Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.46834854T>ACA388150126HTR2Ac.1399A>T (p.Lys467Ter)
c.910A>T (p.Lys304Ter)
c.1147A>T (p.Lys383Ter)
13g.46834854T>CCA388150127HTR2Ac.1399A>G (p.Lys467Glu)
c.910A>G (p.Lys304Glu)
c.1147A>G (p.Lys383Glu)
13g.46834854T>GCA388150128HTR2Ac.1399A>C (p.Lys467Gln)
c.910A>C (p.Lys304Gln)
c.1147A>C (p.Lys383Gln)
13g.46834855T>ACA388150129HTR2Ac.1398A>T (p.Glu466Asp)
c.909A>T (p.Glu303Asp)
c.1146A>T (p.Glu382Asp)
13g.46834855T>CCA483739051HTR2Ac.1398A>G (p.Glu466=)
c.909A>G (p.Glu303=)
c.1146A>G (p.Glu382=)
13g.46834855T>GCA388150130HTR2Ac.1398A>C (p.Glu466Asp)
c.909A>C (p.Glu303Asp)
c.1146A>C (p.Glu382Asp)
13g.46834856T>ACA388150133HTR2Ac.1397A>T (p.Glu466Val)
c.908A>T (p.Glu303Val)
c.1145A>T (p.Glu382Val)
13g.46834856T>CCA388150132HTR2Ac.1397A>G (p.Glu466Gly)
c.908A>G (p.Glu303Gly)
c.1145A>G (p.Glu382Gly)
 COSMIC COSMIC
13g.46834856T>GCA388150131HTR2Ac.1397A>C (p.Glu466Ala)
c.908A>C (p.Glu303Ala)
c.1145A>C (p.Glu382Ala)
13g.46834857C>ACA388150134HTR2Ac.1396G>T (p.Glu466Ter)
c.907G>T (p.Glu303Ter)
c.1144G>T (p.Glu382Ter)
13g.46834857C>GCA388150135HTR2Ac.1396G>C (p.Glu466Gln)
c.907G>C (p.Glu303Gln)
c.1144G>C (p.Glu382Gln)
13g.46834857C>TCA388150136HTR2Ac.1396G>A (p.Glu466Lys)
c.907G>A (p.Glu303Lys)
c.1144G>A (p.Glu382Lys)
 COSMIC COSMIC
13g.46834858A>CCA388150137HTR2Ac.1395T>G (p.Asn465Lys)
c.906T>G (p.Asn302Lys)
c.1143T>G (p.Asn381Lys)
13g.46834858A>GCA483739052HTR2Ac.1395T>C (p.Asn465=)
c.906T>C (p.Asn302=)
c.1143T>C (p.Asn381=)
13g.46834858A>TCA388150138HTR2Ac.1395T>A (p.Asn465Lys)
c.906T>A (p.Asn302Lys)
c.1143T>A (p.Asn381Lys)
13g.46834859T>ACA388150139HTR2Ac.1394A>T (p.Asn465Ile)
c.905A>T (p.Asn302Ile)
c.1142A>T (p.Asn381Ile)
13g.46834859T>CCA388150140HTR2Ac.1394A>G (p.Asn465Ser)
c.905A>G (p.Asn302Ser)
c.1142A>G (p.Asn381Ser)
13g.46834859T>GCA388150141HTR2Ac.1394A>C (p.Asn465Thr)
c.905A>C (p.Asn302Thr)
c.1142A>C (p.Asn381Thr)
13g.46834860T>ACA388150142HTR2Ac.1393A>T (p.Asn465Tyr)
c.904A>T (p.Asn302Tyr)
c.1141A>T (p.Asn381Tyr)
13g.46834860T>CCA6977489HTR2Ac.1393A>G (p.Asn465Asp)
c.904A>G (p.Asn302Asp)
c.1141A>G (p.Asn381Asp)
 dbSNP ExAC gnomAD v4
13g.46834860T>GCA388150143HTR2Ac.1393A>C (p.Asn465His)
c.904A>C (p.Asn302His)
c.1141A>C (p.Asn381His)
13g.46834860T=CA2089283344HTR2Ac.1393A= (p.Asn465=)
c.904A= (p.Asn302=)
c.1141A= (p.Asn381=)
