List of variants in gene CALM3 reported as likely benign

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 119

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HGVS	dbSNP	gnomAD frequency
NM_005184.4(CALM3):c.3+85A>C	rs184847124	0.01506
NM_005184.4(CALM3):c.4-162G>A	rs75486879	0.01311
NM_005184.4(CALM3):c.35-179G>A	rs73940732	0.00938
NM_005184.4(CALM3):c.178+48G>A	rs3729759	0.00652
NM_005184.4(CALM3):c.4-304G>A	rs116318013	0.00399
NM_005184.4(CALM3):c.201G>A (p.Pro67=)	rs34089805	0.00262
NM_005184.4(CALM3):c.35-146G>A	rs186252427	0.00247
NM_005184.4(CALM3):c.306C>T (p.Ser102=)	rs146819515	0.00227
NM_005184.4(CALM3):c.267G>A (p.Ala89=)	rs115265989	0.00146
NM_005184.4(CALM3):c.178+18C>T	rs180722019	0.00108
NM_005184.4(CALM3):c.183C>T (p.Asn61=)	rs3729761	0.00038
NM_005184.4(CALM3):c.-29C>T	rs771975198	0.00019
NM_005184.4(CALM3):c.421+4A>G	rs373529765	0.00017
NM_005184.4(CALM3):c.309C>T (p.Ala103=)	rs200095251	0.00015
NM_005184.4(CALM3):c.*19G>A	rs368104478	0.00013
NM_005184.4(CALM3):c.237C>T (p.Asp79=)	rs147734536	0.00007
NM_005184.4(CALM3):c.444A>T (p.Ala148=)	rs779594484	0.00006
NM_005184.4(CALM3):c.285+17A>G	rs149759804	0.00003
NM_005184.4(CALM3):c.324C>T (p.His108=)	rs45587137	0.00003
NM_005184.4(CALM3):c.35-13C>G	rs369539598	0.00003
NM_005184.4(CALM3):c.12G>A (p.Gln4=)	rs746427314	0.00002
NM_005184.4(CALM3):c.178+17G>A	rs764944151	0.00002
NM_005184.4(CALM3):c.249G>A (p.Glu83=)	rs755348000	0.00002
NM_005184.4(CALM3):c.318G>T (p.Leu106=)	rs773943649	0.00002
NM_005184.4(CALM3):c.35-10C>T	rs748438358	0.00002
NM_005184.4(CALM3):c.354C>T (p.Thr118=)	rs750712140	0.00002
NM_005184.4(CALM3):c.108G>A (p.Val36=)	rs1173698699	0.00001
NM_005184.4(CALM3):c.138A>G (p.Glu46=)	rs1454292329	0.00001
NM_005184.4(CALM3):c.147G>A (p.Leu49=)	rs760657005	0.00001
NM_005184.4(CALM3):c.165G>A (p.Glu55=)	rs764047686	0.00001
NM_005184.4(CALM3):c.178+12A>G	rs753670904	0.00001
NM_005184.4(CALM3):c.179-13C>T	rs764890178	0.00001
NM_005184.4(CALM3):c.179-18C>T	rs761694804	0.00001
NM_005184.4(CALM3):c.24G>A (p.Glu8=)	rs1001080500	0.00001
NM_005184.4(CALM3):c.273T>A (p.Arg91=)	rs559783307	0.00001
NM_005184.4(CALM3):c.286-10C>G	rs375255516	0.00001
NM_005184.4(CALM3):c.286-19C>G	rs1478765429	0.00001
NM_005184.4(CALM3):c.286-4C>G	rs1471091658	0.00001
NM_005184.4(CALM3):c.3+13G>A	rs759824845	0.00001
NM_005184.4(CALM3):c.342G>A (p.Gly114=)	rs202189304	0.00001
NM_005184.4(CALM3):c.35-18T>C	rs780566686	0.00001
NM_005184.4(CALM3):c.360G>A (p.Glu120=)	rs2513645801	0.00001
NM_005184.4(CALM3):c.366G>A (p.Val122=)	rs1261825623	0.00001
NM_005184.4(CALM3):c.384G>A (p.Glu128=)	rs1044212599	0.00001
NM_005184.4(CALM3):c.393C>T (p.Ile131=)	rs751608096	0.00001
NM_005184.4(CALM3):c.402T>C (p.Asp134=)	rs755022859	0.00001
NM_005184.4(CALM3):c.421+14A>G	rs369796184	0.00001
NM_005184.4(CALM3):c.447G>A (p.Lys149=)	rs746647108	0.00001
NM_005184.4(CALM3):c.97T>C (p.Leu33=)	rs375684773	0.00001
NM_005184.4(CALM3):c.*21G>C	rs2229577
NM_005184.4(CALM3):c.*9del	rs758159285
NM_005184.4(CALM3):c.132C>T (p.Pro44=)	rs2513644456
