Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.98922152_98922184delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCCCA2199294747IGF1Rc.2206_2238delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu736=)
c.435_467delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC
n.397_429delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC
c.2269_2301delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu757=)
c.1297_1329delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu433=)
c.871_903delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu291=)
c.2281_2313delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu761=)
c.1843_1875delinsGAAAGGAAGCGGAGAGATGTCATGCAAGTGGCC (p.Glu615=)
15g.98922155_98922186delCA2199294748IGF1Rc.2209_2240del (p.Arg737HisfsTer?)
c.438_469del
n.400_431del
c.2272_2303del (p.Arg758HisfsTer?)
c.1300_1331del (p.Arg434HisfsTer?)
c.874_905del (p.Arg292HisfsTer?)
c.2284_2315del (p.Arg762HisfsTer?)
c.1846_1877del (p.Arg616HisfsTer?)
 dbSNP
15g.98922161_98922167delCA2731817676IGF1Rc.2215_2221del (p.Arg739MetfsTer?)
c.444_450del
n.406_412del
c.2278_2284del (p.Arg760MetfsTer?)
c.1306_1312del (p.Arg436MetfsTer?)
c.880_886del (p.Arg294MetfsTer?)
c.2290_2296del (p.Arg764MetfsTer?)
c.1852_1858del (p.Arg618MetfsTer?)
 dbSNP
15g.98922162G>ACA124314IGF1Rc.2216G>A (p.Arg739Gln)
c.445G>A
n.407G>A
c.2279G>A (p.Arg760Gln)
c.1307G>A (p.Arg436Gln)
c.881G>A (p.Arg294Gln)
c.2291G>A (p.Arg764Gln)
c.1853G>A (p.Arg618Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922162G>CCA393680534IGF1Rc.2216G>C (p.Arg739Pro)
c.445G>C
n.407G>C
c.2279G>C (p.Arg760Pro)
c.1307G>C (p.Arg436Pro)
c.881G>C (p.Arg294Pro)
c.2291G>C (p.Arg764Pro)
c.1853G>C (p.Arg618Pro)
15g.98922162G=CA2199294753IGF1Rc.2216G= (p.Arg739=)
c.445G=
n.407G=
c.2279G= (p.Arg760=)
c.1307G= (p.Arg436=)
c.881G= (p.Arg294=)
c.2291G= (p.Arg764=)
c.1853G= (p.Arg618=)
15g.98922162G>TCA393680533IGF1Rc.2216G>T (p.Arg739Leu)
c.445G>T
n.407G>T
c.2279G>T (p.Arg760Leu)
c.1307G>T (p.Arg436Leu)
c.881G>T (p.Arg294Leu)
c.2291G>T (p.Arg764Leu)
c.1853G>T (p.Arg618Leu)
15g.98922163G>ACA492338369IGF1Rc.2217G>A (p.Arg739=)
c.446G>A
n.408G>A
c.2280G>A (p.Arg760=)
c.1308G>A (p.Arg436=)
c.882G>A (p.Arg294=)
c.2292G>A (p.Arg764=)
c.1854G>A (p.Arg618=)
15g.98922163G>CCA492338371IGF1Rc.2217G>C (p.Arg739=)
c.446G>C
n.408G>C
c.2280G>C (p.Arg760=)
c.1308G>C (p.Arg436=)
c.882G>C (p.Arg294=)
c.2292G>C (p.Arg764=)
c.1854G>C (p.Arg618=)
15g.98922163G>TCA492338374IGF1Rc.2217G>T (p.Arg739=)
c.446G>T
n.408G>T
c.2280G>T (p.Arg760=)
c.1308G>T (p.Arg436=)
c.882G>T (p.Arg294=)
c.2292G>T (p.Arg764=)
c.1854G>T (p.Arg618=)
15g.98922164A>CCA492338378IGF1Rc.2218A>C (p.Arg740=)
c.447A>C
n.409A>C
c.2281A>C (p.Arg761=)
c.1309A>C (p.Arg437=)
c.883A>C (p.Arg295=)
c.2293A>C (p.Arg765=)
c.1855A>C (p.Arg619=)
15g.98922164A>GCA393680535IGF1Rc.2218A>G (p.Arg740Gly)
c.447A>G
n.409A>G
c.2281A>G (p.Arg761Gly)
c.1309A>G (p.Arg437Gly)
c.883A>G (p.Arg295Gly)
c.2293A>G (p.Arg765Gly)
c.1855A>G (p.Arg619Gly)
15g.98922164A>TCA393680536IGF1Rc.2218A>T (p.Arg740Ter)
c.447A>T
n.409A>T
c.2281A>T (p.Arg761Ter)
c.1309A>T (p.Arg437Ter)
c.883A>T (p.Arg295Ter)
c.2293A>T (p.Arg765Ter)
c.1855A>T (p.Arg619Ter)
15g.98922165G>ACA393680538IGF1Rc.2219G>A (p.Arg740Lys)
c.448G>A
n.410G>A
c.2282G>A (p.Arg761Lys)
c.1310G>A (p.Arg437Lys)
c.884G>A (p.Arg295Lys)
c.2294G>A (p.Arg765Lys)
c.1856G>A (p.Arg619Lys)
 gnomAD v4
15g.98922165G>CCA393680540IGF1Rc.2219G>C (p.Arg740Thr)
c.448G>C
n.410G>C
c.2282G>C (p.Arg761Thr)
c.1310G>C (p.Arg437Thr)
c.884G>C (p.Arg295Thr)
c.2294G>C (p.Arg765Thr)
c.1856G>C (p.Arg619Thr)
15g.98922165G>TCA393680542IGF1Rc.2219G>T (p.Arg740Ile)
c.448G>T
n.410G>T
c.2282G>T (p.Arg761Ile)
c.1310G>T (p.Arg437Ile)
c.884G>T (p.Arg295Ile)
c.2294G>T (p.Arg765Ile)
c.1856G>T (p.Arg619Ile)
15g.98922166A>CCA393680543IGF1Rc.2220A>C (p.Arg740Ser)
c.449A>C
n.411A>C
c.2283A>C (p.Arg761Ser)
c.1311A>C (p.Arg437Ser)
c.885A>C (p.Arg295Ser)
c.2295A>C (p.Arg765Ser)
c.1857A>C (p.Arg619Ser)
15g.98922166A>GCA492338393IGF1Rc.2220A>G (p.Arg740=)
c.449A>G
n.411A>G
c.2283A>G (p.Arg761=)
c.1311A>G (p.Arg437=)
c.885A>G (p.Arg295=)
c.2295A>G (p.Arg765=)
c.1857A>G (p.Arg619=)
15g.98922166A>TCA393680544IGF1Rc.2220A>T (p.Arg740Ser)
c.449A>T
n.411A>T
c.2283A>T (p.Arg761Ser)
c.1311A>T (p.Arg437Ser)
c.885A>T (p.Arg295Ser)
c.2295A>T (p.Arg765Ser)
c.1857A>T (p.Arg619Ser)
15g.98922167G>ACA7752351IGF1Rc.2221G>A (p.Asp741Asn)
c.450G>A
n.412G>A
c.2284G>A (p.Asp762Asn)
c.1312G>A (p.Asp438Asn)
c.886G>A (p.Asp296Asn)
c.2296G>A (p.Asp766Asn)
c.1858G>A (p.Asp620Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922167G>CCA393680546IGF1Rc.2221G>C (p.Asp741His)
c.450G>C
n.412G>C
c.2284G>C (p.Asp762His)
c.1312G>C (p.Asp438His)
c.886G>C (p.Asp296His)
c.2296G>C (p.Asp766His)
c.1858G>C (p.Asp620His)
15g.98922167G=CA2199294754IGF1Rc.2221G= (p.Asp741=)
c.450G=
n.412G=
c.2284G= (p.Asp762=)
c.1312G= (p.Asp438=)
c.886G= (p.Asp296=)
c.2296G= (p.Asp766=)
c.1858G= (p.Asp620=)
15g.98922167G>TCA393680548IGF1Rc.2221G>T (p.Asp741Tyr)
c.450G>T
n.412G>T
c.2284G>T (p.Asp762Tyr)
c.1312G>T (p.Asp438Tyr)
c.886G>T (p.Asp296Tyr)
c.2296G>T (p.Asp766Tyr)
c.1858G>T (p.Asp620Tyr)
15g.98922168A>CCA393680550IGF1Rc.2222A>C (p.Asp741Ala)
c.451A>C
n.413A>C
c.2285A>C (p.Asp762Ala)
c.1313A>C (p.Asp438Ala)
c.887A>C (p.Asp296Ala)
c.2297A>C (p.Asp766Ala)
c.1859A>C (p.Asp620Ala)
15g.98922168A>GCA393680551IGF1Rc.2222A>G (p.Asp741Gly)
c.451A>G
n.413A>G
c.2285A>G (p.Asp762Gly)
c.1313A>G (p.Asp438Gly)
c.887A>G (p.Asp296Gly)
c.2297A>G (p.Asp766Gly)
c.1859A>G (p.Asp620Gly)
 gnomAD v4
15g.98922168A>TCA393680553IGF1Rc.2222A>T (p.Asp741Val)
c.451A>T
n.413A>T
c.2285A>T (p.Asp762Val)
c.1313A>T (p.Asp438Val)
c.887A>T (p.Asp296Val)
c.2297A>T (p.Asp766Val)
c.1859A>T (p.Asp620Val)
15g.98922169T>ACA393680555IGF1Rc.2223T>A (p.Asp741Glu)
c.452T>A
n.414T>A
c.2286T>A (p.Asp762Glu)
c.1314T>A (p.Asp438Glu)
c.888T>A (p.Asp296Glu)
c.2298T>A (p.Asp766Glu)
c.1860T>A (p.Asp620Glu)
15g.98922169T>CCA492338413IGF1Rc.2223T>C (p.Asp741=)
c.452T>C
n.414T>C
c.2286T>C (p.Asp762=)
c.1314T>C (p.Asp438=)
c.888T>C (p.Asp296=)
c.2298T>C (p.Asp766=)
c.1860T>C (p.Asp620=)
15g.98922169T>GCA393680557IGF1Rc.2223T>G (p.Asp741Glu)
c.452T>G
n.414T>G
c.2286T>G (p.Asp762Glu)
c.1314T>G (p.Asp438Glu)
c.888T>G (p.Asp296Glu)
c.2298T>G (p.Asp766Glu)
c.1860T>G (p.Asp620Glu)
15g.98922170G>ACA393680559IGF1Rc.2224G>A (p.Val742Ile)
c.453G>A
n.415G>A
c.2287G>A (p.Val763Ile)
c.1315G>A (p.Val439Ile)
c.889G>A (p.Val297Ile)
c.2299G>A (p.Val767Ile)
c.1861G>A (p.Val621Ile)
 gnomAD v4
15g.98922170G>CCA393680562IGF1Rc.2224G>C (p.Val742Leu)
c.453G>C
n.415G>C
c.2287G>C (p.Val763Leu)
c.1315G>C (p.Val439Leu)
c.889G>C (p.Val297Leu)
c.2299G>C (p.Val767Leu)
c.1861G>C (p.Val621Leu)
15g.98922170G>TCA393680560IGF1Rc.2224G>T (p.Val742Phe)
c.453G>T
n.415G>T
c.2287G>T (p.Val763Phe)
c.1315G>T (p.Val439Phe)
c.889G>T (p.Val297Phe)
c.2299G>T (p.Val767Phe)
c.1861G>T (p.Val621Phe)
15g.98922171T>ACA393680564IGF1Rc.2225T>A (p.Val742Asp)
c.454T>A
n.416T>A
c.2288T>A (p.Val763Asp)
c.1316T>A (p.Val439Asp)
c.890T>A (p.Val297Asp)
c.2300T>A (p.Val767Asp)
c.1862T>A (p.Val621Asp)
15g.98922171T>CCA393680565IGF1Rc.2225T>C (p.Val742Ala)
c.454T>C
n.416T>C
c.2288T>C (p.Val763Ala)
c.1316T>C (p.Val439Ala)
c.890T>C (p.Val297Ala)
c.2300T>C (p.Val767Ala)
c.1862T>C (p.Val621Ala)
15g.98922171T>GCA393680567IGF1Rc.2225T>G (p.Val742Gly)
c.454T>G
n.416T>G
c.2288T>G (p.Val763Gly)
c.1316T>G (p.Val439Gly)
c.890T>G (p.Val297Gly)
c.2300T>G (p.Val767Gly)
c.1862T>G (p.Val621Gly)
 gnomAD v4
15g.98922172C>ACA492338428IGF1Rc.2226C>A (p.Val742=)
c.455C>A
n.417C>A
c.2289C>A (p.Val763=)
c.1317C>A (p.Val439=)
c.891C>A (p.Val297=)
c.2301C>A (p.Val767=)
c.1863C>A (p.Val621=)
15g.98922172C>GCA492338431IGF1Rc.2226C>G (p.Val742=)
c.455C>G
n.417C>G
c.2289C>G (p.Val763=)
c.1317C>G (p.Val439=)
c.891C>G (p.Val297=)
c.2301C>G (p.Val767=)
c.1863C>G (p.Val621=)
15g.98922172C>TCA492338433IGF1Rc.2226C>T (p.Val742=)
c.455C>T
n.417C>T
c.2289C>T (p.Val763=)
c.1317C>T (p.Val439=)
c.891C>T (p.Val297=)
c.2301C>T (p.Val767=)
c.1863C>T (p.Val621=)
 dbSNP COSMIC
15g.98922173A>CCA393680569IGF1Rc.2227A>C (p.Met743Leu)
c.456A>C
n.418A>C
c.2290A>C (p.Met764Leu)
c.1318A>C (p.Met440Leu)
c.892A>C (p.Met298Leu)
c.2302A>C (p.Met768Leu)
c.1864A>C (p.Met622Leu)
 gnomAD v4
15g.98922173A>GCA393680570IGF1Rc.2227A>G (p.Met743Val)
c.456A>G
n.418A>G
c.2290A>G (p.Met764Val)
c.1318A>G (p.Met440Val)
c.892A>G (p.Met298Val)
c.2302A>G (p.Met768Val)
