Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.29917485G>ACA412635776IL1RAPL1c.800G>A (p.Cys267Tyr)
c.23G>A (p.Cys8Tyr)
c.422G>A (p.Cys141Tyr)
Xg.29917485G>CCA412635777IL1RAPL1c.800G>C (p.Cys267Ser)
c.23G>C (p.Cys8Ser)
c.422G>C (p.Cys141Ser)
Xg.29917485G>TCA412635778IL1RAPL1c.800G>T (p.Cys267Phe)
c.23G>T (p.Cys8Phe)
c.422G>T (p.Cys141Phe)
Xg.29917486C>ACA412635779IL1RAPL1c.801C>A (p.Cys267Ter)
c.24C>A (p.Cys8Ter)
c.423C>A (p.Cys141Ter)
 gnomAD v4
Xg.29917486C>GCA412635780IL1RAPL1c.801C>G (p.Cys267Trp)
c.24C>G (p.Cys8Trp)
c.423C>G (p.Cys141Trp)
Xg.29917486C>TCA515840617IL1RAPL1c.801C>T (p.Cys267=)
c.24C>T (p.Cys8=)
c.423C>T (p.Cys141=)
Xg.29917487A=CA2421903052IL1RAPL1c.802A= (p.Arg268=)
c.25A= (p.Arg9=)
c.424A= (p.Arg142=)
Xg.29917487A>CCA515840618IL1RAPL1c.802A>C (p.Arg268=)
c.25A>C (p.Arg9=)
c.424A>C (p.Arg142=)
Xg.29917487A>GCA412635781IL1RAPL1c.802A>G (p.Arg268Gly)
c.25A>G (p.Arg9Gly)
c.424A>G (p.Arg142Gly)
 dbSNP gnomAD v2 gnomAD v4
Xg.29917487A>TCA412635782IL1RAPL1c.802A>T (p.Arg268Ter)
c.25A>T (p.Arg9Ter)
c.424A>T (p.Arg142Ter)
Xg.29917488G>ACA412635783IL1RAPL1c.803G>A (p.Arg268Lys)
c.26G>A (p.Arg9Lys)
c.425G>A (p.Arg142Lys)
Xg.29917488G>CCA412635784IL1RAPL1c.803G>C (p.Arg268Thr)
c.26G>C (p.Arg9Thr)
c.425G>C (p.Arg142Thr)
Xg.29917488G>TCA412635785IL1RAPL1c.803G>T (p.Arg268Ile)
c.26G>T (p.Arg9Ile)
c.425G>T (p.Arg142Ile)
 gnomAD v4
Xg.29917489A=CA2421903053IL1RAPL1c.804A= (p.Arg268=)
c.27A= (p.Arg9=)
c.426A= (p.Arg142=)
Xg.29917489A>CCA412635786IL1RAPL1c.804A>C (p.Arg268Ser)
c.27A>C (p.Arg9Ser)
c.426A>C (p.Arg142Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.29917489A>GCA515840619IL1RAPL1c.804A>G (p.Arg268=)
c.27A>G (p.Arg9=)
c.426A>G (p.Arg142=)
Xg.29917489A>TCA412635787IL1RAPL1c.804A>T (p.Arg268Ser)
c.27A>T (p.Arg9Ser)
c.426A>T (p.Arg142Ser)
Xg.29917490G>ACA412635789IL1RAPL1c.805G>A (p.Ala269Thr)
c.28G>A (p.Ala10Thr)
c.427G>A (p.Ala143Thr)
Xg.29917490G>CCA412635790IL1RAPL1c.805G>C (p.Ala269Pro)
c.28G>C (p.Ala10Pro)
c.427G>C (p.Ala143Pro)
Xg.29917490G>TCA412635788IL1RAPL1c.805G>T (p.Ala269Ser)
c.28G>T (p.Ala10Ser)
c.427G>T (p.Ala143Ser)
Xg.29917491C>ACA412635793IL1RAPL1c.806C>A (p.Ala269Asp)
c.29C>A (p.Ala10Asp)
c.428C>A (p.Ala143Asp)
Xg.29917491C>GCA412635791IL1RAPL1c.806C>G (p.Ala269Gly)
c.29C>G (p.Ala10Gly)
c.428C>G (p.Ala143Gly)
Xg.29917491C>TCA412635792IL1RAPL1c.806C>T (p.Ala269Val)
c.29C>T (p.Ala10Val)
c.428C>T (p.Ala143Val)
Xg.29917492T>ACA515840620IL1RAPL1c.807T>A (p.Ala269=)
c.30T>A (p.Ala10=)
c.429T>A (p.Ala143=)
Xg.29917492T>CCA515840621IL1RAPL1c.807T>C (p.Ala269=)
c.30T>C (p.Ala10=)
