"Illumina Laboratory Services, Illumina"[submitter] AND "LPIN2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 326541	NM_001375808.2(LPIN2):c.*3280C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326542	NM_001375808.2(LPIN2):c.*3217A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326543	NM_001375808.2(LPIN2):c.*3139A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326546	NM_001375808.2(LPIN2):c.*3068A>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326547	NM_001375808.2(LPIN2):c.*3015T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326548	NM_001375808.2(LPIN2):c.*2999C>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326549	NM_001375808.2(LPIN2):c.*2946G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326550	NM_001375808.2(LPIN2):c.*2934C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326551	NM_001375808.2(LPIN2):c.*2924del	LPIN2	Deletion (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326552	NM_001375808.2(LPIN2):c.*2923C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326553	NM_001375808.2(LPIN2):c.2890_2893dup	LPIN2	Duplication (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326554	NM_001375808.2(LPIN2):c.*2866A>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326555	NM_001375808.2(LPIN2):c.*2831CA[1]	LPIN2	Microsatellite (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326556	NM_001375808.2(LPIN2):c.*2830C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326557	NM_001375808.2(LPIN2):c.*2822C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326558	NM_001375808.2(LPIN2):c.*2787C>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326559	NM_001375808.2(LPIN2):c.*2759A>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326560	NM_001375808.2(LPIN2):c.*2724A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890343	NM_001375808.2(LPIN2):c.*2710A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326561	NM_001375808.2(LPIN2):c.*2685GAAAAA[1]	LPIN2	Microsatellite (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890344	NM_001375808.2(LPIN2):c.*2605G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890345	NM_001375808.2(LPIN2):c.*2557G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890346	NM_001375808.2(LPIN2):c.*2553G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326562	NM_001375808.2(LPIN2):c.*2493C>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 892144	NM_001375808.2(LPIN2):c.*2417C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326566	NM_001375808.2(LPIN2):c.*2412C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 888702	NM_001375808.2(LPIN2):c.*2391G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326570	NM_001375808.2(LPIN2):c.*2390C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326571	NM_001375808.2(LPIN2):c.*2241T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326572	NM_001375808.2(LPIN2):c.*2216C>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326573	NM_001375808.2(LPIN2):c.2197_2198del	LPIN2	Deletion (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326574	NM_001375808.2(LPIN2):c.*2103G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326575	NM_001375808.2(LPIN2):c.*2076C>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326576	NM_001375808.2(LPIN2):c.*1874C>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326577	NM_001375808.2(LPIN2):c.*1827G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890405	NM_001375808.2(LPIN2):c.*1810A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326578	NM_001375808.2(LPIN2):c.*1742A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326579	NM_001375808.2(LPIN2):c.*1691A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326580	NM_001375808.2(LPIN2):c.*1622T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326581	NM_001375808.2(LPIN2):c.*1586G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326582	NM_001375808.2(LPIN2):c.*1559A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326584	NM_001375808.2(LPIN2):c.*1514G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326583	NM_001375808.2(LPIN2):c.*1514G>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890968	NM_001375808.2(LPIN2):c.*1504T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326585	NM_001375808.2(LPIN2):c.*1502G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 890969	NM_001375808.2(LPIN2):c.*1497C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890970	NM_001375808.2(LPIN2):c.*1494G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890971	NM_001375808.2(LPIN2):c.*1473T>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326586	NM_001375808.2(LPIN2):c.*1462A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890972	NM_001375808.2(LPIN2):c.*1443G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326587	NM_001375808.2(LPIN2):c.*1418G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892201	NM_001375808.2(LPIN2):c.*1417C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892202	NM_001375808.2(LPIN2):c.*1239C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326588	NM_001375808.2(LPIN2):c.*1220G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892203	NM_001375808.2(LPIN2):c.*1199G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326589	NM_001375808.2(LPIN2):c.*1179G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 892204	NM_001375808.2(LPIN2):c.*1157T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892205	NM_001375808.2(LPIN2):c.*1147A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 888769	NM_001375808.2(LPIN2):c.*1146T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326590	NM_001375808.2(LPIN2):c.*1126G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 888770	NM_001375808.2(LPIN2):c.*1104C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 888771	NM_001375808.2(LPIN2):c.*1082G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326591	NM_001375808.2(LPIN2):c.*1077C>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326592	NM_001375808.2(LPIN2):c.*1052T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326593	NM_001375808.2(LPIN2):c.*1027G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326594	NM_001375808.2(LPIN2):c.*1026C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326595	NM_001375808.2(LPIN2):c.*1021G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890475	NM_001375808.2(LPIN2):c.*984T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326596	NM_001375808.2(LPIN2):c.*950A>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326597	NM_001375808.2(LPIN2):c.*947dup	LPIN2	Duplication (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 890476	NM_001375808.2(LPIN2):c.*945G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890477	NM_001375808.2(LPIN2):c.*934G>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326598	NM_001375808.2(LPIN2):c.*903T>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326599	NM_001375808.2(LPIN2):c.*897T>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890478	NM_001375808.2(LPIN2):c.*855A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 891033	NM_001375808.2(LPIN2):c.*850G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GLikely benign
Select item 326600	NM_001375808.2(LPIN2):c.*834G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326601	NM_001375808.2(LPIN2):c.*833G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 891034	NM_001375808.2(LPIN2):c.*828T>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326602	NM_001375808.2(LPIN2):c.*823G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326603	NM_001375808.2(LPIN2):c.*813A>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 891035	NM_001375808.2(LPIN2):c.*810G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 891036	NM_001375808.2(LPIN2):c.*806C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892258	NM_001375808.2(LPIN2):c.*805C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326604	NM_001375808.2(LPIN2):c.*805C>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892259	NM_001375808.2(LPIN2):c.*804G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326605	NM_001375808.2(LPIN2):c.*797T>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326606	NM_001375808.2(LPIN2):c.*796T>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326607	NM_001375808.2(LPIN2):c.*792G>C	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892260	NM_001375808.2(LPIN2):c.*778C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 892261	NM_001375808.2(LPIN2):c.*773C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 888857	NM_001375808.2(LPIN2):c.*772G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326608	NM_001375808.2(LPIN2):c.*767A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326609	NM_001375808.2(LPIN2):c.*725G>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 326610	NM_001375808.2(LPIN2):c.*723A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326611	NM_001375808.2(LPIN2):c.*703dup	LPIN2	Duplication (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 888858	NM_001375808.2(LPIN2):c.*699A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326612	NM_001375808.2(LPIN2):c.*685T>A	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GBenign
Select item 326613	NM_001375808.2(LPIN2):c.*666C>T	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance
Select item 890557	NM_001375808.2(LPIN2):c.*660A>G	LPIN2	Single nucleotide variant (3 prime UTR variant)	Majeed syndrome	GUncertain significance

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