr12:85722164-86332192)x3	LOC126861589, LOC130008342 +3 more	Copy number gain	See cases	GLikely benign
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 2663802	NM_005447.4(RASSF9):c.893_894del (p.Ile298fs)	RASSF9 (I298fs)	Microsatellite (frameshift variant)	Premature coronary artery atherosclerosis	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
Select item 3063243	GRCh37/hg19 12q21.1-21.33(chr12:74887087-90469800)x1	ACSS3, ALX1 +43 more	Copy number loss	not specified	GPathogenic
Select item 980449	GRCh37/hg19 12q21.31-21.32(chr12:85812496-86797077)x3	NTS, MGAT4C +1 more	Copy number gain	not provided	GUncertain significance
Select item 980448	GRCh37/hg19 12q21.31-21.32(chr12:86017618-86786974)x3	RASSF9, MGAT4C +1 more	Copy number gain	not provided	GLikely benign
Select item 980446	GRCh37/hg19 12q21.31(chr12:86223018-86302962)x1	RASSF9, NTS	Copy number loss	not provided	GLikely benign
Select item 815542	GRCh37/hg19 12q21.31(chr12:86173243-86421728)x3	RASSF9, NTS +1 more	Copy number gain	not provided	GUncertain significance
Select item 687328	GRCh37/hg19 12q21.2-22(chr12:77737623-94330526)x1	ACSS3, ALX1 +46 more	Copy number loss	not provided	GPathogenic
Select item 686682	GRCh37/hg19 12q21.31-21.32(chr12:86138213-88183106)x1	MGAT4C, NTS +1 more	Copy number loss	not provided	GUncertain significance
Select item 625562	GRCh37/hg19 12q21.31-21.32(chr12:82183041-88755577)	ALX1, C12orf29 +12 more	Copy number gain	not provided	GPathogenic
Select item 563978	GRCh37/hg19 12q21.31-21.32(chr12:86115942-88186381)x1	MGAT4C, NTS +1 more	Copy number loss	not provided	GUncertain significance
Select item 442061	GRCh37/hg19 12q21.31(chr12:85922052-86231685)x1	RASSF9	Copy number loss	See cases	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic

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Items: 50