ClinVar Miner

List of variants in gene CHRM2, LOC349160 studied for Dilated Cardiomyopathy, Dominant

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Total variants: 148
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HGVS dbSNP gnomAD frequency
NM_001006630.2(CHRM2):c.*295T>A rs8191992 0.59512
NM_001006630.2(CHRM2):c.1197T>C (p.Thr399=) rs34586275 0.00676
NM_001006630.2(CHRM2):c.691G>A (p.Val231Ile) rs76394680 0.00359
NM_001006630.2(CHRM2):c.773A>G (p.Asn258Ser) rs142006633 0.00128
NM_001006630.2(CHRM2):c.1114C>G (p.Pro372Ala) rs138806839 0.00078
NM_001006630.2(CHRM2):c.1050A>G (p.Ser350=) rs60372903 0.00070
NM_001006630.2(CHRM2):c.991A>T (p.Thr331Ser) rs146328962 0.00064
NM_001006630.2(CHRM2):c.860C>G (p.Thr287Ser) rs138193709 0.00053
NM_001006630.2(CHRM2):c.150C>T (p.Val50=) rs144511065 0.00039
NM_001006630.2(CHRM2):c.456C>T (p.Phe152=) rs148163637 0.00038
NM_001006630.2(CHRM2):c.757G>A (p.Asp253Asn) rs140681489 0.00034
NM_001006630.2(CHRM2):c.549T>C (p.Asn183=) rs141951417 0.00031
NM_001006630.2(CHRM2):c.674T>A (p.Val225Asp) rs143952141 0.00031
NM_001006630.2(CHRM2):c.1059T>C (p.Asn353=) rs143722099 0.00019
NM_001006630.2(CHRM2):c.1031T>G (p.Val344Gly) rs139037603 0.00015
NM_001006630.2(CHRM2):c.703C>A (p.Leu235Met) rs138886480 0.00008
NM_001006630.2(CHRM2):c.169G>A (p.Val57Ile) rs143842239 0.00006
NM_001006630.2(CHRM2):c.761G>T (p.Gly254Val) rs368473785 0.00006
NM_001006630.2(CHRM2):c.973A>T (p.Ile325Phe) rs773330734 0.00006
NM_001006630.2(CHRM2):c.384T>C (p.Pro128=) rs375980850 0.00005
NM_001006630.2(CHRM2):c.1074G>C (p.Gln358His) rs747925877 0.00004
NM_001006630.2(CHRM2):c.1088G>A (p.Arg363His) rs147228075 0.00004
NM_001006630.2(CHRM2):c.213C>T (p.Ile71=) rs770495131 0.00004
NM_001006630.2(CHRM2):c.480C>T (p.Leu160=) rs975508576 0.00004
NM_001006630.2(CHRM2):c.570G>A (p.Thr190=) rs777593546 0.00004
NM_001006630.2(CHRM2):c.632G>A (p.Arg211Gln) rs774760812 0.00004
NM_001006630.2(CHRM2):c.756C>T (p.Asp252=) rs531986911 0.00004
NM_001006630.2(CHRM2):c.951T>C (p.Asp317=) rs77845403 0.00004
NM_001006630.2(CHRM2):c.1194C>T (p.Ile398=) rs150776322 0.00003
NM_001006630.2(CHRM2):c.1338C>T (p.Thr446=) rs763752437 0.00003
NM_001006630.2(CHRM2):c.1029C>T (p.Thr343=) rs1481148988 0.00002
NM_001006630.2(CHRM2):c.1389C>T (p.Gly463=) rs573795503 0.00002
NM_001006630.2(CHRM2):c.680A>G (p.Asn227Ser) rs760821552 0.00002
NM_001006630.2(CHRM2):c.885T>C (p.Asn295=) rs1443103188 0.00002
NM_001006630.2(CHRM2):c.1030G>A (p.Val344Met) rs201165506 0.00001
NM_001006630.2(CHRM2):c.1094T>C (p.Ile365Thr) rs1805158684 0.00001
NM_001006630.2(CHRM2):c.1113G>C (p.Gln371His) rs1237014805 0.00001
NM_001006630.2(CHRM2):c.1143G>T (p.Arg381=) rs1227972027 0.00001
NM_001006630.2(CHRM2):c.1180T>C (p.Leu394=) rs781736829 0.00001
NM_001006630.2(CHRM2):c.1251C>A (p.Ile417=) rs770736119 0.00001
