"Ambry Genetics"[submitter] AND "KNDC1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2290340	NM_152643.8(KNDC1):c.20C>A (p.Ala7Asp)	KNDC1 (A7D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522470	NM_152643.8(KNDC1):c.199C>T (p.Arg67Trp)	KNDC1 (R67W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116082	NM_152643.8(KNDC1):c.200G>A (p.Arg67Gln)	KNDC1 (R67Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3289206	NM_152643.8(KNDC1):c.214G>T (p.Ala72Ser)	KNDC1 (A72S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2298054	NM_152643.8(KNDC1):c.217G>T (p.Ala73Ser)	KNDC1 (A73S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116091	NM_152643.8(KNDC1):c.247G>A (p.Asp83Asn)	KNDC1 (D83N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405369	NM_152643.8(KNDC1):c.266C>T (p.Thr89Ile)	KNDC1 (T89I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289195	NM_152643.8(KNDC1):c.277G>A (p.Val93Met)	KNDC1 (V93M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308099	NM_152643.8(KNDC1):c.340G>A (p.Val114Met)	KNDC1 (V114M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321002	NM_152643.8(KNDC1):c.409G>A (p.Val137Met)	KNDC1 (V137M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116113	NM_152643.8(KNDC1):c.487G>A (p.Gly163Arg)	KNDC1 (G163R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2210208	NM_152643.8(KNDC1):c.493C>G (p.Arg165Gly)	KNDC1 (R165G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606870	NM_152643.8(KNDC1):c.494G>A (p.Arg165Gln)	KNDC1 (R165Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341963	NM_152643.8(KNDC1):c.634G>A (p.Glu212Lys)	KNDC1 (E212K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403462	NM_152643.8(KNDC1):c.646C>T (p.Arg216Trp)	KNDC1 (R216W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289196	NM_152643.8(KNDC1):c.647G>T (p.Arg216Leu)	KNDC1 (R216L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116114	NM_152643.8(KNDC1):c.647G>A (p.Arg216Gln)	KNDC1 (R216Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289200	NM_152643.8(KNDC1):c.680G>A (p.Arg227Lys)	KNDC1 (R227K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2591079	NM_152643.8(KNDC1):c.694G>A (p.Asp232Asn)	KNDC1 (D232N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116115	NM_152643.8(KNDC1):c.730G>C (p.Glu244Gln)	KNDC1 (E244Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467028	NM_152643.8(KNDC1):c.730G>A (p.Glu244Lys)	KNDC1 (E244K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116116	NM_152643.8(KNDC1):c.770C>G (p.Ser257Cys)	KNDC1 (S257C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355094	NM_152643.8(KNDC1):c.859C>T (p.Arg287Cys)	KNDC1 (R287C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334849	NM_152643.8(KNDC1):c.860G>C (p.Arg287Pro)	KNDC1 (R287P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254267	NM_152643.8(KNDC1):c.868G>C (p.Gly290Arg)	KNDC1 (G290R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289208	NM_152643.8(KNDC1):c.1022C>T (p.Pro341Leu)	KNDC1 (P341L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260456	NM_152643.8(KNDC1):c.1022C>G (p.Pro341Arg)	KNDC1 (P341R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290168	NM_152643.8(KNDC1):c.1036C>G (p.Leu346Val)	KNDC1 (L346V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529305	NM_152643.8(KNDC1):c.1042A>G (p.Arg348Gly)	KNDC1 (R348G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3289201	NM_152643.8(KNDC1):c.1054C>T (p.Leu352Phe)	KNDC1 (L352F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335117	NM_152643.8(KNDC1):c.1069G>A (p.Ala357Thr)	KNDC1 (A357T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289198	NM_152643.8(KNDC1):c.1123C>T (p.Arg375Trp)	KNDC1 (R375W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611757	NM_152643.8(KNDC1):c.1159C>T (p.Pro387Ser)	KNDC1 (P387S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289202	NM_152643.8(KNDC1):c.1166T>C (p.Val389Ala)	KNDC1 (V389A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2600553	NM_152643.8(KNDC1):c.1171G>A (p.Gly391Ser)	KNDC1 (G391S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289197	NM_152643.8(KNDC1):c.1187C>T (p.Pro396Leu)	KNDC1 (P396L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512092	NM_152643.8(KNDC1):c.1238G>A (p.Arg413Gln)	KNDC1 (R413Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289207	NM_152643.8(KNDC1):c.1249G>A (p.Gly417Ser)	KNDC1 (G417S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116074	NM_152643.8(KNDC1):c.1306G>C (p.Glu436Gln)	KNDC1 (E436Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403525	NM_152643.8(KNDC1):c.1318G>A (p.Ala440Thr)	KNDC1 (A440T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116075	NM_152643.8(KNDC1):c.1319C>T (p.Ala440Val)	KNDC1 (A440V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289203	NM_152643.8(KNDC1):c.1323G>C (p.Glu441Asp)	KNDC1 (E441D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116077	NM_152643.8(KNDC1):c.1373G>A (p.Arg458Gln)	KNDC1 (R458Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116078	NM_152643.8(KNDC1):c.1414G>A (p.Ala472Thr)	KNDC1 (A472T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2316967	NM_152643.8(KNDC1):c.1454T>C (p.Leu485Pro)	KNDC1 (L485P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362612	NM_152643.8(KNDC1):c.1474G>A (p.Glu492Lys)	KNDC1 (E492K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116079	NM_152643.8(KNDC1):c.1657C>T (p.Arg553Cys)	KNDC1 (R553C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116080	NM_152643.8(KNDC1):c.1660A>G (p.Arg554Gly)	KNDC1 (R554G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321327	NM_152643.8(KNDC1):c.1684A>G (p.Met562Val)	KNDC1 (M562V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407702	NM_152643.8(KNDC1):c.1694G>A (p.Arg565His)	KNDC1 (R565H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569082	NM_152643.8(KNDC1):c.1712C>T (p.Pro571Leu)	KNDC1 (P571L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220705	NM_152643.8(KNDC1):c.1718C>T (p.Ala573Val)	KNDC1 (A573V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560380	NM_152643.8(KNDC1):c.1877G>A (p.Ser626Asn)	KNDC1 (S626N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403607	NM_152643.8(KNDC1):c.1933G>A (p.Gly645Arg)	KNDC1 (G645R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2377760	NM_152643.8(KNDC1):c.1934G>T (p.Gly645Val)	KNDC1 (G645V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615874	NM_152643.8(KNDC1):c.1942G>A (p.Ala648Thr)	KNDC1 (A648T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380798	NM_152643.8(KNDC1):c.1963G>A (p.Gly655Ser)	KNDC1 (G655S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2471233	NM_152643.8(KNDC1):c.2014T>C (p.Ser672Pro)	KNDC1 (S672P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347371	NM_152643.8(KNDC1):c.2017G>A (p.Glu673Lys)	KNDC1 (E673K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116083	NM_152643.8(KNDC1):c.2027A>G (p.His676Arg)	KNDC1 (H676R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306119	NM_152643.8(KNDC1):c.2044C>T (p.Leu682Phe)	KNDC1 (L682F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476664	NM_152643.8(KNDC1):c.2048C>A (p.Ala683Glu)	KNDC1 (A683E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408161	NM_152643.8(KNDC1):c.2056G>A (p.Ala686Thr)	KNDC1 (A686T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116084	NM_152643.8(KNDC1):c.2242G>A (p.Ala748Thr)	KNDC1 (A748T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533370	NM_152643.8(KNDC1):c.2252A>G (p.Gln751Arg)	KNDC1 (Q751R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210773	NM_152643.8(KNDC1):c.2335G>C (p.Gly779Arg)	KNDC1 (G779R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409197	NM_152643.8(KNDC1):c.2350G>A (p.Ala784Thr)	KNDC1 (A784T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116085	