Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
21g.43416919C=CA2391216235SIK1c.2175G= (p.Ala725=)
c.2028G= (p.Ala676=)
21g.43416919C>TCA321324363SIK1c.2175G>A (p.Ala725=)
c.2028G>A (p.Ala676=)
 ClinVar dbSNP gnomAD v4
21g.43416920G>ACA321324365SIK1c.2174C>T (p.Ala725Val)
c.2027C>T (p.Ala676Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416920G>CCA410606516SIK1c.2174C>G (p.Ala725Gly)
c.2027C>G (p.Ala676Gly)
21g.43416920G=CA2391216236SIK1c.2174C= (p.Ala725=)
c.2027C= (p.Ala676=)
21g.43416920G>TCA410606517SIK1c.2174C>A (p.Ala725Glu)
c.2027C>A (p.Ala676Glu)
21g.43416921C>ACA410606518SIK1c.2173G>T (p.Ala725Ser)
c.2026G>T (p.Ala676Ser)
21g.43416921C>GCA410606519SIK1c.2173G>C (p.Ala725Pro)
c.2026G>C (p.Ala676Pro)
21g.43416921C>TCA410606520SIK1c.2173G>A (p.Ala725Thr)
c.2026G>A (p.Ala676Thr)
 ClinVar
21g.43416922C=CA2391216237SIK1c.2172G= (p.Ala724=)
c.2025G= (p.Ala675=)
21g.43416922C>TCA321324367SIK1c.2172G>A (p.Ala724=)
c.2025G>A (p.Ala675=)
 ClinVar dbSNP gnomAD v4
21g.43416923G>ACA321324370SIK1c.2171C>T (p.Ala724Val)
c.2024C>T (p.Ala675Val)
 dbSNP gnomAD v3 gnomAD v4
21g.43416923G>CCA410606522SIK1c.2171C>G (p.Ala724Gly)
c.2024C>G (p.Ala675Gly)
21g.43416923G=CA2391216238SIK1c.2171C= (p.Ala724=)
c.2024C= (p.Ala675=)
21g.43416923G>TCA410606521SIK1c.2171C>A (p.Ala724Glu)
c.2024C>A (p.Ala675Glu)
21g.43416924_43416926delCA2739267694SIK1c.2169_2171del (p.Ala724del)
c.2022_2024del (p.Ala675del)
 ClinVar
21g.43416924C>ACA410606523SIK1c.2170G>T (p.Ala724Ser)
c.2023G>T (p.Ala675Ser)
21g.43416924C>GCA410606525SIK1c.2170G>C (p.Ala724Pro)
c.2023G>C (p.Ala675Pro)
21g.43416924C>TCA410606524SIK1c.2170G>A (p.Ala724Thr)
c.2023G>A (p.Ala675Thr)
21g.43416925T>ACA2818014407SIK1c.2169A>T (p.Ser723=)
c.2022A>T (p.Ser674=)
21g.43416925T>CCA2737819887SIK1c.2169A>G (p.Ser723=)
c.2022A>G (p.Ser674=)
 dbSNP
21g.43416925T>GCA1022641456SIK1c.2169A>C (p.Ser723=)
c.2022A>C (p.Ser674=)
 gnomAD v3 gnomAD v4
21g.43416926G>ACA410606526SIK1c.2168C>T (p.Ser723Leu)
c.2021C>T (p.Ser674Leu)
21g.43416926G>CCA410606527SIK1c.2168C>G (p.Ser723Ter)
c.2021C>G (p.Ser674Ter)
21g.43416926G>TCA410606528SIK1c.2168C>A (p.Ser723Ter)
c.2021C>A (p.Ser674Ter)
21g.43416927A>CCA410606529SIK1c.2167T>G (p.Ser723Ala)
c.2020T>G (p.Ser674Ala)
21g.43416927A>GCA410606530SIK1c.2167T>C (p.Ser723Pro)
c.2020T>C (p.Ser674Pro)
