Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.43416738G>ACA2391216180SIK1c.*4C>T (n.*4C>T)
 dbSNP
21g.43416738G=CA2391216179SIK1c.*4C= (n.*4C=)
21g.43416740C=CA2391216181SIK1c.*2G= (n.*2G=)
21g.43416740C>TCA321324227SIK1c.*2G>A (n.*2G>A)
 dbSNP gnomAD v3 gnomAD v4
21g.43416742T>ACA410606150SIK1c.2352A>T (p.Ter784Cys)
c.2205A>T (p.Ter735Cys)
21g.43416742T>CCA410606151SIK1c.2352A>G (p.Ter784Trp)
c.2205A>G (p.Ter735Trp)
21g.43416742T>GCA410606152SIK1c.2352A>C (p.Ter784Cys)
c.2205A>C (p.Ter735Cys)
21g.43416743C>ACA410606153SIK1c.2351G>T (p.Ter784Leu)
c.2204G>T (p.Ter735Leu)
21g.43416743C>GCA410606154SIK1c.2351G>C (p.Ter784Ser)
c.2204G>C (p.Ter735Ser)
21g.43416744A>CCA410606155SIK1c.2350T>G (p.Ter784Gly)
c.2203T>G (p.Ter735Gly)
21g.43416744A>GCA410606156SIK1c.2350T>C (p.Ter784Arg)
c.2203T>C (p.Ter735Arg)
21g.43416744A>TCA410606157SIK1c.2350T>A (p.Ter784Arg)
c.2203T>A (p.Ter735Arg)
21g.43416745C>ACA410606158SIK1c.2349G>T (p.Gln783His)
c.2202G>T (p.Gln734His)
21g.43416745C>GCA410606159SIK1c.2349G>C (p.Gln783His)
c.2202G>C (p.Gln734His)
21g.43416745C>TCA2573129982SIK1c.2349G>A (p.Gln783=)
c.2202G>A (p.Gln734=)
21g.43416746T>ACA410606160SIK1c.2348A>T (p.Gln783Leu)
c.2201A>T (p.Gln734Leu)
21g.43416746T>CCA410606162SIK1c.2348A>G (p.Gln783Arg)
c.2201A>G (p.Gln734Arg)
21g.43416746T>GCA410606161SIK1c.2348A>C (p.Gln783Pro)
c.2201A>C (p.Gln734Pro)
21g.43416747G>ACA410606163SIK1c.2347C>T (p.Gln783Ter)
c.2200C>T (p.Gln734Ter)
21g.43416747G>CCA410606164SIK1c.2347C>G (p.Gln783Glu)
c.2200C>G (p.Gln734Glu)
21g.43416747G>TCA410606165SIK1c.2347C>A (p.Gln783Lys)
c.2200C>A (p.Gln734Lys)
21g.43416749A=CA2391216182SIK1c.2345T= (p.Val782=)
c.2198T= (p.Val733=)
21g.43416749A>CCA410606166SIK1c.2345T>G (p.Val782Gly)
c.2198T>G (p.Val733Gly)
21g.43416749A>GCA410606167SIK1c.2345T>C (p.Val782Ala)
c.2198T>C (p.Val733Ala)
21g.43416749A>TCA321324228SIK1c.2345T>A (p.Val782Glu)
c.2198T>A (p.Val733Glu)
 dbSNP
21g.43416750C>ACA410606168SIK1c.2344G>T (p.Val782Leu)
c.2197G>T (p.Val733Leu)
21g.43416750C>GCA410606169SIK1c.2344G>C (p.Val782Leu)
c.2197G>C (p.Val733Leu)
21g.43416750C>TCA410606170SIK1c.2344G>A (p.Val782Met)
c.2197G>A (p.Val733Met)
21g.43416752A>CCA410606171SIK1c.2342T>G (p.Leu781Arg)
c.2195T>G (p.Leu732Arg)
21g.43416752A>GCA410606172SIK1c.2342T>C (p.Leu781Pro)
c.2195T>C (p.Leu732Pro)
21g.43416752A>TCA410606173SIK1c.2342T>A (p.Leu781Gln)
c.2195T>A (p.Leu732Gln)
21g.43416753G>CCA410606174SIK1c.2341C>G (p.Leu781Val)
c.2194C>G (p.Leu732Val)
 COSMIC
21g.43416753G>TCA410606175SIK1c.2341C>A (p.Leu781Met)
c.2194C>A (p.Leu732Met)
21g.43416754G>ACA2573157445SIK1c.2340C>T (p.Val780=)
c.2193C>T (p.Val731=)