c.1864A>G (p.Met622Val)
15g.98922173A>TCA393680571IGF1Rc.2227A>T (p.Met743Leu)
c.456A>T
n.418A>T
c.2290A>T (p.Met764Leu)
c.1318A>T (p.Met440Leu)
c.892A>T (p.Met298Leu)
c.2302A>T (p.Met768Leu)
c.1864A>T (p.Met622Leu)
 gnomAD v4
15g.98922174T>ACA393680574IGF1Rc.2228T>A (p.Met743Lys)
c.457T>A
n.419T>A
c.2291T>A (p.Met764Lys)
c.1319T>A (p.Met440Lys)
c.893T>A (p.Met298Lys)
c.2303T>A (p.Met768Lys)
c.1865T>A (p.Met622Lys)
15g.98922174T>CCA393680575IGF1Rc.2228T>C (p.Met743Thr)
c.457T>C
n.419T>C
c.2291T>C (p.Met764Thr)
c.1319T>C (p.Met440Thr)
c.893T>C (p.Met298Thr)
c.2303T>C (p.Met768Thr)
c.1865T>C (p.Met622Thr)
 gnomAD v4
15g.98922174T>GCA393680577IGF1Rc.2228T>G (p.Met743Arg)
c.457T>G
n.419T>G
c.2291T>G (p.Met764Arg)
c.1319T>G (p.Met440Arg)
c.893T>G (p.Met298Arg)
c.2303T>G (p.Met768Arg)
c.1865T>G (p.Met622Arg)
15g.98922175G>ACA393680578IGF1Rc.2229G>A (p.Met743Ile)
c.458G>A
n.420G>A
c.2292G>A (p.Met764Ile)
c.1320G>A (p.Met440Ile)
c.894G>A (p.Met298Ile)
c.2304G>A (p.Met768Ile)
c.1866G>A (p.Met622Ile)
 gnomAD v4
15g.98922175G>CCA393680580IGF1Rc.2229G>C (p.Met743Ile)
c.458G>C
n.420G>C
c.2292G>C (p.Met764Ile)
c.1320G>C (p.Met440Ile)
c.894G>C (p.Met298Ile)
c.2304G>C (p.Met768Ile)
c.1866G>C (p.Met622Ile)
15g.98922175G>TCA393680582IGF1Rc.2229G>T (p.Met743Ile)
c.458G>T
n.420G>T
c.2292G>T (p.Met764Ile)
c.1320G>T (p.Met440Ile)
c.894G>T (p.Met298Ile)
c.2304G>T (p.Met768Ile)
c.1866G>T (p.Met622Ile)
15g.98922176C>ACA393680584IGF1Rc.2230C>A (p.Gln744Lys)
c.459C>A
n.421C>A
c.2293C>A (p.Gln765Lys)
c.1321C>A (p.Gln441Lys)
c.895C>A (p.Gln299Lys)
c.2305C>A (p.Gln769Lys)
c.1867C>A (p.Gln623Lys)
15g.98922176C>GCA393680586IGF1Rc.2230C>G (p.Gln744Glu)
c.459C>G
n.421C>G
c.2293C>G (p.Gln765Glu)
c.1321C>G (p.Gln441Glu)
c.895C>G (p.Gln299Glu)
c.2305C>G (p.Gln769Glu)
c.1867C>G (p.Gln623Glu)
15g.98922176C>TCA393680585IGF1Rc.2230C>T (p.Gln744Ter)
c.459C>T
n.421C>T
c.2293C>T (p.Gln765Ter)
c.1321C>T (p.Gln441Ter)
c.895C>T (p.Gln299Ter)
c.2305C>T (p.Gln769Ter)
c.1867C>T (p.Gln623Ter)
 dbSNP gnomAD v4
15g.98922177A>CCA393680588IGF1Rc.2231A>C (p.Gln744Pro)
c.460A>C
n.422A>C
c.2294A>C (p.Gln765Pro)
c.1322A>C (p.Gln441Pro)
c.896A>C (p.Gln299Pro)
c.2306A>C (p.Gln769Pro)
c.1868A>C (p.Gln623Pro)
 gnomAD v4
15g.98922177A>GCA393680590IGF1Rc.2231A>G (p.Gln744Arg)
c.460A>G
n.422A>G
c.2294A>G (p.Gln765Arg)
c.1322A>G (p.Gln441Arg)
c.896A>G (p.Gln299Arg)
c.2306A>G (p.Gln769Arg)
c.1868A>G (p.Gln623Arg)
15g.98922177A>TCA393680592IGF1Rc.2231A>T (p.Gln744Leu)
c.460A>T
n.422A>T
c.2294A>T (p.Gln765Leu)
c.1322A>T (p.Gln441Leu)
c.896A>T (p.Gln299Leu)
c.2306A>T (p.Gln769Leu)
c.1868A>T (p.Gln623Leu)
15g.98922178A=CA2199294755IGF1Rc.2232A= (p.Gln744=)
c.461A=
n.423A=
c.2295A= (p.Gln765=)
c.1323A= (p.Gln441=)
c.897A= (p.Gln299=)
c.2307A= (p.Gln769=)
c.1869A= (p.Gln623=)
15g.98922178A>CCA393680593IGF1Rc.2232A>C (p.Gln744His)
c.461A>C
n.423A>C
c.2295A>C (p.Gln765His)
c.1323A>C (p.Gln441His)
c.897A>C (p.Gln299His)
c.2307A>C (p.Gln769His)
c.1869A>C (p.Gln623His)
15g.98922178A>GCA7752352IGF1Rc.2232A>G (p.Gln744=)
c.461A>G
n.423A>G
c.2295A>G (p.Gln765=)
c.1323A>G (p.Gln441=)
c.897A>G (p.Gln299=)
c.2307A>G (p.Gln769=)
c.1869A>G (p.Gln623=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.98922178A>TCA393680595IGF1Rc.2232A>T (p.Gln744His)
c.461A>T
n.423A>T
c.2295A>T (p.Gln765His)
c.1323A>T (p.Gln441His)
c.897A>T (p.Gln299His)
c.2307A>T (p.Gln769His)
c.1869A>T (p.Gln623His)
15g.98922179G>ACA393680597IGF1Rc.2233G>A (p.Val745Met)
c.462G>A
n.424G>A
c.2296G>A (p.Val766Met)
c.1324G>A (p.Val442Met)
c.898G>A (p.Val300Met)
c.2308G>A (p.Val770Met)
c.1870G>A (p.Val624Met)
 dbSNP
15g.98922179G>CCA393680598IGF1Rc.2233G>C (p.Val745Leu)
c.462G>C
n.424G>C
c.2296G>C (p.Val766Leu)
c.1324G>C (p.Val442Leu)
c.898G>C (p.Val300Leu)
c.2308G>C (p.Val770Leu)
c.1870G>C (p.Val624Leu)
15g.98922179G>TCA393680599IGF1Rc.2233G>T (p.Val745Leu)
c.462G>T
n.424G>T
c.2296G>T (p.Val766Leu)
c.1324G>T (p.Val442Leu)
c.898G>T (p.Val300Leu)
c.2308G>T (p.Val770Leu)
c.1870G>T (p.Val624Leu)
 gnomAD v4
15g.98922180T>ACA393680601IGF1Rc.2234T>A (p.Val745Glu)
c.463T>A
n.425T>A
c.2297T>A (p.Val766Glu)
c.1325T>A (p.Val442Glu)
c.899T>A (p.Val300Glu)
c.2309T>A (p.Val770Glu)
c.1871T>A (p.Val624Glu)
 dbSNP
15g.98922180T>CCA393680602IGF1Rc.2234T>C (p.Val745Ala)
c.463T>C
n.425T>C
c.2297T>C (p.Val766Ala)
c.1325T>C (p.Val442Ala)
c.899T>C (p.Val300Ala)
c.2309T>C (p.Val770Ala)
c.1871T>C (p.Val624Ala)
15g.98922180T>GCA393680603IGF1Rc.2234T>G (p.Val745Gly)
c.463T>G
n.425T>G
c.2297T>G (p.Val766Gly)
c.1325T>G (p.Val442Gly)
c.899T>G (p.Val300Gly)
c.2309T>G (p.Val770Gly)
c.1871T>G (p.Val624Gly)
 dbSNP
15g.98922181G>ACA492338495IGF1Rc.2235G>A (p.Val745=)
c.464G>A
n.426G>A
c.2298G>A (p.Val766=)
c.1326G>A (p.Val442=)
c.900G>A (p.Val300=)
c.2310G>A (p.Val770=)
c.1872G>A (p.Val624=)
15g.98922181G>CCA492338499IGF1Rc.2235G>C (p.Val745=)
c.464G>C
n.426G>C
c.2298G>C (p.Val766=)
c.1326G>C (p.Val442=)
c.900G>C (p.Val300=)
c.2310G>C (p.Val770=)
c.1872G>C (p.Val624=)
15g.98922181G>TCA492338501IGF1Rc.2235G>T (p.Val745=)
c.464G>T
n.426G>T
c.2298G>T (p.Val766=)
c.1326G>T (p.Val442=)
c.900G>T (p.Val300=)
c.2310G>T (p.Val770=)
c.1872G>T (p.Val624=)
15g.98922182G>ACA393680609IGF1Rc.2236G>A (p.Ala746Thr)
c.465G>A
n.427G>A
c.2299G>A (p.Ala767Thr)
c.1327G>A (p.Ala443Thr)
c.901G>A (p.Ala301Thr)
c.2311G>A (p.Ala771Thr)
c.1873G>A (p.Ala625Thr)
 dbSNP
15g.98922182G>CCA393680605IGF1Rc.2236G>C (p.Ala746Pro)
c.465G>C
n.427G>C
c.2299G>C (p.Ala767Pro)
c.1327G>C (p.Ala443Pro)
c.901G>C (p.Ala301Pro)
c.2311G>C (p.Ala771Pro)
c.1873G>C (p.Ala625Pro)
15g.98922182G>TCA393680607IGF1Rc.2236G>T (p.Ala746Ser)
c.465G>T
n.427G>T
c.2299G>T (p.Ala767Ser)
c.1327G>T (p.Ala443Ser)
c.901G>T (p.Ala301Ser)
c.2311G>T (p.Ala771Ser)
c.1873G>T (p.Ala625Ser)
15g.98922183C>ACA393680610IGF1Rc.2237C>A (p.Ala746Asp)
c.466C>A
n.428C>A
c.2300C>A (p.Ala767Asp)
c.1328C>A (p.Ala443Asp)
c.902C>A (p.Ala301Asp)
c.2312C>A (p.Ala771Asp)
c.1874C>A (p.Ala625Asp)
15g.98922183C>GCA393680612IGF1Rc.2237C>G (p.Ala746Gly)
c.466C>G
n.428C>G
c.2300C>G (p.Ala767Gly)
c.1328C>G (p.Ala443Gly)
c.902C>G (p.Ala301Gly)
c.2312C>G (p.Ala771Gly)
c.1874C>G (p.Ala625Gly)
15g.98922183C>TCA393680613IGF1Rc.2237C>T (p.Ala746Val)
c.466C>T
n.428C>T
c.2300C>T (p.Ala767Val)
c.1328C>T (p.Ala443Val)
c.902C>T (p.Ala301Val)
c.2312C>T (p.Ala771Val)
c.1874C>T (p.Ala625Val)
 dbSNP
15g.98922184C>ACA492338519IGF1Rc.2238C>A (p.Ala746=)
c.467C>A
n.429C>A
c.2301C>A (p.Ala767=)
c.1329C>A (p.Ala443=)
c.903C>A (p.Ala301=)
c.2313C>A (p.Ala771=)
c.1875C>A (p.Ala625=)
 dbSNP gnomAD v4
15g.98922184C=CA2199294756IGF1Rc.2238C= (p.Ala746=)
c.467C=
n.429C=
c.2301C= (p.Ala767=)
c.1329C= (p.Ala443=)
c.903C= (p.Ala301=)
c.2313C= (p.Ala771=)
c.1875C= (p.Ala625=)
15g.98922184C>GCA492338521IGF1Rc.2238C>G (p.Ala746=)
c.467C>G
n.429C>G
c.2301C>G (p.Ala767=)
c.1329C>G (p.Ala443=)
c.903C>G (p.Ala301=)
c.2313C>G (p.Ala771=)
c.1875C>G (p.Ala625=)
15g.98922184C>TCA492338523IGF1Rc.2238C>T (p.Ala746=)
c.467C>T
n.429C>T
c.2301C>T (p.Ala767=)
c.1329C>T (p.Ala443=)
c.903C>T (p.Ala301=)
c.2313C>T (p.Ala771=)
c.1875C>T (p.Ala625=)
 dbSNP
15g.98922185A>CCA393680615IGF1Rc.2239A>C (p.Asn747His)
c.468A>C
n.430A>C
c.2302A>C (p.Asn768His)
c.1330A>C (p.Asn444His)
c.904A>C (p.Asn302His)
c.2314A>C (p.Asn772His)
c.1876A>C (p.Asn626His)
15g.98922185A>GCA393680617IGF1Rc.2239A>G (p.Asn747Asp)
c.468A>G
n.430A>G
c.2302A>G (p.Asn768Asp)
c.1330A>G (p.Asn444Asp)
c.904A>G (p.Asn302Asp)
c.2314A>G (p.Asn772Asp)
c.1876A>G (p.Asn626Asp)
15g.98922185A>TCA393680618IGF1Rc.2239A>T (p.Asn747Tyr)
c.468A>T
n.430A>T
c.2302A>T (p.Asn768Tyr)
c.1330A>T (p.Asn444Tyr)
c.904A>T (p.Asn302Tyr)
c.2314A>T (p.Asn772Tyr)
c.1876A>T (p.Asn626Tyr)
15g.98922186A=CA2199294757IGF1Rc.2240A= (p.Asn747=)
c.469A=
n.431A=
c.2303A= (p.Asn768=)
c.1331A= (p.Asn444=)
c.905A= (p.Asn302=)
c.2315A= (p.Asn772=)
c.1877A= (p.Asn626=)
15g.98922186A>CCA393680620IGF1Rc.2240A>C (p.Asn747Thr)
c.469A>C
n.431A>C
c.2303A>C (p.Asn768Thr)
c.1331A>C (p.Asn444Thr)
c.905A>C (p.Asn302Thr)
c.2315A>C (p.Asn772Thr)
c.1877A>C (p.Asn626Thr)
 dbSNP gnomAD v4
15g.98922186A>GCA7752353IGF1Rc.2240A>G (p.Asn747Ser)
c.469A>G
n.431A>G
c.2303A>G (p.Asn768Ser)
c.1331A>G (p.Asn444Ser)
c.905A>G (p.Asn302Ser)
c.2315A>G (p.Asn772Ser)
c.1877A>G (p.Asn626Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922186A>TCA393680622IGF1Rc.2240A>T (p.Asn747Ile)
c.469A>T
n.431A>T
c.2303A>T (p.Asn768Ile)
c.1331A>T (p.Asn444Ile)
c.905A>T (p.Asn302Ile)
c.2315A>T (p.Asn772Ile)
c.1877A>T (p.Asn626Ile)
