ClinVar Miner

List of variants in gene CNGA3 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 202
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HGVS dbSNP gnomAD frequency
NM_001298.2(CNGA3):c.*1351T>G rs28376087 0.03691
NM_001298.3(CNGA3):c.592G>A (p.Glu198Lys) rs2271041 0.01129
NM_001298.3(CNGA3):c.458C>T (p.Thr153Met) rs34314205 0.00836
NM_001298.3(CNGA3):c.215+11A>G rs199755395 0.00490
NM_001298.3(CNGA3):c.1569C>T (p.Asn523=) rs61752503 0.00467
NM_001298.3(CNGA3):c.143C>T (p.Pro48Leu) rs62156348 0.00451
NM_001298.3(CNGA3):c.396-4G>A rs114951127 0.00360
NM_001298.2(CNGA3):c.-383A>G rs143449407 0.00203
NM_001298.3(CNGA3):c.740C>T (p.Thr247Met) rs148616345 0.00158
NM_001298.3(CNGA3):c.198C>T (p.Thr66=) rs139544302 0.00147
NM_001298.3(CNGA3):c.1968G>A (p.Met656Ile) rs147293818 0.00120
NM_001298.3(CNGA3):c.1627G>A (p.Asp543Asn) rs150759499 0.00119
NM_001298.3(CNGA3):c.1618G>A (p.Val540Ile) rs116448158 0.00113
NM_001298.3(CNGA3):c.284C>T (p.Pro95Leu) rs114108462 0.00083
NM_001298.3(CNGA3):c.566+6C>T rs199558955 0.00080
NM_001298.3(CNGA3):c.682G>A (p.Glu228Lys) rs147415641 0.00049
NM_001298.3(CNGA3):c.1863G>A (p.Ala621=) rs181911949 0.00044
NM_001298.3(CNGA3):c.101+17T>C rs367821754 0.00038
NM_001298.3(CNGA3):c.1101T>C (p.Gly367=) rs200069389 0.00034
NM_001298.3(CNGA3):c.180C>T (p.Ser60=) rs372760840 0.00032
NM_001298.3(CNGA3):c.1116C>T (p.Pro372=) rs201649850 0.00031
NM_001298.3(CNGA3):c.210C>T (p.Ile70=) rs145057274 0.00031
NM_001298.3(CNGA3):c.440C>G (p.Thr147Arg) rs144099488 0.00031
NM_001298.3(CNGA3):c.1776C>T (p.Pro592=) rs201637471 0.00027
NM_001298.3(CNGA3):c.211G>A (p.Ala71Thr) rs61756692 0.00026
NM_001298.3(CNGA3):c.307C>T (p.Arg103Cys) rs370581927 0.00025
NM_001298.3(CNGA3):c.1746C>T (p.Asp582=) rs77311157 0.00023
NM_001298.3(CNGA3):c.473C>T (p.Ala158Val) rs138934573 0.00022
NM_001298.3(CNGA3):c.110C>T (p.Ser37Leu) rs141086649 0.00018
NM_001298.3(CNGA3):c.1304C>T (p.Thr435Met) rs758131725 0.00018
NM_001298.3(CNGA3):c.150C>T (p.Ile50=) rs759715897 0.00018
NM_001298.3(CNGA3):c.101+1G>A rs147118493 0.00014
NM_001298.3(CNGA3):c.93C>A (p.Gly31=) rs773541745 0.00013
NM_001298.2(CNGA3):c.-406C>T rs529394802 0.00012
NM_001298.3(CNGA3):c.2005G>C (p.Val669Leu) rs148496805 0.00012
NM_001298.3(CNGA3):c.477C>T (p.Ile159=) rs150944260 0.00012
NM_001298.3(CNGA3):c.734C>T (p.Thr245Met) rs143531659 0.00012
NM_001298.3(CNGA3):c.633T>C (p.Asp211=) rs553995770 0.00011
NM_001298.3(CNGA3):c.129G>A (p.Ser43=) rs372489647 0.00010
NM_001298.3(CNGA3):c.79C>T (p.Arg27Cys) rs149069990 0.00010
NM_001298.3(CNGA3):c.1056C>T (p.Tyr352=) rs372242444 0.00009
NM_001298.3(CNGA3):c.1792C>T (p.Leu598=) rs1018163095 0.00009
