Angptl2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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49 records found for search term Angptl2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405654334	CV3280452	single nucleotide variant	NM_012098.3(ANGPTL2):c.7C>T (p.Pro3Ser)	not specified [RCV004414942]	uncertain significance	9	127108725	127108725	Human		name
597642023	CV3696306	single nucleotide variant	NM_012098.3(ANGPTL2):c.16G>A (p.Val6Met)	not specified [RCV004941818]	uncertain significance	9	127108716	127108716	Human		name
156181252	CV2320784	single nucleotide variant	NM_012098.3(ANGPTL2):c.76G>A (p.Gly26Ser)	not specified [RCV004172621]	uncertain significance	9	127108656	127108656	Human		name
405654361	CV3280460	single nucleotide variant	NM_012098.3(ANGPTL2):c.85G>A (p.Gly29Ser)	not specified [RCV004414950]	uncertain significance	9	127108647	127108647	Human		name
597795817	CV3696353	single nucleotide variant	NM_012098.3(ANGPTL2):c.70G>A (p.Glu24Lys)	not specified [RCV004934980]	likely benign	9	127108662	127108662	Human		name
155917254	CV2236512	single nucleotide variant	NM_012098.3(ANGPTL2):c.226C>G (p.Pro76Ala)	not specified [RCV004110511]	uncertain significance	9	127108506	127108506	Human		name
156069426	CV2292760	single nucleotide variant	NM_012098.3(ANGPTL2):c.176T>C (p.Ile59Thr)	not specified [RCV004154423]	uncertain significance	9	127108556	127108556	Human		name
156389117	CV2373557	single nucleotide variant	NM_012098.3(ANGPTL2):c.193G>A (p.Val65Ile)	not specified [RCV004222659]	uncertain significance	9	127108539	127108539	Human		name
329362267	CV2444527	single nucleotide variant	NM_012098.3(ANGPTL2):c.191G>A (p.Arg64Gln)	not specified [RCV004256755]	uncertain significance	9	127108541	127108541	Human		name
329382817	CV2445542	single nucleotide variant	NM_012098.3(ANGPTL2):c.211G>A (p.Val71Ile)	not specified [RCV004257591]	uncertain significance	9	127108521	127108521	Human		name
405817908	CV3280387	single nucleotide variant	NM_012098.3(ANGPTL2):c.101C>T (p.Ser34Leu)	not specified [RCV004412894]	uncertain significance	9	127108631	127108631	Human		name
405654235	CV3280418	single nucleotide variant	NM_012098.3(ANGPTL2):c.254A>C (p.His85Pro)	not specified [RCV004414908]	uncertain significance	9	127108478	127108478	Human		name
407481668	CV3449787	single nucleotide variant	NM_012098.3(ANGPTL2):c.190C>T (p.Arg64Trp)	not specified [RCV004645184]	uncertain significance	9	127108542	127108542	Human		name
407479612	CV3449809	single nucleotide variant	NM_012098.3(ANGPTL2):c.256A>G (p.Lys86Glu)	not specified [RCV004628745]	uncertain significance	9	127108476	127108476	Human		name
407481674	CV3449820	single nucleotide variant	NM_012098.3(ANGPTL2):c.137G>A (p.Arg46Gln)	not specified [RCV004645211]	uncertain significance	9	127108595	127108595	Human		name
407479615	CV3449831	single nucleotide variant	NM_012098.3(ANGPTL2):c.188A>T (p.Gln63Leu)	not specified [RCV004628748]	uncertain significance	9	127108544	127108544	Human		name
597795812	CV3696334	single nucleotide variant	NM_012098.3(ANGPTL2):c.289C>T (p.Leu97Phe)	not specified [RCV004934978]	uncertain significance	9	127108443	127108443	Human		name
598270119	CV3976320	single nucleotide variant	NM_012098.3(ANGPTL2):c.203C>A (p.Ala68Asp)	not specified [RCV005350038]	uncertain significance	9	127108529	127108529	Human		name
156326119	CV2209572	single nucleotide variant	NM_012098.3(ANGPTL2):c.901C>T (p.Arg301Cys)	not specified [RCV004093677]	uncertain significance	9	127093843	127093843	Human		name
155918676	CV2236883	single nucleotide variant	NM_012098.3(ANGPTL2):c.343G>A (p.Gly115Ser)	not specified [RCV004112637]	uncertain significance	9	127108389	127108389	Human		name
156124652	CV2237397	single nucleotide variant	NM_012098.3(ANGPTL2):c.661C>T (p.Pro221Ser)	not specified [RCV004106369]	uncertain significance	9	127108071	127108071	Human		name
155904400	CV2275914	single nucleotide variant	NM_012098.3(ANGPTL2):c.445C>T (p.Arg149Trp)	not specified [RCV004139570]	uncertain significance	9	127108287	127108287	Human		name
156254957	CV2311574	single nucleotide variant	NM_012098.3(ANGPTL2):c.569C>G (p.Ala190Gly)	not specified [RCV004168388]	uncertain significance	9	127108163	127108163	Human		name
156124316	CV2350098	single nucleotide variant	NM_012098.3(ANGPTL2):c.803C>T (p.Thr268Ile)	not specified [RCV004200020]	uncertain significance	9	127107929	127107929	Human		name