 ClinVar dbSNP
21g.43416755A>CCA410606176SIK1c.2339T>G (p.Val780Gly)
c.2192T>G (p.Val731Gly)
21g.43416755A>GCA410606178SIK1c.2339T>C (p.Val780Ala)
c.2192T>C (p.Val731Ala)
21g.43416755A>TCA410606177SIK1c.2339T>A (p.Val780Asp)
c.2192T>A (p.Val731Asp)
21g.43416756C>ACA410606179SIK1c.2338G>T (p.Val780Phe)
c.2191G>T (p.Val731Phe)
21g.43416756C=CA2391216183SIK1c.2338G= (p.Val780=)
c.2191G= (p.Val731=)
21g.43416756C>GCA410606180SIK1c.2338G>C (p.Val780Leu)
c.2191G>C (p.Val731Leu)
21g.43416756C>TCA410606181SIK1c.2338G>A (p.Val780Ile)
c.2191G>A (p.Val731Ile)
 dbSNP
21g.43416757A>CCA410606182SIK1c.2337T>G (p.Phe779Leu)
c.2190T>G (p.Phe730Leu)
21g.43416757A>TCA410606183SIK1c.2337T>A (p.Phe779Leu)
c.2190T>A (p.Phe730Leu)
21g.43416758A>CCA410606184SIK1c.2336T>G (p.Phe779Cys)
c.2189T>G (p.Phe730Cys)
 gnomAD v4
21g.43416758A>GCA410606185SIK1c.2336T>C (p.Phe779Ser)
c.2189T>C (p.Phe730Ser)
21g.43416758A>TCA410606186SIK1c.2336T>A (p.Phe779Tyr)
c.2189T>A (p.Phe730Tyr)
21g.43416759A>CCA410606187SIK1c.2335T>G (p.Phe779Val)
c.2188T>G (p.Phe730Val)
 gnomAD v4
21g.43416759A>GCA410606188SIK1c.2335T>C (p.Phe779Leu)
c.2188T>C (p.Phe730Leu)
21g.43416759A>TCA410606189SIK1c.2335T>A (p.Phe779Ile)
c.2188T>A (p.Phe730Ile)
21g.43416760C>ACA749584618SIK1c.2334G>T (p.Thr778=)
c.2187G>T (p.Thr729=)
 dbSNP
21g.43416760C=CA2391216184SIK1c.2334G= (p.Thr778=)
c.2187G= (p.Thr729=)
21g.43416760C>TCA321324229SIK1c.2334G>A (p.Thr778=)
c.2187G>A (p.Thr729=)
 ClinVar dbSNP
21g.43416761G>ACA410606192SIK1c.2333C>T (p.Thr778Met)
c.2186C>T (p.Thr729Met)
 ClinVar dbSNP gnomAD v4
21g.43416761G>CCA410606190SIK1c.2333C>G (p.Thr778Arg)
c.2186C>G (p.Thr729Arg)
21g.43416761G=CA2391216185SIK1c.2333C= (p.Thr778=)
c.2186C= (p.Thr729=)
21g.43416761G>TCA410606191SIK1c.2333C>A (p.Thr778Lys)
c.2186C>A (p.Thr729Lys)
21g.43416762T>ACA410606193SIK1c.2332A>T (p.Thr778Ser)
c.2185A>T (p.Thr729Ser)
21g.43416762T>CCA410606194SIK1c.2332A>G (p.Thr778Ala)
c.2185A>G (p.Thr729Ala)
21g.43416762T>GCA410606195SIK1c.2332A>C (p.Thr778Pro)
c.2185A>C (p.Thr729Pro)
21g.43416764C>ACA410606196SIK1c.2330G>T (p.Gly777Val)
c.2183G>T (p.Gly728Val)
21g.43416764C>GCA410606197SIK1c.2330G>C (p.Gly777Ala)
c.2183G>C (p.Gly728Ala)
21g.43416764C>TCA410606198SIK1c.2330G>A (p.Gly777Asp)
c.2183G>A (p.Gly728Asp)
21g.43416765C>ACA410606199SIK1c.2329G>T (p.Gly777Cys)
c.2182G>T (p.Gly728Cys)
21g.43416765C>GCA410606200SIK1c.2329G>C (p.Gly777Arg)
c.2182G>C (p.Gly728Arg)
21g.43416765C>TCA410606201SIK1c.2329G>A (p.Gly777Ser)
c.2182G>A (p.Gly728Ser)
21g.43416767A>CCA410606202SIK1c.2327T>G (p.Leu776Arg)
c.2180T>G (p.Leu727Arg)
21g.43416767A>GCA410606203SIK1c.2327T>C (p.Leu776Pro)