NM_001298.3(CNGA3):c.408G>A (p.Leu136=) rs376332352 0.00008
NM_001298.3(CNGA3):c.1113C>A (p.Pro371=) rs532328081 0.00007
NM_001298.3(CNGA3):c.1861G>A (p.Ala621Thr) rs546831778 0.00007
NM_001298.3(CNGA3):c.216-4C>T rs373583147 0.00006
NM_001298.3(CNGA3):c.489G>A (p.Pro163=) rs557628518 0.00006
NM_001298.3(CNGA3):c.566+11G>A rs377222157 0.00006
NM_001298.3(CNGA3):c.80G>A (p.Arg27His) rs769433253 0.00006
NM_001298.3(CNGA3):c.1305G>A (p.Thr435=) rs150008953 0.00005
NM_001298.3(CNGA3):c.1695G>A (p.Thr565=) rs764338481 0.00005
NM_001298.3(CNGA3):c.1428G>A (p.Thr476=) rs764609891 0.00004
NM_001298.3(CNGA3):c.144G>A (p.Pro48=) rs199670952 0.00004
NM_001298.3(CNGA3):c.1554G>A (p.Glu518=) rs544874644 0.00004
NM_001298.3(CNGA3):c.1857G>A (p.Ala619=) rs370933985 0.00004
NM_001298.3(CNGA3):c.1956C>T (p.Asn652=) rs749868323 0.00004
NM_001298.3(CNGA3):c.2073C>T (p.Asp691=) rs777984739 0.00004
NM_001298.3(CNGA3):c.222G>A (p.Ser74=) rs775081515 0.00004
NM_001298.3(CNGA3):c.224G>A (p.Arg75His) rs371232570 0.00004
NM_001298.3(CNGA3):c.525C>T (p.Ile175=) rs751565950 0.00004
NM_001298.3(CNGA3):c.566+14G>A rs367748425 0.00004
NM_001298.3(CNGA3):c.1413C>T (p.Asn471=) rs771835849 0.00003
NM_001298.3(CNGA3):c.1827C>T (p.Asp609=) rs778279209 0.00003
NM_001298.3(CNGA3):c.216-17C>T rs748117728 0.00003
NM_001298.3(CNGA3):c.395+9C>T rs375494943 0.00003
NM_001298.3(CNGA3):c.396-14C>G rs777304401 0.00003
NM_001298.3(CNGA3):c.519C>T (p.Thr173=) rs763964348 0.00003
NM_001298.3(CNGA3):c.105C>G (p.Ala35=) rs759618030 0.00002
NM_001298.3(CNGA3):c.1350G>A (p.Thr450=) rs377158658 0.00002
NM_001298.3(CNGA3):c.146G>A (p.Gly49Glu) rs771343327 0.00002
NM_001298.3(CNGA3):c.471T>G (p.Asp157Glu) rs199631623 0.00002
NM_001298.3(CNGA3):c.579T>C (p.Asp193=) rs760574115 0.00002
NM_001298.3(CNGA3):c.59C>T (p.Thr20Ile) rs143489966 0.00002
NM_001298.3(CNGA3):c.626C>T (p.Ser209Leu) rs533596832 0.00002
NM_001298.3(CNGA3):c.673+15G>C rs778932631 0.00002
NM_001298.3(CNGA3):c.846C>T (p.Ser282=) rs545024229 0.00002
NM_001298.3(CNGA3):c.102-18G>A rs773593173 0.00001
NM_001298.3(CNGA3):c.1146C>T (p.Val382=) rs756907714 0.00001
NM_001298.3(CNGA3):c.1278C>T (p.Phe426=) rs908538071 0.00001
NM_001298.3(CNGA3):c.1347G>A (p.Lys449=) rs778251470 0.00001
NM_001298.3(CNGA3):c.1368G>A (p.Val456=) rs369892428 0.00001
NM_001298.3(CNGA3):c.1386C>T (p.Asp462=) rs749493667 0.00001
NM_001298.3(CNGA3):c.1437G>A (p.Lys479=) rs1314147707 0.00001
NM_001298.3(CNGA3):c.1614C>T (p.Phe538=) rs762984332 0.00001
NM_001298.3(CNGA3):c.1831C>T (p.Leu611=) rs747855074 0.00001
NM_001298.3(CNGA3):c.183G>A (p.Gly61=) rs767377424 0.00001
NM_001298.3(CNGA3):c.1866C>T (p.Asp622=) rs886056490 0.00001
