ClinVar Miner

List of variants in gene ALPK3 reported as likely benign for not specified

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Gene type:
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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_020778.5(ALPK3):c.4259T>C (p.Leu1420Pro) rs187316 0.20037
NM_020778.5(ALPK3):c.635C>G (p.Thr212Ser) rs3803403 0.19072
NM_020778.5(ALPK3):c.1130G>A (p.Gly377Glu) rs3803405 0.18268
NM_020778.5(ALPK3):c.3628C>T (p.Arg1210Trp) rs55752937 0.02339
NM_020778.5(ALPK3):c.1199A>G (p.Gln400Arg) rs55702300 0.02213
NM_020778.5(ALPK3):c.4064C>A (p.Ala1355Asp) rs34775428 0.01753
NM_020778.5(ALPK3):c.401G>A (p.Arg134His) rs34407151 0.01062
NM_020778.5(ALPK3):c.2595C>T (p.Pro865=) rs114957070 0.00386
NM_020778.5(ALPK3):c.2530C>T (p.Pro844Ser) rs115292211 0.00382
NM_020778.5(ALPK3):c.4474G>A (p.Ala1492Thr) rs114449938 0.00349
NM_020778.5(ALPK3):c.5012C>T (p.Ala1671Val) rs36002219 0.00289
NM_020778.5(ALPK3):c.1336C>A (p.Pro446Thr) rs199986476 0.00202
NM_020778.5(ALPK3):c.3965+11G>A rs117116043 0.00175
NM_020778.5(ALPK3):c.4063G>A (p.Ala1355Thr) rs114686452 0.00171
NM_020778.5(ALPK3):c.135C>T (p.Pro45=) rs369591811 0.00062
NM_020778.5(ALPK3):c.3786C>G (p.Ala1262=) rs202162264 0.00043
NM_020778.5(ALPK3):c.3966-14T>C rs145646854 0.00039
NM_020778.5(ALPK3):c.1737C>T (p.Ser579=) rs115301935 0.00032
NM_020778.5(ALPK3):c.150A>G (p.Ser50=) rs79285448 0.00031
NM_020778.5(ALPK3):c.3702G>A (p.Ala1234=) rs55721004 0.00027
NM_020778.5(ALPK3):c.2528G>A (p.Arg843Gln) rs114988007 0.00024
NM_020778.5(ALPK3):c.-43G>A rs949112384 0.00013
NM_020778.5(ALPK3):c.3735C>T (p.Gly1245=) rs760971774 0.00012
NM_020778.5(ALPK3):c.5064G>A (p.Leu1688=) rs115813516 0.00011
NM_020778.4(ALPK3):c.-30G>T rs370679146 0.00009
NM_020778.5(ALPK3):c.2934A>G (p.Ala978=) rs574248459 0.00009
NM_020778.5(ALPK3):c.182+9A>G rs200942386 0.00007
NM_020778.5(ALPK3):c.4998C>T (p.Gly1666=) rs749593573 0.00007
NM_020778.5(ALPK3):c.-64C>G rs959503280 0.00006
NM_020778.5(ALPK3):c.2649G>A (p.Pro883=) rs115903792 0.00004
NM_020778.5(ALPK3):c.3817+15G>A rs368481088 0.00003
NM_020778.5(ALPK3):c.4308C>T (p.Phe1436=) rs567548946 0.00003
NM_020778.5(ALPK3):c.4723+5G>A rs771461497 0.00003
NM_020778.5(ALPK3):c.4902A>G (p.Gln1634=) rs1390506057 0.00003
NM_020778.5(ALPK3):c.4093+15C>T rs771455330 0.00002
NM_020778.5(ALPK3):c.2421G>A (p.Glu807=) rs150546362 0.00001
NM_020778.5(ALPK3):c.24C>T (p.Ser8=) rs1301150493 0.00001
NM_020778.5(ALPK3):c.2748G>A (p.Leu916=) rs1397241134 0.00001
NM_020778.5(ALPK3):c.3867C>T (p.Ser1289=) rs188837127 0.00001
NM_020778.5(ALPK3):c.4152C>T (p.Thr1384=) rs955410854 0.00001
NM_020778.5(ALPK3):c.4173T>A (p.Gly1391=) rs946844546 0.00001
NM_020778.5(ALPK3):c.648C>G (p.Leu216=) rs142016958 0.00001
NM_020778.5(ALPK3):c.1233G>A (p.Val411=)
NM_020778.5(ALPK3):c.144-16T>C
NM_020778.5(ALPK3):c.1845G>A (p.Lys615=)
NM_020778.5(ALPK3):c.2376T>A (p.Gly792=) rs1057524352
NM_020778.5(ALPK3):c.423-19del rs537375112
NM_020778.5(ALPK3):c.5103C>T (p.Ala1701=) rs527520436

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