Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
 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=)
21g.43416838C=CA2391216207SIK1c.2256G= (p.Leu752=)
c.2109G= (p.Leu703=)
21g.43416838C>TCA321324268SIK1c.2256G>A (p.Leu752=)
c.2109G>A (p.Leu703=)
 dbSNP
21g.43416839A>CCA410606360SIK1c.2255T>G (p.Leu752Arg)
c.2108T>G (p.Leu703Arg)
21g.43416839A>GCA410606359SIK1c.2255T>C (p.Leu752Pro)
c.2108T>C (p.Leu703Pro)
 ClinVar
21g.43416839A>TCA410606361SIK1c.2255T>A (p.Leu752Gln)
c.2108T>A (p.Leu703Gln)
21g.43416840G>CCA410606362SIK1c.2254C>G (p.Leu752Val)
c.2107C>G (p.Leu703Val)
21g.43416840G>TCA410606363SIK1c.2254C>A (p.Leu752Met)
c.2107C>A (p.Leu703Met)
21g.43416841C>ACA410606364SIK1c.2253G>T (p.Arg751Ser)
c.2106G>T (p.Arg702Ser)
21g.43416841C=CA2391216208SIK1c.2253G= (p.Arg751=)
c.2106G= (p.Arg702=)
21g.43416841C>GCA321324272SIK1c.2253G>C (p.Arg751Ser)
c.2106G>C (p.Arg702Ser)
 dbSNP
21g.43416842C>ACA410606365SIK1c.2252G>T (p.Arg751Met)
c.2105G>T (p.Arg702Met)
21g.43416842C=CA2391216209SIK1c.2252G= (p.Arg751=)
c.2105G= (p.Arg702=)
21g.43416842C>GCA410606366SIK1c.2252G>C (p.Arg751Thr)
c.2105G>C (p.Arg702Thr)
 dbSNP
21g.43416842C>TCA410606367SIK1c.2252G>A (p.Arg751Lys)
c.2105G>A (p.Arg702Lys)
21g.43416843T>ACA410606368SIK1c.2251A>T (p.Arg751Trp)
c.2104A>T (p.Arg702Trp)
21g.43416843T>CCA410606369SIK1c.2251A>G (p.Arg751Gly)
c.2104A>G (p.Arg702Gly)
21g.43416843T>GCA2518212919SIK1c.2251A>C (p.Arg751=)
c.2104A>C (p.Arg702=)
21g.43416844G>ACA2580098747SIK1c.2250C>T (p.Ala750=)
c.2103C>T (p.Ala701=)
 ClinVar
21g.43416845G>ACA410606370SIK1c.2249C>T (p.Ala750Val)
c.2102C>T (p.Ala701Val)
21g.43416845G>CCA410606371SIK1c.2249C>G (p.Ala750Gly)
c.2102C>G (p.Ala701Gly)
21g.43416845G>TCA410606372SIK1c.2249C>A (p.Ala750Asp)
c.2102C>A (p.Ala701Asp)
21g.43416846C>ACA410606375SIK1c.2248G>T (p.Ala750Ser)
c.2101G>T (p.Ala701Ser)
21g.43416846C>GCA410606373SIK1c.2248G>C (p.Ala750Pro)
c.2101G>C (p.Ala701Pro)
21g.43416846C>TCA410606374SIK1c.2248G>A (p.Ala750Thr)
c.2101G>A (p.Ala701Thr)
21g.43416847delCA2654732710SIK1c.2248del (p.Ala750ProfsTer22)
c.2101del (p.Ala701ProfsTer22)
 gnomAD v4
21g.43416848A>CCA410606376SIK1c.2246T>G (p.Leu749Arg)
c.2099T>G (p.Leu700Arg)
21g.43416848A>GCA410606377SIK1c.2246T>C (p.Leu749Pro)
c.2099T>C (p.Leu700Pro)