13g.46834861C>ACA483739053HTR2Ac.1392G>T (p.Val464=)
c.903G>T (p.Val301=)
c.1140G>T (p.Val380=)
13g.46834861C>GCA483739055HTR2Ac.1392G>C (p.Val464=)
c.903G>C (p.Val301=)
c.1140G>C (p.Val380=)
13g.46834861C>TCA483739057HTR2Ac.1392G>A (p.Val464=)
c.903G>A (p.Val301=)
c.1140G>A (p.Val380=)
13g.46834862A=CA2089283345HTR2Ac.1391T= (p.Val464=)
c.902T= (p.Val301=)
c.1139T= (p.Val380=)
13g.46834862A>CCA388150144HTR2Ac.1391T>G (p.Val464Gly)
c.902T>G (p.Val301Gly)
c.1139T>G (p.Val380Gly)
 dbSNP
13g.46834862A>GCA388150145HTR2Ac.1391T>C (p.Val464Ala)
c.902T>C (p.Val301Ala)
c.1139T>C (p.Val380Ala)
13g.46834862A>TCA388150146HTR2Ac.1391T>A (p.Val464Glu)
c.902T>A (p.Val301Glu)
c.1139T>A (p.Val380Glu)
13g.46834863C>ACA388150148HTR2Ac.1390G>T (p.Val464Leu)
c.901G>T (p.Val301Leu)
c.1138G>T (p.Val380Leu)
13g.46834863C>GCA388150149HTR2Ac.1390G>C (p.Val464Leu)
c.901G>C (p.Val301Leu)
c.1138G>C (p.Val380Leu)
13g.46834863C>TCA388150147HTR2Ac.1390G>A (p.Val464Met)
c.901G>A (p.Val301Met)
c.1138G>A (p.Val380Met)
13g.46834864T>ACA483739059HTR2Ac.1389A>T (p.Gly463=)
c.900A>T (p.Gly300=)
c.1137A>T (p.Gly379=)
13g.46834864T>CCA483739060HTR2Ac.1389A>G (p.Gly463=)
c.900A>G (p.Gly300=)
c.1137A>G (p.Gly379=)
13g.46834864T>GCA483739061HTR2Ac.1389A>C (p.Gly463=)
c.900A>C (p.Gly300=)
c.1137A>C (p.Gly379=)
13g.46834865C>ACA388150150HTR2Ac.1388G>T (p.Gly463Val)
c.899G>T (p.Gly300Val)
c.1136G>T (p.Gly379Val)
13g.46834865C>GCA388150152HTR2Ac.1388G>C (p.Gly463Ala)
c.899G>C (p.Gly300Ala)
c.1136G>C (p.Gly379Ala)
13g.46834865C>TCA388150151HTR2Ac.1388G>A (p.Gly463Glu)
c.899G>A (p.Gly300Glu)
c.1136G>A (p.Gly379Glu)
13g.46834866C>ACA388150153HTR2Ac.1387G>T (p.Gly463Ter)
c.898G>T (p.Gly300Ter)
c.1135G>T (p.Gly379Ter)
 COSMIC
13g.46834866C=CA2089283346HTR2Ac.1387G= (p.Gly463=)
c.898G= (p.Gly300=)
c.1135G= (p.Gly379=)
13g.46834866C>GCA388150154HTR2Ac.1387G>C (p.Gly463Arg)
c.898G>C (p.Gly300Arg)
c.1135G>C (p.Gly379Arg)
13g.46834866C>TCA6977490HTR2Ac.1387G>A (p.Gly463Arg)
c.898G>A (p.Gly300Arg)
c.1135G>A (p.Gly379Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.46834867G>ACA6977491HTR2Ac.1386C>T (p.Asp462=)
c.897C>T (p.Asp299=)
c.1134C>T (p.Asp378=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.46834867G>CCA388150155HTR2Ac.1386C>G (p.Asp462Glu)
c.897C>G (p.Asp299Glu)
c.1134C>G (p.Asp378Glu)
 dbSNP gnomAD v4
13g.46834867G=CA2089283347HTR2Ac.1386C= (p.Asp462=)
