"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CALM2"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2714374	NM_001743.6(CALM2):c.441_*4del (p.Ala148fs)	CALM2 (A112fs +2 more)	Deletion (frameshift variant)	Long QT syndrome 1	GUncertain significance
Select item 576319	NM_001743.6(CALM2):c.434T>G (p.Met145Arg)	CALM2 (M109R +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 1121205	NM_001743.6(CALM2):c.429A>G (p.Val143=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 1467722	NM_001743.6(CALM2):c.423G>C (p.Glu141Asp)	CALM2 (E105D +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 415527	NM_001743.6(CALM2):c.422-15CTT[2]	CALM2	Microsatellite (intron variant)	Long QT syndrome 1 +1 more	GLikely benign
Select item 2897948	NM_001743.6(CALM2):c.422-9C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2036970	NM_001743.6(CALM2):c.422-12dup	CALM2	Duplication (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2188743	NM_001743.6(CALM2):c.422-12C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1575279	NM_001743.6(CALM2):c.422-13del	CALM2	Deletion (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2191629	NM_001743.6(CALM2):c.422-15C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2145503	NM_001743.6(CALM2):c.421+19C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 384720	NM_001743.6(CALM2):c.421+18A>G	CALM2	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 2729491	NM_001743.6(CALM2):c.421+13G>A	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2721251	NM_001743.6(CALM2):c.421+11C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 458194	NM_001743.6(CALM2):c.421+10T>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1 +1 more	GLikely benign
Select item 2703155	NM_001743.6(CALM2):c.421+8T>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2785081	NM_001743.6(CALM2):c.421+4A>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GUncertain significance
Select item 1043752	NM_001743.6(CALM2):c.421+3A>G	CALM2	Single nucleotide variant (intron variant)	not provided +1 more	GUncertain significance
Select item 1304927	NM_001743.6(CALM2):c.420A>G (p.Glu140=)	CALM2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GUncertain significance
Select item 1606364	NM_001743.6(CALM2):c.417T>C (p.Tyr139=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 1002939	NM_001743.6(CALM2):c.413_416dup (p.Tyr139Ter)	CALM2 (Y103* +2 more)	Duplication (nonsense)	Long QT syndrome 1	GUncertain significance
Select item 650245	NM_001743.6(CALM2):c.414C>A (p.Asn138Lys)	CALM2 (N102K +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 2129105	NM_001743.6(CALM2):c.411A>G (p.Val137=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 448971	NM_001743.6(CALM2):c.400G>A (p.Asp134Asn)	CALM2 (D134N +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 15 +1 more	GConflicting classifications of pathogenicity
Select item 1067140	NM_001743.6(CALM2):c.397G>A (p.Gly133Ser)	CALM2 (G133S +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 955533	NM_001743.6(CALM2):c.395A>G (p.Asp132Gly)	CALM2 (D132G +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GPathogenic
Select item 1456260	NM_001743.6(CALM2):c.394G>T (p.Asp132Tyr)	CALM2 (D180Y +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GPathogenic
Select item 812710	NM_001743.6(CALM2):c.389A>G (p.Asp130Gly)	CALM2 (D130G +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 1398892	NM_001743.6(CALM2):c.388G>A (p.Asp130Asn)	CALM2 (D130N +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GPathogenic
Select item 650556	NM_001743.6(CALM2):c.379A>G (p.Arg127Gly)	CALM2 (R91G +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 2802064	NM_001743.6(CALM2):c.359AAG[1] (p.Glu121del)	CALM2 (E121del +2 more)	Microsatellite (inframe_deletion)	Long QT syndrome 1	GUncertain significance
Select item 458192	NM_001743.6(CALM2):c.348G>A (p.Lys116=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1 +2 more	GLikely benign
Select item 2710832	NM_001743.6(CALM2):c.342A>C (p.Gly114=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 1136043	NM_001743.6(CALM2):c.336C>T (p.Asn112=)	CALM2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 458191	NM_001743.6(CALM2):c.328A>T (p.Met110Leu)	CALM2 (M110L +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1 +1 more	GConflicting classifications of pathogenicity
Select item 956093	NM_001743.6(CALM2):c.319C>T (p.Arg107Cys)	CALM2 (R107C +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1 +1 more	GUncertain significance
Select item 2697885	NM_001743.6(CALM2):c.310G>A (p.Ala104Thr)	CALM2 (A68T +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 2871265	NM_001743.6(CALM2):c.308C>T (p.Ala103Val)	CALM2 (A103V +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 2768970	NM_001743.6(CALM2):c.307G>A (p.Ala103Thr)	CALM2 (A67T +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 1408944	NM_001743.6(CALM2):c.299A>G (p.Tyr100Cys)	CALM2 (Y148C +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 96721	NM_001743.6(CALM2):c.293A>T (p.Asn98Ile)	CALM2 (N98I +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GPathogenic
Select item 96720	NM_001743.6(CALM2):c.293A>G (p.Asn98Ser)	CALM2 (N98S +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1 +1 more	GPathogenic
Select item 2894830	NM_001743.6(CALM2):c.291C>T (p.Gly97=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 183233	NM_001743.6(CALM2):c.287A>T (p.Asp96Val)	CALM2 (D96V +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1 +1 more	GPathogenic
Select item 641544	NM_001743.6(CALM2):c.286G>T (p.Asp96Tyr)	CALM2 (D144Y +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GPathogenic
Select item 2903652	NM_001743.6(CALM2):c.286-6del	CALM2	Deletion (intron variant)	Long QT syndrome 1	GBenign