21g.43416848A>TCA410606378SIK1c.2246T>A (p.Leu749Gln)
c.2099T>A (p.Leu700Gln)
21g.43416849G>ACA2818014365SIK1c.2245C>T (p.Leu749=)
c.2098C>T (p.Leu700=)
21g.43416849G>CCA410606379SIK1c.2245C>G (p.Leu749Val)
c.2098C>G (p.Leu700Val)
21g.43416849G>TCA410606380SIK1c.2245C>A (p.Leu749Met)
c.2098C>A (p.Leu700Met)
21g.43416851C>ACA321324284SIK1c.2243G>T (p.Arg748Leu)
c.2096G>T (p.Arg699Leu)
 ClinVar dbSNP gnomAD v4
21g.43416851C=CA2391216210SIK1c.2243G= (p.Arg748=)
c.2096G= (p.Arg699=)
21g.43416851C>GCA410606381SIK1c.2243G>C (p.Arg748Pro)
c.2096G>C (p.Arg699Pro)
21g.43416851C>TCA321324276SIK1c.2243G>A (p.Arg748His)
c.2096G>A (p.Arg699His)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416852G>ACA321324287SIK1c.2242C>T (p.Arg748Cys)
c.2095C>T (p.Arg699Cys)
 ClinVar dbSNP gnomAD v4
21g.43416852G>CCA410606382SIK1c.2242C>G (p.Arg748Gly)
c.2095C>G (p.Arg699Gly)
21g.43416852G=CA2391216211SIK1c.2242C= (p.Arg748=)
c.2095C= (p.Arg699=)
21g.43416852G>TCA410606383SIK1c.2242C>A (p.Arg748Ser)
c.2095C>A (p.Arg699Ser)
21g.43416854G>ACA410606386SIK1c.2240C>T (p.Pro747Leu)
c.2093C>T (p.Pro698Leu)
21g.43416854G>CCA410606385SIK1c.2240C>G (p.Pro747Arg)
c.2093C>G (p.Pro698Arg)
21g.43416854G>TCA410606384SIK1c.2240C>A (p.Pro747Gln)
c.2093C>A (p.Pro698Gln)
21g.43416855G>ACA410606387SIK1c.2239C>T (p.Pro747Ser)
c.2092C>T (p.Pro698Ser)
21g.43416855G>CCA410606388SIK1c.2239C>G (p.Pro747Ala)
c.2092C>G (p.Pro698Ala)
21g.43416855G>TCA410606389SIK1c.2239C>A (p.Pro747Thr)
c.2092C>A (p.Pro698Thr)
21g.43416856T>CCA2739267692SIK1c.2238A>G (p.Pro746=)
c.2091A>G (p.Pro697=)
 ClinVar
21g.43416856T>GCA2654732711SIK1c.2238A>C (p.Pro746=)
c.2091A>C (p.Pro697=)
 gnomAD v4
21g.43416857G>ACA410606390SIK1c.2237C>T (p.Pro746Leu)
c.2090C>T (p.Pro697Leu)
21g.43416857G>CCA410606391SIK1c.2237C>G (p.Pro746Arg)
c.2090C>G (p.Pro697Arg)
21g.43416857G>TCA410606392SIK1c.2237C>A (p.Pro746Gln)
c.2090C>A (p.Pro697Gln)
21g.43416858G>ACA410606393SIK1c.2236C>T (p.Pro746Ser)
c.2089C>T (p.Pro697Ser)
21g.43416858G>CCA410606394SIK1c.2236C>G (p.Pro746Ala)
c.2089C>G (p.Pro697Ala)
21g.43416858G>TCA410606395SIK1c.2236C>A (p.Pro746Thr)
c.2089C>A (p.Pro697Thr)
21g.43416860G>ACA410606396SIK1c.2234C>T (p.Pro745Leu)
c.2087C>T (p.Pro696Leu)
21g.43416860G>CCA410606397SIK1c.2234C>G (p.Pro745Arg)