c.2180T>C (p.Leu727Pro)
21g.43416767A>TCA410606204SIK1c.2327T>A (p.Leu776Gln)
c.2180T>A (p.Leu727Gln)
21g.43416768G>CCA410606206SIK1c.2326C>G (p.Leu776Val)
c.2179C>G (p.Leu727Val)
21g.43416768G>TCA410606205SIK1c.2326C>A (p.Leu776Ile)
c.2179C>A (p.Leu727Ile)
21g.43416770G>ACA410606207SIK1c.2324C>T (p.Ser775Phe)
c.2177C>T (p.Ser726Phe)
21g.43416770G>CCA410606209SIK1c.2324C>G (p.Ser775Cys)
c.2177C>G (p.Ser726Cys)
21g.43416770G>TCA410606208SIK1c.2324C>A (p.Ser775Tyr)
c.2177C>A (p.Ser726Tyr)
21g.43416771A>CCA410606210SIK1c.2323T>G (p.Ser775Ala)
c.2176T>G (p.Ser726Ala)
21g.43416771A>GCA410606211SIK1c.2323T>C (p.Ser775Pro)
c.2176T>C (p.Ser726Pro)
21g.43416771A>TCA410606212SIK1c.2323T>A (p.Ser775Thr)
c.2176T>A (p.Ser726Thr)
21g.43416772G>CCA410606213SIK1c.2322C>G (p.Cys774Trp)
c.2175C>G (p.Cys725Trp)
21g.43416772G>TCA410606214SIK1c.2322C>A (p.Cys774Ter)
c.2175C>A (p.Cys725Ter)
21g.43416773C>ACA410606215SIK1c.2321G>T (p.Cys774Phe)
c.2174G>T (p.Cys725Phe)
21g.43416773C>GCA410606216SIK1c.2321G>C (p.Cys774Ser)
c.2174G>C (p.Cys725Ser)
 ClinVar dbSNP
21g.43416773C>TCA410606217SIK1c.2321G>A (p.Cys774Tyr)
c.2174G>A (p.Cys725Tyr)
21g.43416774A=CA2391216186SIK1c.2320T= (p.Cys774=)
c.2173T= (p.Cys725=)
21g.43416774A>CCA321324230SIK1c.2320T>G (p.Cys774Gly)
c.2173T>G (p.Cys725Gly)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416774A>GCA410606218SIK1c.2320T>C (p.Cys774Arg)
c.2173T>C (p.Cys725Arg)
 ClinVar dbSNP
21g.43416774A>TCA410606219SIK1c.2320T>A (p.Cys774Ser)
c.2173T>A (p.Cys725Ser)
21g.43416776G>ACA410606222SIK1c.2318C>T (p.Pro773Leu)
c.2171C>T (p.Pro724Leu)
21g.43416776G>CCA410606221SIK1c.2318C>G (p.Pro773Arg)
c.2171C>G (p.Pro724Arg)
21g.43416776G>TCA410606220SIK1c.2318C>A (p.Pro773His)
c.2171C>A (p.Pro724His)
21g.43416777G>ACA410606223SIK1c.2317C>T (p.Pro773Ser)
c.2170C>T (p.Pro724Ser)
 dbSNP gnomAD v4
21g.43416777G>CCA321324233SIK1c.2317C>G (p.Pro773Ala)
c.2170C>G (p.Pro724Ala)
 dbSNP
21g.43416777G=CA2391216187SIK1c.2317C= (p.Pro773=)
c.2170C= (p.Pro724=)
21g.43416777G>TCA410606224SIK1c.2317C>A (p.Pro773Thr)
c.2170C>A (p.Pro724Thr)
21g.43416778C>ACA410606225SIK1c.2316G>T (p.Met772Ile)
c.2169G>T (p.Met723Ile)
21g.43416778C=CA2391216188SIK1c.2316G= (p.Met772=)
c.2169G= (p.Met723=)
21g.43416778C>GCA410606226SIK1c.2316G>C (p.Met772Ile)
c.2169G>C (p.Met723Ile)
21g.43416778C>TCA410606227SIK1c.2316G>A (p.Met772Ile)
c.2169G>A (p.Met723Ile)
 dbSNP gnomAD v4
21g.43416779A>CCA410606228SIK1c.2315T>G (p.Met772Arg)
c.2168T>G (p.Met723Arg)
21g.43416779A>GCA410606229SIK1c.2315T>C (p.Met772Thr)
c.2168T>C (p.Met723Thr)
21g.43416779A>TCA410606230SIK1c.2315T>A (p.Met772Lys)
c.2168T>A (p.Met723Lys)
