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

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Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156851	NM_001015055.2(RTKN):c.1664C>T (p.Pro555Leu)	RTKN (P505L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3156850	NM_001015055.2(RTKN):c.1625G>A (p.Arg542Gln)	RTKN (R492Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333750	NM_001015055.2(RTKN):c.1610C>A (p.Pro537His)	RTKN (P487H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304409	NM_001015055.2(RTKN):c.1610C>G (p.Pro537Arg)	RTKN (P524R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569875	NM_001015055.2(RTKN):c.1597C>T (p.Arg533Cys)	RTKN (R483C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489742	NM_001015055.2(RTKN):c.1565A>T (p.Asp522Val)	RTKN (D522V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209434	NM_001015055.2(RTKN):c.1418G>T (p.Gly473Val)	RTKN (G423V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555192	NM_001015055.2(RTKN):c.1411C>T (p.Arg471Trp)	RTKN (R421W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340040	NM_001015055.2(RTKN):c.1400T>C (p.Ile467Thr)	RTKN (I454T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315638	NM_001015055.2(RTKN):c.1399A>G (p.Ile467Val)	RTKN (I417V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511836	NM_001015055.2(RTKN):c.1363A>G (p.Ile455Val)	RTKN (I455V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613561	NM_001015055.2(RTKN):c.1217G>A (p.Ser406Asn)	RTKN (S356N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481512	NM_001015055.2(RTKN):c.1201C>T (p.Arg401Trp)	RTKN (R388W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254205	NM_001015055.2(RTKN):c.1130G>A (p.Arg377Gln)	RTKN (R377Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315636	NM_001015055.2(RTKN):c.1118A>C (p.Gln373Pro)	RTKN (Q323P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315634	NM_001015055.2(RTKN):c.1099C>T (p.Arg367Trp)	RTKN (R354W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156849	NM_001015055.2(RTKN):c.1027C>T (p.Arg343Trp)	RTKN (R330W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315637	NM_001015055.2(RTKN):c.1018T>G (p.Phe340Val)	RTKN (F327V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401295	NM_001015055.2(RTKN):c.982G>C (p.Ala328Pro)	RTKN (A328P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315633	NM_001015055.2(RTKN):c.896G>A (p.Arg299His)	RTKN (R286H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569951	NM_001015055.2(RTKN):c.895C>G (p.Arg299Gly)	RTKN (R249G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592761	NM_001015055.2(RTKN):c.886G>A (p.Val296Met)	RTKN (V246M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156857	NM_001015055.2(RTKN):c.821G>A (p.Arg274His)	RTKN (R224H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156856	NM_001015055.2(RTKN):c.764G>A (p.Arg255His)	RTKN (R242H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549369	NM_001015055.2(RTKN):c.763C>T (p.Arg255Cys)	RTKN (R255C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412029	NM_001015055.2(RTKN):c.688C>T (p.Arg230Trp)	RTKN (R180W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156855	NM_001015055.2(RTKN):c.683G>A (p.Arg228His)	RTKN (R178H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401319	NM_001015055.2(RTKN):c.625G>A (p.Gly209Ser)	RTKN (G196S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609215	NM_001015055.2(RTKN):c.592G>A (p.Ala198Thr)	RTKN (A185T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364762	NM_001015055.2(RTKN):c.554C>T (p.Ala185Val)	RTKN (A135V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156854	NM_001015055.2(RTKN):c.467G>A (p.Gly156Glu)	RTKN (G106E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345100	NM_001015055.2(RTKN):c.436C>T (p.Arg146Cys)	RTKN (R96C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354105	NM_001015055.2(RTKN):c.393G>A (p.Met131Ile)	RTKN (M118I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156853	NM_001015055.2(RTKN):c.359G>A (p.Arg120Gln)	RTKN (R107Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515289	NM_001015055.2(RTKN):c.355G>T (p.Gly119Cys)	RTKN (G69C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215473	NM_001015055.2(RTKN):c.355G>A (p.Gly119Ser)	RTKN (G69S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216486	NM_001015055.2(RTKN):c.341G>A (p.Arg114His)	RTKN (R114H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313552	NM_001015055.2(RTKN):c.340C>T (p.Arg114Cys)	RTKN (R101C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156852	NM_001015055.2(RTKN):c.310C>T (p.Arg104Trp)	RTKN (R104W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496049	NM_001015055.2(RTKN):c.266T>C (p.Leu89Pro)	RTKN (L89P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212976	NM_001015055.2(RTKN):c.256A>G (p.Met86Val)	RTKN (M36V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329316	NM_001015055.2(RTKN):c.212C>T (p.Ala71Val)	RTKN (A71V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458159	NM_001015055.2(RTKN):c.200A>G (p.Gln67Arg)	RTKN (Q67R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284629	NM_001015055.2(RTKN):c.182C>T (p.Ala61Val)	RTKN (A48V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478092	NM_001015055.2(RTKN):c.141T>G (p.His47Gln)	RTKN (H34Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528128	NM_001015055.2(RTKN):c.137A>G (p.Asp46Gly)	RTKN (D33G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346382	NM_001015055.2(RTKN):c.59T>C (p.Met20Thr)	RTKN (M20T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

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Items: 47