c.2087C>G (p.Pro696Arg)
21g.43416860G>TCA410606398SIK1c.2234C>A (p.Pro745His)
c.2087C>A (p.Pro696His)
21g.43416861G>ACA410606401SIK1c.2233C>T (p.Pro745Ser)
c.2086C>T (p.Pro696Ser)
21g.43416861G>CCA410606399SIK1c.2233C>G (p.Pro745Ala)
c.2086C>G (p.Pro696Ala)
21g.43416861G>TCA410606400SIK1c.2233C>A (p.Pro745Thr)
c.2086C>A (p.Pro696Thr)
21g.43416862C>TCA645601761SIK1c.2232G>A (p.Val744=)
c.2085G>A (p.Val695=)
 COSMIC
21g.43416863A>CCA410606402SIK1c.2231T>G (p.Val744Gly)
c.2084T>G (p.Val695Gly)
21g.43416863A>GCA410606403SIK1c.2231T>C (p.Val744Ala)
c.2084T>C (p.Val695Ala)
21g.43416863A>TCA410606404SIK1c.2231T>A (p.Val744Glu)
c.2084T>A (p.Val695Glu)
21g.43416864C>ACA410606405SIK1c.2230G>T (p.Val744Leu)
c.2083G>T (p.Val695Leu)
21g.43416864C=CA2391216212SIK1c.2230G= (p.Val744=)
c.2083G= (p.Val695=)
21g.43416864C>GCA410606406SIK1c.2230G>C (p.Val744Leu)
c.2083G>C (p.Val695Leu)
 ClinVar
21g.43416864C>TCA321324291SIK1c.2230G>A (p.Val744Met)
c.2083G>A (p.Val695Met)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416865A>CCA2654732712SIK1c.2229T>G (p.Ala743=)
c.2082T>G (p.Ala694=)
 gnomAD v4
21g.43416866G>ACA410606407SIK1c.2228C>T (p.Ala743Val)
c.2081C>T (p.Ala694Val)
21g.43416866G>CCA410606408SIK1c.2228C>G (p.Ala743Gly)
c.2081C>G (p.Ala694Gly)
 dbSNP
21g.43416866G>TCA410606409SIK1c.2228C>A (p.Ala743Asp)
c.2081C>A (p.Ala694Asp)
 dbSNP
21g.43416867C>ACA410606410SIK1c.2227G>T (p.Ala743Ser)
c.2080G>T (p.Ala694Ser)
21g.43416867C=CA2391216213SIK1c.2227G= (p.Ala743=)
c.2080G= (p.Ala694=)
21g.43416867C>GCA410606411SIK1c.2227G>C (p.Ala743Pro)
c.2080G>C (p.Ala694Pro)
21g.43416867C>TCA321324294SIK1c.2227G>A (p.Ala743Thr)
c.2080G>A (p.Ala694Thr)
 ClinVar dbSNP gnomAD v4
21g.43416868G>ACA321324296SIK1c.2226C>T (p.Pro742=)
c.2079C>T (p.Pro693=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416868G>CCA321324300SIK1c.2226C>G (p.Pro742=)
c.2079C>G (p.Pro693=)
 ClinVar dbSNP gnomAD v4
21g.43416868G=CA2391216214SIK1c.2226C= (p.Pro742=)
c.2079C= (p.Pro693=)
21g.43416869G>ACA321324320SIK1c.2225C>T (p.Pro742Leu)
c.2078C>T (p.Pro693Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416869G>CCA410606413SIK1c.2225C>G (p.Pro742Arg)
c.2078C>G (p.Pro693Arg)
21g.43416869G=CA2391216215SIK1c.2225C= (p.Pro742=)
c.2078C= (p.Pro693=)