c.897C= (p.Asp299=)
c.1134C= (p.Asp378=)
13g.46834867G>TCA249253322HTR2Ac.1386C>A (p.Asp462Glu)
c.897C>A (p.Asp299Glu)
c.1134C>A (p.Asp378Glu)
 dbSNP
13g.46834868T>ACA388150156HTR2Ac.1385A>T (p.Asp462Val)
c.896A>T (p.Asp299Val)
c.1133A>T (p.Asp378Val)
 gnomAD v4
13g.46834868T>CCA388150157HTR2Ac.1385A>G (p.Asp462Gly)
c.896A>G (p.Asp299Gly)
c.1133A>G (p.Asp378Gly)
13g.46834868T>GCA388150158HTR2Ac.1385A>C (p.Asp462Ala)
c.896A>C (p.Asp299Ala)
c.1133A>C (p.Asp378Ala)
 COSMIC
13g.46834869C>ACA388150159HTR2Ac.1384G>T (p.Asp462Tyr)
c.895G>T (p.Asp299Tyr)
c.1132G>T (p.Asp378Tyr)
 dbSNP
13g.46834869C=CA2089283348HTR2Ac.1384G= (p.Asp462=)
c.895G= (p.Asp299=)
c.1132G= (p.Asp378=)
13g.46834869C>GCA388150160HTR2Ac.1384G>C (p.Asp462His)
c.895G>C (p.Asp299His)
c.1132G>C (p.Asp378His)
 gnomAD v4
13g.46834869C>TCA6977492HTR2Ac.1384G>A (p.Asp462Asn)
c.895G>A (p.Asp299Asn)
c.1132G>A (p.Asp378Asn)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
13g.46834870G>ACA6977493HTR2Ac.1383C>T (p.Ser461=)
c.894C>T (p.Ser298=)
c.1131C>T (p.Ser377=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834870G>CCA388150161HTR2Ac.1383C>G (p.Ser461Arg)
c.894C>G (p.Ser298Arg)
c.1131C>G (p.Ser377Arg)
13g.46834870G=CA2089283349HTR2Ac.1383C= (p.Ser461=)
c.894C= (p.Ser298=)
c.1131C= (p.Ser377=)
13g.46834870G>TCA388150162HTR2Ac.1383C>A (p.Ser461Arg)
c.894C>A (p.Ser298Arg)
c.1131C>A (p.Ser377Arg)
13g.46834871C>ACA388150165HTR2Ac.1382G>T (p.Ser461Ile)
c.893G>T (p.Ser298Ile)
c.1130G>T (p.Ser377Ile)
13g.46834871C>GCA388150163HTR2Ac.1382G>C (p.Ser461Thr)
c.893G>C (p.Ser298Thr)
c.1130G>C (p.Ser377Thr)
13g.46834871C>TCA388150164HTR2Ac.1382G>A (p.Ser461Asn)
c.893G>A (p.Ser298Asn)
c.1130G>A (p.Ser377Asn)
13g.46834872T>ACA388150166HTR2Ac.1381A>T (p.Ser461Cys)
c.892A>T (p.Ser298Cys)
c.1129A>T (p.Ser377Cys)
13g.46834872T>CCA388150167HTR2Ac.1381A>G (p.Ser461Gly)
c.892A>G (p.Ser298Gly)
c.1129A>G (p.Ser377Gly)
 gnomAD v4
13g.46834872T>GCA388150168HTR2Ac.1381A>C (p.Ser461Arg)
c.892A>C (p.Ser298Arg)
c.1129A>C (p.Ser377Arg)
13g.46834873A=CA2089283350HTR2Ac.1380T= (p.Asn460=)
c.891T= (p.Asn297=)
c.1128T= (p.Asn376=)
13g.46834873A>CCA388150169HTR2Ac.1380T>G (p.Asn460Lys)
c.891T>G (p.Asn297Lys)
c.1128T>G (p.Asn376Lys)
13g.46834873A>GCA483739068HTR2Ac.1380T>C (p.Asn460=)
c.891T>C (p.Asn297=)
c.1128T>C (p.Asn376=)
 dbSNP