Select item 576394	NM_001743.6(CALM2):c.286-10T>A	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2737743	NM_001743.6(CALM2):c.286-13A>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2742234	NM_001743.6(CALM2):c.286-14A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1916943	NM_001743.6(CALM2):c.286-14A>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 422684	NM_001743.6(CALM2):c.286-18_286-17del	CALM2	Microsatellite (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 2918477	NM_001743.6(CALM2):c.286-19A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1649906	NM_001743.6(CALM2):c.285+14_285+20del	CALM2	Deletion (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2175885	NM_001743.6(CALM2):c.285+17A>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 507565	NM_001743.6(CALM2):c.285+16G>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1 +1 more	GLikely benign
Select item 390826	NM_001743.6(CALM2):c.285+16G>C	CALM2	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 2154500	NM_001743.6(CALM2):c.285+9A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 946744	NM_001743.6(CALM2):c.285+5G>A	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1 +1 more	GUncertain significance
Select item 2891837	NM_001743.6(CALM2):c.285+3A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GUncertain significance
Select item 2734184	NM_001743.6(CALM2):c.268T>C (p.Phe90Leu)	CALM2 (F138L +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 1126088	NM_001743.6(CALM2):c.261A>G (p.Arg87=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 2836055	NM_001743.6(CALM2):c.249A>G (p.Glu83=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 854156	NM_001743.6(CALM2):c.247G>A (p.Glu83Lys)	CALM2 (E83K +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 239033	NM_001743.6(CALM2):c.243C>T (p.Asp81=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1 +2 more	GBenign/Likely benign
Select item 239038	NM_001743.6(CALM2):c.240A>T (p.Thr80=)	CALM2	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +3 more	GBenign
Select item 1035607	NM_001743.6(CALM2):c.203A>C (p.Glu68Ala)	CALM2 (E116A +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 1598403	NM_001743.6(CALM2):c.186C>A (p.Gly62=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 1353411	NM_001743.6(CALM2):c.182A>G (p.Asn61Ser)	CALM2 (N25S +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 458190	NM_001743.6(CALM2):c.179-8C>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GUncertain significance
Select item 507892	NM_001743.6(CALM2):c.179-9C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1 +1 more	GLikely benign
Select item 1106661	NM_001743.6(CALM2):c.179-29_179-10del	CALM2	Deletion (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2079422	NM_001743.6(CALM2):c.179-15A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1573840	NM_001743.6(CALM2):c.179-15A>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2136633	NM_001743.6(CALM2):c.178+17G>A	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1585081	NM_001743.6(CALM2):c.178+12A>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2824731	NM_001743.6(CALM2):c.178+10C>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1618635	NM_001743.6(CALM2):c.178+10del	CALM2	Deletion (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2030936	NM_001743.6(CALM2):c.178+9T>A	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2164047	NM_001743.6(CALM2):c.178+7C>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2903536	NM_001743.6(CALM2):c.178+4A>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GUncertain significance
Select item 1101930	NM_001743.6(CALM2):c.165A>G (p.Glu55=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1 +1 more	GLikely benign
Select item 458189	NM_001743.6(CALM2):c.157A>G (p.Ile53Val)	CALM2 (I17V +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GUncertain significance
Select item 2026774	NM_001743.6(CALM2):c.123G>C (p.Gly41=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 759301	NM_001743.6(CALM2):c.123G>A (p.Gly41=)	CALM2	Single nucleotide variant (synonymous variant)	Long QT syndrome 1	GLikely benign
Select item 2813326	NM_001743.6(CALM2):c.105T>C (p.Thr35=)	CALM2	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome 1	GLikely benign
Select item 970445	NM_001743.6(CALM2):c.104C>T (p.Thr35Ile)	CALM2 (T35I +1 more)	Single nucleotide variant (missense variant +1 more)	Long QT syndrome 1 +2 more	GUncertain significance
Select item 429916	NM_001743.6(CALM2):c.79A>T (p.Thr27Ser)	CALM2 (T27S +1 more)	Single nucleotide variant (missense variant +1 more)	Long QT syndrome 1 +1 more	GUncertain significance
Select item 1145883	NM_001743.6(CALM2):c.63C>T (p.Asp21=)	CALM2	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome 1	GLikely benign
Select item 1132401	NM_001743.6(CALM2):c.57A>G (p.Leu19=)	CALM2	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome 1	GLikely benign
Select item 2025116	NM_001743.6(CALM2):c.54A>C (p.Ser18=)	CALM2	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome 1	GUncertain significance
Select item 1423641	NM_001743.6(CALM2):c.35-10_35-7del	CALM2	Microsatellite (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1984624	NM_001743.6(CALM2):c.35-12T>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2733510	NM_001743.6(CALM2):c.35-14T>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1529207	NM_001743.6(CALM2):c.35-15C>G	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2177548	NM_001743.6(CALM2):c.34+19G>T	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1647187	NM_001743.6(CALM2):c.34+17T>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GLikely benign
Select item 1652583	NM_001743.6(CALM2):c.34+12_34+13delinsCT	CALM2	Indel (intron variant)	Long QT syndrome 1	GLikely benign
Select item 2720409	NM_001743.6(CALM2):c.34+5G>C	CALM2	Single nucleotide variant (intron variant)	Long QT syndrome 1	GUncertain significance
Select item 1058419	NM_001743.6(CALM2):c.33A>G (p.Ala11=)	CALM2	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2696320	NM_001743.6(CALM2):c.16A>T (p.Thr6Ser)	CALM2 (T54S +1 more)	Single nucleotide variant (missense variant +1 more)	Long QT syndrome 1	GUncertain significance

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