21g.43416869G>TCA410606412SIK1c.2225C>A (p.Pro742His)
c.2078C>A (p.Pro693His)
21g.43416870G>ACA410606414SIK1c.2224C>T (p.Pro742Ser)
c.2077C>T (p.Pro693Ser)
 COSMIC
21g.43416870G>CCA410606415SIK1c.2224C>G (p.Pro742Ala)
c.2077C>G (p.Pro693Ala)
21g.43416870G>TCA410606416SIK1c.2224C>A (p.Pro742Thr)
c.2077C>A (p.Pro693Thr)
21g.43416872A=CA2391216216SIK1c.2222T= (p.Leu741=)
c.2075T= (p.Leu692=)
21g.43416872A>CCA410606417SIK1c.2222T>G (p.Leu741Arg)
c.2075T>G (p.Leu692Arg)
 ClinVar dbSNP
21g.43416872A>GCA410606418SIK1c.2222T>C (p.Leu741Pro)
c.2075T>C (p.Leu692Pro)
21g.43416872A>TCA410606419SIK1c.2222T>A (p.Leu741His)
c.2075T>A (p.Leu692His)
21g.43416873G>ACA410606420SIK1c.2221C>T (p.Leu741Phe)
c.2074C>T (p.Leu692Phe)
21g.43416873G>CCA410606421SIK1c.2221C>G (p.Leu741Val)
c.2074C>G (p.Leu692Val)
21g.43416873G>TCA410606422SIK1c.2221C>A (p.Leu741Ile)
c.2074C>A (p.Leu692Ile)
21g.43416874G>ACA2739267693SIK1c.2220C>T (p.Ala740=)
c.2073C>T (p.Ala691=)
 ClinVar
21g.43416875G>ACA410606423SIK1c.2219C>T (p.Ala740Val)
c.2072C>T (p.Ala691Val)
21g.43416875G>CCA410606424SIK1c.2219C>G (p.Ala740Gly)
c.2072C>G (p.Ala691Gly)
21g.43416875G>TCA410606425SIK1c.2219C>A (p.Ala740Asp)
c.2072C>A (p.Ala691Asp)
21g.43416876C>ACA410606427SIK1c.2218G>T (p.Ala740Ser)
c.2071G>T (p.Ala691Ser)
21g.43416876C=CA2391216217SIK1c.2218G= (p.Ala740=)
c.2071G= (p.Ala691=)
21g.43416876C>GCA410606426SIK1c.2218G>C (p.Ala740Pro)
c.2071G>C (p.Ala691Pro)
21g.43416876C>TCA321324323SIK1c.2218G>A (p.Ala740Thr)
c.2071G>A (p.Ala691Thr)
 ClinVar dbSNP gnomAD v4
21g.43416877G>ACA321324326SIK1c.2217C>T (p.Thr739=)
c.2070C>T (p.Thr690=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416877G=CA2391216218SIK1c.2217C= (p.Thr739=)
c.2070C= (p.Thr690=)
21g.43416878G>ACA410606428SIK1c.2216C>T (p.Thr739Ile)
c.2069C>T (p.Thr690Ile)
21g.43416878G>CCA410606429SIK1c.2216C>G (p.Thr739Ser)
c.2069C>G (p.Thr690Ser)
21g.43416878G>TCA410606430SIK1c.2216C>A (p.Thr739Asn)
c.2069C>A (p.Thr690Asn)
21g.43416879T>ACA410606431SIK1c.2215A>T (p.Thr739Ser)
c.2068A>T (p.Thr690Ser)
 gnomAD v4
21g.43416879T>CCA410606432SIK1c.2215A>G (p.Thr739Ala)
c.2068A>G (p.Thr690Ala)
21g.43416879T>GCA410606433SIK1c.2215A>C (p.Thr739Pro)
c.2068A>C (p.Thr690Pro)
21g.43416880G>ACA749584756SIK1c.2214C>T (p.Pro738=)