15g.98922187C>ACA393680623IGF1Rc.2241C>A (p.Asn747Lys)
c.470C>A
n.432C>A
c.2304C>A (p.Asn768Lys)
c.1332C>A (p.Asn444Lys)
c.906C>A (p.Asn302Lys)
c.2316C>A (p.Asn772Lys)
c.1878C>A (p.Asn626Lys)
15g.98922187C=CA2199294758IGF1Rc.2241C= (p.Asn747=)
c.470C=
n.432C=
c.2304C= (p.Asn768=)
c.1332C= (p.Asn444=)
c.906C= (p.Asn302=)
c.2316C= (p.Asn772=)
c.1878C= (p.Asn626=)
15g.98922187C>GCA393680625IGF1Rc.2241C>G (p.Asn747Lys)
c.470C>G
n.432C>G
c.2304C>G (p.Asn768Lys)
c.1332C>G (p.Asn444Lys)
c.906C>G (p.Asn302Lys)
c.2316C>G (p.Asn772Lys)
c.1878C>G (p.Asn626Lys)
15g.98922187C>TCA275384254IGF1Rc.2241C>T (p.Asn747=)
c.470C>T
n.432C>T
c.2304C>T (p.Asn768=)
c.1332C>T (p.Asn444=)
c.906C>T (p.Asn302=)
c.2316C>T (p.Asn772=)
c.1878C>T (p.Asn626=)
 dbSNP
15g.98922188A=CA2199294759IGF1Rc.2242A= (p.Thr748=)
c.471A=
n.433A=
c.2305A= (p.Thr769=)
c.1333A= (p.Thr445=)
c.907A= (p.Thr303=)
c.2317A= (p.Thr773=)
c.1879A= (p.Thr627=)
15g.98922188A>CCA393680628IGF1Rc.2242A>C (p.Thr748Pro)
c.471A>C
n.433A>C
c.2305A>C (p.Thr769Pro)
c.1333A>C (p.Thr445Pro)
c.907A>C (p.Thr303Pro)
c.2317A>C (p.Thr773Pro)
c.1879A>C (p.Thr627Pro)
 dbSNP
15g.98922188A>GCA7752354IGF1Rc.2242A>G (p.Thr748Ala)
c.471A>G
n.433A>G
c.2305A>G (p.Thr769Ala)
c.1333A>G (p.Thr445Ala)
c.907A>G (p.Thr303Ala)
c.2317A>G (p.Thr773Ala)
c.1879A>G (p.Thr627Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922188A>TCA393680627IGF1Rc.2242A>T (p.Thr748Ser)
c.471A>T
n.433A>T
c.2305A>T (p.Thr769Ser)
c.1333A>T (p.Thr445Ser)
c.907A>T (p.Thr303Ser)
c.2317A>T (p.Thr773Ser)
c.1879A>T (p.Thr627Ser)
15g.98922189C>ACA7752355IGF1Rc.2243C>A (p.Thr748Asn)
c.472C>A
n.434C>A
c.2306C>A (p.Thr769Asn)
c.1334C>A (p.Thr445Asn)
c.908C>A (p.Thr303Asn)
c.2318C>A (p.Thr773Asn)
c.1880C>A (p.Thr627Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922189C=CA2199294760IGF1Rc.2243C= (p.Thr748=)
c.472C=
n.434C=
c.2306C= (p.Thr769=)
c.1334C= (p.Thr445=)
c.908C= (p.Thr303=)
c.2318C= (p.Thr773=)
c.1880C= (p.Thr627=)
15g.98922189C>GCA275384265IGF1Rc.2243C>G (p.Thr748Ser)
c.472C>G
n.434C>G
c.2306C>G (p.Thr769Ser)
c.1334C>G (p.Thr445Ser)
c.908C>G (p.Thr303Ser)
c.2318C>G (p.Thr773Ser)
c.1880C>G (p.Thr627Ser)
 ClinVar dbSNP gnomAD v4
15g.98922189C>TCA393680631IGF1Rc.2243C>T (p.Thr748Ile)
c.472C>T
n.434C>T
c.2306C>T (p.Thr769Ile)
c.1334C>T (p.Thr445Ile)
c.908C>T (p.Thr303Ile)
c.2318C>T (p.Thr773Ile)
c.1880C>T (p.Thr627Ile)
 gnomAD v4
15g.98922190C>ACA492338560IGF1Rc.2244C>A (p.Thr748=)
c.473C>A
n.435C>A
c.2307C>A (p.Thr769=)
c.1335C>A (p.Thr445=)
c.909C>A (p.Thr303=)
c.2319C>A (p.Thr773=)
c.1881C>A (p.Thr627=)
15g.98922190C=CA2199294761IGF1Rc.2244C= (p.Thr748=)
c.473C=
n.435C=
c.2307C= (p.Thr769=)
c.1335C= (p.Thr445=)
c.909C= (p.Thr303=)
c.2319C= (p.Thr773=)
c.1881C= (p.Thr627=)
15g.98922190C>GCA275384268IGF1Rc.2244C>G (p.Thr748=)
c.473C>G
n.435C>G
c.2307C>G (p.Thr769=)
c.1335C>G (p.Thr445=)
c.909C>G (p.Thr303=)
c.2319C>G (p.Thr773=)
c.1881C>G (p.Thr627=)
 dbSNP
15g.98922190C>TCA492338566IGF1Rc.2244C>T (p.Thr748=)
c.473C>T
n.435C>T
c.2307C>T (p.Thr769=)
c.1335C>T (p.Thr445=)
c.909C>T (p.Thr303=)
c.2319C>T (p.Thr773=)
c.1881C>T (p.Thr627=)
 dbSNP gnomAD v4
15g.98922191A=CA2199294762IGF1Rc.2245A= (p.Thr749=)
c.474A=
n.436A=
c.2308A= (p.Thr770=)
c.1336A= (p.Thr446=)
c.910A= (p.Thr304=)
c.2320A= (p.Thr774=)
c.1882A= (p.Thr628=)
15g.98922191A>CCA393680637IGF1Rc.2245A>C (p.Thr749Pro)
c.474A>C
n.436A>C
c.2308A>C (p.Thr770Pro)
c.1336A>C (p.Thr446Pro)
c.910A>C (p.Thr304Pro)
c.2320A>C (p.Thr774Pro)
c.1882A>C (p.Thr628Pro)
 dbSNP
15g.98922191A>GCA393680634IGF1Rc.2245A>G (p.Thr749Ala)
c.474A>G
n.436A>G
c.2308A>G (p.Thr770Ala)
c.1336A>G (p.Thr446Ala)
c.910A>G (p.Thr304Ala)
c.2320A>G (p.Thr774Ala)
c.1882A>G (p.Thr628Ala)
15g.98922191A>TCA393680635IGF1Rc.2245A>T (p.Thr749Ser)
c.474A>T
n.436A>T
c.2308A>T (p.Thr770Ser)
c.1336A>T (p.Thr446Ser)
c.910A>T (p.Thr304Ser)
c.2320A>T (p.Thr774Ser)
c.1882A>T (p.Thr628Ser)
15g.98922192C>ACA393680638IGF1Rc.2246C>A (p.Thr749Asn)
c.475C>A
n.437C>A
c.2309C>A (p.Thr770Asn)
c.1337C>A (p.Thr446Asn)
c.911C>A (p.Thr304Asn)
c.2321C>A (p.Thr774Asn)
c.1883C>A (p.Thr628Asn)
15g.98922192C=CA2199294763IGF1Rc.2246C= (p.Thr749=)
c.475C=
n.437C=
c.2309C= (p.Thr770=)
c.1337C= (p.Thr446=)
c.911C= (p.Thr304=)
c.2321C= (p.Thr774=)
c.1883C= (p.Thr628=)
15g.98922192C>GCA393680639IGF1Rc.2246C>G (p.Thr749Ser)
c.475C>G
n.437C>G
c.2309C>G (p.Thr770Ser)
c.1337C>G (p.Thr446Ser)
c.911C>G (p.Thr304Ser)
c.2321C>G (p.Thr774Ser)
c.1883C>G (p.Thr628Ser)
15g.98922192C>TCA393680640IGF1Rc.2246C>T (p.Thr749Ile)
c.475C>T
n.437C>T
c.2309C>T (p.Thr770Ile)
c.1337C>T (p.Thr446Ile)
c.911C>T (p.Thr304Ile)
c.2321C>T (p.Thr774Ile)
c.1883C>T (p.Thr628Ile)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.98922193C>ACA492338582IGF1Rc.2247C>A (p.Thr749=)
c.476C>A
n.438C>A
c.2310C>A (p.Thr770=)
c.1338C>A (p.Thr446=)
c.912C>A (p.Thr304=)
c.2322C>A (p.Thr774=)
c.1884C>A (p.Thr628=)
 dbSNP
15g.98922193C>GCA492338584IGF1Rc.2247C>G (p.Thr749=)
c.476C>G
n.438C>G
c.2310C>G (p.Thr770=)
c.1338C>G (p.Thr446=)
c.912C>G (p.Thr304=)
c.2322C>G (p.Thr774=)
c.1884C>G (p.Thr628=)
15g.98922193C>TCA492338586IGF1Rc.2247C>T (p.Thr749=)
c.476C>T
n.438C>T
c.2310C>T (p.Thr770=)
c.1338C>T (p.Thr446=)
c.912C>T (p.Thr304=)
c.2322C>T (p.Thr774=)
c.1884C>T (p.Thr628=)
 dbSNP COSMIC
15g.98922194A=CA2199294764IGF1Rc.2248A= (p.Met750=)
c.477A=
n.439A=
c.2311A= (p.Met771=)
c.1339A= (p.Met447=)
c.913A= (p.Met305=)
c.2323A= (p.Met775=)
c.1885A= (p.Met629=)
15g.98922194A>CCA393680644IGF1Rc.2248A>C (p.Met750Leu)
c.477A>C
n.439A>C
c.2311A>C (p.Met771Leu)
c.1339A>C (p.Met447Leu)
c.913A>C (p.Met305Leu)
c.2323A>C (p.Met775Leu)
c.1885A>C (p.Met629Leu)
15g.98922194A>GCA275384271IGF1Rc.2248A>G (p.Met750Val)
c.477A>G
n.439A>G
c.2311A>G (p.Met771Val)
c.1339A>G (p.Met447Val)
c.913A>G (p.Met305Val)
c.2323A>G (p.Met775Val)
c.1885A>G (p.Met629Val)
 dbSNP gnomAD v2 gnomAD v4
15g.98922194A>TCA393680642IGF1Rc.2248A>T (p.Met750Leu)
c.477A>T
n.439A>T
c.2311A>T (p.Met771Leu)
c.1339A>T (p.Met447Leu)
c.913A>T (p.Met305Leu)
c.2323A>T (p.Met775Leu)
c.1885A>T (p.Met629Leu)
15g.98922195T>ACA393680646IGF1Rc.2249T>A (p.Met750Lys)
c.478T>A
n.440T>A
c.2312T>A (p.Met771Lys)
c.1340T>A (p.Met447Lys)
c.914T>A (p.Met305Lys)
c.2324T>A (p.Met775Lys)
c.1886T>A (p.Met629Lys)
15g.98922195T>CCA393680647IGF1Rc.2249T>C (p.Met750Thr)
c.478T>C
n.440T>C
c.2312T>C (p.Met771Thr)
c.1340T>C (p.Met447Thr)
c.914T>C (p.Met305Thr)
c.2324T>C (p.Met775Thr)
c.1886T>C (p.Met629Thr)
15g.98922195T>GCA393680648IGF1Rc.2249T>G (p.Met750Arg)
c.478T>G
n.440T>G
c.2312T>G (p.Met771Arg)
c.1340T>G (p.Met447Arg)
c.914T>G (p.Met305Arg)
c.2324T>G (p.Met775Arg)
c.1886T>G (p.Met629Arg)
15g.98922196G>ACA393680650IGF1Rc.2250G>A (p.Met750Ile)
c.479G>A
n.441G>A
c.2313G>A (p.Met771Ile)
c.1341G>A (p.Met447Ile)
c.915G>A (p.Met305Ile)
c.2325G>A (p.Met775Ile)
c.1887G>A (p.Met629Ile)
 dbSNP
15g.98922196G>CCA393680652IGF1Rc.2250G>C (p.Met750Ile)
c.479G>C
n.441G>C
c.2313G>C (p.Met771Ile)
c.1341G>C (p.Met447Ile)
c.915G>C (p.Met305Ile)
c.2325G>C (p.Met775Ile)
c.1887G>C (p.Met629Ile)
15g.98922196G=CA2199294765IGF1Rc.2250G= (p.Met750=)
c.479G=
n.441G=
c.2313G= (p.Met771=)
c.1341G= (p.Met447=)
c.915G= (p.Met305=)
c.2325G= (p.Met775=)
c.1887G= (p.Met629=)
15g.98922196G>TCA393680654IGF1Rc.2250G>T (p.Met750Ile)
c.479G>T
n.441G>T
c.2313G>T (p.Met771Ile)
c.1341G>T (p.Met447Ile)
c.915G>T (p.Met305Ile)
c.2325G>T (p.Met775Ile)
c.1887G>T (p.Met629Ile)
15g.98922197T>ACA393680656IGF1Rc.2251T>A (p.Ser751Thr)
c.480T>A
n.442T>A
c.2314T>A (p.Ser772Thr)
c.1342T>A (p.Ser448Thr)
c.916T>A (p.Ser306Thr)
c.2326T>A (p.Ser776Thr)
c.1888T>A (p.Ser630Thr)
15g.98922197T>CCA393680659IGF1Rc.2251T>C (p.Ser751Pro)
c.480T>C
n.442T>C
c.2314T>C (p.Ser772Pro)
c.1342T>C (p.Ser448Pro)
c.916T>C (p.Ser306Pro)
c.2326T>C (p.Ser776Pro)
c.1888T>C (p.Ser630Pro)
15g.98922197T>GCA393680657IGF1Rc.2251T>G (p.Ser751Ala)
c.480T>G
n.442T>G
c.2314T>G (p.Ser772Ala)
c.1342T>G (p.Ser448Ala)
c.916T>G (p.Ser306Ala)
c.2326T>G (p.Ser776Ala)
c.1888T>G (p.Ser630Ala)
15g.98922198C>ACA393680660IGF1Rc.2252C>A (p.Ser751Tyr)
c.481C>A
n.443C>A
c.2315C>A (p.Ser772Tyr)
c.1343C>A (p.Ser448Tyr)
c.917C>A (p.Ser306Tyr)
c.2327C>A (p.Ser776Tyr)
c.1889C>A (p.Ser630Tyr)
15g.98922198C>GCA393680662IGF1Rc.2252C>G (p.Ser751Cys)
c.481C>G
n.443C>G
c.2315C>G (p.Ser772Cys)
c.1343C>G (p.Ser448Cys)
c.917C>G (p.Ser306Cys)
c.2327C>G (p.Ser776Cys)
c.1889C>G (p.Ser630Cys)
 gnomAD v4
15g.98922198C>TCA393680664IGF1Rc.2252C>T (p.Ser751Phe)
c.481C>T
n.443C>T
