"Ambry Genetics"[submitter] AND "TNS2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2282143	NM_170754.4(TNS2):c.104G>A (p.Arg35Gln)	TNS2, TNS2-AS1 (R35Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3327801	NM_170754.4(TNS2):c.160G>A (p.Asp54Asn)	TNS2, TNS2-AS1 (D54N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542738	NM_170754.4(TNS2):c.277C>T (p.Pro93Ser)	TNS2, TNS2-AS1 (P93S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548494	NM_170754.4(TNS2):c.284G>A (p.Arg95Lys)	TNS2, TNS2-AS1 (R72K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2278903	NM_170754.4(TNS2):c.287G>A (p.Arg96His)	TNS2, TNS2-AS1 (R106H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304837	NM_170754.4(TNS2):c.319A>G (p.Asn107Asp)	TNS2, TNS2-AS1 (N117D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286315	NM_170754.4(TNS2):c.421T>G (p.Leu141Val)	TNS2, TNS2-AS1 (L151V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410907	NM_170754.4(TNS2):c.446C>T (p.Pro149Leu)	TNS2, TNS2-AS1 (P149L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556661	NM_170754.4(TNS2):c.508C>G (p.Arg170Gly)	TNS2, TNS2-AS1 (R170G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548670	NM_170754.4(TNS2):c.654G>T (p.Trp218Cys)	TNS2 (W195C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329612	NM_170754.4(TNS2):c.679G>A (p.Val227Ile)	TNS2 (V227I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1492852	NM_170754.4(TNS2):c.682G>A (p.Val228Ile)	TNS2 (V104I +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2741717	NM_170754.4(TNS2):c.764C>T (p.Ala255Val)	TNS2 (A131V +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3180842	NM_170754.4(TNS2):c.805G>A (p.Glu269Lys)	TNS2 (E269K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262381	NM_170754.4(TNS2):c.812A>G (p.Lys271Arg)	TNS2 (K271R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373054	NM_170754.4(TNS2):c.817G>A (p.Ala273Thr)	TNS2 (A149T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618338	NM_170754.4(TNS2):c.827T>A (p.Leu276Gln)	TNS2 (L152Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180843	NM_170754.4(TNS2):c.830A>G (p.Gln277Arg)	TNS2 (Q153R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1968329	NM_170754.4(TNS2):c.841C>T (p.Arg281Cys)	TNS2 (R157C +3 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3327807	NM_170754.4(TNS2):c.894C>G (p.Asn298Lys)	TNS2 (N174K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508582	NM_170754.4(TNS2):c.968C>A (p.Pro323His)	TNS2 (P323H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463466	NM_170754.4(TNS2):c.1046A>G (p.Gln349Arg)	TNS2 (Q225R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180822	NM_170754.4(TNS2):c.1084G>A (p.Gly362Ser)	TNS2 (G362S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1492086	NM_170754.4(TNS2):c.1126A>G (p.Thr376Ala)	TNS2 (T376A +3 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3180823	NM_170754.4(TNS2):c.1145T>G (p.Phe382Cys)	TNS2 (F382C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2068657	NM_170754.4(TNS2):c.1213G>A (p.Glu405Lys)	TNS2 (E281K +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3180824	NM_170754.4(TNS2):c.1301C>A (p.Pro434Gln)	TNS2 (P310Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1442913	NM_170754.4(TNS2):c.1319T>C (p.Val440Ala)	TNS2 (V440A +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2321789	NM_170754.4(TNS2):c.1355G>A (p.Arg452His)	TNS2 (R328H +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2527739	NM_170754.4(TNS2):c.1367A>G (p.Tyr456Cys)	TNS2 (Y332C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392223	NM_170754.4(TNS2):c.1372A>G (p.Asn458Asp)	TNS2 (N458D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291073	NM_170754.4(TNS2):c.1384C>G (p.His462Asp)	TNS2 (H462D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319163	NM_170754.4(TNS2):c.1423C>T (p.Arg475Trp)	TNS2 (R351W +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1699313	NM_170754.4(TNS2):c.1424G>A (p.Arg475Gln)	TNS2 (R351Q +5 more)	Single nucleotide variant (missense variant)	Nephrotic syndrome +2 more	GUncertain significance