21g.43416780T>ACA410606231SIK1c.2314A>T (p.Met772Leu)
c.2167A>T (p.Met723Leu)
21g.43416780T>CCA410606232SIK1c.2314A>G (p.Met772Val)
c.2167A>G (p.Met723Val)
21g.43416780T>GCA410606233SIK1c.2314A>C (p.Met772Leu)
c.2167A>C (p.Met723Leu)
21g.43416782A>CCA410606234SIK1c.2312T>G (p.Leu771Arg)
c.2165T>G (p.Leu722Arg)
21g.43416782A>GCA410606236SIK1c.2312T>C (p.Leu771Pro)
c.2165T>C (p.Leu722Pro)
21g.43416782A>TCA410606235SIK1c.2312T>A (p.Leu771Gln)
c.2165T>A (p.Leu722Gln)
21g.43416783G>ACA645601759SIK1c.2311C>T (p.Leu771=)
c.2164C>T (p.Leu722=)
 ClinVar dbSNP COSMIC
21g.43416783G>CCA410606237SIK1c.2311C>G (p.Leu771Val)
c.2164C>G (p.Leu722Val)
21g.43416783G>TCA410606238SIK1c.2311C>A (p.Leu771Met)
c.2164C>A (p.Leu722Met)
21g.43416784G>CCA410606239SIK1c.2310C>G (p.Asp770Glu)
c.2163C>G (p.Asp721Glu)
21g.43416784G>TCA410606240SIK1c.2310C>A (p.Asp770Glu)
c.2163C>A (p.Asp721Glu)
21g.43416785T>ACA410606241SIK1c.2309A>T (p.Asp770Val)
c.2162A>T (p.Asp721Val)
21g.43416785T>CCA410606242SIK1c.2309A>G (p.Asp770Gly)
c.2162A>G (p.Asp721Gly)
21g.43416785T>GCA410606243SIK1c.2309A>C (p.Asp770Ala)
c.2162A>C (p.Asp721Ala)
21g.43416786C>ACA410606244SIK1c.2308G>T (p.Asp770Tyr)
c.2161G>T (p.Asp721Tyr)
21g.43416786C=CA2391216189SIK1c.2308G= (p.Asp770=)
c.2161G= (p.Asp721=)
21g.43416786C>GCA410606245SIK1c.2308G>C (p.Asp770His)
c.2161G>C (p.Asp721His)
21g.43416786C>TCA410606246SIK1c.2308G>A (p.Asp770Asn)
c.2161G>A (p.Asp721Asn)
 dbSNP
21g.43416787C>ACA410606247SIK1c.2307G>T (p.Glu769Asp)
c.2160G>T (p.Glu720Asp)
21g.43416787C>GCA410606248SIK1c.2307G>C (p.Glu769Asp)
c.2160G>C (p.Glu720Asp)
21g.43416788T>ACA410606249SIK1c.2306A>T (p.Glu769Val)
c.2159A>T (p.Glu720Val)
21g.43416788T>CCA410606250SIK1c.2306A>G (p.Glu769Gly)
c.2159A>G (p.Glu720Gly)
21g.43416788T>GCA410606251SIK1c.2306A>C (p.Glu769Ala)
c.2159A>C (p.Glu720Ala)
21g.43416789C>ACA410606252SIK1c.2305G>T (p.Glu769Ter)
c.2158G>T (p.Glu720Ter)
21g.43416789C=CA2391216190SIK1c.2305G= (p.Glu769=)
c.2158G= (p.Glu720=)
21g.43416789C>GCA410606253SIK1c.2305G>C (p.Glu769Gln)
c.2158G>C (p.Glu720Gln)
21g.43416789C>TCA321324242SIK1c.2305G>A (p.Glu769Lys)
c.2158G>A (p.Glu720Lys)
 ClinVar dbSNP COSMIC
21g.43416790C>ACA410606254SIK1c.2304G>T (p.Met768Ile)
c.2157G>T (p.Met719Ile)
21g.43416790C>GCA410606255SIK1c.2304G>C (p.Met768Ile)
c.2157G>C (p.Met719Ile)
21g.43416790C>TCA410606256SIK1c.2304G>A (p.Met768Ile)
c.2157G>A (p.Met719Ile)
21g.43416791A>CCA410606257SIK1c.2303T>G (p.Met768Arg)
c.2156T>G (p.Met719Arg)
21g.43416791A>GCA410606258SIK1c.2303T>C (p.Met768Thr)
c.2156T>C (p.Met719Thr)
21g.43416791A>TCA410606259SIK1c.2303T>A (p.Met768Lys)
c.2156T>A (p.Met719Lys)