NM_001298.3(CNGA3):c.1902G>T (p.Gly634=) rs916798917 0.00001
NM_001298.3(CNGA3):c.2049C>T (p.Pro683=) rs923799882 0.00001
NM_001298.3(CNGA3):c.215+10C>T rs1401326236 0.00001
NM_001298.3(CNGA3):c.225C>T (p.Arg75=) rs200404774 0.00001
NM_001298.3(CNGA3):c.246G>A (p.Arg82=) rs1460177858 0.00001
NM_001298.3(CNGA3):c.267C>T (p.His89=) rs367951775 0.00001
NM_001298.3(CNGA3):c.285G>A (p.Pro95=) rs1469543969 0.00001
NM_001298.3(CNGA3):c.395+10G>A rs367602506 0.00001
NM_001298.3(CNGA3):c.459G>A (p.Thr153=) rs764028648 0.00001
NM_001298.3(CNGA3):c.474G>A (p.Ala158=) rs774720490 0.00001
NM_001298.3(CNGA3):c.566+17G>A rs745879257 0.00001
NM_001298.3(CNGA3):c.567-11G>T rs1201696750 0.00001
NM_001298.3(CNGA3):c.673+7G>A rs753973144 0.00001
NM_001298.3(CNGA3):c.681C>T (p.Leu227=) rs1176637666 0.00001
NM_001298.3(CNGA3):c.735G>A (p.Thr245=) rs181616312 0.00001
NM_001298.3(CNGA3):c.741G>A (p.Thr247=) rs765663301 0.00001
NM_001298.3(CNGA3):c.781C>T (p.Leu261=) rs1329749192 0.00001
NM_001298.3(CNGA3):c.939C>T (p.Ile313=) rs138545096 0.00001
NM_001298.3(CNGA3):c.978G>A (p.Lys326=) rs1313791180 0.00001
NM_001298.3(CNGA3):c.1002C>T (p.Ser334=) rs746731732
NM_001298.3(CNGA3):c.101+14_101+23dup
NM_001298.3(CNGA3):c.102-16A>C rs2279859
NM_001298.3(CNGA3):c.102-17_102-16inv
NM_001298.3(CNGA3):c.102-4C>T
NM_001298.3(CNGA3):c.1080C>T (p.Thr360=)
NM_001298.3(CNGA3):c.1107C>A (p.Thr369=)
NM_001298.3(CNGA3):c.1107C>T (p.Thr369=)
NM_001298.3(CNGA3):c.1158G>A (p.Leu386=)
NM_001298.3(CNGA3):c.1194T>C (p.Asn398=) rs778001158
NM_001298.3(CNGA3):c.1200C>T (p.Gly400=)
NM_001298.3(CNGA3):c.1212G>A (p.Ser404=)
NM_001298.3(CNGA3):c.1260C>A (p.Ile420=)
NM_001298.3(CNGA3):c.1269C>T (p.Tyr423=)
NM_001298.3(CNGA3):c.129G>T (p.Ser43=) rs372489647
NM_001298.3(CNGA3):c.1332G>A (p.Leu444=)
NM_001298.3(CNGA3):c.1338C>T (p.Ala446=)
NM_001298.3(CNGA3):c.1443C>T (p.Arg481=)
NM_001298.3(CNGA3):c.1461G>A (p.Glu487=) rs1455338995
NM_001298.3(CNGA3):c.1486C>T (p.Leu496=) rs747895951
NM_001298.3(CNGA3):c.1551G>A (p.Lys517=)
NM_001298.3(CNGA3):c.1584C>A (p.Ala528=) rs207462093
NM_001298.3(CNGA3):c.1596T>C (p.Asp532=)
NM_001298.3(CNGA3):c.159G>A (p.Glu53=)
NM_001298.3(CNGA3):c.1608C>G (p.Thr536=) rs2104249310
NM_001298.3(CNGA3):c.1629T>C (p.Asp543=)
NM_001298.3(CNGA3):c.1641C>T (p.Phe547=) rs104893617
NM_001298.3(CNGA3):c.1704C>T (p.Ile568=) rs2104249861
NM_001298.3(CNGA3):c.1725C>T (p.Asp575=) rs148867596
NM_001298.3(CNGA3):c.1764C>T (p.Leu588=) rs2104250218
NM_001298.3(CNGA3):c.1800G>A (p.Glu600=)
NM_001298.3(CNGA3):c.1848G>A (p.Leu616=)
NM_001298.3(CNGA3):c.1860C>T (p.Gly620=)
NM_001298.3(CNGA3):c.1881G>A (p.Glu627=) rs2104250749