21g.43416927A>TCA410606531SIK1c.2167T>A (p.Ser723Thr)
c.2020T>A (p.Ser674Thr)
21g.43416928G>ACA321324381SIK1c.2166C>T (p.Ala722=)
c.2019C>T (p.Ala673=)
 ClinVar dbSNP
21g.43416928G=CA2391216239SIK1c.2166C= (p.Ala722=)
c.2019C= (p.Ala673=)
21g.43416929G>ACA410606532SIK1c.2165C>T (p.Ala722Val)
c.2018C>T (p.Ala673Val)
21g.43416929G>CCA410606533SIK1c.2165C>G (p.Ala722Gly)
c.2018C>G (p.Ala673Gly)
21g.43416929G=CA2391216240SIK1c.2165C= (p.Ala722=)
c.2018C= (p.Ala673=)
21g.43416929G>TCA410606534SIK1c.2165C>A (p.Ala722Asp)
c.2018C>A (p.Ala673Asp)
 ClinVar dbSNP
21g.43416930C>ACA410606535SIK1c.2164G>T (p.Ala722Ser)
c.2017G>T (p.Ala673Ser)
21g.43416930C>GCA410606536SIK1c.2164G>C (p.Ala722Pro)
c.2017G>C (p.Ala673Pro)
21g.43416930C>TCA410606537SIK1c.2164G>A (p.Ala722Thr)
c.2017G>A (p.Ala673Thr)
21g.43416932A=CA2391216241SIK1c.2162T= (p.Val721=)
c.2015T= (p.Val672=)
21g.43416932A>CCA410606538SIK1c.2162T>G (p.Val721Gly)
c.2015T>G (p.Val672Gly)
 dbSNP
21g.43416932A>GCA410606540SIK1c.2162T>C (p.Val721Ala)
c.2015T>C (p.Val672Ala)
 dbSNP
21g.43416932A>TCA410606539SIK1c.2162T>A (p.Val721Glu)
c.2015T>A (p.Val672Glu)
 dbSNP
21g.43416933C>ACA321324384SIK1c.2161G>T (p.Val721Leu)
c.2014G>T (p.Val672Leu)
 ClinVar dbSNP
21g.43416933C=CA2391216242SIK1c.2161G= (p.Val721=)
c.2014G= (p.Val672=)
21g.43416933C>GCA410606541SIK1c.2161G>C (p.Val721Leu)
c.2014G>C (p.Val672Leu)
21g.43416933C>TCA410606542SIK1c.2161G>A (p.Val721Met)
c.2014G>A (p.Val672Met)
 ClinVar dbSNP
21g.43416934C>ACA321324388SIK1c.2160G>T (p.Pro720=)
c.2013G>T (p.Pro671=)
 ClinVar dbSNP gnomAD v4
21g.43416934C=CA2391216244SIK1c.2160G= (p.Pro720=)
c.2013G= (p.Pro671=)
21g.43416934C>GCA749584815SIK1c.2160G>C (p.Pro720=)
c.2013G>C (p.Pro671=)
 dbSNP
21g.43416934C>TCA749584817SIK1c.2160G>A (p.Pro720=)
c.2013G>A (p.Pro671=)
 ClinVar dbSNP
21g.43416934_43416935delinsCGCA2391216243SIK1c.2159_2160delinsCG (p.Pro720=)
c.2012_2013delinsCG (p.Pro671=)
21g.43416935G>ACA321324392SIK1c.2159C>T (p.Pro720Leu)
c.2012C>T (p.Pro671Leu)
 ClinVar dbSNP gnomAD v4
21g.43416935G>CCA410606543SIK1c.2159C>G (p.Pro720Arg)
c.2012C>G (p.Pro671Arg)
21g.43416935G=CA2391216246SIK1c.2159C= (p.Pro720=)
c.2012C= (p.Pro671=)
21g.43416935G>TCA410606544SIK1c.2159C>A (p.Pro720Gln)
c.2012C>A (p.Pro671Gln)
21g.43416938delCA2391216245SIK1c.2159del (p.Pro720ArgfsTer?)
c.2012del (p.Pro671ArgfsTer?)