c.2067C>T (p.Pro689=)
 dbSNP
21g.43416880G=CA2391216219SIK1c.2214C= (p.Pro738=)
c.2067C= (p.Pro689=)
21g.43416881G>ACA410606434SIK1c.2213C>T (p.Pro738Leu)
c.2066C>T (p.Pro689Leu)
21g.43416881G>CCA410606435SIK1c.2213C>G (p.Pro738Arg)
c.2066C>G (p.Pro689Arg)
21g.43416881G>TCA410606436SIK1c.2213C>A (p.Pro738His)
c.2066C>A (p.Pro689His)
21g.43416882G>ACA410606439SIK1c.2212C>T (p.Pro738Ser)
c.2065C>T (p.Pro689Ser)
21g.43416882G>CCA410606438SIK1c.2212C>G (p.Pro738Ala)
c.2065C>G (p.Pro689Ala)
 gnomAD v4
21g.43416882G>TCA410606437SIK1c.2212C>A (p.Pro738Thr)
c.2065C>A (p.Pro689Thr)
21g.43416883G>ACA321324329SIK1c.2211C>T (p.Gly737=)
c.2064C>T (p.Gly688=)
 ClinVar dbSNP
21g.43416883G=CA2391216220SIK1c.2211C= (p.Gly737=)
c.2064C= (p.Gly688=)
21g.43416884C>ACA410606440SIK1c.2210G>T (p.Gly737Val)
c.2063G>T (p.Gly688Val)
 COSMIC
21g.43416884C>GCA410606441SIK1c.2210G>C (p.Gly737Ala)
c.2063G>C (p.Gly688Ala)
21g.43416884C>TCA410606442SIK1c.2210G>A (p.Gly737Asp)
c.2063G>A (p.Gly688Asp)
21g.43416885C>ACA410606443SIK1c.2209G>T (p.Gly737Cys)
c.2062G>T (p.Gly688Cys)
 dbSNP
21g.43416885C=CA2391216221SIK1c.2209G= (p.Gly737=)
c.2062G= (p.Gly688=)
21g.43416885C>GCA410606444SIK1c.2209G>C (p.Gly737Arg)
c.2062G>C (p.Gly688Arg)
21g.43416885C>TCA321324332SIK1c.2209G>A (p.Gly737Ser)
c.2062G>A (p.Gly688Ser)
 ClinVar dbSNP gnomAD v4
21g.43416886G>ACA321324333SIK1c.2208C>T (p.Thr736=)
c.2061C>T (p.Thr687=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416886G>CCA321324336SIK1c.2208C>G (p.Thr736=)
c.2061C>G (p.Thr687=)
 ClinVar dbSNP
21g.43416886G=CA2391216222SIK1c.2208C= (p.Thr736=)
c.2061C= (p.Thr687=)
21g.43416887G>ACA410606445SIK1c.2207C>T (p.Thr736Ile)
c.2060C>T (p.Thr687Ile)
21g.43416887G>CCA410606446SIK1c.2207C>G (p.Thr736Ser)
c.2060C>G (p.Thr687Ser)
21g.43416887G>TCA410606447SIK1c.2207C>A (p.Thr736Asn)
c.2060C>A (p.Thr687Asn)
21g.43416888T>ACA410606448SIK1c.2206A>T (p.Thr736Ser)
c.2059A>T (p.Thr687Ser)
21g.43416888T>CCA410606449SIK1c.2206A>G (p.Thr736Ala)
c.2059A>G (p.Thr687Ala)
21g.43416888T>GCA410606450SIK1c.2206A>C (p.Thr736Pro)
c.2059A>C (p.Thr687Pro)
21g.43416890C>ACA410606451SIK1c.2204G>T (p.Gly735Val)
c.2057G>T (p.Gly686Val)
21g.43416890C=CA2391216223SIK1c.2204G= (p.Gly735=)
c.2057G= (p.Gly686=)
21g.43416890C>GCA410606452SIK1c.2204G>C (p.Gly735Ala)