c.2315C>T (p.Ser772Phe)
c.1343C>T (p.Ser448Phe)
c.917C>T (p.Ser306Phe)
c.2327C>T (p.Ser776Phe)
c.1889C>T (p.Ser630Phe)
 ClinVar dbSNP
15g.98922199C>ACA492338626IGF1Rc.2253C>A (p.Ser751=)
c.482C>A
n.444C>A
c.2316C>A (p.Ser772=)
c.1344C>A (p.Ser448=)
c.918C>A (p.Ser306=)
c.2328C>A (p.Ser776=)
c.1890C>A (p.Ser630=)
15g.98922199C>GCA492338624IGF1Rc.2253C>G (p.Ser751=)
c.482C>G
n.444C>G
c.2316C>G (p.Ser772=)
c.1344C>G (p.Ser448=)
c.918C>G (p.Ser306=)
c.2328C>G (p.Ser776=)
c.1890C>G (p.Ser630=)
15g.98922199C>TCA492338622IGF1Rc.2253C>T (p.Ser751=)
c.482C>T
n.444C>T
c.2316C>T (p.Ser772=)
c.1344C>T (p.Ser448=)
c.918C>T (p.Ser306=)
c.2328C>T (p.Ser776=)
c.1890C>T (p.Ser630=)
 gnomAD v4
15g.98922200A>CCA393680666IGF1Rc.2254A>C (p.Ser752Arg)
c.483A>C
n.445A>C
c.2317A>C (p.Ser773Arg)
c.1345A>C (p.Ser449Arg)
c.919A>C (p.Ser307Arg)
c.2329A>C (p.Ser777Arg)
c.1891A>C (p.Ser631Arg)
15g.98922200A>GCA393680667IGF1Rc.2254A>G (p.Ser752Gly)
c.483A>G
n.445A>G
c.2317A>G (p.Ser773Gly)
c.1345A>G (p.Ser449Gly)
c.919A>G (p.Ser307Gly)
c.2329A>G (p.Ser777Gly)
c.1891A>G (p.Ser631Gly)
15g.98922200A>TCA393680669IGF1Rc.2254A>T (p.Ser752Cys)
c.483A>T
n.445A>T
c.2317A>T (p.Ser773Cys)
c.1345A>T (p.Ser449Cys)
c.919A>T (p.Ser307Cys)
c.2329A>T (p.Ser777Cys)
c.1891A>T (p.Ser631Cys)
 dbSNP
15g.98922201G>ACA393680671IGF1Rc.2255G>A (p.Ser752Asn)
c.484G>A
n.446G>A
c.2318G>A (p.Ser773Asn)
c.1346G>A (p.Ser449Asn)
c.920G>A (p.Ser307Asn)
c.2330G>A (p.Ser777Asn)
c.1892G>A (p.Ser631Asn)
15g.98922201G>CCA393680672IGF1Rc.2255G>C (p.Ser752Thr)
c.484G>C
n.446G>C
c.2318G>C (p.Ser773Thr)
c.1346G>C (p.Ser449Thr)
c.920G>C (p.Ser307Thr)
c.2330G>C (p.Ser777Thr)
c.1892G>C (p.Ser631Thr)
15g.98922201G>TCA393680674IGF1Rc.2255G>T (p.Ser752Ile)
c.484G>T
n.446G>T
c.2318G>T (p.Ser773Ile)
c.1346G>T (p.Ser449Ile)
c.920G>T (p.Ser307Ile)
c.2330G>T (p.Ser777Ile)
c.1892G>T (p.Ser631Ile)
 gnomAD v4
15g.98922202C>ACA393680676IGF1Rc.2256C>A (p.Ser752Arg)
c.485C>A
n.447C>A
c.2319C>A (p.Ser773Arg)
c.1347C>A (p.Ser449Arg)
c.921C>A (p.Ser307Arg)
c.2331C>A (p.Ser777Arg)
c.1893C>A (p.Ser631Arg)
15g.98922202C=CA2199294766IGF1Rc.2256C= (p.Ser752=)
c.485C=
n.447C=
c.2319C= (p.Ser773=)
c.1347C= (p.Ser449=)
c.921C= (p.Ser307=)
c.2331C= (p.Ser777=)
c.1893C= (p.Ser631=)
15g.98922202C>GCA393680677IGF1Rc.2256C>G (p.Ser752Arg)
c.485C>G
n.447C>G
c.2319C>G (p.Ser773Arg)
c.1347C>G (p.Ser449Arg)
c.921C>G (p.Ser307Arg)
c.2331C>G (p.Ser777Arg)
c.1893C>G (p.Ser631Arg)
15g.98922202C>TCA492338648IGF1Rc.2256C>T (p.Ser752=)
c.485C>T
n.447C>T
c.2319C>T (p.Ser773=)
c.1347C>T (p.Ser449=)
c.921C>T (p.Ser307=)
c.2331C>T (p.Ser777=)
c.1893C>T (p.Ser631=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922203C>ACA492338654IGF1Rc.2257C>A (p.Arg753=)
c.486C>A
n.448C>A
c.2320C>A (p.Arg774=)
c.1348C>A (p.Arg450=)
c.922C>A (p.Arg308=)
c.2332C>A (p.Arg778=)
c.1894C>A (p.Arg632=)
15g.98922203C=CA2199294767IGF1Rc.2257C= (p.Arg753=)
c.486C=
n.448C=
c.2320C= (p.Arg774=)
c.1348C= (p.Arg450=)
c.922C= (p.Arg308=)
c.2332C= (p.Arg778=)
c.1894C= (p.Arg632=)
15g.98922203C>GCA393680680IGF1Rc.2257C>G (p.Arg753Gly)
c.486C>G
n.448C>G
c.2320C>G (p.Arg774Gly)
c.1348C>G (p.Arg450Gly)
c.922C>G (p.Arg308Gly)
c.2332C>G (p.Arg778Gly)
c.1894C>G (p.Arg632Gly)
 dbSNP gnomAD v2 gnomAD v4
15g.98922203C>TCA393680679IGF1Rc.2257C>T (p.Arg753Ter)
c.486C>T
n.448C>T
c.2320C>T (p.Arg774Ter)
c.1348C>T (p.Arg450Ter)
c.922C>T (p.Arg308Ter)
c.2332C>T (p.Arg778Ter)
c.1894C>T (p.Arg632Ter)
 ClinVar dbSNP gnomAD v4
15g.98922204G>ACA275384274IGF1Rc.2258G>A (p.Arg753Gln)
c.487G>A
n.449G>A
c.2321G>A (p.Arg774Gln)
c.1349G>A (p.Arg450Gln)
c.923G>A (p.Arg308Gln)
c.2333G>A (p.Arg778Gln)
c.1895G>A (p.Arg632Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922204G>CCA393680683IGF1Rc.2258G>C (p.Arg753Pro)
c.487G>C
n.449G>C
c.2321G>C (p.Arg774Pro)
c.1349G>C (p.Arg450Pro)
c.923G>C (p.Arg308Pro)
c.2333G>C (p.Arg778Pro)
c.1895G>C (p.Arg632Pro)
 gnomAD v4
15g.98922204G=CA2199294768IGF1Rc.2258G= (p.Arg753=)
c.487G=
n.449G=
c.2321G= (p.Arg774=)
c.1349G= (p.Arg450=)
c.923G= (p.Arg308=)
c.2333G= (p.Arg778=)
c.1895G= (p.Arg632=)
15g.98922204G>TCA393680684IGF1Rc.2258G>T (p.Arg753Leu)
c.487G>T
n.449G>T
c.2321G>T (p.Arg774Leu)
c.1349G>T (p.Arg450Leu)
c.923G>T (p.Arg308Leu)
c.2333G>T (p.Arg778Leu)
c.1895G>T (p.Arg632Leu)
15g.98922205A=CA2199294769IGF1Rc.2259A= (p.Arg753=)
c.488A=
n.450A=
c.2322A= (p.Arg774=)
c.1350A= (p.Arg450=)
c.924A= (p.Arg308=)
c.2334A= (p.Arg778=)
c.1896A= (p.Arg632=)
15g.98922205A>CCA275384277IGF1Rc.2259A>C (p.Arg753=)
c.488A>C
n.450A>C
c.2322A>C (p.Arg774=)
c.1350A>C (p.Arg450=)
c.924A>C (p.Arg308=)
c.2334A>C (p.Arg778=)
c.1896A>C (p.Arg632=)
 dbSNP gnomAD v4
15g.98922205A>GCA492338667IGF1Rc.2259A>G (p.Arg753=)
c.488A>G
n.450A>G
c.2322A>G (p.Arg774=)
c.1350A>G (p.Arg450=)
c.924A>G (p.Arg308=)
c.2334A>G (p.Arg778=)
c.1896A>G (p.Arg632=)
15g.98922205A>TCA492338672IGF1Rc.2259A>T (p.Arg753=)
c.488A>T
n.450A>T
c.2322A>T (p.Arg774=)
c.1350A>T (p.Arg450=)
c.924A>T (p.Arg308=)
c.2334A>T (p.Arg778=)
c.1896A>T (p.Arg632=)
 ClinVar
15g.98922206A>CCA393680686IGF1Rc.2260A>C (p.Ser754Arg)
c.489A>C
n.451A>C
c.2323A>C (p.Ser775Arg)
c.1351A>C (p.Ser451Arg)
c.925A>C (p.Ser309Arg)
c.2335A>C (p.Ser779Arg)
c.1897A>C (p.Ser633Arg)
15g.98922206A>GCA393680688IGF1Rc.2260A>G (p.Ser754Gly)
c.489A>G
n.451A>G
c.2323A>G (p.Ser775Gly)
c.1351A>G (p.Ser451Gly)
c.925A>G (p.Ser309Gly)
c.2335A>G (p.Ser779Gly)
c.1897A>G (p.Ser633Gly)
15g.98922206A>TCA393680690IGF1Rc.2260A>T (p.Ser754Cys)
c.489A>T
n.451A>T
c.2323A>T (p.Ser775Cys)
c.1351A>T (p.Ser451Cys)
c.925A>T (p.Ser309Cys)
c.2335A>T (p.Ser779Cys)
c.1897A>T (p.Ser633Cys)
15g.98922207G>ACA393680692IGF1Rc.2261G>A (p.Ser754Asn)
c.490G>A
n.452G>A
c.2324G>A (p.Ser775Asn)
c.1352G>A (p.Ser451Asn)
c.926G>A (p.Ser309Asn)
c.2336G>A (p.Ser779Asn)
c.1898G>A (p.Ser633Asn)
15g.98922207G>CCA393680695IGF1Rc.2261G>C (p.Ser754Thr)
c.490G>C
n.452G>C
c.2324G>C (p.Ser775Thr)
c.1352G>C (p.Ser451Thr)
c.926G>C (p.Ser309Thr)
c.2336G>C (p.Ser779Thr)
c.1898G>C (p.Ser633Thr)
15g.98922207G>TCA393680693IGF1Rc.2261G>T (p.Ser754Ile)
c.490G>T
n.452G>T
c.2324G>T (p.Ser775Ile)
c.1352G>T (p.Ser451Ile)
c.926G>T (p.Ser309Ile)
c.2336G>T (p.Ser779Ile)
c.1898G>T (p.Ser633Ile)
15g.98922208C>ACA393680696IGF1Rc.2262C>A (p.Ser754Arg)
c.491C>A
n.453C>A
c.2325C>A (p.Ser775Arg)
c.1353C>A (p.Ser451Arg)
c.927C>A (p.Ser309Arg)
c.2337C>A (p.Ser779Arg)
c.1899C>A (p.Ser633Arg)
15g.98922208C>GCA393680698IGF1Rc.2262C>G (p.Ser754Arg)
c.491C>G
n.453C>G
c.2325C>G (p.Ser775Arg)
c.1353C>G (p.Ser451Arg)
c.927C>G (p.Ser309Arg)
c.2337C>G (p.Ser779Arg)
c.1899C>G (p.Ser633Arg)
15g.98922208C>TCA492338698IGF1Rc.2262C>T (p.Ser754=)
c.491C>T
n.453C>T
c.2325C>T (p.Ser775=)
c.1353C>T (p.Ser451=)
c.927C>T (p.Ser309=)
c.2337C>T (p.Ser779=)
c.1899C>T (p.Ser633=)
 dbSNP
15g.98922209A>CCA492338701IGF1Rc.2263A>C (p.Arg755=)
c.492A>C
n.454A>C
c.2326A>C (p.Arg776=)
c.1354A>C (p.Arg452=)
c.928A>C (p.Arg310=)
c.2338A>C (p.Arg780=)
c.1900A>C (p.Arg634=)
15g.98922209A>GCA393680700IGF1Rc.2263A>G (p.Arg755Gly)
c.492A>G
n.454A>G
c.2326A>G (p.Arg776Gly)
c.1354A>G (p.Arg452Gly)
c.928A>G (p.Arg310Gly)
c.2338A>G (p.Arg780Gly)
c.1900A>G (p.Arg634Gly)
15g.98922209A>TCA393680701IGF1Rc.2263A>T (p.Arg755Trp)
c.492A>T
n.454A>T
c.2326A>T (p.Arg776Trp)
c.1354A>T (p.Arg452Trp)
c.928A>T (p.Arg310Trp)
c.2338A>T (p.Arg780Trp)
c.1900A>T (p.Arg634Trp)
15g.98922210G>ACA393680707IGF1Rc.2264G>A (p.Arg755Lys)
c.493G>A
n.455G>A
c.2327G>A (p.Arg776Lys)
c.1355G>A (p.Arg452Lys)
c.929G>A (p.Arg310Lys)
c.2339G>A (p.Arg780Lys)
c.1901G>A (p.Arg634Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922210G>CCA393680703IGF1Rc.2264G>C (p.Arg755Thr)
c.493G>C
n.455G>C
c.2327G>C (p.Arg776Thr)
c.1355G>C (p.Arg452Thr)
c.929G>C (p.Arg310Thr)
c.2339G>C (p.Arg780Thr)
c.1901G>C (p.Arg634Thr)
15g.98922210G=CA2199294770IGF1Rc.2264G= (p.Arg755=)
c.493G=
n.455G=
c.2327G= (p.Arg776=)
c.1355G= (p.Arg452=)
c.929G= (p.Arg310=)
c.2339G= (p.Arg780=)
c.1901G= (p.Arg634=)
15g.98922210G>TCA393680705IGF1Rc.2264G>T (p.Arg755Met)
c.493G>T
n.455G>T
c.2327G>T (p.Arg776Met)
c.1355G>T (p.Arg452Met)
c.929G>T (p.Arg310Met)
c.2339G>T (p.Arg780Met)
c.1901G>T (p.Arg634Met)
15g.98922211G>ACA492338714IGF1Rc.2265G>A (p.Arg755=)
c.494G>A
n.456G>A
c.2328G>A (p.Arg776=)
c.1356G>A (p.Arg452=)
c.930G>A (p.Arg310=)
c.2340G>A (p.Arg780=)
c.1902G>A (p.Arg634=)
15g.98922211G>CCA393680708IGF1Rc.2265G>C (p.Arg755Ser)
c.494G>C
n.456G>C
c.2328G>C (p.Arg776Ser)
c.1356G>C (p.Arg452Ser)
c.930G>C (p.Arg310Ser)