 dbSNP
21g.43416936G>ACA321324395SIK1c.2158C>T (p.Pro720Ser)
c.2011C>T (p.Pro671Ser)
 dbSNP
21g.43416936G>CCA410606545SIK1c.2158C>G (p.Pro720Ala)
c.2011C>G (p.Pro671Ala)
21g.43416936G=CA2391216247SIK1c.2158C= (p.Pro720=)
c.2011C= (p.Pro671=)
21g.43416936G>TCA410606546SIK1c.2158C>A (p.Pro720Thr)
c.2011C>A (p.Pro671Thr)
21g.43416937G>ACA749584822SIK1c.2157C>T (p.Ser719=)
c.2010C>T (p.Ser670=)
 dbSNP
21g.43416937G=CA2391216248SIK1c.2157C= (p.Ser719=)
c.2010C= (p.Ser670=)
21g.43416938G>ACA410606548SIK1c.2156C>T (p.Ser719Phe)
c.2009C>T (p.Ser670Phe)
 gnomAD v4
21g.43416938G>CCA410606549SIK1c.2156C>G (p.Ser719Cys)
c.2009C>G (p.Ser670Cys)
21g.43416938G>TCA410606547SIK1c.2156C>A (p.Ser719Tyr)
c.2009C>A (p.Ser670Tyr)
21g.43416939A>CCA410606550SIK1c.2155T>G (p.Ser719Ala)
c.2008T>G (p.Ser670Ala)
21g.43416939A>GCA410606551SIK1c.2155T>C (p.Ser719Pro)
c.2008T>C (p.Ser670Pro)
21g.43416939A>TCA410606552SIK1c.2155T>A (p.Ser719Thr)
c.2008T>A (p.Ser670Thr)
21g.43416939_43416941delinsACGCA2391216249SIK1c.2153_2155delinsCGT (p.Ala718=)
c.2006_2008delinsCGT (p.Ala669=)
21g.43416940C=CA2391216251SIK1c.2154G= (p.Ala718=)
c.2007G= (p.Ala669=)
21g.43416940C>TCA321324398SIK1c.2154G>A (p.Ala718=)
c.2007G>A (p.Ala669=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416943_43416944delCA2391216250SIK1c.2153_2154del (p.Ala718ValfsTer?)
c.2006_2007del (p.Ala669ValfsTer?)
 dbSNP
21g.43416941G>ACA321324401SIK1c.2153C>T (p.Ala718Val)
c.2006C>T (p.Ala669Val)
 ClinVar dbSNP
21g.43416941G>CCA410606553SIK1c.2153C>G (p.Ala718Gly)
c.2006C>G (p.Ala669Gly)
21g.43416941G=CA2391216252SIK1c.2153C= (p.Ala718=)
c.2006C= (p.Ala669=)
21g.43416941G>TCA410606554SIK1c.2153C>A (p.Ala718Glu)
c.2006C>A (p.Ala669Glu)
21g.43416942C>ACA410606555SIK1c.2152G>T (p.Ala718Ser)
c.2005G>T (p.Ala669Ser)
21g.43416942C=CA2391216253SIK1c.2152G= (p.Ala718=)
c.2005G= (p.Ala669=)
21g.43416942C>GCA410606556SIK1c.2152G>C (p.Ala718Pro)
c.2005G>C (p.Ala669Pro)
21g.43416942C>TCA321324406SIK1c.2152G>A (p.Ala718Thr)
c.2005G>A (p.Ala669Thr)
 ClinVar dbSNP gnomAD v4
21g.43416943G>ACA321324409SIK1c.2151C>T (p.Gly717=)
c.2004C>T (p.Gly668=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416943G>CCA2499225949SIK1c.2151C>G (p.Gly717=)
c.2004C>G (p.Gly668=)
 ClinVar dbSNP
21g.43416943G=CA2391216254SIK1c.2151C= (p.Gly717=)
c.2004C= (p.Gly668=)
21g.43416944C>ACA410606557SIK1c.2150G>T (p.Gly717Val)
c.2003G>T (p.Gly668Val)
21g.43416944C>GCA410606558SIK1c.2150G>C (p.Gly717Ala)
c.2003G>C (p.Gly668Ala)
21g.43416944C>TCA410606559SIK1c.2150G>A (p.Gly717Asp)
c.2003G>A (p.Gly668Asp)
21g.43416945C>ACA410606560SIK1c.2149G>T (p.Gly717Cys)
c.2002G>T (p.Gly668Cys)
21g.43416945C=CA2391216255SIK1c.2149G= (p.Gly717=)
c.2002G= (p.Gly668=)