13g.46834873A>TCA388150170HTR2Ac.1380T>A (p.Asn460Lys)
c.891T>A (p.Asn297Lys)
c.1128T>A (p.Asn376Lys)
13g.46834874T>ACA388150172HTR2Ac.1379A>T (p.Asn460Ile)
c.890A>T (p.Asn297Ile)
c.1127A>T (p.Asn376Ile)
13g.46834874T>CCA6977494HTR2Ac.1379A>G (p.Asn460Ser)
c.890A>G (p.Asn297Ser)
c.1127A>G (p.Asn376Ser)
 dbSNP ExAC
13g.46834874T>GCA388150174HTR2Ac.1379A>C (p.Asn460Thr)
c.890A>C (p.Asn297Thr)
c.1127A>C (p.Asn376Thr)
13g.46834874T=CA2089283351HTR2Ac.1379A= (p.Asn460=)
c.890A= (p.Asn297=)
c.1127A= (p.Asn376=)
13g.46834875T>ACA388150176HTR2Ac.1378A>T (p.Asn460Tyr)
c.889A>T (p.Asn297Tyr)
c.1126A>T (p.Asn376Tyr)
13g.46834875T>CCA388150177HTR2Ac.1378A>G (p.Asn460Asp)
c.889A>G (p.Asn297Asp)
c.1126A>G (p.Asn376Asp)
13g.46834875T>GCA388150178HTR2Ac.1378A>C (p.Asn460His)
c.889A>C (p.Asn297His)
c.1126A>C (p.Asn376His)
13g.46834876G>ACA483739069HTR2Ac.1377C>T (p.Asp459=)
c.888C>T (p.Asp296=)
c.1125C>T (p.Asp375=)
 gnomAD v4
13g.46834876G>CCA388150180HTR2Ac.1377C>G (p.Asp459Glu)
c.888C>G (p.Asp296Glu)
c.1125C>G (p.Asp375Glu)
13g.46834876G>TCA388150182HTR2Ac.1377C>A (p.Asp459Glu)
c.888C>A (p.Asp296Glu)
c.1125C>A (p.Asp375Glu)
 gnomAD v4
13g.46834877T>ACA388150184HTR2Ac.1376A>T (p.Asp459Val)
c.887A>T (p.Asp296Val)
c.1124A>T (p.Asp375Val)
13g.46834877T>CCA388150186HTR2Ac.1376A>G (p.Asp459Gly)
c.887A>G (p.Asp296Gly)
c.1124A>G (p.Asp375Gly)
13g.46834877T>GCA388150187HTR2Ac.1376A>C (p.Asp459Ala)
c.887A>C (p.Asp296Ala)
c.1124A>C (p.Asp375Ala)
13g.46834878C>ACA388150190HTR2Ac.1375G>T (p.Asp459Tyr)
c.886G>T (p.Asp296Tyr)
c.1123G>T (p.Asp375Tyr)
13g.46834878C>GCA388150191HTR2Ac.1375G>C (p.Asp459His)
c.886G>C (p.Asp296His)
c.1123G>C (p.Asp375His)
13g.46834878C>TCA388150193HTR2Ac.1375G>A (p.Asp459Asn)
c.886G>A (p.Asp296Asn)
c.1123G>A (p.Asp375Asn)
13g.46834879T>ACA388150195HTR2Ac.1374A>T (p.Lys458Asn)
c.885A>T (p.Lys295Asn)
c.1122A>T (p.Lys374Asn)
13g.46834879T>CCA483739073HTR2Ac.1374A>G (p.Lys458=)
c.885A>G (p.Lys295=)
c.1122A>G (p.Lys374=)
 dbSNP
13g.46834879T>GCA388150196HTR2Ac.1374A>C (p.Lys458Asn)
c.885A>C (p.Lys295Asn)
c.1122A>C (p.Lys374Asn)
13g.46834879T=CA2089283352HTR2Ac.1374A= (p.Lys458=)
c.885A= (p.Lys295=)
c.1122A= (p.Lys374=)
13g.46834880T>ACA388150199HTR2Ac.1373A>T (p.Lys458Ile)
c.884A>T (p.Lys295Ile)
c.1121A>T (p.Lys374Ile)
13g.46834880T>CCA388150200HTR2Ac.1373A>G (p.Lys458Arg)
c.884A>G (p.Lys295Arg)