21g.43416792T>ACA410606260SIK1c.2302A>T (p.Met768Leu)
c.2155A>T (p.Met719Leu)
21g.43416792T>CCA410606261SIK1c.2302A>G (p.Met768Val)
c.2155A>G (p.Met719Val)
 ClinVar
21g.43416792T>GCA410606262SIK1c.2302A>C (p.Met768Leu)
c.2155A>C (p.Met719Leu)
21g.43416793C>ACA410606263SIK1c.2301G>T (p.Glu767Asp)
c.2154G>T (p.Glu718Asp)
21g.43416793C>GCA410606264SIK1c.2301G>C (p.Glu767Asp)
c.2154G>C (p.Glu718Asp)
21g.43416794T>ACA410606267SIK1c.2300A>T (p.Glu767Val)
c.2153A>T (p.Glu718Val)
21g.43416794T>CCA410606266SIK1c.2300A>G (p.Glu767Gly)
c.2153A>G (p.Glu718Gly)
21g.43416794T>GCA410606265SIK1c.2300A>C (p.Glu767Ala)
c.2153A>C (p.Glu718Ala)
21g.43416795C>ACA410606270SIK1c.2299G>T (p.Glu767Ter)
c.2152G>T (p.Glu718Ter)
21g.43416795C>GCA410606268SIK1c.2299G>C (p.Glu767Gln)
c.2152G>C (p.Glu718Gln)
21g.43416795C>TCA410606269SIK1c.2299G>A (p.Glu767Lys)
c.2152G>A (p.Glu718Lys)
21g.43416796A>CCA410606271SIK1c.2298T>G (p.Cys766Trp)
c.2151T>G (p.Cys717Trp)
 gnomAD v4
21g.43416796A>TCA410606272SIK1c.2298T>A (p.Cys766Ter)
c.2151T>A (p.Cys717Ter)
21g.43416797C>ACA410606273SIK1c.2297G>T (p.Cys766Phe)
c.2150G>T (p.Cys717Phe)
21g.43416797C>GCA410606274SIK1c.2297G>C (p.Cys766Ser)
c.2150G>C (p.Cys717Ser)
21g.43416797C>TCA410606275SIK1c.2297G>A (p.Cys766Tyr)
c.2150G>A (p.Cys717Tyr)
21g.43416798A>CCA410606276SIK1c.2296T>G (p.Cys766Gly)
c.2149T>G (p.Cys717Gly)
 gnomAD v4
21g.43416798A>GCA410606277SIK1c.2296T>C (p.Cys766Arg)
c.2149T>C (p.Cys717Arg)
21g.43416798A>TCA410606278SIK1c.2296T>A (p.Cys766Ser)
c.2149T>A (p.Cys717Ser)
21g.43416799G>ACA645601760SIK1c.2295C>T (p.Asp765=)
c.2148C>T (p.Asp716=)
 COSMIC
21g.43416799G>CCA410606279SIK1c.2295C>G (p.Asp765Glu)
c.2148C>G (p.Asp716Glu)
21g.43416799G>TCA410606280SIK1c.2295C>A (p.Asp765Glu)
c.2148C>A (p.Asp716Glu)
21g.43416800T>ACA410606282SIK1c.2294A>T (p.Asp765Val)
c.2147A>T (p.Asp716Val)
21g.43416800T>CCA410606283SIK1c.2294A>G (p.Asp765Gly)
c.2147A>G (p.Asp716Gly)
 gnomAD v4
21g.43416800T>GCA410606281SIK1c.2294A>C (p.Asp765Ala)
c.2147A>C (p.Asp716Ala)
 gnomAD v4
21g.43416801C>ACA321324244SIK1c.2293G>T (p.Asp765Tyr)
c.2146G>T (p.Asp716Tyr)
 ClinVar dbSNP gnomAD v4
21g.43416801C=CA2391216191SIK1c.2293G= (p.Asp765=)
c.2146G= (p.Asp716=)
21g.43416801C>GCA410606284SIK1c.2293G>C (p.Asp765His)
c.2146G>C (p.Asp716His)
21g.43416801C>TCA321324247SIK1c.2293G>A (p.Asp765Asn)
c.2146G>A (p.Asp716Asn)
 dbSNP
21g.43416802C=CA2391216192SIK1c.2292G= (p.Gly764=)
c.2145G= (p.Gly715=)
21g.43416802C>TCA749584666SIK1c.2292G>A (p.Gly764=)
c.2145G>A (p.Gly715=)
 dbSNP
21g.43416803C>ACA410606285SIK1c.2291G>T (p.Gly764Val)
c.2144G>T (p.Gly715Val)
21g.43416803C=CA2391216193SIK1c.2291G= (p.Gly764=)
c.2144G= (p.Gly715=)