21g.43416945C>GCA410606561SIK1c.2149G>C (p.Gly717Arg)
c.2002G>C (p.Gly668Arg)
21g.43416945C>TCA321324414SIK1c.2149G>A (p.Gly717Ser)
c.2002G>A (p.Gly668Ser)
 ClinVar dbSNP gnomAD v4
21g.43416946G>ACA321324417SIK1c.2148C>T (p.Thr716=)
c.2001C>T (p.Thr667=)
 ClinVar dbSNP gnomAD v4
21g.43416946G>CCA2739267695SIK1c.2148C>G (p.Thr716=)
c.2001C>G (p.Thr667=)
 ClinVar
21g.43416946G=CA2391216256SIK1c.2148C= (p.Thr716=)
c.2001C= (p.Thr667=)
21g.43416947G>ACA410606562SIK1c.2147C>T (p.Thr716Ile)
c.2000C>T (p.Thr667Ile)
21g.43416947G>CCA410606563SIK1c.2147C>G (p.Thr716Ser)
c.2000C>G (p.Thr667Ser)
21g.43416947G>TCA410606564SIK1c.2147C>A (p.Thr716Asn)
c.2000C>A (p.Thr667Asn)
21g.43416948T>ACA410606565SIK1c.2146A>T (p.Thr716Ser)
c.1999A>T (p.Thr667Ser)
21g.43416948T>CCA410606566SIK1c.2146A>G (p.Thr716Ala)
c.1999A>G (p.Thr667Ala)
21g.43416948T>GCA410606567SIK1c.2146A>C (p.Thr716Pro)
c.1999A>C (p.Thr667Pro)
21g.43416949C>ACA410606568SIK1c.2145G>T (p.Gln715His)
c.1998G>T (p.Gln666His)
21g.43416949C>GCA410606569SIK1c.2145G>C (p.Gln715His)
c.1998G>C (p.Gln666His)
21g.43416950T>ACA410606570SIK1c.2144A>T (p.Gln715Leu)
c.1997A>T (p.Gln666Leu)
21g.43416950T>CCA410606571SIK1c.2144A>G (p.Gln715Arg)
c.1997A>G (p.Gln666Arg)
 dbSNP gnomAD v3 gnomAD v4
21g.43416950T>GCA410606572SIK1c.2144A>C (p.Gln715Pro)
c.1997A>C (p.Gln666Pro)
21g.43416950T=CA2391216257SIK1c.2144A= (p.Gln715=)
c.1997A= (p.Gln666=)
21g.43416951G>ACA410606574SIK1c.2143C>T (p.Gln715Ter)
c.1996C>T (p.Gln666Ter)
21g.43416951G>CCA410606575SIK1c.2143C>G (p.Gln715Glu)
c.1996C>G (p.Gln666Glu)
21g.43416951G>TCA410606573SIK1c.2143C>A (p.Gln715Lys)
c.1996C>A (p.Gln666Lys)
21g.43416952C=CA2391216258SIK1c.2142G= (p.Leu714=)
c.1995G= (p.Leu665=)
21g.43416952C>TCA321324422SIK1c.2142G>A (p.Leu714=)
c.1995G>A (p.Leu665=)
 ClinVar dbSNP
21g.43416953A>CCA410606576SIK1c.2141T>G (p.Leu714Arg)
c.1994T>G (p.Leu665Arg)
21g.43416953A>GCA410606578SIK1c.2141T>C (p.Leu714Pro)
c.1994T>C (p.Leu665Pro)
21g.43416953A>TCA410606577SIK1c.2141T>A (p.Leu714Gln)
c.1994T>A (p.Leu665Gln)
21g.43416954G>CCA410606579SIK1c.2140C>G (p.Leu714Val)
c.1993C>G (p.Leu665Val)
21g.43416954G>TCA410606580SIK1c.2140C>A (p.Leu714Met)
c.1993C>A (p.Leu665Met)
21g.43416955G>ACA749584844SIK1c.2139C>T (p.Leu713=)
c.1992C>T (p.Leu664=)
 ClinVar dbSNP
21g.43416955G=CA2391216259SIK1c.2139C= (p.Leu713=)
c.1992C= (p.Leu664=)
21g.43416956A=CA2391216260SIK1c.2138T= (p.Leu713=)
c.1991T= (p.Leu664=)
21g.43416956A>CCA410606581SIK1c.2138T>G (p.Leu713Arg)
c.1991T>G (p.Leu664Arg)
 dbSNP
21g.43416956A>GCA410606582SIK1c.2138T>C (p.Leu713Pro)
c.1991T>C (p.Leu664Pro)
21g.43416956A>TCA410606583SIK1c.2138T>A (p.Leu713His)
c.1991T>A (p.Leu664His)