c.2340G>C (p.Arg780Ser)
c.1902G>C (p.Arg634Ser)
15g.98922211G=CA2199294771IGF1Rc.2265G= (p.Arg755=)
c.494G=
n.456G=
c.2328G= (p.Arg776=)
c.1356G= (p.Arg452=)
c.930G= (p.Arg310=)
c.2340G= (p.Arg780=)
c.1902G= (p.Arg634=)
15g.98922211G>TCA7752356IGF1Rc.2265G>T (p.Arg755Ser)
c.494G>T
n.456G>T
c.2328G>T (p.Arg776Ser)
c.1356G>T (p.Arg452Ser)
c.930G>T (p.Arg310Ser)
c.2340G>T (p.Arg780Ser)
c.1902G>T (p.Arg634Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.98922212A>CCA393680711IGF1Rc.2266A>C (p.Asn756His)
c.495A>C
n.457A>C
c.2329A>C (p.Asn777His)
c.1357A>C (p.Asn453His)
c.931A>C (p.Asn311His)
c.2341A>C (p.Asn781His)
c.1903A>C (p.Asn635His)
15g.98922212A>GCA393680713IGF1Rc.2266A>G (p.Asn756Asp)
c.495A>G
n.457A>G
c.2329A>G (p.Asn777Asp)
c.1357A>G (p.Asn453Asp)
c.931A>G (p.Asn311Asp)
c.2341A>G (p.Asn781Asp)
c.1903A>G (p.Asn635Asp)
15g.98922212A>TCA393680714IGF1Rc.2266A>T (p.Asn756Tyr)
c.495A>T
n.457A>T
c.2329A>T (p.Asn777Tyr)
c.1357A>T (p.Asn453Tyr)
c.931A>T (p.Asn311Tyr)
c.2341A>T (p.Asn781Tyr)
c.1903A>T (p.Asn635Tyr)
15g.98922213A=CA2199294772IGF1Rc.2267A= (p.Asn756=)
c.496A=
n.458A=
c.2330A= (p.Asn777=)
c.1358A= (p.Asn453=)
c.932A= (p.Asn311=)
c.2342A= (p.Asn781=)
c.1904A= (p.Asn635=)
15g.98922213A>CCA393680716IGF1Rc.2267A>C (p.Asn756Thr)
c.496A>C
n.458A>C
c.2330A>C (p.Asn777Thr)
c.1358A>C (p.Asn453Thr)
c.932A>C (p.Asn311Thr)
c.2342A>C (p.Asn781Thr)
c.1904A>C (p.Asn635Thr)
15g.98922213A>GCA275384289IGF1Rc.2267A>G (p.Asn756Ser)
c.496A>G
n.458A>G
c.2330A>G (p.Asn777Ser)
c.1358A>G (p.Asn453Ser)
c.932A>G (p.Asn311Ser)
c.2342A>G (p.Asn781Ser)
c.1904A>G (p.Asn635Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922213A>TCA393680718IGF1Rc.2267A>T (p.Asn756Ile)
c.496A>T
n.458A>T
c.2330A>T (p.Asn777Ile)
c.1358A>T (p.Asn453Ile)
c.932A>T (p.Asn311Ile)
c.2342A>T (p.Asn781Ile)
c.1904A>T (p.Asn635Ile)
15g.98922214C>ACA393680720IGF1Rc.2268C>A (p.Asn756Lys)
c.497C>A
n.459C>A
c.2331C>A (p.Asn777Lys)
c.1359C>A (p.Asn453Lys)
c.933C>A (p.Asn311Lys)
c.2343C>A (p.Asn781Lys)
c.1905C>A (p.Asn635Lys)
15g.98922214C>GCA393680721IGF1Rc.2268C>G (p.Asn756Lys)
c.497C>G
n.459C>G
c.2331C>G (p.Asn777Lys)
c.1359C>G (p.Asn453Lys)
c.933C>G (p.Asn311Lys)
c.2343C>G (p.Asn781Lys)
c.1905C>G (p.Asn635Lys)
15g.98922214C>TCA492338737IGF1Rc.2268C>T (p.Asn756=)
c.497C>T
n.459C>T
c.2331C>T (p.Asn777=)
c.1359C>T (p.Asn453=)
c.933C>T (p.Asn311=)
c.2343C>T (p.Asn781=)
c.1905C>T (p.Asn635=)
 dbSNP
15g.98922215A>CCA393680723IGF1Rc.2269A>C (p.Thr757Pro)
c.498A>C
n.460A>C
c.2332A>C (p.Thr778Pro)
c.1360A>C (p.Thr454Pro)
c.934A>C (p.Thr312Pro)
c.2344A>C (p.Thr782Pro)
c.1906A>C (p.Thr636Pro)
15g.98922215A>GCA393680725IGF1Rc.2269A>G (p.Thr757Ala)
c.498A>G
n.460A>G
c.2332A>G (p.Thr778Ala)
c.1360A>G (p.Thr454Ala)
c.934A>G (p.Thr312Ala)
c.2344A>G (p.Thr782Ala)
c.1906A>G (p.Thr636Ala)
15g.98922215A>TCA393680726IGF1Rc.2269A>T (p.Thr757Ser)
c.498A>T
n.460A>T
c.2332A>T (p.Thr778Ser)
c.1360A>T (p.Thr454Ser)
c.934A>T (p.Thr312Ser)
c.2344A>T (p.Thr782Ser)
c.1906A>T (p.Thr636Ser)
15g.98922216C>ACA393680732IGF1Rc.2270C>A (p.Thr757Asn)
c.499C>A
n.461C>A
c.2333C>A (p.Thr778Asn)
c.1361C>A (p.Thr454Asn)
c.935C>A (p.Thr312Asn)
c.2345C>A (p.Thr782Asn)
c.1907C>A (p.Thr636Asn)
15g.98922216C=CA2199294773IGF1Rc.2270C= (p.Thr757=)
c.499C=
n.461C=
c.2333C= (p.Thr778=)
c.1361C= (p.Thr454=)
c.935C= (p.Thr312=)
c.2345C= (p.Thr782=)
c.1907C= (p.Thr636=)
15g.98922216C>GCA393680728IGF1Rc.2270C>G (p.Thr757Ser)
c.499C>G
n.461C>G
c.2333C>G (p.Thr778Ser)
c.1361C>G (p.Thr454Ser)
c.935C>G (p.Thr312Ser)
c.2345C>G (p.Thr782Ser)
c.1907C>G (p.Thr636Ser)
15g.98922216C>TCA393680730IGF1Rc.2270C>T (p.Thr757Ile)
c.499C>T
n.461C>T
c.2333C>T (p.Thr778Ile)
c.1361C>T (p.Thr454Ile)
c.935C>T (p.Thr312Ile)
c.2345C>T (p.Thr782Ile)
c.1907C>T (p.Thr636Ile)
 dbSNP gnomAD v3 gnomAD v4
15g.98922217C>ACA492338753IGF1Rc.2271C>A (p.Thr757=)
c.500C>A
n.462C>A
c.2334C>A (p.Thr778=)
c.1362C>A (p.Thr454=)
c.936C>A (p.Thr312=)
c.2346C>A (p.Thr782=)
c.1908C>A (p.Thr636=)
15g.98922217C>GCA492338758IGF1Rc.2271C>G (p.Thr757=)
c.500C>G
n.462C>G
c.2334C>G (p.Thr778=)
c.1362C>G (p.Thr454=)
c.936C>G (p.Thr312=)
c.2346C>G (p.Thr782=)
c.1908C>G (p.Thr636=)
15g.98922217C>TCA492338755IGF1Rc.2271C>T (p.Thr757=)
c.500C>T
n.462C>T
c.2334C>T (p.Thr778=)
c.1362C>T (p.Thr454=)
c.936C>T (p.Thr312=)
c.2346C>T (p.Thr782=)
c.1908C>T (p.Thr636=)
 gnomAD v4
15g.98922218A>CCA393680733IGF1Rc.2272A>C (p.Thr758Pro)
c.501A>C
n.463A>C
c.2335A>C (p.Thr779Pro)
c.1363A>C (p.Thr455Pro)
c.937A>C (p.Thr313Pro)
c.2347A>C (p.Thr783Pro)
c.1909A>C (p.Thr637Pro)
15g.98922218A>GCA393680736IGF1Rc.2272A>G (p.Thr758Ala)
c.501A>G
n.463A>G
c.2335A>G (p.Thr779Ala)
c.1363A>G (p.Thr455Ala)
c.937A>G (p.Thr313Ala)
c.2347A>G (p.Thr783Ala)
c.1909A>G (p.Thr637Ala)
15g.98922218A>TCA393680734IGF1Rc.2272A>T (p.Thr758Ser)
c.501A>T
n.463A>T
c.2335A>T (p.Thr779Ser)
c.1363A>T (p.Thr455Ser)
c.937A>T (p.Thr313Ser)
c.2347A>T (p.Thr783Ser)
c.1909A>T (p.Thr637Ser)
15g.98922219C>ACA393680738IGF1Rc.2273C>A (p.Thr758Lys)
c.502C>A
n.464C>A
c.2336C>A (p.Thr779Lys)
c.1364C>A (p.Thr455Lys)
c.938C>A (p.Thr313Lys)
c.2348C>A (p.Thr783Lys)
c.1910C>A (p.Thr637Lys)
 gnomAD v4
15g.98922219C=CA2199294774IGF1Rc.2273C= (p.Thr758=)
c.502C=
n.464C=
c.2336C= (p.Thr779=)
c.1364C= (p.Thr455=)
c.938C= (p.Thr313=)
c.2348C= (p.Thr783=)
c.1910C= (p.Thr637=)
15g.98922219C>GCA393680740IGF1Rc.2273C>G (p.Thr758Arg)
c.502C>G
n.464C>G
c.2336C>G (p.Thr779Arg)
c.1364C>G (p.Thr455Arg)
c.938C>G (p.Thr313Arg)
c.2348C>G (p.Thr783Arg)
c.1910C>G (p.Thr637Arg)
15g.98922219C>TCA7752357IGF1Rc.2273C>T (p.Thr758Met)
c.502C>T
n.464C>T
c.2336C>T (p.Thr779Met)
c.1364C>T (p.Thr455Met)
c.938C>T (p.Thr313Met)
c.2348C>T (p.Thr783Met)
c.1910C>T (p.Thr637Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922220G>ACA7752358IGF1Rc.2274G>A (p.Thr758=)
c.503G>A
n.465G>A
c.2337G>A (p.Thr779=)
c.1365G>A (p.Thr455=)
c.939G>A (p.Thr313=)
c.2349G>A (p.Thr783=)
c.1911G>A (p.Thr637=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922220G>CCA492338780IGF1Rc.2274G>C (p.Thr758=)
c.503G>C
n.465G>C
c.2337G>C (p.Thr779=)
c.1365G>C (p.Thr455=)
c.939G>C (p.Thr313=)
c.2349G>C (p.Thr783=)
c.1911G>C (p.Thr637=)
15g.98922220G=CA2199294775IGF1Rc.2274G= (p.Thr758=)
c.503G=
n.465G=
c.2337G= (p.Thr779=)
c.1365G= (p.Thr455=)
c.939G= (p.Thr313=)
c.2349G= (p.Thr783=)
c.1911G= (p.Thr637=)
15g.98922220G>TCA492338783IGF1Rc.2274G>T (p.Thr758=)
c.503G>T
n.465G>T
c.2337G>T (p.Thr779=)
c.1365G>T (p.Thr455=)
c.939G>T (p.Thr313=)
c.2349G>T (p.Thr783=)
c.1911G>T (p.Thr637=)
15g.98922221G>ACA393680741IGF1Rc.2275G>A (p.Ala759Thr)
c.504G>A
n.466G>A
c.2338G>A (p.Ala780Thr)
c.1366G>A (p.Ala456Thr)
c.940G>A (p.Ala314Thr)
c.2350G>A (p.Ala784Thr)
c.1912G>A (p.Ala638Thr)
 dbSNP gnomAD v4
15g.98922221G>CCA393680743IGF1Rc.2275G>C (p.Ala759Pro)
c.504G>C
n.466G>C
c.2338G>C (p.Ala780Pro)
c.1366G>C (p.Ala456Pro)
c.940G>C (p.Ala314Pro)
c.2350G>C (p.Ala784Pro)
c.1912G>C (p.Ala638Pro)
 dbSNP
15g.98922221G>TCA393680744IGF1Rc.2275G>T (p.Ala759Ser)
c.504G>T
n.466G>T
c.2338G>T (p.Ala780Ser)
c.1366G>T (p.Ala456Ser)
c.940G>T (p.Ala314Ser)
c.2350G>T (p.Ala784Ser)
c.1912G>T (p.Ala638Ser)
15g.98922222C>ACA393680745IGF1Rc.2276C>A (p.Ala759Asp)
c.505C>A
n.467C>A
c.2339C>A (p.Ala780Asp)
c.1367C>A (p.Ala456Asp)
c.941C>A (p.Ala314Asp)
c.2351C>A (p.Ala784Asp)
c.1913C>A (p.Ala638Asp)
 dbSNP
15g.98922222C=CA2199294776IGF1Rc.2276C= (p.Ala759=)
c.505C=
n.467C=
c.2339C= (p.Ala780=)
c.1367C= (p.Ala456=)
c.941C= (p.Ala314=)
c.2351C= (p.Ala784=)
c.1913C= (p.Ala638=)
15g.98922222C>GCA7752359IGF1Rc.2276C>G (p.Ala759Gly)
c.505C>G
n.467C>G
c.2339C>G (p.Ala780Gly)
c.1367C>G (p.Ala456Gly)
c.941C>G (p.Ala314Gly)
c.2351C>G (p.Ala784Gly)
c.1913C>G (p.Ala638Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922222C>TCA393680746IGF1Rc.2276C>T (p.Ala759Val)
c.505C>T
n.467C>T
c.2339C>T (p.Ala780Val)
c.1367C>T (p.Ala456Val)
c.941C>T (p.Ala314Val)
c.2351C>T (p.Ala784Val)
c.1913C>T (p.Ala638Val)
 dbSNP gnomAD v3 gnomAD v4
15g.98922223C>ACA492338800IGF1Rc.2277C>A (p.Ala759=)
c.506C>A
n.468C>A
c.2340C>A (p.Ala780=)
c.1368C>A (p.Ala456=)
c.942C>A (p.Ala314=)
c.2352C>A (p.Ala784=)
c.1914C>A (p.Ala638=)
15g.98922223C=CA2199294777IGF1Rc.2277C= (p.Ala759=)
c.506C=
n.468C=
c.2340C= (p.Ala780=)
c.1368C= (p.Ala456=)
c.942C= (p.Ala314=)
c.2352C= (p.Ala784=)
c.1914C= (p.Ala638=)
15g.98922223C>GCA492338804IGF1Rc.2277C>G (p.Ala759=)
c.506C>G
n.468C>G
c.2340C>G (p.Ala780=)
c.1368C>G (p.Ala456=)
c.942C>G (p.Ala314=)
c.2352C>G (p.Ala784=)
c.1914C>G (p.Ala638=)