NM_001006630.2(CHRM2):c.1329C>T (p.Cys443=) rs187298017 0.00001
NM_001006630.2(CHRM2):c.1363C>A (p.Leu455Ile) rs1470994649 0.00001
NM_001006630.2(CHRM2):c.154C>T (p.Arg52Cys) rs1011147170 0.00001
NM_001006630.2(CHRM2):c.186A>G (p.Leu62=) rs760443842 0.00001
NM_001006630.2(CHRM2):c.227C>G (p.Ser76Cys) rs1440850408 0.00001
NM_001006630.2(CHRM2):c.426G>A (p.Met142Ile) rs142493466 0.00001
NM_001006630.2(CHRM2):c.525G>A (p.Glu175=) rs576281726 0.00001
NM_001006630.2(CHRM2):c.537G>A (p.Gln179=) rs150934226 0.00001
NM_001006630.2(CHRM2):c.569C>T (p.Thr190Met) rs1394629702 0.00001
NM_001006630.2(CHRM2):c.597G>A (p.Val199=) rs769572164 0.00001
NM_001006630.2(CHRM2):c.618T>C (p.Tyr206=) rs141382037 0.00001
NM_001006630.2(CHRM2):c.686A>G (p.Asp229Gly) rs762688022 0.00001
NM_001006630.2(CHRM2):c.735T>C (p.Asn245=) rs1263310656 0.00001
NM_001006630.2(CHRM2):c.911A>T (p.Asp304Val) rs778284565 0.00001
NM_001006630.2(CHRM2):c.914A>G (p.Glu305Gly) rs915877356 0.00001
NM_001006630.2(CHRM2):c.101G>T (p.Ser34Ile) rs1805074915
NM_001006630.2(CHRM2):c.1020T>A (p.Thr340=) rs764893658
NM_001006630.2(CHRM2):c.1020T>C (p.Thr340=)
NM_001006630.2(CHRM2):c.1021A>G (p.Asn341Asp)
NM_001006630.2(CHRM2):c.1031T>C (p.Val344Ala) rs139037603
NM_001006630.2(CHRM2):c.1032G>T (p.Val344=)
NM_001006630.2(CHRM2):c.1036G>T (p.Val346Leu) rs1455067791
NM_001006630.2(CHRM2):c.1054C>A (p.Gln352Lys)
NM_001006630.2(CHRM2):c.106G>T (p.Val36Leu)
NM_001006630.2(CHRM2):c.1074G>A (p.Gln358=) rs747925877
NM_001006630.2(CHRM2):c.1074G>T (p.Gln358His) rs747925877
NM_001006630.2(CHRM2):c.1087C>T (p.Arg363Cys)
NM_001006630.2(CHRM2):c.1107T>G (p.Thr369=)
NM_001006630.2(CHRM2):c.1135C>T (p.Pro379Ser) rs36044268
NM_001006630.2(CHRM2):c.1140C>T (p.Ser380=)
NM_001006630.2(CHRM2):c.1141C>T (p.Arg381Trp)
NM_001006630.2(CHRM2):c.1142G>A (p.Arg381Gln) rs1432230108
NM_001006630.2(CHRM2):c.1142G>T (p.Arg381Leu)
NM_001006630.2(CHRM2):c.1148A>G (p.Lys383Arg)
NM_001006630.2(CHRM2):c.116T>A (p.Ile39Asn)
NM_001006630.2(CHRM2):c.1203C>T (p.Ala401=) rs2131136011
NM_001006630.2(CHRM2):c.120G>C (p.Gly40=)
NM_001006630.2(CHRM2):c.1243C>T (p.Pro415Ser) rs1584929720
NM_001006630.2(CHRM2):c.1245T>G (p.Pro415=)
NM_001006630.2(CHRM2):c.1248C>G (p.Cys416Trp) rs2131136215
NM_001006630.2(CHRM2):c.1259C>G (p.Thr420Ser) rs758947846
NM_001006630.2(CHRM2):c.1263G>A (p.Val421=)
NM_001006630.2(CHRM2):c.1286G>C (p.Cys429Ser) rs1805176312
NM_001006630.2(CHRM2):c.1303A>G (p.Ile435Val)
NM_001006630.2(CHRM2):c.1323A>T (p.Ala441=)
NM_001006630.2(CHRM2):c.1326T>C (p.Leu442=)
NM_001006630.2(CHRM2):c.1368G>T (p.Met456Ile) rs139832815
NM_001006630.2(CHRM2):c.1372C>T (p.His458Tyr)
NM_001006630.2(CHRM2):c.1389C>A (p.Gly463=) rs573795503
NM_001006630.2(CHRM2):c.1394C>T (p.Thr465Ile) rs202195493
NM_001006630.2(CHRM2):c.171C>T (p.Val57=)
NM_001006630.2(CHRM2):c.17del (p.Asn6fs)
