ClinVar Miner

List of variants in gene KIAA1549 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_001164665.2(KIAA1549):c.3708G>T (p.Pro1236=) rs7802841 0.71421
NM_001164665.2(KIAA1549):c.2973C>T (p.Tyr991=) rs6969074 0.54454
NM_001164665.2(KIAA1549):c.1849A>G (p.Arg617Gly) rs2774962 0.52408
NM_001164665.2(KIAA1549):c.2546C>T (p.Ser849Leu) rs2251220 0.43675
NM_001164665.2(KIAA1549):c.1955C>T (p.Pro652Leu) rs2774960 0.41799
NM_001164665.2(KIAA1549):c.1456C>G (p.Pro486Ala) rs2718131 0.21208
NM_001164665.2(KIAA1549):c.5136C>T (p.Pro1712=) rs12707399 0.09704
NM_001164665.2(KIAA1549):c.2301T>C (p.Thr767=) rs61746879 0.08707
NM_001164665.2(KIAA1549):c.3036C>T (p.Ser1012=) rs16873582 0.08470
NM_001164665.2(KIAA1549):c.2800G>A (p.Asp934Asn) rs2150283 0.05297
NM_001164665.2(KIAA1549):c.2666G>T (p.Gly889Val) rs2354336 0.05287
NM_001164665.2(KIAA1549):c.1940C>G (p.Ser647Cys) rs61734132 0.05285
NM_001164665.2(KIAA1549):c.4033-11G>C rs10227679 0.04084
NM_001164665.2(KIAA1549):c.42G>A (p.Glu14=) rs536040543 0.02962
NM_001164665.2(KIAA1549):c.2799C>T (p.Val933=) rs61995719 0.02724
NM_001164665.2(KIAA1549):c.3461-15C>T rs117618554 0.02338
NM_001164665.2(KIAA1549):c.3195C>T (p.Thr1065=) rs10277735 0.01777
NM_001164665.2(KIAA1549):c.2523C>T (p.Asp841=) rs6962973 0.01475
NM_001164665.2(KIAA1549):c.958G>A (p.Asp320Asn) rs61978615 0.01092
NM_001164665.2(KIAA1549):c.3593A>G (p.Gln1198Arg) rs144488000 0.01007
NM_001164665.2(KIAA1549):c.875C>T (p.Pro292Leu) rs140890453 0.00764
NM_001164665.2(KIAA1549):c.4716C>T (p.Ile1572=) rs28523576 0.00683
NM_001164665.2(KIAA1549):c.1769C>T (p.Thr590Met) rs144262582 0.00620
NM_001164665.2(KIAA1549):c.658G>C (p.Ala220Pro) rs79731548 0.00602
NM_001164665.2(KIAA1549):c.4532G>C (p.Ser1511Thr) rs61744110 0.00589
NM_001164665.2(KIAA1549):c.4648G>A (p.Val1550Ile) rs116788555 0.00585
NM_001164665.2(KIAA1549):c.3052A>T (p.Ile1018Leu) rs185695096 0.00534
NM_001164665.2(KIAA1549):c.1399G>A (p.Val467Ile) rs61736034 0.00519
NM_001164665.2(KIAA1549):c.4930-14A>G rs80130913 0.00514
NM_001164665.2(KIAA1549):c.261C>T (p.His87=) rs141812444 0.00418
NM_001164665.2(KIAA1549):c.3453C>T (p.Ile1151=) rs61744112 0.00408
NM_001164665.2(KIAA1549):c.5662G>A (p.Gly1888Ser) rs115152294 0.00399
NM_001164665.2(KIAA1549):c.2770G>A (p.Val924Met) rs148827805 0.00397
NM_001164665.2(KIAA1549):c.4158G>A (p.Thr1386=) rs142709120 0.00351
NM_001164665.2(KIAA1549):c.5157C>T (p.Pro1719=) rs148849089 0.00307
NM_001164665.2(KIAA1549):c.1123A>G (p.Thr375Ala) rs144913038 0.00303
NM_001164665.2(KIAA1549):c.2713G>C (p.Ala905Pro) rs148007950 0.00295
NM_001164665.2(KIAA1549):c.130C>T (p.Leu44=) rs188225028 0.00291
NM_001164665.2(KIAA1549):c.2640C>T (p.Ser880=) rs115066019 0.00287
NM_001164665.2(KIAA1549):c.1656C>T (p.Ser552=) rs113045455 0.00233
NM_001164665.2(KIAA1549):c.4552-20dup rs536450000 0.00231
NM_001164665.2(KIAA1549):c.5186G>A (p.Arg1729Lys) rs60797311 0.00231
NM_001164665.2(KIAA1549):c.5520C>A (p.Ile1840=) rs372228871 0.00189
