"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CALR3"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1141144	NM_145046.5(CALR3):c.1152T>G (p.Leu384=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1046730	NM_145046.5(CALR3):c.1147G>A (p.Glu383Lys)	CALR3 (E383K)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 2187624	NM_145046.5(CALR3):c.1134T>A (p.Phe378Leu)	CALR3 (F378L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 573600	NM_145046.5(CALR3):c.1129_1132del (p.Gln377fs)	CALR3 (Q377fs)	Microsatellite (frameshift variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 847573	NM_145046.5(CALR3):c.1131A>G (p.Gln377=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2771166	NM_145046.5(CALR3):c.1129C>A (p.Gln377Lys)	CALR3 (Q377K)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 574380	NM_145046.5(CALR3):c.1129C>G (p.Gln377Glu)	CALR3 (Q377E)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 471788	NM_145046.5(CALR3):c.1120T>G (p.Tyr374Asp)	CALR3 (Y374D)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2727546	NM_145046.5(CALR3):c.1114G>T (p.Glu372Ter)	CALR3 (E372*)	Single nucleotide variant (nonsense)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 539147	NM_145046.5(CALR3):c.1114G>C (p.Glu372Gln)	CALR3 (E372Q)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 410622	NM_145046.5(CALR3):c.1114G>A (p.Glu372Lys)	CALR3 (E372K)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2076510	NM_145046.5(CALR3):c.1113C>T (p.His371=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 699312	NM_145046.5(CALR3):c.1110G>A (p.Arg370=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 471787	NM_145046.5(CALR3):c.1104T>A (p.Ile368=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1556217	NM_145046.5(CALR3):c.1095G>A (p.Ser365=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1152522	NM_145046.5(CALR3):c.1095G>C (p.Ser365=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 647084	NM_145046.5(CALR3):c.1094C>T (p.Ser365Leu)	CALR3 (S365L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 696721	NM_145046.5(CALR3):c.1089G>T (p.Leu363=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 539148	NM_145046.5(CALR3):c.1087C>T (p.Leu363=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GBenign
Select item 1569295	NM_145046.5(CALR3):c.1080G>A (p.Glu360=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 410621	NM_145046.5(CALR3):c.1069G>A (p.Glu357Lys)	CALR3 (E357K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2724046	NM_145046.5(CALR3):c.1068C>T (p.Arg356=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1510882	NM_145046.5(CALR3):c.1067G>A (p.Arg356His)	CALR3 (R356H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 416237	NM_145046.5(CALR3):c.1067G>T (p.Arg356Leu)	CALR3 (R356L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19 +3 more	GBenign
Select item 660734	NM_145046.5(CALR3):c.1066C>T (p.Arg356Cys)	CALR3 (R356C)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2185592	NM_145046.5(CALR3):c.1064C>T (p.Ala355Val)	CALR3 (A355V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2169185	NM_145046.5(CALR3):c.1058A>G (p.Lys353Arg)	CALR3 (K353R)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2181550	NM_145046.5(CALR3):c.1043C>A (p.Ala348Asp)	CALR3 (A348D)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2088111	NM_145046.5(CALR3):c.1036A>G (p.Ile346Val)	CALR3 (I346V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2975311	NM_145046.5(CALR3):c.1013G>T (p.Gly338Val)	CALR3 (G338V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 721429	NM_145046.5(CALR3):c.1012-10_1012-9del	CALR3	Deletion (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 241948	NM_145046.5(CALR3):c.1012-9T>C	CALR3	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2919208	NM_145046.5(CALR3):c.1011+16T>A	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1586728	NM_145046.5(CALR3):c.1011+12G>T	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2082200	NM_145046.5(CALR3):c.1011+11C>T	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 471786	NM_145046.5(CALR3):c.1003G>A (p.Glu335Lys)	CALR3 (E335K)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2046984	NM_145046.5(CALR3):c.1002C>T (p.Gly334=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2184630	NM_145046.5(CALR3):c.992C>T (p.Ala331Val)	CALR3 (A331V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2728251	NM_145046.5(CALR3):c.973G>A (p.Ala325Thr)	CALR3 (A325T)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 496549	NM_145046.5(CALR3):c.972C>T (p.Tyr324=)	CALR3	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GBenign
Select item 2693793	NM_145046.5(CALR3):c.969G>A (p.Glu323=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1480417	NM_145046.5(CALR3):c.962A>G (p.Asp321Gly)	CALR3 (D321G)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1343388	NM_145046.5(CALR3):c.961G>A (p.Asp321Asn)	CALR3 (D321N)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2819597	NM_145046.5(CALR3):c.960T>C (p.Asp320=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2153289	NM_145046.5(CALR3):c.941A>G (p.Asp314Gly)	CALR3 (D314G)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1009504	NM_145046.5(CALR3):c.941A>T (p.Asp314Val)	CALR3 (D314V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1421633	NM_145046.5(CALR3):c.923G>T (p.Arg308Ile)	CALR3 (R308I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1386119	NM_145046.5(CALR3):c.923G>A (p.Arg308Lys)	CALR3 (R308K)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1586529	NM_145046.5(CALR3):c.918+16C>T	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 651507	NM_145046.5(CALR3):c.916C>A (p.Gln306Lys)	CALR3 (Q306K)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1958259	NM_145046.5(CALR3):c.896C>T (p.Ala299Val)	CALR3 (A299V)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 2819601	NM_145046.5(CALR3):c.891T>C (p.Ile297=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 220787	NM_145046.5(CALR3):c.861G>A (p.Thr287=)	CALR3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2149510	NM_145046.5(CALR3):c.860C>T (p.Thr287Met)	CALR3 (T287M)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1083470	NM_145046.5(CALR3):c.858G>A (p.Leu286=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2728849	NM_145046.5(CALR3):c.852C>G (p.Asp284Glu)	CALR3 (D284E)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 192182	NM_145046.5(CALR3):c.850G>A (p.Asp284Asn)	CALR3 (D284N)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 1556893	NM_145046.5(CALR3):c.849C>T (p.Thr283=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 416239	NM_145046.5(CALR3):c.848C>T (p.Thr283Ile)	CALR3 (T283I)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19 +3 more	GConflicting classifications of pathogenicity
Select item 520244	NM_145046.5(CALR3):c.833G>A (p.Arg278His)	CALR3 (R278H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19 +1 more	GUncertain significance
Select item 471795	NM_145046.5(CALR3):c.832C>T (p.Arg278Cys)	CALR3 (R278C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 192183	NM_145046.5(CALR3):c.820G>A (p.Val274Ile)	CALR3 (V274I)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign
Select item 1153594	NM_145046.5(CALR3):c.816A>G (p.Lys272=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2919357	NM_145046.5(CALR3):c.813T>C (p.His271=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GBenign
Select item 410618	NM_145046.5(CALR3):c.787G>C (p.Asp263His)	CALR3 (D263H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 575883	NM_145046.5(CALR3):c.787-3C>G	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1170536	NM_145046.5(CALR3):c.787-14dup	CALR3	Duplication (intron variant)	Hypertrophic cardiomyopathy 19	GBenign
Select item 1139868	NM_145046.5(CALR3):c.787-8del	CALR3	Deletion (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1650886	NM_145046.5(CALR3):c.787-11T>G	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1602442	NM_145046.5(CALR3):c.786+18A>T	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2080464	NM_145046.5(CALR3):c.786+14_786+15del	CALR3	Deletion (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1604563	NM_145046.5(CALR3):c.786+9C>A	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1481153	NM_145046.5(CALR3):c.786+3G>T	CALR3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 699281	NM_145046.5(CALR3):c.780G>A (p.Pro260=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 241952	NM_145046.5(CALR3):c.780G>T (p.Pro260=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2148217	NM_145046.5(CALR3):c.779C>T (p.Pro260Leu)	CALR3 (P260L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19 +1 more	GUncertain significance
Select item 1603406	NM_145046.5(CALR3):c.777C>A (p.Pro259=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2906896	NM_145046.5(CALR3):c.770A>C (p.Gln257Pro)	CALR3 (Q257P)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 3018700	NM_145046.5(CALR3):c.766C>T (p.Leu256Phe)	CALR3 (L256F)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1151361	NM_145046.5(CALR3):c.761C>T (p.Pro254Leu)	CALR3 (P254L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 695896	NM_145046.5(CALR3):c.759G>A (p.Ala253=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2053221	NM_145046.5(CALR3):c.743A>C (p.Asp248Ala)	CALR3 (D248A)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 766534	NM_145046.5(CALR3):c.741G>C (p.Leu247=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 577806	NM_145046.5(CALR3):c.740T>A (p.Leu247Gln)	CALR3 (L247Q)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 471794	NM_145046.5(CALR3):c.738C>T (p.Asp246=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 956606	NM_145046.5(CALR3):c.733G>A (p.Gly245Ser)	CALR3 (G245S)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 471793	NM_145046.5(CALR3):c.732C>T (p.Asn244=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1481634	NM_145046.5(CALR3):c.728G>A (p.Trp243Ter)	CALR3 (W243*)	Single nucleotide variant (nonsense)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1948948	NM_145046.5(CALR3):c.724G>C (p.Asp242His)	CALR3 (D242H)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 659042	NM_145046.5(CALR3):c.724G>A (p.Asp242Asn)	CALR3 (D242N)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1466533	NM_145046.5(CALR3):c.723C>A (p.Ser241Arg)	CALR3 (S241R)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 584207	NC_000019.9:g.(?_16593553)_(16606960_?)dup	CALR3, LOC125371488	Duplication	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 848653	NM_145046.5(CALR3):c.714C>T (p.Ser238=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 576202	NM_145046.5(CALR3):c.710C>G (p.Thr237Ser)	CALR3 (T237S)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 1106327	NM_145046.5(CALR3):c.705C>T (p.Ala235=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 1404174	NM_145046.5(CALR3):c.703G>A (p.Ala235Thr)	CALR3 (A235T)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance
Select item 496548	NM_145046.5(CALR3):c.702C>T (p.Asp234=)	CALR3	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 471792	NM_145046.5(CALR3):c.691C>G (p.His231Asp)	CALR3 (H231D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2081057	NM_145046.5(CALR3):c.690G>A (p.Lys230=)	CALR3	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 19	GLikely benign
Select item 2052375	NM_145046.5(CALR3):c.681C>A (p.Asp227Glu)	CALR3 (D227E)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 19	GUncertain significance

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