ClinVar Miner

List of variants in gene CHST3 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 127
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HGVS dbSNP gnomAD frequency
NM_004273.5(CHST3):c.*1899G>A rs17297481 0.08826
NM_004273.5(CHST3):c.*3555G>A rs4148951 0.04774
NM_004273.5(CHST3):c.*3039C>T rs74145519 0.04770
NM_004273.5(CHST3):c.*4770G>A rs4148953 0.04304
NM_004273.5(CHST3):c.*1370G>A rs60924680 0.03944
NM_004273.5(CHST3):c.*2026A>G rs115545740 0.03755
NM_004273.5(CHST3):c.*1006T>C rs116018996 0.02989
NM_004273.5(CHST3):c.-274G>T rs146305825 0.02017
NM_004273.5(CHST3):c.*1425C>T rs80269486 0.01869
NM_004273.5(CHST3):c.*1101T>G rs116999241 0.01828
NM_004273.5(CHST3):c.*1426T>C rs76062174 0.01720
NM_004273.5(CHST3):c.*255C>T rs114569872 0.01583
NM_004273.5(CHST3):c.*483G>A rs113283291 0.01271
NM_004273.5(CHST3):c.*3666G>A rs113342172 0.01185
NM_004273.5(CHST3):c.*2391C>T rs116391584 0.00817
NM_004273.5(CHST3):c.*1823G>C rs116289781 0.00816
NM_004273.5(CHST3):c.*2163A>G rs114563668 0.00816
NM_004273.5(CHST3):c.*2826G>A rs114457501 0.00816
NM_004273.5(CHST3):c.*3890C>T rs79559408 0.00815
NM_004273.5(CHST3):c.*4095A>G rs114800040 0.00815
NM_004273.5(CHST3):c.*203A>G rs77359818 0.00814
NM_004273.5(CHST3):c.1173C>A (p.Ile391=) rs115579748 0.00763
NM_004273.5(CHST3):c.108C>G (p.Val36=) rs77124584 0.00681
NM_004273.5(CHST3):c.561G>C (p.Val187=) rs147804585 0.00480
NM_004273.5(CHST3):c.1428C>T (p.Phe476=) rs75845750 0.00421
NM_004273.5(CHST3):c.*7C>T rs202242499 0.00123
NM_004273.5(CHST3):c.1197C>T (p.Asp399=) rs184636110 0.00097
NM_004273.5(CHST3):c.959C>G (p.Thr320Ser) rs535309495 0.00077
NM_004273.5(CHST3):c.1251G>C (p.Thr417=) rs140411224 0.00072
NM_004273.5(CHST3):c.1135C>T (p.Leu379=) rs564028722 0.00049
NM_004273.5(CHST3):c.348G>T (p.Glu116Asp) rs144885813 0.00048
NM_004273.5(CHST3):c.528G>A (p.Pro176=) rs373748456 0.00039
NM_004273.5(CHST3):c.1003G>A (p.Glu335Lys) rs150466838 0.00038
NM_004273.5(CHST3):c.1363C>G (p.Leu455Val) rs374954414 0.00018
NM_004273.5(CHST3):c.114C>T (p.Ile38=) rs374590185 0.00016
NM_004273.5(CHST3):c.570C>T (p.Asp190=) rs367857089 0.00013
NM_004273.5(CHST3):c.423G>A (p.Thr141=) rs376107245 0.00011
NM_004273.5(CHST3):c.624G>A (p.Thr208=) rs145440508 0.00006
NM_004273.5(CHST3):c.540C>T (p.Asn180=) rs748812857 0.00004
NM_004273.5(CHST3):c.306C>A (p.Gly102=) rs776007496 0.00003
NM_004273.5(CHST3):c.447C>T (p.Gly149=) rs995812238 0.00003
NM_004273.5(CHST3):c.1056G>C (p.Ala352=) rs779966805 0.00002
NM_004273.5(CHST3):c.111C>T (p.Phe37=) rs371428228 0.00001
NM_004273.5(CHST3):c.1134G>A (p.Pro378=) rs893941954 0.00001
NM_004273.5(CHST3):c.1167C>T (p.Ala389=) rs1380183951 0.00001
NM_004273.5(CHST3):c.486C>T (p.Phe162=) rs774188997 0.00001
NM_004273.5(CHST3):c.72C>T (p.Tyr24=) rs542040061 0.00001
NM_004273.5(CHST3):c.861C>G (p.Ala287=) rs1489540204 0.00001
NM_004273.5(CHST3):c.942C>T (p.Phe314=) rs1010927640 0.00001
NM_004273.5(CHST3):c.*1447C>A rs76808415
NM_004273.5(CHST3):c.*1978GT[4] rs150678709
NM_004273.5(CHST3):c.*2126A>C rs7072219
NM_004273.5(CHST3):c.*2349A>C rs4148948
NM_004273.5(CHST3):c.*2718G>A rs115489836