Select item 2593667	NM_170754.4(TNS2):c.1430C>T (p.Pro477Leu)	TNS2 (P477L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327809	NM_170754.4(TNS2):c.1445C>T (p.Pro482Leu)	TNS2 (P482L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2062677	NM_170754.4(TNS2):c.1463G>A (p.Arg488Gln)	TNS2 (R364Q +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3180825	NM_170754.4(TNS2):c.1478C>T (p.Thr493Ile)	TNS2 (T470I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286161	NM_170754.4(TNS2):c.1513C>G (p.Pro505Ala)	TNS2 (P515A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334404	NM_170754.4(TNS2):c.1568C>T (p.Pro523Leu)	TNS2 (P533L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2054155	NM_170754.4(TNS2):c.1582C>G (p.Pro528Ala)	TNS2 (P538A +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2353854	NM_170754.4(TNS2):c.1588C>T (p.Arg530Trp)	TNS2 (R540W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327804	NM_170754.4(TNS2):c.1678G>A (p.Glu560Lys)	TNS2 (E569K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209850	NM_170754.4(TNS2):c.1729C>G (p.His577Asp)	TNS2 (H577D +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180826	NM_170754.4(TNS2):c.1752T>G (p.His584Gln)	TNS2 (H460Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598890	NM_170754.4(TNS2):c.1768C>T (p.Arg590Cys)	TNS2 (R466C +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2217941	NM_170754.4(TNS2):c.1784G>A (p.Arg595His)	TNS2 (R605H +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514141	NM_170754.4(TNS2):c.1795C>T (p.Arg599Trp)	TNS2 (R599W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180827	NM_170754.4(TNS2):c.1796G>A (p.Arg599Gln)	TNS2 (R475Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474206	NM_170754.4(TNS2):c.1807G>A (p.Gly603Arg)	TNS2 (G479R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495292	NM_170754.4(TNS2):c.1831C>T (p.Arg611Trp)	TNS2 (R611W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327802	NM_170754.4(TNS2):c.1865C>G (p.Ala622Gly)	TNS2 (A498G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495552	NM_170754.4(TNS2):c.1871G>A (p.Gly624Glu)	TNS2 (G500E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180828	NM_170754.4(TNS2):c.1934G>A (p.Arg645Gln)	TNS2 (R521Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324862	NM_170754.4(TNS2):c.1937C>G (p.Ser646Trp)	TNS2 (S646W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532760	NM_170754.4(TNS2):c.1996T>C (p.Phe666Leu)	TNS2 (F643L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334792	NM_170754.4(TNS2):c.2020C>T (p.Arg674Trp)	TNS2 (R550W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370308	NM_170754.4(TNS2):c.2036T>C (p.Leu679Pro)	TNS2 (L679P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2908822	NM_170754.4(TNS2):c.2048G>A (p.Gly683Glu)	TNS2 (G559E +4 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3327808	NM_170754.4(TNS2):c.2114A>G (p.Tyr705Cys)	TNS2 (Y714C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1971735	NM_170754.4(TNS2):c.2296G>A (p.Glu766Lys)	TNS2 (E766K +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2395642	NM_170754.4(TNS2):c.2323G>A (p.Glu775Lys)	TNS2 (E785K +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3180829	NM_170754.4(TNS2):c.2396G>A (p.Cys799Tyr)	TNS2 (C776Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599125	NM_170754.4(TNS2):c.2419C>T (p.His807Tyr)	TNS2 (H683Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376490	NM_170754.4(TNS2):c.2540A>C (p.Glu847Ala)	TNS2 (E847A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180830	NM_170754.4(TNS2):c.2576T>C (p.Leu859Ser)	TNS2 (L735S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2151206	NM_170754.4(TNS2):c.2630C>T (p.Pro877Leu)	TNS2 (P753L +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3180832	NM_170754.4(TNS2):c.2782G>C (p.Asp928His)	TNS2 (D804H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180833	NM_170754.4(TNS2):c.2830G>A (p.Glu944Lys)	TNS2 (E921K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1990955	NM_170754.4(TNS2):c.2831A>C (p.Glu944Ala)	TNS2 (E944A +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3327805	NM_170754.4(TNS2):c.2863G>C (p.Gly955Arg)	TNS2 (G964R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359306	NM_170754.4(TNS2):c.2863G>A (p.Gly955Arg)	TNS2 (G831R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327800	NM_170754.4(TNS2):c.2869G>A (p.Ala957Thr)	TNS2 (A943T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237026	NM_170754.4(TNS2):c.2975C>A (p.Pro992Gln)	TNS2 (P1002Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511895	NM_170754.4(TNS2):c.2990A>G (p.Asp997Gly)	TNS2 (D983G +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1959074	NM_170754.4(TNS2):c.2995G>A (p.Ala999Thr)	TNS2 (A999T +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2329289	NM_170754.4(TNS2):c.3019A>T (p.Thr1007Ser)	TNS2 (T1017S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2142956	NM_170754.4(TNS2):c.3037C>T (p.Arg1013Cys)	TNS2 (R1013C +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2297054	NM_170754.4(TNS2):c.3058C>T (p.Pro1020Ser)	TNS2 (P896S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260265	NM_170754.4(TNS2):c.3067C>A (p.Pro1023Thr)	TNS2 (P1033T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242411	NM_170754.4(TNS2):c.3073G>A (p.Asp1025Asn)	TNS2 (D1025N +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2319785	NM_170754.4(TNS2):c.3077G>A (p.Ser1026Asn)	TNS2 (S902N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399694	NM_170754.4(TNS2):c.3143C>T (p.Pro1048Leu)	TNS2 (P1048L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595458	NM_170754.4(TNS2):c.3197A>G (p.Asn1066Ser)	TNS2 (N942S +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 806895	NM_170754.4(TNS2):c.3248G>A (p.Gly1083Glu)	TNS2 (G959E +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1973007	NM_170754.4(TNS2):c.3287C>T (p.Ser1096Leu)	TNS2 (S1106L +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2519638	NM_170754.4(TNS2):c.3289C>T (p.Pro1097Ser)	TNS2 (P1097S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271660	NM_170754.4(TNS2):c.3307C>T (p.His1103Tyr)	TNS2 (H979Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221196	NM_170754.4(TNS2):c.3322G>A (p.Ala1108Thr)	TNS2 (A1108T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454357	NM_170754.4(TNS2):c.3403G>C (p.Asp1135His)	TNS2 (D1135H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180834	NM_170754.4(TNS2):c.3410C>A (p.Ser1137Tyr)	TNS2 (S1123Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180835	NM_170754.4(TNS2):c.3553C>G (p.Pro1185Ala)	TNS2 (P1162A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2191468	NM_170754.4(TNS2):c.3563A>G (p.Gln1188Arg)	TNS2 (Q1188R +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3180836	NM_170754.4(TNS2):c.3659C>T (p.Pro1220Leu)	TNS2 (P1206L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376774	NM_170754.4(TNS2):c.3679G>A (p.Ala1227Thr)	TNS2 (A1103T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180837	NM_170754.4(TNS2):c.3706C>T (p.Pro1236Ser)	TNS2 (P1236S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180838	NM_170754.4(TNS2):c.3730C>T (p.Arg1244Cys)	TNS2 (R1230C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236961	NM_170754.4(TNS2):c.3769G>A (p.Ala1257Thr)	TNS2 (A1133T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327806	NM_170754.4(TNS2):c.3785A>G (p.Asn1262Ser)	TNS2 (N1138S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2077960	NM_170754.4(TNS2):c.3787A>T (p.Met1263Leu)	TNS2 (M1263L +5 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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