NM_001298.3(CNGA3):c.1890G>A (p.Val630=) rs753877028
NM_001298.3(CNGA3):c.189C>A (p.Gly63=) rs1574375785
NM_001298.3(CNGA3):c.1929G>A (p.Arg643=)
NM_001298.3(CNGA3):c.1941C>T (p.Leu647=)
NM_001298.3(CNGA3):c.1950G>A (p.Glu650=)
NM_001298.3(CNGA3):c.1986C>G (p.Leu662=) rs2104251268
NM_001298.3(CNGA3):c.1989C>T (p.Ser663=)
NM_001298.3(CNGA3):c.2017G>A (p.Gly673Arg)
NM_001298.3(CNGA3):c.2019G>A (p.Gly673=)
NM_001298.3(CNGA3):c.2019G>T (p.Gly673=)
NM_001298.3(CNGA3):c.2052G>A (p.Gly684=)
NM_001298.3(CNGA3):c.2076A>G (p.Lys692=)
NM_001298.3(CNGA3):c.215+46T>A rs58990587
NM_001298.3(CNGA3):c.215+7G>C
NM_001298.3(CNGA3):c.216-12G>C
NM_001298.3(CNGA3):c.27C>A (p.Ser9=)
NM_001298.3(CNGA3):c.336C>T (p.Ser112=)
NM_001298.3(CNGA3):c.354G>A (p.Gln118=) rs771785153
NM_001298.3(CNGA3):c.393A>G (p.Arg131=) rs2104206079
NM_001298.3(CNGA3):c.395+10G>C rs367602506
NM_001298.3(CNGA3):c.395+14AAG[2] rs1357183420
NM_001298.3(CNGA3):c.395+19G>C
NM_001298.3(CNGA3):c.396-13T>C
NM_001298.3(CNGA3):c.405C>G (p.Pro135=)
NM_001298.3(CNGA3):c.441G>C (p.Thr147=) rs754767905
NM_001298.3(CNGA3):c.441G>T (p.Thr147=) rs754767905
NM_001298.3(CNGA3):c.449+11A>T
NM_001298.3(CNGA3):c.449+16C>G
NM_001298.3(CNGA3):c.449+19A>C
NM_001298.3(CNGA3):c.450-20G>A
NM_001298.3(CNGA3):c.453G>A (p.Lys151=)
NM_001298.3(CNGA3):c.471T>C (p.Asp157=)
NM_001298.3(CNGA3):c.483G>A (p.Val161=)
NM_001298.3(CNGA3):c.48C>G (p.Leu16=) rs374845812
NM_001298.3(CNGA3):c.495C>T (p.Ser165=) rs1692738790
NM_001298.3(CNGA3):c.519C>G (p.Thr173=)
NM_001298.3(CNGA3):c.531G>C (p.Leu177=)
NM_001298.3(CNGA3):c.566+10del rs2104230065
NM_001298.3(CNGA3):c.566+7G>A rs374306710
NM_001298.3(CNGA3):c.567-12T>C
NM_001298.3(CNGA3):c.567-13A>C rs373527569
NM_001298.3(CNGA3):c.567-13A>G
NM_001298.3(CNGA3):c.567-4T>G rs2104235482
NM_001298.3(CNGA3):c.588G>A (p.Gln196=)
NM_001298.3(CNGA3):c.591C>T (p.Ser197=)
NM_001298.3(CNGA3):c.597C>T (p.Tyr199=)
NM_001298.3(CNGA3):c.600G>C (p.Leu200=)
NM_001298.3(CNGA3):c.627G>A (p.Ser209=)
NM_001298.3(CNGA3):c.636C>T (p.Val212=)
NM_001298.3(CNGA3):c.645C>G (p.Val215=)
NM_001298.3(CNGA3):c.654G>C (p.Val218=) rs771894602
NM_001298.3(CNGA3):c.674-7T>G
NM_001298.3(CNGA3):c.702T>C (p.Ser234=)
NM_001298.3(CNGA3):c.717G>A (p.Leu239=) rs924715004
NM_001298.3(CNGA3):c.753G>T (p.Leu251=) rs62156349
NM_001298.3(CNGA3):c.777C>A (p.Thr259=) rs138921037
NM_001298.3(CNGA3):c.777C>T (p.Thr259=) rs138921037
NM_001298.3(CNGA3):c.796G>A (p.Val266Met) rs536335712
NM_001298.3(CNGA3):c.835C>T (p.Leu279=)
NM_001298.3(CNGA3):c.852C>T (p.Leu284=)
NM_001298.3(CNGA3):c.921C>A (p.Val307=) rs2104246133
NM_001298.3(CNGA3):c.927C>T (p.Tyr309=)

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