NM_004273.5(CHST3):c.*3090T>A rs76750860
NM_004273.5(CHST3):c.*3701AG[1] rs200054447
NM_004273.5(CHST3):c.*3884A>G rs77908871
NM_004273.5(CHST3):c.-270del rs538907004
NM_004273.5(CHST3):c.1017G>A (p.Gln339=)
NM_004273.5(CHST3):c.1060C>T (p.Leu354=)
NM_004273.5(CHST3):c.1128C>T (p.Arg376=)
NM_004273.5(CHST3):c.1129G>A (p.Gly377Arg)
NM_004273.5(CHST3):c.1143G>A (p.Lys381=) rs2131776355
NM_004273.5(CHST3):c.1185G>A (p.Pro395=) rs1455730645
NM_004273.5(CHST3):c.1185G>T (p.Pro395=)
NM_004273.5(CHST3):c.1251G>A (p.Thr417=)
NM_004273.5(CHST3):c.1254G>A (p.Gln418=)
NM_004273.5(CHST3):c.1260C>T (p.Asn420=)
NM_004273.5(CHST3):c.1263C>G (p.Ser421=)
NM_004273.5(CHST3):c.1263C>T (p.Ser421=)
NM_004273.5(CHST3):c.1266G>A (p.Ser422=) rs372291815
NM_004273.5(CHST3):c.1275C>T (p.Phe425=)
NM_004273.5(CHST3):c.1293C>T (p.Ser431=)
NM_004273.5(CHST3):c.1326C>T (p.Ala442=)
NM_004273.5(CHST3):c.1332C>T (p.Cys444=)
NM_004273.5(CHST3):c.1350C>G (p.Leu450=)
NM_004273.5(CHST3):c.1365G>A (p.Leu455=)
NM_004273.5(CHST3):c.1368G>C (p.Ala456=)
NM_004273.5(CHST3):c.1380C>T (p.Ala460=) rs369055984
NM_004273.5(CHST3):c.1404C>T (p.Ser468=)
NM_004273.5(CHST3):c.1408C>T (p.Leu470=)
NM_004273.5(CHST3):c.141-14C>T
NM_004273.5(CHST3):c.141-17C>T
NM_004273.5(CHST3):c.168C>G (p.Pro56=) rs1840047159
NM_004273.5(CHST3):c.175C>T (p.Leu59=)
NM_004273.5(CHST3):c.195C>T (p.Thr65=) rs759935618
NM_004273.5(CHST3):c.201A>T (p.Pro67=)
NM_004273.5(CHST3):c.243C>T (p.Ser81=)
NM_004273.5(CHST3):c.255A>T (p.Ser85=)
NM_004273.5(CHST3):c.279T>C (p.Arg93=)
NM_004273.5(CHST3):c.306C>T (p.Gly102=) rs776007496
NM_004273.5(CHST3):c.327C>T (p.Ala109=)
NM_004273.5(CHST3):c.348G>A (p.Glu116=) rs144885813
NM_004273.5(CHST3):c.360G>A (p.Glu120=)
NM_004273.5(CHST3):c.36G>A (p.Arg12=)
NM_004273.5(CHST3):c.378G>C (p.Pro126=)
NM_004273.5(CHST3):c.378G>T (p.Pro126=)
NM_004273.5(CHST3):c.381C>T (p.Ala127=) rs769338504
NM_004273.5(CHST3):c.382G>C (p.Val128Leu) rs563761692
NM_004273.5(CHST3):c.384G>A (p.Val128=)
NM_004273.5(CHST3):c.480C>T (p.Tyr160=)
NM_004273.5(CHST3):c.48C>T (p.His16=) rs574784635
NM_004273.5(CHST3):c.492G>A (p.Pro164=)
NM_004273.5(CHST3):c.534C>T (p.Gly178=)
NM_004273.5(CHST3):c.549C>T (p.Gly183=)
NM_004273.5(CHST3):c.54G>T (p.Leu18=)
NM_004273.5(CHST3):c.552G>A (p.Ser184=)
NM_004273.5(CHST3):c.588C>T (p.Phe196=)
NM_004273.5(CHST3):c.591G>A (p.Leu197=)
NM_004273.5(CHST3):c.594C>T (p.Cys198=)
NM_004273.5(CHST3):c.618C>T (p.Phe206=)
NM_004273.5(CHST3):c.633C>G (p.Pro211=)
NM_004273.5(CHST3):c.666G>C (p.Arg222=)
NM_004273.5(CHST3):c.681C>G (p.Ser227=) rs1840057937
NM_004273.5(CHST3):c.705G>C (p.Thr235=)
NM_004273.5(CHST3):c.711C>T (p.Phe237=)
NM_004273.5(CHST3):c.720G>A (p.Lys240=)
NM_004273.5(CHST3):c.759C>T (p.Gly253=)
NM_004273.5(CHST3):c.780C>T (p.Ala260=)
NM_004273.5(CHST3):c.795C>G (p.Arg265=)
NM_004273.5(CHST3):c.840G>A (p.Leu280=)
NM_004273.5(CHST3):c.849G>C (p.Leu283=)
NM_004273.5(CHST3):c.903C>G (p.Arg301=)
NM_004273.5(CHST3):c.906C>T (p.Asp302=)
NM_004273.5(CHST3):c.915C>A (p.Ala305=)
NM_004273.5(CHST3):c.945C>T (p.Ala315=)
NM_004273.5(CHST3):c.993C>T (p.Asp331=)

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