NM_001164665.2(KIAA1549):c.885C>T (p.Asp295=) rs79934303 0.00167
NM_001164665.2(KIAA1549):c.1155C>T (p.Ser385=) rs140043575 0.00157
NM_001164665.2(KIAA1549):c.2105T>A (p.Leu702Gln) rs141831128 0.00157
NM_001164665.2(KIAA1549):c.1802C>T (p.Ser601Leu) rs149565300 0.00132
NM_001164665.2(KIAA1549):c.660G>A (p.Ala220=) rs77986377 0.00116
NM_001164665.2(KIAA1549):c.404C>A (p.Pro135His) rs79234060 0.00113
NM_001164665.2(KIAA1549):c.2689G>A (p.Asp897Asn) rs141705276 0.00112
NM_001164665.2(KIAA1549):c.1746C>T (p.Ala582=) rs148743027 0.00106
NM_001164665.2(KIAA1549):c.3276+9A>G rs369690093 0.00088
NM_001164665.2(KIAA1549):c.2879-19G>T rs372555864 0.00087
NM_001164665.2(KIAA1549):c.4184G>A (p.Ser1395Asn) rs139412672 0.00086
NM_001164665.2(KIAA1549):c.2688C>T (p.Leu896=) rs144765229 0.00074
NM_001164665.2(KIAA1549):c.4164G>A (p.Ser1388=) rs183617317 0.00074
NM_001164665.2(KIAA1549):c.2761C>T (p.Leu921=) rs143475803 0.00073
NM_001164665.2(KIAA1549):c.819A>G (p.Leu273=) rs144704761 0.00073
NM_001164665.2(KIAA1549):c.2181C>T (p.Leu727=) rs201109912 0.00072
NM_001164665.2(KIAA1549):c.2710G>A (p.Ala904Thr) rs117908080 0.00070
NM_001164665.2(KIAA1549):c.4743C>T (p.Ser1581=) rs372552870 0.00055
NM_001164665.2(KIAA1549):c.1854T>C (p.Gly618=) rs61732262 0.00053
NM_001164665.2(KIAA1549):c.5469C>T (p.His1823=) rs565452410 0.00048
NM_001164665.2(KIAA1549):c.2100C>T (p.Ser700=) rs3735012 0.00044
NM_001164665.2(KIAA1549):c.1344C>T (p.Ala448=) rs183368912 0.00039
NM_001164665.2(KIAA1549):c.2314C>T (p.Pro772Ser) rs200244255 0.00026
NM_001164665.2(KIAA1549):c.5294+6G>A rs117006285 0.00025
NM_001164665.2(KIAA1549):c.4428G>A (p.Pro1476=) rs145725555 0.00024
NM_001164665.2(KIAA1549):c.2525C>T (p.Ala842Val) rs202114551 0.00018
NM_001164665.2(KIAA1549):c.1652C>G (p.Ser551Cys) rs369401473 0.00016
NM_001164665.2(KIAA1549):c.1398C>T (p.Ser466=) rs572555872 0.00014
NM_001164665.2(KIAA1549):c.5253C>T (p.Tyr1751=) rs376589057 0.00013
NM_001164665.2(KIAA1549):c.2716A>G (p.Ser906Gly) rs201853693 0.00011
NM_001164665.2(KIAA1549):c.3834T>C (p.Gly1278=) rs185026022 0.00004
NM_001164665.2(KIAA1549):c.1740G>A (p.Ser580=) rs185123082 0.00001
NM_001164665.2(KIAA1549):c.201G>A (p.Pro67=) rs533338378 0.00001
NM_001164665.2(KIAA1549):c.4033-19G>A rs558572322 0.00001
NM_001164665.2(KIAA1549):c.1090A>G (p.Thr364Ala) rs59985563
NM_001164665.2(KIAA1549):c.2316C>T (p.Pro772=) rs61746877
NM_001164665.2(KIAA1549):c.3269C>A (p.Thr1090Lys) rs377595061
NM_001164665.2(KIAA1549):c.3847+14del rs541855481
NM_001164665.2(KIAA1549):c.4257G>C (p.Thr1419=) rs146930653
NM_001164665.2(KIAA1549):c.4380C>A (p.His1460Gln) rs138395431
NM_001164665.2(KIAA1549):c.462C>G (p.Asp154Glu) rs191728209
NM_001164665.2(KIAA1549):c.462C>T (p.Asp154=) rs191728209
NM_001164665.2(KIAA1549):c.4775+11del rs747636400
NM_001164665.2(KIAA1549):c.5523G>A (p.Pro1841=) rs199869689
NM_001164665.2(KIAA1549):c.710G>T (p.Arg237Leu) rs112263100

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