21g.43416803C>GCA410606286SIK1c.2291G>C (p.Gly764Ala)
c.2144G>C (p.Gly715Ala)
21g.43416803C>TCA410606287SIK1c.2291G>A (p.Gly764Glu)
c.2144G>A (p.Gly715Glu)
 dbSNP
21g.43416804C>ACA410606288SIK1c.2290G>T (p.Gly764Trp)
c.2143G>T (p.Gly715Trp)
21g.43416804C>GCA410606290SIK1c.2290G>C (p.Gly764Arg)
c.2143G>C (p.Gly715Arg)
21g.43416804C>TCA410606289SIK1c.2290G>A (p.Gly764Arg)
c.2143G>A (p.Gly715Arg)
21g.43416805C>ACA410606291SIK1c.2289G>T (p.Gln763His)
c.2142G>T (p.Gln714His)
21g.43416805C>GCA410606292SIK1c.2289G>C (p.Gln763His)
c.2142G>C (p.Gln714His)
21g.43416805C>TCA2654732708SIK1c.2289G>A (p.Gln763=)
c.2142G>A (p.Gln714=)
 gnomAD v4
21g.43416806T>ACA410606293SIK1c.2288A>T (p.Gln763Leu)
c.2141A>T (p.Gln714Leu)
 gnomAD v4
21g.43416806T>CCA410606294SIK1c.2288A>G (p.Gln763Arg)
c.2141A>G (p.Gln714Arg)
21g.43416806T>GCA410606295SIK1c.2288A>C (p.Gln763Pro)
c.2141A>C (p.Gln714Pro)
 gnomAD v4
21g.43416807G>ACA410606297SIK1c.2287C>T (p.Gln763Ter)
c.2140C>T (p.Gln714Ter)
21g.43416807G>CCA410606298SIK1c.2287C>G (p.Gln763Glu)
c.2140C>G (p.Gln714Glu)
21g.43416807G>TCA410606296SIK1c.2287C>A (p.Gln763Lys)
c.2140C>A (p.Gln714Lys)
21g.43416808C=CA2391216194SIK1c.2286G= (p.Leu762=)
c.2139G= (p.Leu713=)
21g.43416808C>TCA749584676SIK1c.2286G>A (p.Leu762=)
c.2139G>A (p.Leu713=)
 dbSNP gnomAD v4
21g.43416809A>CCA410606299SIK1c.2285T>G (p.Leu762Arg)
c.2138T>G (p.Leu713Arg)
21g.43416809A>GCA410606301SIK1c.2285T>C (p.Leu762Pro)
c.2138T>C (p.Leu713Pro)
21g.43416809A>TCA410606300SIK1c.2285T>A (p.Leu762Gln)
c.2138T>A (p.Leu713Gln)
21g.43416810G>ACA2818014358SIK1c.2284C>T (p.Leu762=)
c.2137C>T (p.Leu713=)
21g.43416810G>CCA410606302SIK1c.2284C>G (p.Leu762Val)
c.2137C>G (p.Leu713Val)
21g.43416810G>TCA410606303SIK1c.2284C>A (p.Leu762Met)
c.2137C>A (p.Leu713Met)
21g.43416811C=CA2391216195SIK1c.2283G= (p.Leu761=)
c.2136G= (p.Leu712=)
21g.43416811C>TCA321324250SIK1c.2283G>A (p.Leu761=)
c.2136G>A (p.Leu712=)
 dbSNP
21g.43416812A>CCA410606304SIK1c.2282T>G (p.Leu761Arg)
c.2135T>G (p.Leu712Arg)
21g.43416812A>GCA410606305SIK1c.2282T>C (p.Leu761Pro)
c.2135T>C (p.Leu712Pro)
21g.43416812A>TCA410606306SIK1c.2282T>A (p.Leu761Gln)
c.2135T>A (p.Leu712Gln)
21g.43416813G>CCA410606307SIK1c.2281C>G (p.Leu761Val)
c.2134C>G (p.Leu712Val)
21g.43416813G>TCA410606308SIK1c.2281C>A (p.Leu761Met)
c.2134C>A (p.Leu712Met)
21g.43416814C>ACA321324253SIK1c.2280G>T (p.Gly760=)
c.2133G>T (p.Gly711=)
 dbSNP
21g.43416814C=CA2391216196SIK1c.2280G= (p.Gly760=)
c.2133G= (p.Gly711=)
21g.43416815C>ACA410606309SIK1c.2279G>T (p.Gly760Val)
c.2132G>T (p.Gly711Val)
 dbSNP
21g.43416815C=CA2391216197SIK1c.2279G= (p.Gly760=)
c.2132G= (p.Gly711=)