NM_001006630.2(CHRM2):c.180C>T (p.Tyr60=) rs2131131055
NM_001006630.2(CHRM2):c.217G>A (p.Gly73Ser)
NM_001006630.2(CHRM2):c.219T>C (p.Gly73=)
NM_001006630.2(CHRM2):c.234C>T (p.Asn78=) rs760006520
NM_001006630.2(CHRM2):c.247T>G (p.Tyr83Asp) rs1192304125
NM_001006630.2(CHRM2):c.256A>G (p.Ile86Val)
NM_001006630.2(CHRM2):c.257T>C (p.Ile86Thr)
NM_001006630.2(CHRM2):c.2T>A (p.Met1Lys)
NM_001006630.2(CHRM2):c.348C>T (p.Ile116=)
NM_001006630.2(CHRM2):c.34C>T (p.Leu12=)
NM_001006630.2(CHRM2):c.351C>T (p.Ile117=)
NM_001006630.2(CHRM2):c.357T>C (p.Phe119=)
NM_001006630.2(CHRM2):c.385C>G (p.Leu129Val)
NM_001006630.2(CHRM2):c.403C>T (p.Arg135Trp)
NM_001006630.2(CHRM2):c.404G>A (p.Arg135Gln)
NM_001006630.2(CHRM2):c.415A>G (p.Met139Val)
NM_001006630.2(CHRM2):c.416T>A (p.Met139Lys) rs757844531
NM_001006630.2(CHRM2):c.44C>A (p.Thr15Lys) rs1805069679
NM_001006630.2(CHRM2):c.454T>G (p.Phe152Val) rs2131132038
NM_001006630.2(CHRM2):c.457A>G (p.Ile153Val)
NM_001006630.2(CHRM2):c.486G>T (p.Trp162Cys) rs2131132222
NM_001006630.2(CHRM2):c.501G>C (p.Gly167=)
NM_001006630.2(CHRM2):c.502G>A (p.Val168Met)
NM_001006630.2(CHRM2):c.532A>C (p.Ile178Leu)
NM_001006630.2(CHRM2):c.576T>C (p.Ile192=) rs1293483630
NM_001006630.2(CHRM2):c.577G>A (p.Ala193Thr) rs1805107459
NM_001006630.2(CHRM2):c.579A>C (p.Ala193=)
NM_001006630.2(CHRM2):c.594A>G (p.Pro198=) rs558678081
NM_001006630.2(CHRM2):c.622C>T (p.His208Tyr) rs1196291053
NM_001006630.2(CHRM2):c.629C>T (p.Ser210Phe) rs1563128628
NM_001006630.2(CHRM2):c.638G>A (p.Ser213Asn)
NM_001006630.2(CHRM2):c.639C>T (p.Ser213=)
NM_001006630.2(CHRM2):c.645C>T (p.Ser215=) rs2131132940
NM_001006630.2(CHRM2):c.652A>G (p.Lys218Glu) rs2131132962
NM_001006630.2(CHRM2):c.652AAG[1] (p.Lys219del)
NM_001006630.2(CHRM2):c.673G>A (p.Val225Ile)
NM_001006630.2(CHRM2):c.692T>C (p.Val231Ala)
NM_001006630.2(CHRM2):c.709C>G (p.Gln237Glu)
NM_001006630.2(CHRM2):c.713G>C (p.Gly238Ala)
NM_001006630.2(CHRM2):c.716G>A (p.Arg239Lys)
NM_001006630.2(CHRM2):c.720A>G (p.Ile240Met) rs1805119053
NM_001006630.2(CHRM2):c.727C>A (p.Pro243Thr)
NM_001006630.2(CHRM2):c.794C>T (p.Ala265Val) rs1554437349
NM_001006630.2(CHRM2):c.829G>A (p.Gly277Arg)
NM_001006630.2(CHRM2):c.830G>A (p.Gly277Glu)
NM_001006630.2(CHRM2):c.874G>A (p.Val292Ile) rs1805134418
NM_001006630.2(CHRM2):c.874_882del (p.Val292_Ser294del) rs1454380573
NM_001006630.2(CHRM2):c.897T>C (p.Asp299=)
NM_001006630.2(CHRM2):c.8A>G (p.Asn3Ser)
NM_001006630.2(CHRM2):c.916A>C (p.Asn306His)
NM_001006630.2(CHRM2):c.927C>T (p.Ser309=) rs770969121
NM_001006630.2(CHRM2):c.935T>A (p.Leu312Gln) rs200017653
NM_001006630.2(CHRM2):c.943T>C (p.Ser315Pro)
NM_001006630.2(CHRM2):c.952G>A (p.Glu318Lys)
NM_001006630.2(CHRM2):c.954G>A (p.Glu318=) rs1442558581
NM_001006630.2(CHRM2):c.991A>C (p.Thr331Pro) rs146328962

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