 gnomAD v4
15g.98922223C>TCA7752360IGF1Rc.2277C>T (p.Ala759=)
c.506C>T
n.468C>T
c.2340C>T (p.Ala780=)
c.1368C>T (p.Ala456=)
c.942C>T (p.Ala314=)
c.2352C>T (p.Ala784=)
c.1914C>T (p.Ala638=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922224G>ACA7752361IGF1Rc.2278G>A (p.Ala760Thr)
c.507G>A
n.469G>A
c.2341G>A (p.Ala781Thr)
c.1369G>A (p.Ala457Thr)
c.943G>A (p.Ala315Thr)
c.2353G>A (p.Ala785Thr)
c.1915G>A (p.Ala639Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.98922224G>CCA393680749IGF1Rc.2278G>C (p.Ala760Pro)
c.507G>C
n.469G>C
c.2341G>C (p.Ala781Pro)
c.1369G>C (p.Ala457Pro)
c.943G>C (p.Ala315Pro)
c.2353G>C (p.Ala785Pro)
c.1915G>C (p.Ala639Pro)
 dbSNP
15g.98922224G=CA2199294778IGF1Rc.2278G= (p.Ala760=)
c.507G=
n.469G=
c.2341G= (p.Ala781=)
c.1369G= (p.Ala457=)
c.943G= (p.Ala315=)
c.2353G= (p.Ala785=)
c.1915G= (p.Ala639=)
15g.98922224G>TCA393680750IGF1Rc.2278G>T (p.Ala760Ser)
c.507G>T
n.469G>T
c.2341G>T (p.Ala781Ser)
c.1369G>T (p.Ala457Ser)
c.943G>T (p.Ala315Ser)
c.2353G>T (p.Ala785Ser)
c.1915G>T (p.Ala639Ser)
 dbSNP gnomAD v2 gnomAD v4
15g.98922225C>ACA393680751IGF1Rc.2279C>A (p.Ala760Glu)
c.508C>A
n.470C>A
c.2342C>A (p.Ala781Glu)
c.1370C>A (p.Ala457Glu)
c.944C>A (p.Ala315Glu)
c.2354C>A (p.Ala785Glu)
c.1916C>A (p.Ala639Glu)
15g.98922225C=CA2199294779IGF1Rc.2279C= (p.Ala760=)
c.508C=
n.470C=
c.2342C= (p.Ala781=)
c.1370C= (p.Ala457=)
c.944C= (p.Ala315=)
c.2354C= (p.Ala785=)
c.1916C= (p.Ala639=)
15g.98922225C>GCA393680753IGF1Rc.2279C>G (p.Ala760Gly)
c.508C>G
n.470C>G
c.2342C>G (p.Ala781Gly)
c.1370C>G (p.Ala457Gly)
c.944C>G (p.Ala315Gly)
c.2354C>G (p.Ala785Gly)
c.1916C>G (p.Ala639Gly)
 dbSNP gnomAD v2 gnomAD v4
15g.98922225C>TCA393680754IGF1Rc.2279C>T (p.Ala760Val)
c.508C>T
n.470C>T
c.2342C>T (p.Ala781Val)
c.1370C>T (p.Ala457Val)
c.944C>T (p.Ala315Val)
c.2354C>T (p.Ala785Val)
c.1916C>T (p.Ala639Val)
 dbSNP gnomAD v3 gnomAD v4
15g.98922226A>CCA492338824IGF1Rc.2280A>C (p.Ala760=)
c.509A>C
n.471A>C
c.2343A>C (p.Ala781=)
c.1371A>C (p.Ala457=)
c.945A>C (p.Ala315=)
c.2355A>C (p.Ala785=)
c.1917A>C (p.Ala639=)
15g.98922226A>GCA492338827IGF1Rc.2280A>G (p.Ala760=)
c.509A>G
n.471A>G
c.2343A>G (p.Ala781=)
c.1371A>G (p.Ala457=)
c.945A>G (p.Ala315=)
c.2355A>G (p.Ala785=)
c.1917A>G (p.Ala639=)
15g.98922226A>TCA492338830IGF1Rc.2280A>T (p.Ala760=)
c.509A>T
n.471A>T
c.2343A>T (p.Ala781=)
c.1371A>T (p.Ala457=)
c.945A>T (p.Ala315=)
c.2355A>T (p.Ala785=)
c.1917A>T (p.Ala639=)
 dbSNP
15g.98922227G>ACA393680757IGF1Rc.2281G>A (p.Asp761Asn)
c.510G>A
n.472G>A
c.2344G>A (p.Asp782Asn)
c.1372G>A (p.Asp458Asn)
c.946G>A (p.Asp316Asn)
c.2356G>A (p.Asp786Asn)
c.1918G>A (p.Asp640Asn)
 dbSNP
15g.98922227G>CCA393680758IGF1Rc.2281G>C (p.Asp761His)
c.510G>C
n.472G>C
c.2344G>C (p.Asp782His)
c.1372G>C (p.Asp458His)
c.946G>C (p.Asp316His)
c.2356G>C (p.Asp786His)
c.1918G>C (p.Asp640His)
 dbSNP
15g.98922227G>TCA393680759IGF1Rc.2281G>T (p.Asp761Tyr)
c.510G>T
n.472G>T
c.2344G>T (p.Asp782Tyr)
c.1372G>T (p.Asp458Tyr)
c.946G>T (p.Asp316Tyr)
c.2356G>T (p.Asp786Tyr)
c.1918G>T (p.Asp640Tyr)
15g.98922228A=CA2199294780IGF1Rc.2282A= (p.Asp761=)
c.511A=
n.473A=
c.2345A= (p.Asp782=)
c.1373A= (p.Asp458=)
c.947A= (p.Asp316=)
c.2357A= (p.Asp786=)
c.1919A= (p.Asp640=)
15g.98922228A>CCA393680761IGF1Rc.2282A>C (p.Asp761Ala)
c.511A>C
n.473A>C
c.2345A>C (p.Asp782Ala)
c.1373A>C (p.Asp458Ala)
c.947A>C (p.Asp316Ala)
c.2357A>C (p.Asp786Ala)
c.1919A>C (p.Asp640Ala)
15g.98922228A>GCA393680763IGF1Rc.2282A>G (p.Asp761Gly)
c.511A>G
n.473A>G
c.2345A>G (p.Asp782Gly)
c.1373A>G (p.Asp458Gly)
c.947A>G (p.Asp316Gly)
c.2357A>G (p.Asp786Gly)
c.1919A>G (p.Asp640Gly)
 dbSNP gnomAD v2 gnomAD v4
15g.98922228A>TCA393680764IGF1Rc.2282A>T (p.Asp761Val)
c.511A>T
n.473A>T
c.2345A>T (p.Asp782Val)
c.1373A>T (p.Asp458Val)
c.947A>T (p.Asp316Val)
c.2357A>T (p.Asp786Val)
c.1919A>T (p.Asp640Val)
15g.98922229C>ACA393680766IGF1Rc.2283C>A (p.Asp761Glu)
c.512C>A
n.474C>A
c.2346C>A (p.Asp782Glu)
c.1374C>A (p.Asp458Glu)
c.948C>A (p.Asp316Glu)
c.2358C>A (p.Asp786Glu)
c.1920C>A (p.Asp640Glu)
 dbSNP
15g.98922229C>GCA393680767IGF1Rc.2283C>G (p.Asp761Glu)
c.512C>G
n.474C>G
c.2346C>G (p.Asp782Glu)
c.1374C>G (p.Asp458Glu)
c.948C>G (p.Asp316Glu)
c.2358C>G (p.Asp786Glu)
c.1920C>G (p.Asp640Glu)
15g.98922229C>TCA492338849IGF1Rc.2283C>T (p.Asp761=)
c.512C>T
n.474C>T
c.2346C>T (p.Asp782=)
c.1374C>T (p.Asp458=)
c.948C>T (p.Asp316=)
c.2358C>T (p.Asp786=)
c.1920C>T (p.Asp640=)
15g.98922230A>CCA393680773IGF1Rc.2284A>C (p.Thr762Pro)
c.513A>C
n.475A>C
c.2347A>C (p.Thr783Pro)
c.1375A>C (p.Thr459Pro)
c.949A>C (p.Thr317Pro)
c.2359A>C (p.Thr787Pro)
c.1921A>C (p.Thr641Pro)
15g.98922230A>GCA393680772IGF1Rc.2284A>G (p.Thr762Ala)
c.513A>G
n.475A>G
c.2347A>G (p.Thr783Ala)
c.1375A>G (p.Thr459Ala)
c.949A>G (p.Thr317Ala)
c.2359A>G (p.Thr787Ala)
c.1921A>G (p.Thr641Ala)
 gnomAD v4
15g.98922230A>TCA393680770IGF1Rc.2284A>T (p.Thr762Ser)
c.513A>T
n.475A>T
c.2347A>T (p.Thr783Ser)
c.1375A>T (p.Thr459Ser)
c.949A>T (p.Thr317Ser)
c.2359A>T (p.Thr787Ser)
c.1921A>T (p.Thr641Ser)
15g.98922231C>ACA7752362IGF1Rc.2285C>A (p.Thr762Asn)
c.514C>A
n.476C>A
c.2348C>A (p.Thr783Asn)
c.1376C>A (p.Thr459Asn)
c.950C>A (p.Thr317Asn)
c.2360C>A (p.Thr787Asn)
c.1922C>A (p.Thr641Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.98922231C=CA2199294781IGF1Rc.2285C= (p.Thr762=)
c.514C=
n.476C=
c.2348C= (p.Thr783=)
c.1376C= (p.Thr459=)
c.950C= (p.Thr317=)
c.2360C= (p.Thr787=)
c.1922C= (p.Thr641=)
15g.98922231C>GCA393680774IGF1Rc.2285C>G (p.Thr762Ser)
c.514C>G
n.476C>G
c.2348C>G (p.Thr783Ser)
c.1376C>G (p.Thr459Ser)
c.950C>G (p.Thr317Ser)
c.2360C>G (p.Thr787Ser)
c.1922C>G (p.Thr641Ser)
15g.98922231C>TCA275384313IGF1Rc.2285C>T (p.Thr762Ile)
c.514C>T
n.476C>T
c.2348C>T (p.Thr783Ile)
c.1376C>T (p.Thr459Ile)
c.950C>T (p.Thr317Ile)
c.2360C>T (p.Thr787Ile)
c.1922C>T (p.Thr641Ile)
 dbSNP gnomAD v2 gnomAD v4
15g.98922232C>ACA492338865IGF1Rc.2286C>A (p.Thr762=)
c.515C>A
n.477C>A
c.2349C>A (p.Thr783=)
c.1377C>A (p.Thr459=)
c.951C>A (p.Thr317=)
c.2361C>A (p.Thr787=)
c.1923C>A (p.Thr641=)
15g.98922232C>GCA492338867IGF1Rc.2286C>G (p.Thr762=)
c.515C>G
n.477C>G
c.2349C>G (p.Thr783=)
c.1377C>G (p.Thr459=)
c.951C>G (p.Thr317=)
c.2361C>G (p.Thr787=)
c.1923C>G (p.Thr641=)
 gnomAD v4
15g.98922232C>TCA492338870IGF1Rc.2286C>T (p.Thr762=)
c.515C>T
n.477C>T
c.2349C>T (p.Thr783=)
c.1377C>T (p.Thr459=)
c.951C>T (p.Thr317=)
c.2361C>T (p.Thr787=)
c.1923C>T (p.Thr641=)
 gnomAD v4
15g.98922233T>ACA393680778IGF1Rc.2287T>A (p.Tyr763Asn)
c.516T>A
n.478T>A
c.2350T>A (p.Tyr784Asn)
c.1378T>A (p.Tyr460Asn)
c.952T>A (p.Tyr318Asn)
c.2362T>A (p.Tyr788Asn)
c.1924T>A (p.Tyr642Asn)
 gnomAD v4
15g.98922233T>CCA393680779IGF1Rc.2287T>C (p.Tyr763His)
c.516T>C
n.478T>C
c.2350T>C (p.Tyr784His)
c.1378T>C (p.Tyr460His)
c.952T>C (p.Tyr318His)
c.2362T>C (p.Tyr788His)
c.1924T>C (p.Tyr642His)
15g.98922233T>GCA393680780IGF1Rc.2287T>G (p.Tyr763Asp)
c.516T>G
n.478T>G
c.2350T>G (p.Tyr784Asp)
c.1378T>G (p.Tyr460Asp)
c.952T>G (p.Tyr318Asp)
c.2362T>G (p.Tyr788Asp)
c.1924T>G (p.Tyr642Asp)
15g.98922234A=CA2199294782IGF1Rc.2288A= (p.Tyr763=)
c.517A=
n.479A=
c.2351A= (p.Tyr784=)
c.1379A= (p.Tyr460=)
c.953A= (p.Tyr318=)
c.2363A= (p.Tyr788=)
c.1925A= (p.Tyr642=)
15g.98922234A>CCA393680782IGF1Rc.2288A>C (p.Tyr763Ser)
c.517A>C
n.479A>C
c.2351A>C (p.Tyr784Ser)
c.1379A>C (p.Tyr460Ser)
c.953A>C (p.Tyr318Ser)
c.2363A>C (p.Tyr788Ser)
c.1925A>C (p.Tyr642Ser)
15g.98922234A>GCA275384317IGF1Rc.2288A>G (p.Tyr763Cys)
c.517A>G
n.479A>G
c.2351A>G (p.Tyr784Cys)
c.1379A>G (p.Tyr460Cys)
c.953A>G (p.Tyr318Cys)
c.2363A>G (p.Tyr788Cys)
c.1925A>G (p.Tyr642Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.98922234A>TCA393680783IGF1Rc.2288A>T (p.Tyr763Phe)
c.517A>T
n.479A>T
c.2351A>T (p.Tyr784Phe)
c.1379A>T (p.Tyr460Phe)
c.953A>T (p.Tyr318Phe)
c.2363A>T (p.Tyr788Phe)
c.1925A>T (p.Tyr642Phe)
15g.98922237_98922239delCA2630564856IGF1Rc.2291_2293del (p.Asn764del)
c.520_522del
n.482_484del
c.2354_2356del (p.Asn785del)
c.1382_1384del (p.Asn461del)
c.956_958del (p.Asn319del)
c.2366_2368del (p.Asn789del)
c.1928_1930del (p.Asn643del)
 gnomAD v4
15g.98922235C>ACA393680785IGF1Rc.2289C>A (p.Tyr763Ter)
c.518C>A
n.480C>A
c.2352C>A (p.Tyr784Ter)
c.1380C>A (p.Tyr460Ter)
c.954C>A (p.Tyr318Ter)
c.2364C>A (p.Tyr788Ter)
c.1926C>A (p.Tyr642Ter)
15g.98922235C>GCA393680786IGF1Rc.2289C>G (p.Tyr763Ter)
c.518C>G
n.480C>G
c.2352C>G (p.Tyr784Ter)
c.1380C>G (p.Tyr460Ter)
c.954C>G (p.Tyr318Ter)
c.2364C>G (p.Tyr788Ter)
c.1926C>G (p.Tyr642Ter)
15g.98922235C>TCA492338890IGF1Rc.2289C>T (p.Tyr763=)