155933239	CV2399286	single nucleotide variant	NM_012098.3(ANGPTL2):c.887C>T (p.Pro296Leu)	not specified [RCV004242581]	uncertain significance	9	127093857	127093857	Human		name
401772247	CV2687461	single nucleotide variant	NM_012098.3(ANGPTL2):c.775C>T (p.Pro259Ser)	not specified [RCV004300703]	uncertain significance	9	127107957	127107957	Human		name
401858233	CV2774246	single nucleotide variant	NM_012098.3(ANGPTL2):c.314C>T (p.Thr105Met)	not specified [RCV004347614]	uncertain significance	9	127108418	127108418	Human		name
401891106	CV2778647	single nucleotide variant	NM_012098.3(ANGPTL2):c.578A>T (p.Gln193Leu)	not specified [RCV004344290]	uncertain significance	9	127108154	127108154	Human		name
405654243	CV3280421	single nucleotide variant	NM_012098.3(ANGPTL2):c.309C>G (p.Ile103Met)	not specified [RCV004414911]	uncertain significance	9	127108423	127108423	Human		name
405654304	CV3280441	single nucleotide variant	NM_012098.3(ANGPTL2):c.664C>T (p.Pro222Ser)	not specified [RCV004414931]	uncertain significance	9	127108068	127108068	Human		name
407479608	CV3449798	single nucleotide variant	NM_012098.3(ANGPTL2):c.757C>A (p.Pro253Thr)	not specified [RCV004628743]	uncertain significance	9	127107975	127107975	Human		name
597795806	CV3696314	single nucleotide variant	NM_012098.3(ANGPTL2):c.952G>A (p.Val318Ile)	not specified [RCV004934976]	uncertain significance	9	127093792	127093792	Human		name
597795809	CV3696326	single nucleotide variant	NM_012098.3(ANGPTL2):c.635C>T (p.Pro212Leu)	not specified [RCV004934977]	uncertain significance	9	127108097	127108097	Human		name
597642330	CV3696363	single nucleotide variant	NM_012098.3(ANGPTL2):c.502G>A (p.Asp168Asn)	not specified [RCV004941847]	uncertain significance	9	127108230	127108230	Human		name
597642376	CV3696372	single nucleotide variant	NM_012098.3(ANGPTL2):c.440G>A (p.Arg147His)	not specified [RCV004941855]	uncertain significance	9	127108292	127108292	Human		name
597795829	CV3696380	single nucleotide variant	NM_012098.3(ANGPTL2):c.300G>C (p.Lys100Asn)	not specified [RCV004934984]	uncertain significance	9	127108432	127108432	Human		name
598235745	CV3976325	single nucleotide variant	NM_012098.3(ANGPTL2):c.446G>A (p.Arg149Gln)	not specified [RCV005363718]	uncertain significance	9	127108286	127108286	Human		name
598270142	CV3976334	single nucleotide variant	NM_012098.3(ANGPTL2):c.306G>C (p.Gln102His)	not specified [RCV005350043]	uncertain significance	9	127108426	127108426	Human		name
598270161	CV3976344	single nucleotide variant	NM_012098.3(ANGPTL2):c.667C>T (p.Arg223Trp)	not specified [RCV005350047]	uncertain significance	9	127108065	127108065	Human		name
156108760	CV2211053	single nucleotide variant	NM_012098.3(ANGPTL2):c.1195C>T (p.Arg399Cys)	not specified [RCV004088234]	uncertain significance	9	127091757	127091757	Human		name
156364052	CV2262763	single nucleotide variant	NM_012098.3(ANGPTL2):c.1375C>T (p.Arg459Trp)	not specified [RCV004130939]	uncertain significance	9	127089046	127089046	Human		name
156345249	CV2372893	single nucleotide variant	NM_012098.3(ANGPTL2):c.1469A>G (p.Asn490Ser)	not specified [RCV004223938]	uncertain significance	9	127088952	127088952	Human		name
401773478	CV2709330	single nucleotide variant	NM_012098.3(ANGPTL2):c.1267C>T (p.His423Tyr)	not specified [RCV004316479]	uncertain significance	9	127091685	127091685	Human		name
401863748	CV2770643	single nucleotide variant	NM_012098.3(ANGPTL2):c.1378A>G (p.Ser460Gly)	not specified [RCV004349695]	uncertain significance	9	127089043	127089043	Human		name
405654168	CV3280395	single nucleotide variant	NM_012098.3(ANGPTL2):c.1237G>A (p.Gly413Ser)	not specified [RCV004414885]	uncertain significance	9	127091715	127091715	Human		name
597642065	CV3696320	single nucleotide variant	NM_012098.3(ANGPTL2):c.1154G>A (p.Arg385His)	not specified [RCV004941825]	uncertain significance	9	127091798	127091798	Human		name
597642103	CV3696344	single nucleotide variant	NM_012098.3(ANGPTL2):c.1186C>T (p.Arg396Trp)	not specified [RCV004941831]	uncertain significance	9	127091766	127091766	Human		name
598235808	CV3976350	single nucleotide variant	NM_012098.3(ANGPTL2):c.1108G>A (p.Glu370Lys)	not specified [RCV005363728]	uncertain significance	9	127091844	127091844	Human		name
598213200	CV3976360	single nucleotide variant	NM_012098.3(ANGPTL2):c.1171G>A (p.Glu391Lys)	not specified [RCV005358952]	uncertain significance	9	127091781	127091781	Human		name

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