ClinVar Miner

List of variants in gene CALR3 reported as likely benign for cardiovascular disorder

Included ClinVar conditions (1435):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
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HGVS dbSNP gnomAD frequency
NM_145046.5(CALR3):c.861G>A (p.Thr287=) rs118131979 0.01186
NM_145046.5(CALR3):c.125A>G (p.Asn42Ser) rs149634686 0.00123
NM_145046.5(CALR3):c.398-6T>C rs376479901 0.00118
NM_145046.5(CALR3):c.245A>G (p.Lys82Arg) rs142951029 0.00083
NM_145046.5(CALR3):c.60C>G (p.Thr20=) rs370721650 0.00029
NM_145046.5(CALR3):c.761C>T (p.Pro254Leu) rs761736548 0.00021
NM_145046.5(CALR3):c.639A>G (p.Glu213=) rs377026384 0.00017
NM_145046.5(CALR3):c.215G>A (p.Gly72Asp) rs182376945 0.00014
NM_145046.5(CALR3):c.780G>A (p.Pro260=) rs775009764 0.00012
NM_145046.5(CALR3):c.378G>A (p.Ser126=) rs374869347 0.00011
NM_145046.5(CALR3):c.787-11T>G rs199588341 0.00011
NM_145046.5(CALR3):c.511C>T (p.Leu171=) rs752204583 0.00009
NM_145046.5(CALR3):c.849C>T (p.Thr283=) rs142902333 0.00007
NM_145046.5(CALR3):c.159G>A (p.Ser53=) rs372912264 0.00006
NM_145046.5(CALR3):c.1089G>T (p.Leu363=) rs201203591 0.00004
NM_145046.5(CALR3):c.786+9C>A rs1159720687 0.00004
NM_145046.5(CALR3):c.918+16C>T rs777906520 0.00004
NM_145046.5(CALR3):c.193+17G>A rs921498420 0.00003
NM_145046.5(CALR3):c.642G>A (p.Ser214=) rs200669493 0.00003
NM_145046.5(CALR3):c.1110G>A (p.Arg370=) rs774421614 0.00002
NM_145046.5(CALR3):c.249G>A (p.Pro83=) rs570064234 0.00002
NM_145046.5(CALR3):c.398-11C>A rs546157618 0.00002
NM_145046.5(CALR3):c.627G>A (p.Thr209=) rs777454147 0.00002
NM_145046.5(CALR3):c.648T>C (p.Asp216=) rs372889302 0.00002
NM_145046.5(CALR3):c.732C>T (p.Asn244=) rs201198066 0.00002
NM_145046.5(CALR3):c.1080G>A (p.Glu360=) rs752458256 0.00001
NM_145046.5(CALR3):c.156G>A (p.Ser52=) rs779192527 0.00001
NM_145046.5(CALR3):c.216C>T (p.Gly72=) rs577809057 0.00001
NM_145046.5(CALR3):c.271C>T (p.Leu91=) rs765069343 0.00001
NM_145046.5(CALR3):c.291A>G (p.Val97=) rs1056692608 0.00001
NM_145046.5(CALR3):c.398-17G>C rs779762872 0.00001
NM_145046.5(CALR3):c.398-9T>C rs1344157973 0.00001
NM_145046.5(CALR3):c.492+9T>C rs780317722 0.00001
NM_145046.5(CALR3):c.493-15C>G rs775571848 0.00001
NM_145046.5(CALR3):c.546T>C (p.Tyr182=) rs369476772 0.00001
NM_145046.5(CALR3):c.633G>A (p.Pro211=) rs748099861 0.00001
NM_145046.5(CALR3):c.705C>T (p.Ala235=) rs1330398267 0.00001
NM_145046.5(CALR3):c.759G>A (p.Ala253=) rs1011639048 0.00001
NM_145046.5(CALR3):c.786+18A>T rs780747845 0.00001
NM_145046.5(CALR3):c.858G>A (p.Leu286=) rs1275633743 0.00001
NM_145046.5(CALR3):c.1002C>T (p.Gly334=)
NM_145046.5(CALR3):c.1011+11C>T
NM_145046.5(CALR3):c.1011+12G>T rs777158814
NM_145046.5(CALR3):c.1011+16T>A
NM_145046.5(CALR3):c.1012-10_1012-9del rs1358738890
NM_145046.5(CALR3):c.1068C>T (p.Arg356=)
NM_145046.5(CALR3):c.1095G>A (p.Ser365=) rs200844516
NM_145046.5(CALR3):c.1095G>C (p.Ser365=) rs200844516
NM_145046.5(CALR3):c.1104T>A (p.Ile368=) rs1555775535
NM_145046.5(CALR3):c.1113C>T (p.His371=)
NM_145046.5(CALR3):c.1114G>C (p.Glu372Gln) rs140440387
NM_145046.5(CALR3):c.1152T>G (p.Leu384=) rs1443146127
NM_145046.5(CALR3):c.129C>T (p.Asp43=) rs1599723855
NM_145046.5(CALR3):c.193+15A>G
NM_145046.5(CALR3):c.193+15_193+16del
NM_145046.5(CALR3):c.194-14T>A
NM_145046.5(CALR3):c.195T>C (p.Gly65=) rs1599721013
NM_145046.5(CALR3):c.239G>C (p.Arg80Pro) rs746369368
NM_145046.5(CALR3):c.273G>A (p.Leu91=) rs759314483
NM_145046.5(CALR3):c.30C>T (p.Ala10=)
NM_145046.5(CALR3):c.345A>G (p.Ala115=) rs2122142658
NM_145046.5(CALR3):c.387T>C (p.Tyr129=) rs2122142562
NM_145046.5(CALR3):c.397+11G>A
NM_145046.5(CALR3):c.397+13G>A
NM_145046.5(CALR3):c.397+7T>A
NM_145046.5(CALR3):c.398-15T>A
NM_145046.5(CALR3):c.398-20G>A
NM_145046.5(CALR3):c.516C>T (p.Tyr172=)
NM_145046.5(CALR3):c.579C>T (p.Ser193=)
NM_145046.5(CALR3):c.604T>C (p.Leu202=)
NM_145046.5(CALR3):c.63C>G (p.Val21=) rs1163504118
NM_145046.5(CALR3):c.679-3dup rs756560192
NM_145046.5(CALR3):c.690G>A (p.Lys230=)
NM_145046.5(CALR3):c.6C>G (p.Ala2=)
NM_145046.5(CALR3):c.738C>T (p.Asp246=) rs780488544
NM_145046.5(CALR3):c.741G>C (p.Leu247=) rs1188902703
NM_145046.5(CALR3):c.777C>A (p.Pro259=) rs143252466
NM_145046.5(CALR3):c.780G>T (p.Pro260=) rs775009764
NM_145046.5(CALR3):c.786+14_786+15del
NM_145046.5(CALR3):c.787-8del rs1267486642
NM_145046.5(CALR3):c.816A>G (p.Lys272=) rs2122128398
NM_145046.5(CALR3):c.891T>C (p.Ile297=)
NM_145046.5(CALR3):c.91+15C>T
NM_145046.5(CALR3):c.960T>C (p.Asp320=)
NM_145046.5(CALR3):c.969G>A (p.Glu323=)

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