21g.43416957G>ACA410606586SIK1c.2137C>T (p.Leu713Phe)
c.1990C>T (p.Leu664Phe)
21g.43416957G>CCA410606585SIK1c.2137C>G (p.Leu713Val)
c.1990C>G (p.Leu664Val)
 ClinVar dbSNP
21g.43416957G>TCA410606584SIK1c.2137C>A (p.Leu713Ile)
c.1990C>A (p.Leu664Ile)
21g.43416958T>GCA1022641482SIK1c.2136A>C (p.Pro712=)
c.1989A>C (p.Pro663=)
 gnomAD v3 gnomAD v4
21g.43416959G>ACA410606587SIK1c.2135C>T (p.Pro712Leu)
c.1988C>T (p.Pro663Leu)
 dbSNP
21g.43416959G>CCA410606588SIK1c.2135C>G (p.Pro712Arg)
c.1988C>G (p.Pro663Arg)
21g.43416959G=CA2391216261SIK1c.2135C= (p.Pro712=)
c.1988C= (p.Pro663=)
21g.43416959G>TCA410606589SIK1c.2135C>A (p.Pro712Gln)
c.1988C>A (p.Pro663Gln)
 ClinVar
21g.43416960G>ACA321324426SIK1c.2134C>T (p.Pro712Ser)
c.1987C>T (p.Pro663Ser)
 dbSNP
21g.43416960G>CCA410606590SIK1c.2134C>G (p.Pro712Ala)
c.1987C>G (p.Pro663Ala)
21g.43416960G=CA2391216262SIK1c.2134C= (p.Pro712=)
c.1987C= (p.Pro663=)
21g.43416960G>TCA410606591SIK1c.2134C>A (p.Pro712Thr)
c.1987C>A (p.Pro663Thr)
21g.43416961G>CCA2573157449SIK1c.2133C>G (p.Pro711=)
c.1986C>G (p.Pro662=)
 ClinVar dbSNP
21g.43416962G>ACA410606592SIK1c.2132C>T (p.Pro711Leu)
c.1985C>T (p.Pro662Leu)
21g.43416962G>CCA410606594SIK1c.2132C>G (p.Pro711Arg)
c.1985C>G (p.Pro662Arg)
 ClinVar dbSNP
21g.43416962G=CA2391216263SIK1c.2132C= (p.Pro711=)
c.1985C= (p.Pro662=)
21g.43416962G>TCA410606593SIK1c.2132C>A (p.Pro711His)
c.1985C>A (p.Pro662His)
21g.43416962_43416963insCCA2818014408SIK1c.2131_2132insG (p.Pro711ArgfsTer?)
c.1984_1985insG (p.Pro662ArgfsTer?)
21g.43416963G>ACA410606595SIK1c.2131C>T (p.Pro711Ser)
c.1984C>T (p.Pro662Ser)
21g.43416963G>CCA410606596SIK1c.2131C>G (p.Pro711Ala)
c.1984C>G (p.Pro662Ala)
21g.43416963G>TCA410606597SIK1c.2131C>A (p.Pro711Thr)
c.1984C>A (p.Pro662Thr)
21g.43416964C=CA2391216264SIK1c.2130G= (p.Pro710=)
c.1983G= (p.Pro661=)
21g.43416964C>TCA749584854SIK1c.2130G>A (p.Pro710=)
c.1983G>A (p.Pro661=)
 ClinVar dbSNP gnomAD v4
21g.43416965G>ACA410606598SIK1c.2129C>T (p.Pro710Leu)
c.1982C>T (p.Pro661Leu)
 ClinVar dbSNP COSMIC
21g.43416965G>CCA410606599SIK1c.2129C>G (p.Pro710Arg)
c.1982C>G (p.Pro661Arg)
21g.43416965G=CA2391216265SIK1c.2129C= (p.Pro710=)
c.1982C= (p.Pro661=)
21g.43416965G>TCA410606600SIK1c.2129C>A (p.Pro710Gln)
c.1982C>A (p.Pro661Gln)
21g.43416966G>ACA410606601SIK1c.2128C>T (p.Pro710Ser)
c.1981C>T (p.Pro661Ser)
21g.43416966G>CCA410606602SIK1c.2128C>G (p.Pro710Ala)
c.1981C>G (p.Pro661Ala)
21g.43416966G>TCA410606603SIK1c.2128C>A (p.Pro710Thr)
c.1981C>A (p.Pro661Thr)
 gnomAD v4
21g.43416967C=CA2391216266SIK1c.2127G= (p.Leu709=)
c.1980G= (p.Leu660=)
21g.43416967C>TCA749584859SIK1c.2127G>A (p.Leu709=)
c.1980G>A (p.Leu660=)
 ClinVar dbSNP
21g.43416968A=CA2391216267SIK1c.2126T= (p.Leu709=)
