"Ambry Genetics"[submitter] AND "RTKN2"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156861	NM_145307.4(RTKN2):c.1792A>T (p.Ile598Phe)	RTKN2 (I598F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458926	NM_145307.4(RTKN2):c.1792A>G (p.Ile598Val)	RTKN2 (I598V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310230	NM_145307.4(RTKN2):c.1783A>G (p.Ile595Val)	RTKN2 (I595V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350440	NM_145307.4(RTKN2):c.1742A>G (p.Asn581Ser)	RTKN2 (N581S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2360634	NM_145307.4(RTKN2):c.1676C>T (p.Pro559Leu)	RTKN2 (P559L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454197	NM_145307.4(RTKN2):c.1672G>A (p.Ala558Thr)	RTKN2 (A558T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552281	NM_145307.4(RTKN2):c.1657C>G (p.Gln553Glu)	RTKN2 (Q553E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603606	NM_145307.4(RTKN2):c.1645A>G (p.Met549Val)	RTKN2 (M549V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377779	NM_145307.4(RTKN2):c.1594A>G (p.Lys532Glu)	RTKN2 (K532E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397012	NM_145307.4(RTKN2):c.1496G>A (p.Gly499Glu)	RTKN2 (G499E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332618	NM_145307.4(RTKN2):c.1270G>A (p.Ala424Thr)	RTKN2 (A424T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156860	NM_145307.4(RTKN2):c.1202G>A (p.Cys401Tyr)	RTKN2 (C401Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156859	NM_145307.4(RTKN2):c.1109C>A (p.Thr370Asn)	RTKN2 (T370N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156858	NM_145307.4(RTKN2):c.1100A>G (p.Gln367Arg)	RTKN2 (Q367R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346325	NM_145307.4(RTKN2):c.1099C>G (p.Gln367Glu)	RTKN2 (Q367E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370214	NM_145307.4(RTKN2):c.1043A>G (p.Asp348Gly)	RTKN2 (D348G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611296	NM_145307.4(RTKN2):c.972G>T (p.Glu324Asp)	RTKN2 (E324D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556087	NM_145307.4(RTKN2):c.949C>T (p.Leu317Phe)	RTKN2 (L317F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215677	NM_145307.4(RTKN2):c.893T>C (p.Met298Thr)	RTKN2 (M298T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258016	NM_145307.4(RTKN2):c.818T>C (p.Met273Thr)	RTKN2 (M273T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224697	NM_145307.4(RTKN2):c.758A>G (p.His253Arg)	RTKN2 (H253R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274881	NM_145307.4(RTKN2):c.731A>G (p.Glu244Gly)	RTKN2 (E244G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156869	NM_145307.4(RTKN2):c.692T>A (p.Val231Glu)	RTKN2 (V231E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156867	NM_145307.4(RTKN2):c.688G>C (p.Gly230Arg)	RTKN2 (G230R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156866	NM_145307.4(RTKN2):c.674G>A (p.Ser225Asn)	RTKN2 (S225N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156865	NM_145307.4(RTKN2):c.605G>A (p.Ser202Asn)	RTKN2 (S202N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261691	NM_145307.4(RTKN2):c.560C>T (p.Thr187Ile)	RTKN2 (T187I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156864	NM_145307.4(RTKN2):c.526G>C (p.Val176Leu)	RTKN2 (V176L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249553	NM_145307.4(RTKN2):c.520G>A (p.Val174Met)	RTKN2 (V174M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403005	NM_145307.4(RTKN2):c.242A>G (p.Asn81Ser)	LINC02621, RTKN2 (N81S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551701	NM_145307.4(RTKN2):c.145G>T (p.Asp49Tyr)	LINC02621, RTKN2 (D49Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156870	NM_145307.4(RTKN2):c.91G>A (p.Glu31Lys)	LINC02621, RTKN2 (E31K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156863	NM_145307.4(RTKN2):c.49C>G (p.Pro17Ala)	LINC02621, RTKN2 (P17A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3156862	NM_145307.4(RTKN2):c.43G>T (p.Gly15Trp)	LINC02621, RTKN2 (G15W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34