21g.43416815C>GCA410606310SIK1c.2279G>C (p.Gly760Ala)
c.2132G>C (p.Gly711Ala)
21g.43416815C>TCA410606311SIK1c.2279G>A (p.Gly760Glu)
c.2132G>A (p.Gly711Glu)
 ClinVar dbSNP
21g.43416816C>ACA410606314SIK1c.2278G>T (p.Gly760Trp)
c.2131G>T (p.Gly711Trp)
21g.43416816C>GCA410606312SIK1c.2278G>C (p.Gly760Arg)
c.2131G>C (p.Gly711Arg)
21g.43416816C>TCA410606313SIK1c.2278G>A (p.Gly760Arg)
c.2131G>A (p.Gly711Arg)
21g.43416818A>CCA410606315SIK1c.2276T>G (p.Leu759Arg)
c.2129T>G (p.Leu710Arg)
21g.43416818A>GCA410606316SIK1c.2276T>C (p.Leu759Pro)
c.2129T>C (p.Leu710Pro)
21g.43416818A>TCA410606317SIK1c.2276T>A (p.Leu759Gln)
c.2129T>A (p.Leu710Gln)
21g.43416819G>CCA410606318SIK1c.2275C>G (p.Leu759Val)
c.2128C>G (p.Leu710Val)
21g.43416819G>TCA410606319SIK1c.2275C>A (p.Leu759Met)
c.2128C>A (p.Leu710Met)
21g.43416820G>ACA2818014360SIK1c.2274C>T (p.Pro758=)
c.2127C>T (p.Pro709=)
21g.43416821G>ACA410606320SIK1c.2273C>T (p.Pro758Leu)
c.2126C>T (p.Pro709Leu)
 COSMIC
21g.43416821G>CCA410606321SIK1c.2273C>G (p.Pro758Arg)
c.2126C>G (p.Pro709Arg)
21g.43416821G>TCA410606322SIK1c.2273C>A (p.Pro758His)
c.2126C>A (p.Pro709His)
21g.43416822G>ACA410606323SIK1c.2272C>T (p.Pro758Ser)
c.2125C>T (p.Pro709Ser)
 ClinVar dbSNP
21g.43416822G>CCA410606324SIK1c.2272C>G (p.Pro758Ala)
c.2125C>G (p.Pro709Ala)
21g.43416822G=CA2391216198SIK1c.2272C= (p.Pro758=)
c.2125C= (p.Pro709=)
21g.43416822G>TCA410606325SIK1c.2272C>A (p.Pro758Thr)
c.2125C>A (p.Pro709Thr)
21g.43416823C>ACA410606326SIK1c.2271G>T (p.Glu757Asp)
c.2124G>T (p.Glu708Asp)
21g.43416823C=CA2391216199SIK1c.2271G= (p.Glu757=)
c.2124G= (p.Glu708=)
21g.43416823C>GCA410606327SIK1c.2271G>C (p.Glu757Asp)
c.2124G>C (p.Glu708Asp)
21g.43416823C>TCA749584699SIK1c.2271G>A (p.Glu757=)
c.2124G>A (p.Glu708=)
 dbSNP
21g.43416824T>ACA410606328SIK1c.2270A>T (p.Glu757Val)
c.2123A>T (p.Glu708Val)
21g.43416824T>CCA410606329SIK1c.2270A>G (p.Glu757Gly)
c.2123A>G (p.Glu708Gly)
21g.43416824T>GCA410606330SIK1c.2270A>C (p.Glu757Ala)
c.2123A>C (p.Glu708Ala)
21g.43416825C>ACA410606331SIK1c.2269G>T (p.Glu757Ter)
c.2122G>T (p.Glu708Ter)
21g.43416825C>GCA410606332SIK1c.2269G>C (p.Glu757Gln)
c.2122G>C (p.Glu708Gln)
21g.43416825C>TCA410606333SIK1c.2269G>A (p.Glu757Lys)
c.2122G>A (p.Glu708Lys)
21g.43416826A>CCA410606335SIK1c.2268T>G (p.Cys756Trp)
c.2121T>G (p.Cys707Trp)
21g.43416826A>TCA410606334SIK1c.2268T>A (p.Cys756Ter)
c.2121T>A (p.Cys707Ter)
21g.43416827C>ACA410606336SIK1c.2267G>T (p.Cys756Phe)
c.2120G>T (p.Cys707Phe)
21g.43416827C>GCA410606337SIK1c.2267G>C (p.Cys756Ser)
c.2120G>C (p.Cys707Ser)
21g.43416827C>TCA410606338SIK1c.2267G>A (p.Cys756Tyr)
c.2120G>A (p.Cys707Tyr)