c.1979T= (p.Leu660=)
21g.43416968A>CCA410606604SIK1c.2126T>G (p.Leu709Arg)
c.1979T>G (p.Leu660Arg)
21g.43416968A>GCA321324439SIK1c.2126T>C (p.Leu709Pro)
c.1979T>C (p.Leu660Pro)
 ClinVar dbSNP
21g.43416968A>TCA410606605SIK1c.2126T>A (p.Leu709Gln)
c.1979T>A (p.Leu660Gln)
21g.43416969G>ACA749584864SIK1c.2125C>T (p.Leu709=)
c.1978C>T (p.Leu660=)
 dbSNP
21g.43416969G>CCA410606606SIK1c.2125C>G (p.Leu709Val)
c.1978C>G (p.Leu660Val)
21g.43416969G=CA2391216268SIK1c.2125C= (p.Leu709=)
c.1978C= (p.Leu660=)
21g.43416969G>TCA410606607SIK1c.2125C>A (p.Leu709Met)
c.1978C>A (p.Leu660Met)
21g.43416971A>CCA410606608SIK1c.2123T>G (p.Leu708Arg)
c.1976T>G (p.Leu659Arg)
21g.43416971A>GCA410606609SIK1c.2123T>C (p.Leu708Pro)
c.1976T>C (p.Leu659Pro)
 ClinVar
21g.43416971A>TCA410606610SIK1c.2123T>A (p.Leu708Gln)
c.1976T>A (p.Leu659Gln)
21g.43416972G>CCA410606611SIK1c.2122C>G (p.Leu708Val)
c.1975C>G (p.Leu659Val)
21g.43416972G>TCA410606612SIK1c.2122C>A (p.Leu708Met)
c.1975C>A (p.Leu659Met)
21g.43416973C=CA2391216269SIK1c.2121G= (p.Pro707=)
c.1974G= (p.Pro658=)
21g.43416973C>TCA321324447SIK1c.2121G>A (p.Pro707=)
c.1974G>A (p.Pro658=)
 ClinVar dbSNP gnomAD v4
21g.43416974G>ACA321324450SIK1c.2120C>T (p.Pro707Leu)
c.1973C>T (p.Pro658Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416974G>CCA410606613SIK1c.2120C>G (p.Pro707Arg)
c.1973C>G (p.Pro658Arg)
21g.43416974G=CA2391216270SIK1c.2120C= (p.Pro707=)
c.1973C= (p.Pro658=)
21g.43416974G>TCA410606614SIK1c.2120C>A (p.Pro707Gln)
c.1973C>A (p.Pro658Gln)
21g.43416975G>ACA410606615SIK1c.2119C>T (p.Pro707Ser)
c.1972C>T (p.Pro658Ser)
21g.43416975G>CCA410606616SIK1c.2119C>G (p.Pro707Ala)
c.1972C>G (p.Pro658Ala)
21g.43416975G>TCA410606617SIK1c.2119C>A (p.Pro707Thr)
c.1972C>A (p.Pro658Thr)
21g.43416976G>ACA321324454SIK1c.2118C>T (p.Leu706=)
c.1971C>T (p.Leu657=)
 ClinVar dbSNP
21g.43416976G>CCA2391216271SIK1c.2118C>G (p.Leu706=)
c.1971C>G (p.Leu657=)
 dbSNP
21g.43416976G=CA2391216272SIK1c.2118C= (p.Leu706=)
c.1971C= (p.Leu657=)
21g.43416976G>TCA645601763SIK1c.2118C>A (p.Leu706=)
c.1971C>A (p.Leu657=)
 dbSNP COSMIC
21g.43416977A>CCA410606619SIK1c.2117T>G (p.Leu706Arg)
c.1970T>G (p.Leu657Arg)
21g.43416977A>GCA410606620SIK1c.2117T>C (p.Leu706Pro)
c.1970T>C (p.Leu657Pro)
21g.43416977A>TCA410606618SIK1c.2117T>A (p.Leu706His)
c.1970T>A (p.Leu657His)
 ClinVar
21g.43416978G>ACA410606621SIK1c.2116C>T (p.Leu706Phe)
c.1969C>T (p.Leu657Phe)
21g.43416978G>CCA410606622SIK1c.2116C>G (p.Leu706Val)
c.1969C>G (p.Leu657Val)
21g.43416978G>TCA410606623SIK1c.2116C>A (p.Leu706Ile)
c.1969C>A (p.Leu657Ile)
21g.43416979C>TCA2580098759SIK1c.2115G>A (p.Gly705=)
c.1968G>A (p.Gly656=)
 ClinVar
21g.43416980C>ACA410606624SIK1c.2114G>T (p.Gly705Val)