c.2057G>C (p.Gly686Ala)
21g.43416890C>TCA321324346SIK1c.2204G>A (p.Gly735Asp)
c.2057G>A (p.Gly686Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416891C>ACA410606453SIK1c.2203G>T (p.Gly735Cys)
c.2056G>T (p.Gly686Cys)
21g.43416891C>GCA410606454SIK1c.2203G>C (p.Gly735Arg)
c.2056G>C (p.Gly686Arg)
21g.43416891C>TCA410606455SIK1c.2203G>A (p.Gly735Ser)
c.2056G>A (p.Gly686Ser)
21g.43416892A=CA2391216224SIK1c.2202T= (p.Ile734=)
c.2055T= (p.Ile685=)
21g.43416892A>CCA410606456SIK1c.2202T>G (p.Ile734Met)
c.2055T>G (p.Ile685Met)
21g.43416892A>GCA321324348SIK1c.2202T>C (p.Ile734=)
c.2055T>C (p.Ile685=)
 ClinVar dbSNP
21g.43416893A=CA2391216225SIK1c.2201T= (p.Ile734=)
c.2054T= (p.Ile685=)
21g.43416893A>CCA410606457SIK1c.2201T>G (p.Ile734Ser)
c.2054T>G (p.Ile685Ser)
 gnomAD v4
21g.43416893A>GCA321324351SIK1c.2201T>C (p.Ile734Thr)
c.2054T>C (p.Ile685Thr)
 ClinVar dbSNP
21g.43416893A>TCA410606458SIK1c.2201T>A (p.Ile734Asn)
c.2054T>A (p.Ile685Asn)
21g.43416894T>ACA410606459SIK1c.2200A>T (p.Ile734Phe)
c.2053A>T (p.Ile685Phe)
21g.43416894T>CCA410606460SIK1c.2200A>G (p.Ile734Val)
c.2053A>G (p.Ile685Val)
21g.43416894T>GCA410606461SIK1c.2200A>C (p.Ile734Leu)
c.2053A>C (p.Ile685Leu)
 ClinVar
21g.43416895G>CCA410606463SIK1c.2199C>G (p.His733Gln)
c.2052C>G (p.His684Gln)
21g.43416895G>TCA410606462SIK1c.2199C>A (p.His733Gln)
c.2052C>A (p.His684Gln)
21g.43416896T>ACA410606464SIK1c.2198A>T (p.His733Leu)
c.2051A>T (p.His684Leu)
21g.43416896T>CCA410606466SIK1c.2198A>G (p.His733Arg)
c.2051A>G (p.His684Arg)
21g.43416896T>GCA410606465SIK1c.2198A>C (p.His733Pro)
c.2051A>C (p.His684Pro)
21g.43416897G>ACA410606467SIK1c.2197C>T (p.His733Tyr)
c.2050C>T (p.His684Tyr)
21g.43416897G>CCA410606468SIK1c.2197C>G (p.His733Asp)
c.2050C>G (p.His684Asp)
21g.43416897G>TCA410606469SIK1c.2197C>A (p.His733Asn)
c.2050C>A (p.His684Asn)
21g.43416898C=CA2391216226SIK1c.2196G= (p.Leu732=)
c.2049G= (p.Leu683=)
21g.43416898C>TCA321324355SIK1c.2196G>A (p.Leu732=)
c.2049G>A (p.Leu683=)
 ClinVar dbSNP
21g.43416899A=CA2391216227SIK1c.2195T= (p.Leu732=)
c.2048T= (p.Leu683=)
21g.43416899A>CCA410606470SIK1c.2195T>G (p.Leu732Arg)
c.2048T>G (p.Leu683Arg)
 ClinVar
21g.43416899A>GCA410606471SIK1c.2195T>C (p.Leu732Pro)
c.2048T>C (p.Leu683Pro)
 dbSNP
