Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.29917476A>CCA412635759IL1RAPL1c.791A>C (p.Asn264Thr)
c.14A>C (p.Asn5Thr)
c.413A>C (p.Asn138Thr)
Xg.29917476A>GCA412635758IL1RAPL1c.791A>G (p.Asn264Ser)
c.14A>G (p.Asn5Ser)
c.413A>G (p.Asn138Ser)
Xg.29917476A>TCA412635757IL1RAPL1c.791A>T (p.Asn264Ile)
c.14A>T (p.Asn5Ile)
c.413A>T (p.Asn138Ile)
Xg.29917477T>ACA412635760IL1RAPL1c.792T>A (p.Asn264Lys)
c.15T>A (p.Asn5Lys)
c.414T>A (p.Asn138Lys)
Xg.29917477T>CCA515840609IL1RAPL1c.792T>C (p.Asn264=)
c.15T>C (p.Asn5=)
c.414T>C (p.Asn138=)
Xg.29917477T>GCA412635761IL1RAPL1c.792T>G (p.Asn264Lys)
c.15T>G (p.Asn5Lys)
c.414T>G (p.Asn138Lys)
Xg.29917478C>ACA412635762IL1RAPL1c.793C>A (p.Leu265Ile)
c.16C>A (p.Leu6Ile)
c.415C>A (p.Leu139Ile)
Xg.29917478C>GCA412635763IL1RAPL1c.793C>G (p.Leu265Val)
c.16C>G (p.Leu6Val)
c.415C>G (p.Leu139Val)
gnomAD v4
Xg.29917478C>TCA515840610IL1RAPL1c.793C>T (p.Leu265=)
c.16C>T (p.Leu6=)
c.415C>T (p.Leu139=)
Xg.29917479T>ACA412635764IL1RAPL1c.794T>A (p.Leu265Gln)
c.17T>A (p.Leu6Gln)
c.416T>A (p.Leu139Gln)
Xg.29917479T>CCA412635765IL1RAPL1c.794T>C (p.Leu265Pro)
c.17T>C (p.Leu6Pro)
c.416T>C (p.Leu139Pro)
Xg.29917479T>GCA412635766IL1RAPL1c.794T>G (p.Leu265Arg)
c.17T>G (p.Leu6Arg)
c.416T>G (p.Leu139Arg)
Xg.29917480A>CCA515840611IL1RAPL1c.795A>C (p.Leu265=)
c.18A>C (p.Leu6=)
c.417A>C (p.Leu139=)
Xg.29917480A>GCA515840612IL1RAPL1c.795A>G (p.Leu265=)
c.18A>G (p.Leu6=)
c.417A>G (p.Leu139=)
Xg.29917480A>TCA515840613IL1RAPL1c.795A>T (p.Leu265=)
c.18A>T (p.Leu6=)
c.417A>T (p.Leu139=)
Xg.29917481A>CCA412635767IL1RAPL1c.796A>C (p.Thr266Pro)
c.19A>C (p.Thr7Pro)
c.418A>C (p.Thr140Pro)
Xg.29917481A>GCA412635768IL1RAPL1c.796A>G (p.Thr266Ala)
c.19A>G (p.Thr7Ala)
c.418A>G (p.Thr140Ala)
Xg.29917481A>TCA412635769IL1RAPL1c.796A>T (p.Thr266Ser)
c.19A>T (p.Thr7Ser)
c.418A>T (p.Thr140Ser)
Xg.29917482C>ACA412635770IL1RAPL1c.797C>A (p.Thr266Asn)
c.20C>A (p.Thr7Asn)
c.419C>A (p.Thr140Asn)
Xg.29917482C>GCA412635771IL1RAPL1c.797C>G (p.Thr266Ser)
c.20C>G (p.Thr7Ser)
c.419C>G (p.Thr140Ser)
Xg.29917482C>TCA412635772IL1RAPL1c.797C>T (p.Thr266Ile)
c.20C>T (p.Thr7Ile)
c.419C>T (p.Thr140Ile)
Xg.29917483C>ACA515840614IL1RAPL1c.798C>A (p.Thr266=)
c.21C>A (p.Thr7=)
c.420C>A (p.Thr140=)
gnomAD v4
Xg.29917483C>GCA515840615IL1RAPL1c.798C>G (p.Thr266=)
c.21C>G (p.Thr7=)
c.420C>G (p.Thr140=)
Xg.29917483C>TCA515840616IL1RAPL1c.798C>T (p.Thr266=)
c.21C>T (p.Thr7=)
c.420C>T (p.Thr140=)
Xg.29917484T>ACA412635775IL1RAPL1c.799T>A (p.Cys267Ser)
c.22T>A (p.Cys8Ser)
c.421T>A (p.Cys141Ser)
Xg.29917484T>CCA412635773IL1RAPL1c.799T>C (p.Cys267Arg)
c.22T>C (p.Cys8Arg)
c.421T>C (p.Cys141Arg)
Xg.29917484T>GCA412635774IL1RAPL1c.799T>G (p.Cys267Gly)
c.22T>G (p.Cys8Gly)
c.421T>G (p.Cys141Gly)
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)

Number of alleles fetched