c.1967G>T (p.Gly656Val)
21g.43416980C=CA2391216273SIK1c.2114G= (p.Gly705=)
c.1967G= (p.Gly656=)
21g.43416980C>GCA410606625SIK1c.2114G>C (p.Gly705Ala)
c.1967G>C (p.Gly656Ala)
21g.43416980C>TCA410606626SIK1c.2114G>A (p.Gly705Glu)
c.1967G>A (p.Gly656Glu)
 ClinVar dbSNP
21g.43416981C>ACA410606627SIK1c.2113G>T (p.Gly705Trp)
c.1966G>T (p.Gly656Trp)
21g.43416981C>GCA410606629SIK1c.2113G>C (p.Gly705Arg)
c.1966G>C (p.Gly656Arg)
21g.43416981C>TCA410606628SIK1c.2113G>A (p.Gly705Arg)
c.1966G>A (p.Gly656Arg)
21g.43416982C=CA2391216274SIK1c.2112G= (p.Ser704=)
c.1965G= (p.Ser655=)
21g.43416982C>GCA2573157451SIK1c.2112G>C (p.Ser704=)
c.1965G>C (p.Ser655=)
 ClinVar dbSNP
21g.43416982C>TCA321324457SIK1c.2112G>A (p.Ser704=)
c.1965G>A (p.Ser655=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
21g.43416983G>ACA410606630SIK1c.2111C>T (p.Ser704Leu)
c.1964C>T (p.Ser655Leu)
 ClinVar dbSNP COSMIC
21g.43416983G>CCA410606631SIK1c.2111C>G (p.Ser704Trp)
c.1964C>G (p.Ser655Trp)
21g.43416983G=CA2391216275SIK1c.2111C= (p.Ser704=)
c.1964C= (p.Ser655=)
21g.43416983G>TCA410606632SIK1c.2111C>A (p.Ser704Ter)
c.1964C>A (p.Ser655Ter)
21g.43416984A>CCA410606633SIK1c.2110T>G (p.Ser704Ala)
c.1963T>G (p.Ser655Ala)
21g.43416984A>GCA410606635SIK1c.2110T>C (p.Ser704Pro)
c.1963T>C (p.Ser655Pro)
21g.43416984A>TCA410606634SIK1c.2110T>A (p.Ser704Thr)
c.1963T>A (p.Ser655Thr)
21g.43416985C=CA2391216276SIK1c.2109G= (p.Thr703=)
c.1962G= (p.Thr654=)
21g.43416985C>TCA321324468SIK1c.2109G>A (p.Thr703=)
c.1962G>A (p.Thr654=)
 ClinVar dbSNP gnomAD v4
21g.43416986G>ACA410606636SIK1c.2108C>T (p.Thr703Met)
c.1961C>T (p.Thr654Met)
 ClinVar dbSNP gnomAD v4
21g.43416986G>CCA410606637SIK1c.2108C>G (p.Thr703Arg)
c.1961C>G (p.Thr654Arg)
21g.43416986G=CA2391216277SIK1c.2108C= (p.Thr703=)
c.1961C= (p.Thr654=)
21g.43416986G>TCA410606638SIK1c.2108C>A (p.Thr703Lys)
c.1961C>A (p.Thr654Lys)
21g.43416987T>ACA410606639SIK1c.2107A>T (p.Thr703Ser)
c.1960A>T (p.Thr654Ser)
 gnomAD v4
21g.43416987T>CCA410606640SIK1c.2107A>G (p.Thr703Ala)
c.1960A>G (p.Thr654Ala)
21g.43416987T>GCA410606641SIK1c.2107A>C (p.Thr703Pro)
c.1960A>C (p.Thr654Pro)
 gnomAD v4
21g.43416989A>CCA410606642SIK1c.2105T>G (p.Leu702Arg)
c.1958T>G (p.Leu653Arg)
21g.43416989A>GCA410606643SIK1c.2105T>C (p.Leu702Pro)
c.1958T>C (p.Leu653Pro)
21g.43416989A>TCA410606644SIK1c.2105T>A (p.Leu702His)
c.1958T>A (p.Leu653His)
21g.43416990G>ACA410606645SIK1c.2104C>T (p.Leu702Phe)
c.1957C>T (p.Leu653Phe)
21g.43416990G>CCA410606646SIK1c.2104C>G (p.Leu702Val)
c.1957C>G (p.Leu653Val)
21g.43416990G=CA2391216278SIK1c.2104C= (p.Leu702=)
c.1957C= (p.Leu653=)
21g.43416990G>TCA410606647SIK1c.2104C>A (p.Leu702Ile)
c.1957C>A (p.Leu653Ile)
 ClinVar dbSNP