NM_005184.4(CALM3):c.144G>A (p.Glu48=)	rs1599758683
NM_005184.4(CALM3):c.147G>T (p.Leu49=)	rs760657005
NM_005184.4(CALM3):c.159C>A (p.Ile53=)	rs375106354
NM_005184.4(CALM3):c.159C>T (p.Ile53=)	rs375106354
NM_005184.4(CALM3):c.171T>C (p.Asp57=)
NM_005184.4(CALM3):c.174A>G (p.Ala58=)	rs2122245693
NM_005184.4(CALM3):c.178+16C>T
NM_005184.4(CALM3):c.179-14del	rs577585466
NM_005184.4(CALM3):c.192T>A (p.Ile64=)	rs2513644964
NM_005184.4(CALM3):c.213C>T (p.Thr71=)	rs1568666350
NM_005184.4(CALM3):c.222C>A (p.Ala74=)
NM_005184.4(CALM3):c.246T>C (p.Ser82=)	rs2513645054
NM_005184.4(CALM3):c.252G>A (p.Glu84=)
NM_005184.4(CALM3):c.27G>A (p.Gln9=)	rs1971731867
NM_005184.4(CALM3):c.285+16C>T
NM_005184.4(CALM3):c.286-7C>A
NM_005184.4(CALM3):c.286-8dup	rs2122249132
NM_005184.4(CALM3):c.3+11C>T	rs2122211406
NM_005184.4(CALM3):c.3+14G>C	rs1326371138
NM_005184.4(CALM3):c.3+17G>A	rs982176814
NM_005184.4(CALM3):c.3+18G>A	rs767873951
NM_005184.4(CALM3):c.3+19T>G	rs2065869954
NM_005184.4(CALM3):c.3+20C>T
NM_005184.4(CALM3):c.333G>A (p.Thr111=)
NM_005184.4(CALM3):c.333G>C (p.Thr111=)	rs1274089736
NM_005184.4(CALM3):c.336C>T (p.Asn112=)	rs887745567
NM_005184.4(CALM3):c.337C>T (p.Leu113=)	rs2513645767
NM_005184.4(CALM3):c.339G>A (p.Leu113=)	rs143699789
NM_005184.4(CALM3):c.339G>C (p.Leu113=)	rs143699789
NM_005184.4(CALM3):c.339G>T (p.Leu113=)
NM_005184.4(CALM3):c.34+11T>C	rs1971732200
NM_005184.4(CALM3):c.34+16C>T
NM_005184.4(CALM3):c.34+7C>G	rs2122231385
NM_005184.4(CALM3):c.35-13C>A	rs369539598
NM_005184.4(CALM3):c.35-14C>A	rs370430097
NM_005184.4(CALM3):c.35-14C>T	rs370430097
NM_005184.4(CALM3):c.35-16C>T
NM_005184.4(CALM3):c.35-18T>G	rs780566686
NM_005184.4(CALM3):c.35-19C>T	rs757777400
NM_005184.4(CALM3):c.35-9T>C	rs1262949304
NM_005184.4(CALM3):c.354C>G (p.Thr118=)	rs750712140
NM_005184.4(CALM3):c.363G>A (p.Glu121=)	rs758692040
NM_005184.4(CALM3):c.387T>A (p.Ala129=)	rs1271316314
NM_005184.4(CALM3):c.387T>C (p.Ala129=)	rs1271316314
NM_005184.4(CALM3):c.4-17C>G	rs370333318
NM_005184.4(CALM3):c.4-5T>C	rs2122231200
NM_005184.4(CALM3):c.4-6T>C	rs2513641150
NM_005184.4(CALM3):c.411C>T (p.Val137=)	rs1599759588
NM_005184.4(CALM3):c.421+10G>T	rs2513645953
NM_005184.4(CALM3):c.421+16G>A	rs1367034954
NM_005184.4(CALM3):c.421+16G>C
NM_005184.4(CALM3):c.421+16G>T
NM_005184.4(CALM3):c.421+18T>C	rs745577081
NM_005184.4(CALM3):c.422-20C>G	rs757183576
NM_005184.4(CALM3):c.422-5C>T	rs2513646331
NM_005184.4(CALM3):c.422-7T>C	rs1971813201
NM_005184.4(CALM3):c.422-7_422-3del
NM_005184.4(CALM3):c.422-8C>T	rs1317120997
NM_005184.4(CALM3):c.422-9A>G
NM_005184.4(CALM3):c.429A>G (p.Val143=)	rs2122252253
NM_005184.4(CALM3):c.51C>T (p.Phe17=)	rs1272522747
NM_005184.4(CALM3):c.57C>A (p.Leu19=)	rs1476616729
NM_005184.4(CALM3):c.66G>A (p.Lys22=)	rs2122245298
NM_005184.4(CALM3):c.72A>G (p.Gly24=)	rs2122245344
NM_005184.4(CALM3):c.75T>C (p.Asp25=)	rs2513644344
NM_005184.4(CALM3):c.81T>C (p.Thr27=)	rs773251048
NM_005184.4(CALM3):c.9C>T (p.Asp3=)

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