c.1121A>G (p.Lys374Arg)
13g.46834880T>GCA388150202HTR2Ac.1373A>C (p.Lys458Thr)
c.884A>C (p.Lys295Thr)
c.1121A>C (p.Lys374Thr)
13g.46834881T>ACA388150208HTR2Ac.1372A>T (p.Lys458Ter)
c.883A>T (p.Lys295Ter)
c.1120A>T (p.Lys374Ter)
13g.46834881T>CCA388150206HTR2Ac.1372A>G (p.Lys458Glu)
c.883A>G (p.Lys295Glu)
c.1120A>G (p.Lys374Glu)
13g.46834881T>GCA388150204HTR2Ac.1372A>C (p.Lys458Gln)
c.883A>C (p.Lys295Gln)
c.1120A>C (p.Lys374Gln)
13g.46834882A>CCA483739077HTR2Ac.1371T>G (p.Ser457=)
c.882T>G (p.Ser294=)
c.1119T>G (p.Ser373=)
13g.46834882A>GCA483739078HTR2Ac.1371T>C (p.Ser457=)
c.882T>C (p.Ser294=)
c.1119T>C (p.Ser373=)
 gnomAD v4
13g.46834882A>TCA483739079HTR2Ac.1371T>A (p.Ser457=)
c.882T>A (p.Ser294=)
c.1119T>A (p.Ser373=)
13g.46834883G>ACA388150210HTR2Ac.1370C>T (p.Ser457Phe)
c.881C>T (p.Ser294Phe)
c.1118C>T (p.Ser373Phe)
13g.46834883G>CCA388150211HTR2Ac.1370C>G (p.Ser457Cys)
c.881C>G (p.Ser294Cys)
c.1118C>G (p.Ser373Cys)
13g.46834883G>TCA388150213HTR2Ac.1370C>A (p.Ser457Tyr)
c.881C>A (p.Ser294Tyr)
c.1118C>A (p.Ser373Tyr)
13g.46834884A>CCA388150216HTR2Ac.1369T>G (p.Ser457Ala)
c.880T>G (p.Ser294Ala)
c.1117T>G (p.Ser373Ala)
13g.46834884A>GCA388150217HTR2Ac.1369T>C (p.Ser457Pro)
c.880T>C (p.Ser294Pro)
c.1117T>C (p.Ser373Pro)
13g.46834884A>TCA388150218HTR2Ac.1369T>A (p.Ser457Thr)
c.880T>A (p.Ser294Thr)
c.1117T>A (p.Ser373Thr)
13g.46834885_46834886insCTAAACA2622958750HTR2Ac.1369_1370insTAGTT (p.Ser457LeufsTer10)
c.880_881insTAGTT (p.Ser294LeufsTer10)
c.1117_1118insTAGTT (p.Ser373LeufsTer10)
 gnomAD v4
13g.46834885A>CCA483739081HTR2Ac.1368T>G (p.Ala456=)
c.879T>G (p.Ala293=)
c.1116T>G (p.Ala372=)
13g.46834885A>GCA483739082HTR2Ac.1368T>C (p.Ala456=)
c.879T>C (p.Ala293=)
c.1116T>C (p.Ala372=)
13g.46834885A>TCA483739083HTR2Ac.1368T>A (p.Ala456=)
c.879T>A (p.Ala293=)
c.1116T>A (p.Ala372=)
13g.46834886G>ACA388150219HTR2Ac.1367C>T (p.Ala456Val)
c.878C>T (p.Ala293Val)
c.1115C>T (p.Ala372Val)
 dbSNP gnomAD v2 gnomAD v4
13g.46834886G>CCA388150221HTR2Ac.1367C>G (p.Ala456Gly)
c.878C>G (p.Ala293Gly)
c.1115C>G (p.Ala372Gly)
13g.46834886G=CA2089283353HTR2Ac.1367C= (p.Ala456=)
c.878C= (p.Ala293=)
c.1115C= (p.Ala372=)
13g.46834886G>TCA388150223HTR2Ac.1367C>A (p.Ala456Asp)
c.878C>A (p.Ala293Asp)
c.1115C>A (p.Ala372Asp)
13g.46834887C>ACA249253342HTR2Ac.1366G>T (p.Ala456Ser)
c.877G>T (p.Ala293Ser)
