ClinVar Miner

List of variants in gene ANKIB1 reported as uncertain significance for not specified

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_019004.2(ANKIB1):c.3008G>T (p.Cys1003Phe) rs199967517 0.00040
NM_019004.2(ANKIB1):c.2860A>G (p.Ser954Gly) rs201087382 0.00023
NM_019004.2(ANKIB1):c.390G>T (p.Gln130His) rs201516787 0.00019
NM_019004.2(ANKIB1):c.200G>A (p.Gly67Asp) rs200441644 0.00015
NM_019004.2(ANKIB1):c.665G>A (p.Arg222Gln) rs761679571 0.00015
NM_019004.2(ANKIB1):c.1315A>G (p.Asn439Asp) rs774182703 0.00007
NM_019004.2(ANKIB1):c.2362C>G (p.Pro788Ala) rs748896469 0.00005
NM_019004.2(ANKIB1):c.1772G>A (p.Arg591Gln) rs776841813 0.00004
NM_019004.2(ANKIB1):c.770C>G (p.Ala257Gly) rs1310289996 0.00004
NM_019004.2(ANKIB1):c.3029G>T (p.Gly1010Val) rs199578051 0.00003
NM_019004.2(ANKIB1):c.3086T>C (p.Val1029Ala) rs376253765 0.00003
NM_019004.2(ANKIB1):c.2296T>C (p.Phe766Leu) rs527486645 0.00002
NM_019004.2(ANKIB1):c.2372A>G (p.Asp791Gly) rs1442778451 0.00002
NM_019004.2(ANKIB1):c.2486G>A (p.Arg829His) rs756805504 0.00002
NM_019004.2(ANKIB1):c.2911G>A (p.Gly971Ser) rs1360836511 0.00002
NM_019004.2(ANKIB1):c.824C>G (p.Ser275Cys) rs762211381 0.00002
NM_019004.2(ANKIB1):c.1319C>T (p.Thr440Ile) rs759314504 0.00001
NM_019004.2(ANKIB1):c.1321T>C (p.Ser441Pro) rs1481227852 0.00001
NM_019004.2(ANKIB1):c.2413A>G (p.Ser805Gly) rs775363363 0.00001
NM_019004.2(ANKIB1):c.2422C>T (p.Arg808Cys) rs746928096 0.00001
NM_019004.2(ANKIB1):c.2485C>T (p.Arg829Cys) rs1361399149 0.00001
NM_019004.2(ANKIB1):c.2642A>G (p.Asn881Ser) rs752657143 0.00001
NM_019004.2(ANKIB1):c.2698C>T (p.Pro900Ser) rs1485822377 0.00001
NM_019004.2(ANKIB1):c.2803G>T (p.Asp935Tyr) rs376497678 0.00001
NM_019004.2(ANKIB1):c.2897A>G (p.Asn966Ser) rs1039112752 0.00001
NM_019004.2(ANKIB1):c.2968C>G (p.Pro990Ala) rs1187271425 0.00001
NM_019004.2(ANKIB1):c.3185C>T (p.Ala1062Val) rs2484457687 0.00001
NM_019004.2(ANKIB1):c.652G>A (p.Ala218Thr) rs779731136 0.00001
NM_019004.2(ANKIB1):c.1174A>G (p.Ile392Val)
NM_019004.2(ANKIB1):c.1657A>G (p.Lys553Glu) rs2484434551
NM_019004.2(ANKIB1):c.1691G>A (p.Arg564Lys)
NM_019004.2(ANKIB1):c.1750G>A (p.Glu584Lys)
NM_019004.2(ANKIB1):c.183A>G (p.Ile61Met) rs2536262615
NM_019004.2(ANKIB1):c.2024C>T (p.Thr675Ile)
NM_019004.2(ANKIB1):c.2101C>A (p.Pro701Thr) rs746389506
NM_019004.2(ANKIB1):c.2327G>A (p.Arg776His) rs776777318
NM_019004.2(ANKIB1):c.2345G>A (p.Ser782Asn) rs1296052951
NM_019004.2(ANKIB1):c.2372A>C (p.Asp791Ala)
NM_019004.2(ANKIB1):c.2387G>T (p.Ser796Ile) rs2484453027
NM_019004.2(ANKIB1):c.2480C>T (p.Ser827Phe)
NM_019004.2(ANKIB1):c.2492A>G (p.Tyr831Cys)
NM_019004.2(ANKIB1):c.2614G>A (p.Asp872Asn)
NM_019004.2(ANKIB1):c.2693C>G (p.Ser898Cys) rs1804945623
NM_019004.2(ANKIB1):c.2776G>A (p.Gly926Arg) rs752507458
NM_019004.2(ANKIB1):c.284C>T (p.Ser95Phe)
NM_019004.2(ANKIB1):c.2943C>A (p.Asn981Lys)
NM_019004.2(ANKIB1):c.2957C>T (p.Ala986Val)
NM_019004.2(ANKIB1):c.3022T>A (p.Ser1008Thr) rs200370929
NM_019004.2(ANKIB1):c.3032T>C (p.Val1011Ala)
NM_019004.2(ANKIB1):c.304C>T (p.Arg102Cys)
NM_019004.2(ANKIB1):c.305G>T (p.Arg102Leu)
NM_019004.2(ANKIB1):c.3082A>G (p.Ser1028Gly) rs1357056400
NM_019004.2(ANKIB1):c.3085G>A (p.Val1029Ile) rs2484457474
NM_019004.2(ANKIB1):c.313C>T (p.Arg105Cys)
NM_019004.2(ANKIB1):c.3181G>A (p.Glu1061Lys)
NM_019004.2(ANKIB1):c.3200A>G (p.Asp1067Gly) rs2484457717
NM_019004.2(ANKIB1):c.328G>C (p.Asp110His)
NM_019004.2(ANKIB1):c.388C>G (p.Gln130Glu) rs1463525996
NM_019004.2(ANKIB1):c.391G>C (p.Gly131Arg)
NM_019004.2(ANKIB1):c.404G>A (p.Arg135Lys)
NM_019004.2(ANKIB1):c.564A>C (p.Gln188His)
NM_019004.2(ANKIB1):c.670C>A (p.Pro224Thr) rs1405842985
NM_019004.2(ANKIB1):c.864G>A (p.Met288Ile) rs2536323259
NM_019004.2(ANKIB1):c.890A>G (p.Asn297Ser)
NM_019004.2(ANKIB1):c.931A>G (p.Thr311Ala) rs1221532659
NM_019004.2(ANKIB1):c.992G>T (p.Ser331Ile) rs754461918

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