c.518C>T
n.480C>T
c.2352C>T (p.Tyr784=)
c.1380C>T (p.Tyr460=)
c.954C>T (p.Tyr318=)
c.2364C>T (p.Tyr788=)
c.1926C>T (p.Tyr642=)
15g.98922236A>CCA393680788IGF1Rc.2290A>C (p.Asn764His)
c.519A>C
n.481A>C
c.2353A>C (p.Asn785His)
c.1381A>C (p.Asn461His)
c.955A>C (p.Asn319His)
c.2365A>C (p.Asn789His)
c.1927A>C (p.Asn643His)
15g.98922236A>GCA393680789IGF1Rc.2290A>G (p.Asn764Asp)
c.519A>G
n.481A>G
c.2353A>G (p.Asn785Asp)
c.1381A>G (p.Asn461Asp)
c.955A>G (p.Asn319Asp)
c.2365A>G (p.Asn789Asp)
c.1927A>G (p.Asn643Asp)
15g.98922236A>TCA393680791IGF1Rc.2290A>T (p.Asn764Tyr)
c.519A>T
n.481A>T
c.2353A>T (p.Asn785Tyr)
c.1381A>T (p.Asn461Tyr)
c.955A>T (p.Asn319Tyr)
c.2365A>T (p.Asn789Tyr)
c.1927A>T (p.Asn643Tyr)
15g.98922237A=CA2199294783IGF1Rc.2291A= (p.Asn764=)
c.520A=
n.482A=
c.2354A= (p.Asn785=)
c.1382A= (p.Asn461=)
c.956A= (p.Asn319=)
c.2366A= (p.Asn789=)
c.1928A= (p.Asn643=)
15g.98922237A>CCA7752363IGF1Rc.2291A>C (p.Asn764Thr)
c.520A>C
n.482A>C
c.2354A>C (p.Asn785Thr)
c.1382A>C (p.Asn461Thr)
c.956A>C (p.Asn319Thr)
c.2366A>C (p.Asn789Thr)
c.1928A>C (p.Asn643Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922237A>GCA393680793IGF1Rc.2291A>G (p.Asn764Ser)
c.520A>G
n.482A>G
c.2354A>G (p.Asn785Ser)
c.1382A>G (p.Asn461Ser)
c.956A>G (p.Asn319Ser)
c.2366A>G (p.Asn789Ser)
c.1928A>G (p.Asn643Ser)
 dbSNP gnomAD v4
15g.98922237A>TCA393680794IGF1Rc.2291A>T (p.Asn764Ile)
c.520A>T
n.482A>T
c.2354A>T (p.Asn785Ile)
c.1382A>T (p.Asn461Ile)
c.956A>T (p.Asn319Ile)
c.2366A>T (p.Asn789Ile)
c.1928A>T (p.Asn643Ile)
15g.98922238C>ACA393680796IGF1Rc.2292C>A (p.Asn764Lys)
c.521C>A
n.483C>A
c.2355C>A (p.Asn785Lys)
c.1383C>A (p.Asn461Lys)
c.957C>A (p.Asn319Lys)
c.2367C>A (p.Asn789Lys)
c.1929C>A (p.Asn643Lys)
15g.98922238C>GCA393680798IGF1Rc.2292C>G (p.Asn764Lys)
c.521C>G
n.483C>G
c.2355C>G (p.Asn785Lys)
c.1383C>G (p.Asn461Lys)
c.957C>G (p.Asn319Lys)
c.2367C>G (p.Asn789Lys)
c.1929C>G (p.Asn643Lys)
15g.98922238C>TCA492338906IGF1Rc.2292C>T (p.Asn764=)
c.521C>T
n.483C>T
c.2355C>T (p.Asn785=)
c.1383C>T (p.Asn461=)
c.957C>T (p.Asn319=)
c.2367C>T (p.Asn789=)
c.1929C>T (p.Asn643=)
 dbSNP
15g.98922239A>CCA393680800IGF1Rc.2293A>C (p.Ile765Leu)
c.522A>C
n.484A>C
c.2356A>C (p.Ile786Leu)
c.1384A>C (p.Ile462Leu)
c.958A>C (p.Ile320Leu)
c.2368A>C (p.Ile790Leu)
c.1930A>C (p.Ile644Leu)
15g.98922239A>GCA393680801IGF1Rc.2293A>G (p.Ile765Val)
c.522A>G
n.484A>G
c.2356A>G (p.Ile786Val)
c.1384A>G (p.Ile462Val)
c.958A>G (p.Ile320Val)
c.2368A>G (p.Ile790Val)
c.1930A>G (p.Ile644Val)
 gnomAD v4
15g.98922239A>TCA393680803IGF1Rc.2293A>T (p.Ile765Phe)
c.522A>T
n.484A>T
c.2356A>T (p.Ile786Phe)
c.1384A>T (p.Ile462Phe)
c.958A>T (p.Ile320Phe)
c.2368A>T (p.Ile790Phe)
c.1930A>T (p.Ile644Phe)
15g.98922240T>ACA7752364IGF1Rc.2294T>A (p.Ile765Asn)
c.523T>A
n.485T>A
c.2357T>A (p.Ile786Asn)
c.1385T>A (p.Ile462Asn)
c.959T>A (p.Ile320Asn)
c.2369T>A (p.Ile790Asn)
c.1931T>A (p.Ile644Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.98922240T>CCA393680805IGF1Rc.2294T>C (p.Ile765Thr)
c.523T>C
n.485T>C
c.2357T>C (p.Ile786Thr)
c.1385T>C (p.Ile462Thr)
c.959T>C (p.Ile320Thr)
c.2369T>C (p.Ile790Thr)
c.1931T>C (p.Ile644Thr)
 dbSNP
15g.98922240T>GCA393680806IGF1Rc.2294T>G (p.Ile765Ser)
c.523T>G
n.485T>G
c.2357T>G (p.Ile786Ser)
c.1385T>G (p.Ile462Ser)
c.959T>G (p.Ile320Ser)
c.2369T>G (p.Ile790Ser)
c.1931T>G (p.Ile644Ser)
15g.98922240T=CA2199294784IGF1Rc.2294T= (p.Ile765=)
c.523T=
n.485T=
c.2357T= (p.Ile786=)
c.1385T= (p.Ile462=)
c.959T= (p.Ile320=)
c.2369T= (p.Ile790=)
c.1931T= (p.Ile644=)
15g.98922241C>ACA492338932IGF1Rc.2295C>A (p.Ile765=)
c.524C>A
n.486C>A
c.2358C>A (p.Ile786=)
c.1386C>A (p.Ile462=)
c.960C>A (p.Ile320=)
c.2370C>A (p.Ile790=)
c.1932C>A (p.Ile644=)
15g.98922241C>GCA393680808IGF1Rc.2295C>G (p.Ile765Met)
c.524C>G
n.486C>G
c.2358C>G (p.Ile786Met)
c.1386C>G (p.Ile462Met)
c.960C>G (p.Ile320Met)
c.2370C>G (p.Ile790Met)
c.1932C>G (p.Ile644Met)
15g.98922241C>TCA492338927IGF1Rc.2295C>T (p.Ile765=)
c.524C>T
n.486C>T
c.2358C>T (p.Ile786=)
c.1386C>T (p.Ile462=)
c.960C>T (p.Ile320=)
c.2370C>T (p.Ile790=)
c.1932C>T (p.Ile644=)
 dbSNP
15g.98922242A>CCA393680809IGF1Rc.2296A>C (p.Thr766Pro)
c.525A>C
n.487A>C
c.2359A>C (p.Thr787Pro)
c.1387A>C (p.Thr463Pro)
c.961A>C (p.Thr321Pro)
c.2371A>C (p.Thr791Pro)
c.1933A>C (p.Thr645Pro)
15g.98922242A>GCA393680811IGF1Rc.2296A>G (p.Thr766Ala)
c.525A>G
n.487A>G
c.2359A>G (p.Thr787Ala)
c.1387A>G (p.Thr463Ala)
c.961A>G (p.Thr321Ala)
c.2371A>G (p.Thr791Ala)
c.1933A>G (p.Thr645Ala)
15g.98922242A>TCA393680813IGF1Rc.2296A>T (p.Thr766Ser)
c.525A>T
n.487A>T
c.2359A>T (p.Thr787Ser)
c.1387A>T (p.Thr463Ser)
c.961A>T (p.Thr321Ser)
c.2371A>T (p.Thr791Ser)
c.1933A>T (p.Thr645Ser)
15g.98922243C>ACA393680816IGF1Rc.2297C>A (p.Thr766Asn)
n.488C>A
c.2360C>A (p.Thr787Asn)
c.1388C>A (p.Thr463Asn)
c.962C>A (p.Thr321Asn)
c.2372C>A (p.Thr791Asn)
c.1934C>A (p.Thr645Asn)
15g.98922243C>GCA393680817IGF1Rc.2297C>G (p.Thr766Ser)
n.488C>G
c.2360C>G (p.Thr787Ser)
c.1388C>G (p.Thr463Ser)
c.962C>G (p.Thr321Ser)
c.2372C>G (p.Thr791Ser)
c.1934C>G (p.Thr645Ser)
15g.98922243C>TCA393680814IGF1Rc.2297C>T (p.Thr766Ile)
n.488C>T
c.2360C>T (p.Thr787Ile)
c.1388C>T (p.Thr463Ile)
c.962C>T (p.Thr321Ile)
c.2372C>T (p.Thr791Ile)
c.1934C>T (p.Thr645Ile)
15g.98922244C>ACA492338952IGF1Rc.2298C>A (p.Thr766=)
n.489C>A
c.2361C>A (p.Thr787=)
c.1389C>A (p.Thr463=)
c.963C>A (p.Thr321=)
c.2373C>A (p.Thr791=)
c.1935C>A (p.Thr645=)
 dbSNP
15g.98922244C=CA2199294785IGF1Rc.2298C= (p.Thr766=)
n.489C=
c.2361C= (p.Thr787=)
c.1389C= (p.Thr463=)
c.963C= (p.Thr321=)
c.2373C= (p.Thr791=)
c.1935C= (p.Thr645=)
15g.98922244C>GCA492338957IGF1Rc.2298C>G (p.Thr766=)
n.489C>G
c.2361C>G (p.Thr787=)
c.1389C>G (p.Thr463=)
c.963C>G (p.Thr321=)
c.2373C>G (p.Thr791=)
c.1935C>G (p.Thr645=)
15g.98922244C>TCA200789IGF1Rc.2298C>T (p.Thr766=)
n.489C>T
c.2361C>T (p.Thr787=)
c.1389C>T (p.Thr463=)
c.963C>T (p.Thr321=)
c.2373C>T (p.Thr791=)
c.1935C>T (p.Thr645=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922245G>ACA275384334IGF1Rc.2299G>A (p.Asp767Asn)
n.490G>A
c.2362G>A (p.Asp788Asn)
c.1390G>A (p.Asp464Asn)
c.964G>A (p.Asp322Asn)
c.2374G>A (p.Asp792Asn)
c.1936G>A (p.Asp646Asn)
 dbSNP gnomAD v4
15g.98922245G>CCA393680820IGF1Rc.2299G>C (p.Asp767His)
n.490G>C
c.2362G>C (p.Asp788His)
c.1390G>C (p.Asp464His)
c.964G>C (p.Asp322His)
c.2374G>C (p.Asp792His)
c.1936G>C (p.Asp646His)
 dbSNP
15g.98922245G=CA2199294786IGF1Rc.2299G= (p.Asp767=)
n.490G=
c.2362G= (p.Asp788=)
c.1390G= (p.Asp464=)
c.964G= (p.Asp322=)
c.2374G= (p.Asp792=)
c.1936G= (p.Asp646=)
15g.98922245G>TCA393680822IGF1Rc.2299G>T (p.Asp767Tyr)
n.490G>T
c.2362G>T (p.Asp788Tyr)
c.1390G>T (p.Asp464Tyr)
c.964G>T (p.Asp322Tyr)
c.2374G>T (p.Asp792Tyr)
c.1936G>T (p.Asp646Tyr)
15g.98922246A>CCA393680825IGF1Rc.2300A>C (p.Asp767Ala)
n.491A>C
c.2363A>C (p.Asp788Ala)
c.1391A>C (p.Asp464Ala)
c.965A>C (p.Asp322Ala)
c.2375A>C (p.Asp792Ala)
c.1937A>C (p.Asp646Ala)
15g.98922246A>GCA393680826IGF1Rc.2300A>G (p.Asp767Gly)
n.491A>G
c.2363A>G (p.Asp788Gly)
c.1391A>G (p.Asp464Gly)
c.965A>G (p.Asp322Gly)
c.2375A>G (p.Asp792Gly)
c.1937A>G (p.Asp646Gly)
15g.98922246A>TCA393680828IGF1Rc.2300A>T (p.Asp767Val)
n.491A>T
c.2363A>T (p.Asp788Val)
c.1391A>T (p.Asp464Val)
c.965A>T (p.Asp322Val)
c.2375A>T (p.Asp792Val)
c.1937A>T (p.Asp646Val)
15g.98922246_98922247delinsACCA2199294787IGF1Rc.2300_2301delinsAC (p.Asp767=)
n.491_492delinsAC
c.2363_2364delinsAC (p.Asp788=)
c.1391_1392delinsAC (p.Asp464=)
c.965_966delinsAC (p.Asp322=)
c.2375_2376delinsAC (p.Asp792=)
c.1937_1938delinsAC (p.Asp646=)
15g.98922247C>ACA393680829IGF1Rc.2301C>A (p.Asp767Glu)
n.492C>A
c.2364C>A (p.Asp788Glu)
c.1392C>A (p.Asp464Glu)
c.966C>A (p.Asp322Glu)
c.2376C>A (p.Asp792Glu)
c.1938C>A (p.Asp646Glu)
 dbSNP
15g.98922247C=CA2199294788IGF1Rc.2301C= (p.Asp767=)
n.492C=
c.2364C= (p.Asp788=)
c.1392C= (p.Asp464=)
c.966C= (p.Asp322=)
c.2376C= (p.Asp792=)
c.1938C= (p.Asp646=)
15g.98922247C>GCA393680831IGF1Rc.2301C>G (p.Asp767Glu)
n.492C>G
c.2364C>G (p.Asp788Glu)
c.1392C>G (p.Asp464Glu)
c.966C>G (p.Asp322Glu)
c.2376C>G (p.Asp792Glu)
c.1938C>G (p.Asp646Glu)
15g.98922247C>TCA492338975IGF1Rc.2301C>T (p.Asp767=)
n.492C>T
c.2364C>T (p.Asp788=)
c.1392C>T (p.Asp464=)
c.966C>T (p.Asp322=)
c.2376C>T (p.Asp792=)
c.1938C>T (p.Asp646=)
15g.98922249delCA717747601IGF1Rc.2303del (p.Pro768ArgfsTer?)
n.494del
c.2366del (p.Pro789ArgfsTer?)
c.1394del (p.Pro465ArgfsTer?)
c.968del (p.Pro323ArgfsTer?)
c.2378del (p.Pro793ArgfsTer?)
c.1940del (p.Pro647ArgfsTer?)