21g.43416899A>TCA410606472SIK1c.2195T>A (p.Leu732Gln)
c.2048T>A (p.Leu683Gln)
21g.43416900G>CCA410606474SIK1c.2194C>G (p.Leu732Val)
c.2047C>G (p.Leu683Val)
21g.43416900G=CA2391216228SIK1c.2194C= (p.Leu732=)
c.2047C= (p.Leu683=)
21g.43416900G>TCA410606473SIK1c.2194C>A (p.Leu732Met)
c.2047C>A (p.Leu683Met)
 dbSNP
21g.43416901G>ACA321324358SIK1c.2193C>T (p.His731=)
c.2046C>T (p.His682=)
 ClinVar dbSNP gnomAD v4
21g.43416901G>CCA410606475SIK1c.2193C>G (p.His731Gln)
c.2046C>G (p.His682Gln)
21g.43416901G=CA2391216229SIK1c.2193C= (p.His731=)
c.2046C= (p.His682=)
21g.43416901G>TCA410606476SIK1c.2193C>A (p.His731Gln)
c.2046C>A (p.His682Gln)
 gnomAD v4
21g.43416902T>ACA410606477SIK1c.2192A>T (p.His731Leu)
c.2045A>T (p.His682Leu)
 COSMIC
21g.43416902T>CCA410606478SIK1c.2192A>G (p.His731Arg)
c.2045A>G (p.His682Arg)
21g.43416902T>GCA410606479SIK1c.2192A>C (p.His731Pro)
c.2045A>C (p.His682Pro)
21g.43416903G>ACA410606480SIK1c.2191C>T (p.His731Tyr)
c.2044C>T (p.His682Tyr)
 ClinVar dbSNP
21g.43416903G>CCA410606482SIK1c.2191C>G (p.His731Asp)
c.2044C>G (p.His682Asp)
21g.43416903G=CA2391216230SIK1c.2191C= (p.His731=)
c.2044C= (p.His682=)
21g.43416903G>TCA410606481SIK1c.2191C>A (p.His731Asn)
c.2044C>A (p.His682Asn)
 ClinVar dbSNP
21g.43416904T>GCA2818014403SIK1c.2190A>C (p.Thr730=)
c.2043A>C (p.Thr681=)
21g.43416905G>ACA410606483SIK1c.2189C>T (p.Thr730Ile)
c.2042C>T (p.Thr681Ile)
 ClinVar
21g.43416905G>CCA410606484SIK1c.2189C>G (p.Thr730Arg)
c.2042C>G (p.Thr681Arg)
21g.43416905G>TCA410606485SIK1c.2189C>A (p.Thr730Lys)
c.2042C>A (p.Thr681Lys)
21g.43416906T>ACA410606486SIK1c.2188A>T (p.Thr730Ser)
c.2041A>T (p.Thr681Ser)
 ClinVar dbSNP
21g.43416906T>CCA410606487SIK1c.2188A>G (p.Thr730Ala)
c.2041A>G (p.Thr681Ala)
21g.43416906T>GCA410606488SIK1c.2188A>C (p.Thr730Pro)
c.2041A>C (p.Thr681Pro)
21g.43416906T=CA2391216231SIK1c.2188A= (p.Thr730=)
c.2041A= (p.Thr681=)
21g.43416907G>CCA410606489SIK1c.2187C>G (p.Asp729Glu)
c.2040C>G (p.Asp680Glu)
21g.43416907G>TCA410606490SIK1c.2187C>A (p.Asp729Glu)
c.2040C>A (p.Asp680Glu)
21g.43416908T>ACA410606491SIK1c.2186A>T (p.Asp729Val)
c.2039A>T (p.Asp680Val)
21g.43416908T>CCA410606492SIK1c.2186A>G (p.Asp729Gly)
c.2039A>G (p.Asp680Gly)
21g.43416908T>GCA410606493SIK1c.2186A>C (p.Asp729Ala)
c.2039A>C (p.Asp680Ala)