21g.43416992A>CCA410606650SIK1c.2102T>G (p.Leu701Arg)
c.1955T>G (p.Leu652Arg)
21g.43416992A>GCA410606649SIK1c.2102T>C (p.Leu701Pro)
c.1955T>C (p.Leu652Pro)
21g.43416992A>TCA410606648SIK1c.2102T>A (p.Leu701His)
c.1955T>A (p.Leu652His)
21g.43416993G>ACA410606651SIK1c.2101C>T (p.Leu701Phe)
c.1954C>T (p.Leu652Phe)
21g.43416993G>CCA410606652SIK1c.2101C>G (p.Leu701Val)
c.1954C>G (p.Leu652Val)
21g.43416993G>TCA410606653SIK1c.2101C>A (p.Leu701Ile)
c.1954C>A (p.Leu652Ile)
21g.43416995G>ACA410606654SIK1c.2099C>T (p.Thr700Ile)
c.1952C>T (p.Thr651Ile)
 ClinVar
21g.43416995G>CCA410606655SIK1c.2099C>G (p.Thr700Ser)
c.1952C>G (p.Thr651Ser)
21g.43416995G>TCA410606656SIK1c.2099C>A (p.Thr700Asn)
c.1952C>A (p.Thr651Asn)
21g.43416996T>ACA410606657SIK1c.2098A>T (p.Thr700Ser)
c.1951A>T (p.Thr651Ser)
21g.43416996T>CCA410606658SIK1c.2098A>G (p.Thr700Ala)
c.1951A>G (p.Thr651Ala)
 dbSNP
21g.43416996T>GCA410606659SIK1c.2098A>C (p.Thr700Pro)
c.1951A>C (p.Thr651Pro)
21g.43416996T=CA2391216279SIK1c.2098A= (p.Thr700=)
c.1951A= (p.Thr651=)
21g.43416997G>CCA410606660SIK1c.2097C>G (p.Ser699Arg)
c.1950C>G (p.Ser650Arg)
21g.43416997G>TCA410606661SIK1c.2097C>A (p.Ser699Arg)
c.1950C>A (p.Ser650Arg)
21g.43416998C>ACA410606662SIK1c.2096G>T (p.Ser699Ile)
c.1949G>T (p.Ser650Ile)
21g.43416998C>GCA410606663SIK1c.2096G>C (p.Ser699Thr)
c.1949G>C (p.Ser650Thr)
21g.43416998C>TCA410606664SIK1c.2096G>A (p.Ser699Asn)
c.1949G>A (p.Ser650Asn)
21g.43416999T>ACA410606666SIK1c.2095A>T (p.Ser699Cys)
c.1948A>T (p.Ser650Cys)
21g.43416999T>CCA410606667SIK1c.2095A>G (p.Ser699Gly)
c.1948A>G (p.Ser650Gly)
21g.43416999T>GCA410606665SIK1c.2095A>C (p.Ser699Arg)
c.1948A>C (p.Ser650Arg)
21g.43417001G>ACA321324477SIK1c.2093C>T (p.Pro698Leu)
c.1946C>T (p.Pro649Leu)
 ClinVar dbSNP
21g.43417001G>CCA410606668SIK1c.2093C>G (p.Pro698Arg)
c.1946C>G (p.Pro649Arg)
21g.43417001G=CA2391216280SIK1c.2093C= (p.Pro698=)
c.1946C= (p.Pro649=)
21g.43417001G>TCA410606669SIK1c.2093C>A (p.Pro698His)
c.1946C>A (p.Pro649His)
21g.43417002G>ACA410606670SIK1c.2092C>T (p.Pro698Ser)
c.1945C>T (p.Pro649Ser)
 dbSNP
21g.43417002G>CCA410606671SIK1c.2092C>G (p.Pro698Ala)
c.1945C>G (p.Pro649Ala)
21g.43417002G=CA2391216281SIK1c.2092C= (p.Pro698=)
c.1945C= (p.Pro649=)
21g.43417002G>TCA410606672SIK1c.2092C>A (p.Pro698Thr)
c.1945C>A (p.Pro649Thr)
21g.43417003G>ACA321324478SIK1c.2091C>T (p.Leu697=)
c.1944C>T (p.Leu648=)
 ClinVar dbSNP
21g.43417003G=CA2391216282SIK1c.2091C= (p.Leu697=)
c.1944C= (p.Leu648=)
21g.43417004A>CCA410606673SIK1c.2090T>G (p.Leu697Arg)
c.1943T>G (p.Leu648Arg)
21g.43417004A>GCA410606674SIK1c.2090T>C (p.Leu697Pro)
c.1943T>C (p.Leu648Pro)
21g.43417004A>TCA410606675SIK1c.2090T>A (p.Leu697His)
c.1943T>A (p.Leu648His)

Number of alleles fetched