21g.43416828A>CCA410606339SIK1c.2266T>G (p.Cys756Gly)
c.2119T>G (p.Cys707Gly)
 gnomAD v4
21g.43416828A>GCA410606340SIK1c.2266T>C (p.Cys756Arg)
c.2119T>C (p.Cys707Arg)
21g.43416828A>TCA410606341SIK1c.2266T>A (p.Cys756Ser)
c.2119T>A (p.Cys707Ser)
21g.43416829A>CCA2654732709SIK1c.2265T>G (p.Gly755=)
c.2118T>G (p.Gly706=)
 gnomAD v4
21g.43416830C>ACA410606342SIK1c.2264G>T (p.Gly755Val)
c.2117G>T (p.Gly706Val)
21g.43416830C=CA2391216200SIK1c.2264G= (p.Gly755=)
c.2117G= (p.Gly706=)
21g.43416830C>GCA410606344SIK1c.2264G>C (p.Gly755Ala)
c.2117G>C (p.Gly706Ala)
21g.43416830C>TCA410606343SIK1c.2264G>A (p.Gly755Asp)
c.2117G>A (p.Gly706Asp)
 dbSNP
21g.43416831C>ACA410606345SIK1c.2263G>T (p.Gly755Cys)
c.2116G>T (p.Gly706Cys)
21g.43416831C>GCA410606346SIK1c.2263G>C (p.Gly755Arg)
c.2116G>C (p.Gly706Arg)
 ClinVar
21g.43416831C>TCA410606347SIK1c.2263G>A (p.Gly755Ser)
c.2116G>A (p.Gly706Ser)
21g.43416832T>ACA321324257SIK1c.2262A>T (p.Pro754=)
c.2115A>T (p.Pro705=)
 dbSNP
21g.43416832T>GCA2391216202SIK1c.2262A>C (p.Pro754=)
c.2115A>C (p.Pro705=)
 dbSNP gnomAD v4
21g.43416832T=CA2391216201SIK1c.2262A= (p.Pro754=)
c.2115A= (p.Pro705=)
21g.43416833G>ACA410606348SIK1c.2261C>T (p.Pro754Leu)
c.2114C>T (p.Pro705Leu)
 dbSNP
21g.43416833G>CCA410606349SIK1c.2261C>G (p.Pro754Arg)
c.2114C>G (p.Pro705Arg)
21g.43416833G=CA2391216203SIK1c.2261C= (p.Pro754=)
c.2114C= (p.Pro705=)
21g.43416833G>TCA410606350SIK1c.2261C>A (p.Pro754Gln)
c.2114C>A (p.Pro705Gln)
21g.43416834G>ACA410606351SIK1c.2260C>T (p.Pro754Ser)
c.2113C>T (p.Pro705Ser)
21g.43416834G>CCA410606352SIK1c.2260C>G (p.Pro754Ala)
c.2113C>G (p.Pro705Ala)
21g.43416834G>TCA410606353SIK1c.2260C>A (p.Pro754Thr)
c.2113C>A (p.Pro705Thr)
21g.43416836G>ACA410606354SIK1c.2258C>T (p.Ala753Val)
c.2111C>T (p.Ala704Val)
 ClinVar dbSNP
21g.43416836G>CCA410606356SIK1c.2258C>G (p.Ala753Gly)
c.2111C>G (p.Ala704Gly)
 ClinVar dbSNP gnomAD v4
21g.43416836G=CA2391216204SIK1c.2258C= (p.Ala753=)
c.2111C= (p.Ala704=)
21g.43416836G>TCA410606355SIK1c.2258C>A (p.Ala753Asp)
c.2111C>A (p.Ala704Asp)
 dbSNP
21g.43416837C>ACA321324264SIK1c.2257G>T (p.Ala753Ser)
c.2110G>T (p.Ala704Ser)
 ClinVar dbSNP
21g.43416837C=CA2391216206SIK1c.2257G= (p.Ala753=)
c.2110G= (p.Ala704=)
21g.43416837C>GCA410606358SIK1c.2257G>C (p.Ala753Pro)
c.2110G>C (p.Ala704Pro)
21g.43416837C>TCA410606357SIK1c.2257G>A (p.Ala753Thr)
c.2110G>A (p.Ala704Thr)
 dbSNP gnomAD v3 gnomAD v4
21g.43416837_43416838delinsATCA915952648SIK1c.2256_2257delinsAT (p.Ala753Ser)
c.2109_2110delinsAT (p.Ala704Ser)
 ClinVar dbSNP
21g.43416837_43416838delinsCCCA2391216205SIK1c.2256_2257delinsGG (p.Leu752=)
c.2109_2110delinsGG (p.Leu703=)

Number of alleles fetched