21g.43416909C>ACA410606494SIK1c.2185G>T (p.Asp729Tyr)
c.2038G>T (p.Asp680Tyr)
21g.43416909C>GCA410606496SIK1c.2185G>C (p.Asp729His)
c.2038G>C (p.Asp680His)
21g.43416909C>TCA410606495SIK1c.2185G>A (p.Asp729Asn)
c.2038G>A (p.Asp680Asn)
21g.43416911A=CA2391216232SIK1c.2183T= (p.Leu728=)
c.2036T= (p.Leu679=)
21g.43416911A>CCA410606497SIK1c.2183T>G (p.Leu728Arg)
c.2036T>G (p.Leu679Arg)
21g.43416911A>GCA410606498SIK1c.2183T>C (p.Leu728Pro)
c.2036T>C (p.Leu679Pro)
21g.43416911A>TCA410606499SIK1c.2183T>A (p.Leu728Gln)
c.2036T>A (p.Leu679Gln)
 dbSNP
21g.43416912G>ACA321324359SIK1c.2182C>T (p.Leu728=)
c.2035C>T (p.Leu679=)
 ClinVar dbSNP
21g.43416912G>CCA410606500SIK1c.2182C>G (p.Leu728Val)
c.2035C>G (p.Leu679Val)
21g.43416912G=CA2391216233SIK1c.2182C= (p.Leu728=)
c.2035C= (p.Leu679=)
21g.43416912G>TCA410606501SIK1c.2182C>A (p.Leu728Met)
c.2035C>A (p.Leu679Met)
21g.43416913G>TCA2818014405SIK1c.2181C>A (p.Leu727=)
c.2034C>A (p.Leu678=)
21g.43416914A>CCA410606502SIK1c.2180T>G (p.Leu727Arg)
c.2033T>G (p.Leu678Arg)
21g.43416914A>GCA410606503SIK1c.2180T>C (p.Leu727Pro)
c.2033T>C (p.Leu678Pro)
21g.43416914A>TCA410606504SIK1c.2180T>A (p.Leu727His)
c.2033T>A (p.Leu678His)
21g.43416915G>ACA410606505SIK1c.2179C>T (p.Leu727Phe)
c.2032C>T (p.Leu678Phe)
 ClinVar dbSNP
21g.43416915G>CCA410606506SIK1c.2179C>G (p.Leu727Val)
c.2032C>G (p.Leu678Val)
21g.43416915G=CA2391216234SIK1c.2179C= (p.Leu727=)
c.2032C= (p.Leu678=)
21g.43416915G>TCA410606507SIK1c.2179C>A (p.Leu727Ile)
c.2032C>A (p.Leu678Ile)
21g.43416916C>ACA410606508SIK1c.2178G>T (p.Gln726His)
c.2031G>T (p.Gln677His)
21g.43416916C>GCA410606509SIK1c.2178G>C (p.Gln726His)
c.2031G>C (p.Gln677His)
21g.43416917T>ACA410606510SIK1c.2177A>T (p.Gln726Leu)
c.2030A>T (p.Gln677Leu)
21g.43416917T>CCA410606512SIK1c.2177A>G (p.Gln726Arg)
c.2030A>G (p.Gln677Arg)
21g.43416917T>GCA410606511SIK1c.2177A>C (p.Gln726Pro)
c.2030A>C (p.Gln677Pro)
21g.43416918G>ACA410606513SIK1c.2176C>T (p.Gln726Ter)
c.2029C>T (p.Gln677Ter)
21g.43416918G>CCA410606514SIK1c.2176C>G (p.Gln726Glu)
c.2029C>G (p.Gln677Glu)
21g.43416918G>TCA410606515SIK1c.2176C>A (p.Gln726Lys)
c.2029C>A (p.Gln677Lys)
21g.43416924_43416946delCA645601762SIK1c.2154_2176del (p.Ser719AlafsTer?)
c.2007_2029del (p.Ser670AlafsTer?)
 COSMIC

Number of alleles fetched