NM_152643.8(KNDC1):c.2360C>T (p.Thr787Met)	KNDC1 (T787M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116087	NM_152643.8(KNDC1):c.2372C>T (p.Ala791Val)	KNDC1 (A791V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335037	NM_152643.8(KNDC1):c.2390G>A (p.Gly797Glu)	KNDC1 (G797E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347519	NM_152643.8(KNDC1):c.2393C>T (p.Pro798Leu)	KNDC1 (P798L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535962	NM_152643.8(KNDC1):c.2395G>A (p.Ala799Thr)	KNDC1 (A799T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116088	NM_152643.8(KNDC1):c.2402C>T (p.Pro801Leu)	KNDC1 (P801L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276735	NM_152643.8(KNDC1):c.2405T>A (p.Ile802Asn)	KNDC1 (I802N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307815	NM_152643.8(KNDC1):c.2406C>G (p.Ile802Met)	KNDC1 (I802M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462905	NM_152643.8(KNDC1):c.2425G>A (p.Gly809Arg)	KNDC1 (G809R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257771	NM_152643.8(KNDC1):c.2425G>C (p.Gly809Arg)	KNDC1 (G809R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116089	NM_152643.8(KNDC1):c.2440G>A (p.Asp814Asn)	KNDC1 (D814N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212266	NM_152643.8(KNDC1):c.2441A>C (p.Asp814Ala)	KNDC1 (D814A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395600	NM_152643.8(KNDC1):c.2443G>A (p.Ala815Thr)	KNDC1 (A815T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3116090	NM_152643.8(KNDC1):c.2459C>T (p.Thr820Met)	KNDC1 (T820M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244325	NM_152643.8(KNDC1):c.2470G>A (p.Gly824Ser)	KNDC1 (G824S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358892	NM_152643.8(KNDC1):c.2480A>C (p.His827Pro)	KNDC1 (H827P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271272	NM_152643.8(KNDC1):c.2488A>G (p.Lys830Glu)	KNDC1 (K830E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289189	NM_152643.8(KNDC1):c.2519C>T (p.Pro840Leu)	KNDC1 (P840L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218823	NM_152643.8(KNDC1):c.2527G>C (p.Glu843Gln)	KNDC1 (E843Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267398	NM_152643.8(KNDC1):c.2555C>G (p.Ala852Gly)	KNDC1 (A852G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116092	NM_152643.8(KNDC1):c.2578C>A (p.Pro860Thr)	KNDC1 (P860T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399054	NM_152643.8(KNDC1):c.2611G>C (p.Asp871His)	KNDC1 (D871H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116093	NM_152643.8(KNDC1):c.2615G>A (p.Arg872Gln)	KNDC1 (R872Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592788	NM_152643.8(KNDC1):c.2635G>C (p.Val879Leu)	KNDC1 (V879L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116094	NM_152643.8(KNDC1):c.2641G>A (p.Ala881Thr)	KNDC1 (A881T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2253229	NM_152643.8(KNDC1):c.2650C>T (p.Leu884Phe)	KNDC1 (L884F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607442	NM_152643.8(KNDC1):c.2749C>G (p.Leu917Val)	KNDC1 (L917V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289199	NM_152643.8(KNDC1):c.2755A>G (p.Met919Val)	KNDC1 (M919V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382987	NM_152643.8(KNDC1):c.2769C>G (p.Ile923Met)	KNDC1 (I923M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611111	NM_152643.8(KNDC1):c.2773G>A (p.Ala925Thr)	KNDC1 (A925T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557437	NM_152643.8(KNDC1):c.2879A>G (p.Asn960Ser)	KNDC1 (N960S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116096	NM_152643.8(KNDC1):c.2894C>T (p.Pro965Leu)	KNDC1 (P965L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374613	NM_152643.8(KNDC1):c.2911G>A (p.Glu971Lys)	KNDC1 (E971K)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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