 dbSNP
15g.98922248C>ACA393680833IGF1Rc.2302C>A (p.Pro768Thr)
n.493C>A
c.2365C>A (p.Pro789Thr)
c.1393C>A (p.Pro465Thr)
c.967C>A (p.Pro323Thr)
c.2377C>A (p.Pro793Thr)
c.1939C>A (p.Pro647Thr)
15g.98922248C=CA2199294789IGF1Rc.2302C= (p.Pro768=)
n.493C=
c.2365C= (p.Pro789=)
c.1393C= (p.Pro465=)
c.967C= (p.Pro323=)
c.2377C= (p.Pro793=)
c.1939C= (p.Pro647=)
15g.98922248C>GCA7752365IGF1Rc.2302C>G (p.Pro768Ala)
n.493C>G
c.2365C>G (p.Pro789Ala)
c.1393C>G (p.Pro465Ala)
c.967C>G (p.Pro323Ala)
c.2377C>G (p.Pro793Ala)
c.1939C>G (p.Pro647Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.98922248C>TCA393680835IGF1Rc.2302C>T (p.Pro768Ser)
n.493C>T
c.2365C>T (p.Pro789Ser)
c.1393C>T (p.Pro465Ser)
c.967C>T (p.Pro323Ser)
c.2377C>T (p.Pro793Ser)
c.1939C>T (p.Pro647Ser)
 gnomAD v4
15g.98922249C>ACA393680837IGF1Rc.2303C>A (p.Pro768Gln)
n.494C>A
c.2366C>A (p.Pro789Gln)
c.1394C>A (p.Pro465Gln)
c.968C>A (p.Pro323Gln)
c.2378C>A (p.Pro793Gln)
c.1940C>A (p.Pro647Gln)
15g.98922249C=CA2199294790IGF1Rc.2303C= (p.Pro768=)
n.494C=
c.2366C= (p.Pro789=)
c.1394C= (p.Pro465=)
c.968C= (p.Pro323=)
c.2378C= (p.Pro793=)
c.1940C= (p.Pro647=)
15g.98922249C>GCA393680839IGF1Rc.2303C>G (p.Pro768Arg)
n.494C>G
c.2366C>G (p.Pro789Arg)
c.1394C>G (p.Pro465Arg)
c.968C>G (p.Pro323Arg)
c.2378C>G (p.Pro793Arg)
c.1940C>G (p.Pro647Arg)
15g.98922249C>TCA7752366IGF1Rc.2303C>T (p.Pro768Leu)
n.494C>T
c.2366C>T (p.Pro789Leu)
c.1394C>T (p.Pro465Leu)
c.968C>T (p.Pro323Leu)
c.2378C>T (p.Pro793Leu)
c.1940C>T (p.Pro647Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922250G>ACA7752367IGF1Rc.2304G>A (p.Pro768=)
n.495G>A
c.2367G>A (p.Pro789=)
c.1395G>A (p.Pro465=)
c.969G>A (p.Pro323=)
c.2379G>A (p.Pro793=)
c.1941G>A (p.Pro647=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.98922250G>CCA492339988IGF1Rc.2304G>C (p.Pro768=)
n.495G>C
c.2367G>C (p.Pro789=)
c.1395G>C (p.Pro465=)
c.969G>C (p.Pro323=)
c.2379G>C (p.Pro793=)
c.1941G>C (p.Pro647=)
 dbSNP
15g.98922250G=CA2199294791IGF1Rc.2304G= (p.Pro768=)
n.495G=
c.2367G= (p.Pro789=)
c.1395G= (p.Pro465=)
c.969G= (p.Pro323=)
c.2379G= (p.Pro793=)
c.1941G= (p.Pro647=)
15g.98922250G>TCA492339989IGF1Rc.2304G>T (p.Pro768=)
n.495G>T
c.2367G>T (p.Pro789=)
c.1395G>T (p.Pro465=)
c.969G>T (p.Pro323=)
c.2379G>T (p.Pro793=)
c.1941G>T (p.Pro647=)
 dbSNP gnomAD v4
15g.98922251G>ACA393680845IGF1Rc.2305G>A (p.Glu769Lys)
n.496G>A
c.2368G>A (p.Glu790Lys)
c.1396G>A (p.Glu466Lys)
c.970G>A (p.Glu324Lys)
c.2380G>A (p.Glu794Lys)
c.1942G>A (p.Glu648Lys)
15g.98922251G>CCA393680841IGF1Rc.2305G>C (p.Glu769Gln)
n.496G>C
c.2368G>C (p.Glu790Gln)
c.1396G>C (p.Glu466Gln)
c.970G>C (p.Glu324Gln)
c.2380G>C (p.Glu794Gln)
c.1942G>C (p.Glu648Gln)
 dbSNP
15g.98922251G>TCA393680843IGF1Rc.2305G>T (p.Glu769Ter)
n.496G>T
c.2368G>T (p.Glu790Ter)
c.1396G>T (p.Glu466Ter)
c.970G>T (p.Glu324Ter)
c.2380G>T (p.Glu794Ter)
c.1942G>T (p.Glu648Ter)
15g.98922252A>CCA393680847IGF1Rc.2306A>C (p.Glu769Ala)
n.497A>C
c.2369A>C (p.Glu790Ala)
c.1397A>C (p.Glu466Ala)
c.971A>C (p.Glu324Ala)
c.2381A>C (p.Glu794Ala)
c.1943A>C (p.Glu648Ala)
15g.98922252A>GCA393680849IGF1Rc.2306A>G (p.Glu769Gly)
n.497A>G
c.2369A>G (p.Glu790Gly)
c.1397A>G (p.Glu466Gly)
c.971A>G (p.Glu324Gly)
c.2381A>G (p.Glu794Gly)
c.1943A>G (p.Glu648Gly)
15g.98922252A>TCA393680850IGF1Rc.2306A>T (p.Glu769Val)
n.497A>T
c.2369A>T (p.Glu790Val)
c.1397A>T (p.Glu466Val)
c.971A>T (p.Glu324Val)
c.2381A>T (p.Glu794Val)
c.1943A>T (p.Glu648Val)
15g.98922253A>CCA393680852IGF1Rc.2307A>C (p.Glu769Asp)
n.498A>C
c.2370A>C (p.Glu790Asp)
c.1398A>C (p.Glu466Asp)
c.972A>C (p.Glu324Asp)
c.2382A>C (p.Glu794Asp)
c.1944A>C (p.Glu648Asp)
15g.98922253A>GCA492339998IGF1Rc.2307A>G (p.Glu769=)
n.498A>G
c.2370A>G (p.Glu790=)
c.1398A>G (p.Glu466=)
c.972A>G (p.Glu324=)
c.2382A>G (p.Glu794=)
c.1944A>G (p.Glu648=)
 gnomAD v4
15g.98922253A>TCA393680853IGF1Rc.2307A>T (p.Glu769Asp)
n.498A>T
c.2370A>T (p.Glu790Asp)
c.1398A>T (p.Glu466Asp)
c.972A>T (p.Glu324Asp)
c.2382A>T (p.Glu794Asp)
c.1944A>T (p.Glu648Asp)
15g.98922254G>ACA393680855IGF1Rc.2308G>A (p.Glu770Lys)
n.499G>A
c.2371G>A (p.Glu791Lys)
c.1399G>A (p.Glu467Lys)
c.973G>A (p.Glu325Lys)
c.2383G>A (p.Glu795Lys)
c.1945G>A (p.Glu649Lys)
 dbSNP gnomAD v3 gnomAD v4
15g.98922254G>CCA393680856IGF1Rc.2308G>C (p.Glu770Gln)
n.499G>C
c.2371G>C (p.Glu791Gln)
c.1399G>C (p.Glu467Gln)
c.973G>C (p.Glu325Gln)
c.2383G>C (p.Glu795Gln)
c.1945G>C (p.Glu649Gln)
15g.98922254G=CA2199294792IGF1Rc.2308G= (p.Glu770=)
n.499G=
c.2371G= (p.Glu791=)
c.1399G= (p.Glu467=)
c.973G= (p.Glu325=)
c.2383G= (p.Glu795=)
c.1945G= (p.Glu649=)
15g.98922254G>TCA393680857IGF1Rc.2308G>T (p.Glu770Ter)
n.499G>T
c.2371G>T (p.Glu791Ter)
c.1399G>T (p.Glu467Ter)
c.973G>T (p.Glu325Ter)
c.2383G>T (p.Glu795Ter)
c.1945G>T (p.Glu649Ter)
15g.98922255A>CCA393680859IGF1Rc.2309A>C (p.Glu770Ala)
n.500A>C
c.2372A>C (p.Glu791Ala)
c.1400A>C (p.Glu467Ala)
c.974A>C (p.Glu325Ala)
c.2384A>C (p.Glu795Ala)
c.1946A>C (p.Glu649Ala)
15g.98922255A>GCA393680861IGF1Rc.2309A>G (p.Glu770Gly)
n.500A>G
c.2372A>G (p.Glu791Gly)
c.1400A>G (p.Glu467Gly)
c.974A>G (p.Glu325Gly)
c.2384A>G (p.Glu795Gly)
c.1946A>G (p.Glu649Gly)
15g.98922255A>TCA393680863IGF1Rc.2309A>T (p.Glu770Val)
n.500A>T
c.2372A>T (p.Glu791Val)
c.1400A>T (p.Glu467Val)
c.974A>T (p.Glu325Val)
c.2384A>T (p.Glu795Val)
c.1946A>T (p.Glu649Val)
15g.98922256G>ACA492340007IGF1Rc.2310G>A (p.Glu770=)
n.501G>A
c.2373G>A (p.Glu791=)
c.1401G>A (p.Glu467=)
c.975G>A (p.Glu325=)
c.2385G>A (p.Glu795=)
c.1947G>A (p.Glu649=)
15g.98922256G>CCA393680864IGF1Rc.2310G>C (p.Glu770Asp)
n.501G>C
c.2373G>C (p.Glu791Asp)
c.1401G>C (p.Glu467Asp)
c.975G>C (p.Glu325Asp)
c.2385G>C (p.Glu795Asp)
c.1947G>C (p.Glu649Asp)
15g.98922256G>TCA393680865IGF1Rc.2310G>T (p.Glu770Asp)
n.501G>T
c.2373G>T (p.Glu791Asp)
c.1401G>T (p.Glu467Asp)
c.975G>T (p.Glu325Asp)
c.2385G>T (p.Glu795Asp)
c.1947G>T (p.Glu649Asp)
15g.98922257C>ACA393680866IGF1Rc.2311C>A (p.Leu771Met)
n.502C>A
c.2374C>A (p.Leu792Met)
c.1402C>A (p.Leu468Met)
c.976C>A (p.Leu326Met)
c.2386C>A (p.Leu796Met)
c.1948C>A (p.Leu650Met)
 gnomAD v4
15g.98922257C=CA2199294793IGF1Rc.2311C= (p.Leu771=)
n.502C=
c.2374C= (p.Leu792=)
c.1402C= (p.Leu468=)
c.976C= (p.Leu326=)
c.2386C= (p.Leu796=)
c.1948C= (p.Leu650=)
15g.98922257C>GCA7752368IGF1Rc.2311C>G (p.Leu771Val)
n.502C>G
c.2374C>G (p.Leu792Val)
c.1402C>G (p.Leu468Val)
c.976C>G (p.Leu326Val)
c.2386C>G (p.Leu796Val)
c.1948C>G (p.Leu650Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.98922257C>TCA492340013IGF1Rc.2311C>T (p.Leu771=)
n.502C>T
c.2374C>T (p.Leu792=)
c.1402C>T (p.Leu468=)
c.976C>T (p.Leu326=)
c.2386C>T (p.Leu796=)
c.1948C>T (p.Leu650=)
15g.98922258T>ACA393680868IGF1Rc.2312T>A (p.Leu771Gln)
n.503T>A
c.2375T>A (p.Leu792Gln)
c.1403T>A (p.Leu468Gln)
c.977T>A (p.Leu326Gln)
c.2387T>A (p.Leu796Gln)
c.1949T>A (p.Leu650Gln)
15g.98922258T>CCA393680870IGF1Rc.2312T>C (p.Leu771Pro)
n.503T>C
c.2375T>C (p.Leu792Pro)
c.1403T>C (p.Leu468Pro)
c.977T>C (p.Leu326Pro)
c.2387T>C (p.Leu796Pro)
c.1949T>C (p.Leu650Pro)
15g.98922258T>GCA393680872IGF1Rc.2312T>G (p.Leu771Arg)
n.503T>G
c.2375T>G (p.Leu792Arg)
c.1403T>G (p.Leu468Arg)
c.977T>G (p.Leu326Arg)
c.2387T>G (p.Leu796Arg)
c.1949T>G (p.Leu650Arg)
15g.98922259G>ACA492340021IGF1Rc.2313G>A (p.Leu771=)
n.504G>A
c.2376G>A (p.Leu792=)
c.1404G>A (p.Leu468=)
c.978G>A (p.Leu326=)
c.2388G>A (p.Leu796=)
c.1950G>A (p.Leu650=)
15g.98922259G>CCA492340023IGF1Rc.2313G>C (p.Leu771=)
n.504G>C
c.2376G>C (p.Leu792=)
c.1404G>C (p.Leu468=)
c.978G>C (p.Leu326=)
c.2388G>C (p.Leu796=)
c.1950G>C (p.Leu650=)
15g.98922259G>TCA492340020IGF1Rc.2313G>T (p.Leu771=)
n.504G>T
c.2376G>T (p.Leu792=)
c.1404G>T (p.Leu468=)
c.978G>T (p.Leu326=)
c.2388G>T (p.Leu796=)
c.1950G>T (p.Leu650=)
15g.98922260G>ACA393680874IGF1Rc.2314G>A (p.Glu772Lys)
n.505G>A
c.2377G>A (p.Glu793Lys)
c.1405G>A (p.Glu469Lys)
c.979G>A (p.Glu327Lys)
c.2389G>A (p.Glu797Lys)
c.1951G>A (p.Glu651Lys)
 dbSNP
15g.98922260G>CCA393680875IGF1Rc.2314G>C (p.Glu772Gln)
n.505G>C
c.2377G>C (p.Glu793Gln)
c.1405G>C (p.Glu469Gln)
c.979G>C (p.Glu327Gln)
c.2389G>C (p.Glu797Gln)
c.1951G>C (p.Glu651Gln)
15g.98922260G>TCA393680877IGF1Rc.2314G>T (p.Glu772Ter)
n.505G>T
c.2377G>T (p.Glu793Ter)
c.1405G>T (p.Glu469Ter)
c.979G>T (p.Glu327Ter)
c.2389G>T (p.Glu797Ter)
c.1951G>T (p.Glu651Ter)
15g.98922261A=CA2199294794IGF1Rc.2315A= (p.Glu772=)
n.506A=
c.2378A= (p.Glu793=)
c.1406A= (p.Glu469=)
c.980A= (p.Glu327=)
c.2390A= (p.Glu797=)
c.1952A= (p.Glu651=)
15g.98922261A>CCA393680879IGF1Rc.2315A>C (p.Glu772Ala)
n.506A>C
c.2378A>C (p.Glu793Ala)
c.1406A>C (p.Glu469Ala)
c.980A>C (p.Glu327Ala)
c.2390A>C (p.Glu797Ala)
c.1952A>C (p.Glu651Ala)
15g.98922261A>GCA393680880IGF1Rc.2315A>G (p.Glu772Gly)
n.506A>G
c.2378A>G (p.Glu793Gly)
c.1406A>G (p.Glu469Gly)
c.980A>G (p.Glu327Gly)
c.2390A>G (p.Glu797Gly)
c.1952A>G (p.Glu651Gly)
 dbSNP gnomAD v2 gnomAD v4
15g.98922261A>TCA393680882IGF1Rc.2315A>T (p.Glu772Val)
n.506A>T
c.2378A>T (p.Glu793Val)
c.1406A>T (p.Glu469Val)
c.980A>T (p.Glu327Val)
c.2390A>T (p.Glu797Val)
c.1952A>T (p.Glu651Val)
15g.98922262G>ACA492340032IGF1Rc.2316G>A (p.Glu772=)
n.507G>A
c.2379G>A (p.Glu793=)
c.1407G>A (p.Glu469=)
c.981G>A (p.Glu327=)
c.2391G>A (p.Glu797=)
c.1953G>A (p.Glu651=)
15g.98922262G>CCA393680884IGF1Rc.2316G>C (p.Glu772Asp)
n.507G>C
c.2379G>C (p.Glu793Asp)
c.1407G>C (p.Glu469Asp)
c.981G>C (p.Glu327Asp)
c.2391G>C (p.Glu797Asp)
c.1953G>C (p.Glu651Asp)
 dbSNP
15g.98922262G>TCA393680885IGF1Rc.2316G>T (p.Glu772Asp)
n.507G>T
c.2379G>T (p.Glu793Asp)
c.1407G>T (p.Glu469Asp)
c.981G>T (p.Glu327Asp)
c.2391G>T (p.Glu797Asp)
c.1953G>T (p.Glu651Asp)

Number of alleles fetched