c.429T>C (p.Ala143=)
Xg.29917492T>GCA515840622IL1RAPL1c.807T>G (p.Ala269=)
c.30T>G (p.Ala10=)
c.429T>G (p.Ala143=)
Xg.29917493T>ACA412635794IL1RAPL1c.808T>A (p.Phe270Ile)
c.31T>A (p.Phe11Ile)
c.430T>A (p.Phe144Ile)
Xg.29917493T>CCA412635795IL1RAPL1c.808T>C (p.Phe270Leu)
c.31T>C (p.Phe11Leu)
c.430T>C (p.Phe144Leu)
 gnomAD v4
Xg.29917493T>GCA412635796IL1RAPL1c.808T>G (p.Phe270Val)
c.31T>G (p.Phe11Val)
c.430T>G (p.Phe144Val)
Xg.29917494T>ACA412635797IL1RAPL1c.809T>A (p.Phe270Tyr)
c.32T>A (p.Phe11Tyr)
c.431T>A (p.Phe144Tyr)
Xg.29917494T>CCA412635798IL1RAPL1c.809T>C (p.Phe270Ser)
c.32T>C (p.Phe11Ser)
c.431T>C (p.Phe144Ser)
Xg.29917494T>GCA412635799IL1RAPL1c.809T>G (p.Phe270Cys)
c.32T>G (p.Phe11Cys)
c.431T>G (p.Phe144Cys)
 gnomAD v4
Xg.29917495C>ACA412635800IL1RAPL1c.810C>A (p.Phe270Leu)
c.33C>A (p.Phe11Leu)
c.432C>A (p.Phe144Leu)
Xg.29917495C>GCA412635801IL1RAPL1c.810C>G (p.Phe270Leu)
c.33C>G (p.Phe11Leu)
c.432C>G (p.Phe144Leu)
Xg.29917495C>TCA515840623IL1RAPL1c.810C>T (p.Phe270=)
c.33C>T (p.Phe11=)
c.432C>T (p.Phe144=)
 gnomAD v4
Xg.29917496T>ACA412635802IL1RAPL1c.811T>A (p.Phe271Ile)
c.34T>A (p.Phe12Ile)
c.433T>A (p.Phe145Ile)
Xg.29917496T>CCA412635803IL1RAPL1c.811T>C (p.Phe271Leu)
c.34T>C (p.Phe12Leu)
c.433T>C (p.Phe145Leu)
Xg.29917496T>GCA412635804IL1RAPL1c.811T>G (p.Phe271Val)
c.34T>G (p.Phe12Val)
c.433T>G (p.Phe145Val)
Xg.29917497T>ACA412635805IL1RAPL1c.812T>A (p.Phe271Tyr)
c.35T>A (p.Phe12Tyr)
c.434T>A (p.Phe145Tyr)
Xg.29917497T>CCA412635807IL1RAPL1c.812T>C (p.Phe271Ser)
c.35T>C (p.Phe12Ser)
c.434T>C (p.Phe145Ser)
Xg.29917497T>GCA412635806IL1RAPL1c.812T>G (p.Phe271Cys)
c.35T>G (p.Phe12Cys)
c.434T>G (p.Phe145Cys)
Xg.29917498T>ACA412635808IL1RAPL1c.813T>A (p.Phe271Leu)
c.36T>A (p.Phe12Leu)
c.435T>A (p.Phe145Leu)
Xg.29917498T>CCA515840624IL1RAPL1c.813T>C (p.Phe271=)
c.36T>C (p.Phe12=)
c.435T>C (p.Phe145=)
Xg.29917498T>GCA412635809IL1RAPL1c.813T>G (p.Phe271Leu)
c.36T>G (p.Phe12Leu)
c.435T>G (p.Phe145Leu)
Xg.29917499G>ACA412635810IL1RAPL1c.814G>A (p.Gly272Arg)
c.37G>A (p.Gly13Arg)
c.436G>A (p.Gly146Arg)
Xg.29917499G>CCA412635811IL1RAPL1c.814G>C (p.Gly272Arg)
c.37G>C (p.Gly13Arg)
c.436G>C (p.Gly146Arg)
 dbSNP
Xg.29917499G=CA2421903054IL1RAPL1c.814G= (p.Gly272=)
c.37G= (p.Gly13=)
c.436G= (p.Gly146=)
Xg.29917499G>TCA412635812IL1RAPL1c.814G>T (p.Gly272Trp)
c.37G>T (p.Gly13Trp)
c.436G>T (p.Gly146Trp)
Xg.29917500G>ACA412635813IL1RAPL1c.815G>A (p.Gly272Glu)
c.38G>A (p.Gly13Glu)
c.437G>A (p.Gly146Glu)
Xg.29917500G>CCA412635814IL1RAPL1c.815G>C (p.Gly272Ala)
c.38G>C (p.Gly13Ala)
c.437G>C (p.Gly146Ala)
 COSMIC COSMIC

Number of alleles fetched