c.1114G>T (p.Ala372Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46834887C=CA2089283354HTR2Ac.1366G= (p.Ala456=)
c.877G= (p.Ala293=)
c.1114G= (p.Ala372=)
13g.46834887C>GCA388150225HTR2Ac.1366G>C (p.Ala456Pro)
c.877G>C (p.Ala293Pro)
c.1114G>C (p.Ala372Pro)
 dbSNP
13g.46834887C>TCA388150227HTR2Ac.1366G>A (p.Ala456Thr)
c.877G>A (p.Ala293Thr)
c.1114G>A (p.Ala372Thr)
 gnomAD v4
13g.46834888C>ACA388150232HTR2Ac.1365G>T (p.Glu455Asp)
c.876G>T (p.Glu292Asp)
c.1113G>T (p.Glu371Asp)
13g.46834888C=CA2089283355HTR2Ac.1365G= (p.Glu455=)
c.876G= (p.Glu292=)
c.1113G= (p.Glu371=)
13g.46834888C>GCA388150231HTR2Ac.1365G>C (p.Glu455Asp)
c.876G>C (p.Glu292Asp)
c.1113G>C (p.Glu371Asp)
 COSMIC
13g.46834888C>TCA6977495HTR2Ac.1365G>A (p.Glu455=)
c.876G>A (p.Glu292=)
c.1113G>A (p.Glu371=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834889T>ACA388150234HTR2Ac.1364A>T (p.Glu455Val)
c.875A>T (p.Glu292Val)
c.1112A>T (p.Glu371Val)
13g.46834889T>CCA388150235HTR2Ac.1364A>G (p.Glu455Gly)
c.875A>G (p.Glu292Gly)
c.1112A>G (p.Glu371Gly)
13g.46834889T>GCA388150237HTR2Ac.1364A>C (p.Glu455Ala)
c.875A>C (p.Glu292Ala)
c.1112A>C (p.Glu371Ala)
13g.46834890C>ACA388150239HTR2Ac.1363G>T (p.Glu455Ter)
c.874G>T (p.Glu292Ter)
c.1111G>T (p.Glu371Ter)
13g.46834890C>GCA388150241HTR2Ac.1363G>C (p.Glu455Gln)
c.874G>C (p.Glu292Gln)
c.1111G>C (p.Glu371Gln)
13g.46834890C>TCA388150242HTR2Ac.1363G>A (p.Glu455Lys)
c.874G>A (p.Glu292Lys)
c.1111G>A (p.Glu371Lys)
13g.46834891T>ACA388150246HTR2Ac.1362A>T (p.Glu454Asp)
c.873A>T (p.Glu291Asp)
c.1110A>T (p.Glu370Asp)
13g.46834891T>CCA483739088HTR2Ac.1362A>G (p.Glu454=)
c.873A>G (p.Glu291=)
c.1110A>G (p.Glu370=)
13g.46834891T>GCA388150245HTR2Ac.1362A>C (p.Glu454Asp)
c.873A>C (p.Glu291Asp)
c.1110A>C (p.Glu370Asp)
 COSMIC
13g.46834892T>ACA388150248HTR2Ac.1361A>T (p.Glu454Val)
c.872A>T (p.Glu291Val)
c.1109A>T (p.Glu370Val)
 gnomAD v4
13g.46834892T>CCA388150250HTR2Ac.1361A>G (p.Glu454Gly)
c.872A>G (p.Glu291Gly)
c.1109A>G (p.Glu370Gly)
13g.46834892T>GCA388150251HTR2Ac.1361A>C (p.Glu454Ala)
c.872A>C (p.Glu291Ala)
c.1109A>C (p.Glu370Ala)
13g.46834893C>ACA388150253HTR2Ac.1360G>T (p.Glu454Ter)
c.871G>T (p.Glu291Ter)
c.1108G>T (p.Glu370Ter)
 COSMIC COSMIC
13g.46834893C=CA2089283356HTR2Ac.1360G= (p.Glu454=)
c.871G= (p.Glu291=)
c.1108G= (p.Glu370=)
13g.46834893C>GCA6977496HTR2Ac.1360G>C (p.Glu454Gln)
c.871G>C (p.Glu291Gln)
c.1108G>C (p.Glu370Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834893C>TCA388150256HTR2Ac.1360G>A (p.Glu454Lys)
c.871G>A (p.Glu291Lys)
c.1108G>A (p.Glu370Lys)
13g.46834894A>CCA483739092HTR2Ac.1359T>G (p.Ser453=)
c.870T>G (p.Ser290=)
c.1107T>G (p.Ser369=)
13g.46834894A>GCA483739094HTR2Ac.1359T>C (p.Ser453=)
c.870T>C (p.Ser290=)
c.1107T>C (p.Ser369=)
13g.46834894A>TCA483739093HTR2Ac.1359T>A (p.Ser453=)
c.870T>A (p.Ser290=)
c.1107T>A (p.Ser369=)
13g.46834895G>ACA249253349HTR2Ac.1358C>T (p.Ser453Phe)
c.869C>T (p.Ser290Phe)
c.1106C>T (p.Ser369Phe)
 dbSNP gnomAD v3 gnomAD v4
13g.46834895G>CCA6977497HTR2Ac.1358C>G (p.Ser453Cys)
c.869C>G (p.Ser290Cys)
c.1106C>G (p.Ser369Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834895G=CA2089283357HTR2Ac.1358C= (p.Ser453=)
c.869C= (p.Ser290=)
c.1106C= (p.Ser369=)
13g.46834895G>TCA388150258HTR2Ac.1358C>A (p.Ser453Tyr)
c.869C>A (p.Ser290Tyr)
c.1106C>A (p.Ser369Tyr)
13g.46834896A=CA2089283358HTR2Ac.1357T= (p.Ser453=)
c.868T= (p.Ser290=)
c.1105T= (p.Ser369=)
13g.46834896A>CCA388150261HTR2Ac.1357T>G (p.Ser453Ala)
c.868T>G (p.Ser290Ala)
c.1105T>G (p.Ser369Ala)
13g.46834896A>GCA388150262HTR2Ac.1357T>C (p.Ser453Pro)
c.868T>C (p.Ser290Pro)
c.1105T>C (p.Ser369Pro)
13g.46834896A>TCA6977498HTR2Ac.1357T>A (p.Ser453Thr)
c.868T>A (p.Ser290Thr)
c.1105T>A (p.Ser369Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834897A>CCA388150265HTR2Ac.1356T>G (p.His452Gln)
c.867T>G (p.His289Gln)
c.1104T>G (p.His368Gln)
13g.46834897A>GCA483739096HTR2Ac.1356T>C (p.His452=)
c.867T>C (p.His289=)
c.1104T>C (p.His368=)
13g.46834897A>TCA388150266HTR2Ac.1356T>A (p.His452Gln)
c.867T>A (p.His289Gln)
c.1104T>A (p.His368Gln)
 gnomAD v4
13g.46834898T>ACA6977499HTR2Ac.1355A>T (p.His452Leu)
c.866A>T (p.His289Leu)
c.1103A>T (p.His368Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834898T>CCA249253350HTR2Ac.1355A>G (p.His452Arg)
c.866A>G (p.His289Arg)
c.1103A>G (p.His368Arg)
 dbSNP gnomAD v4
13g.46834898T>GCA388150270HTR2Ac.1355A>C (p.His452Pro)
c.866A>C (p.His289Pro)
c.1103A>C (p.His368Pro)
 dbSNP gnomAD v4
13g.46834898T=CA2089283359HTR2Ac.1355A= (p.His452=)
c.866A= (p.His289=)
c.1103A= (p.His368=)
13g.46834899G>ACA6977500HTR2Ac.1354C>T (p.His452Tyr)
c.865C>T (p.His289Tyr)
c.1102C>T (p.His368Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834899G>CCA388150272HTR2Ac.1354C>G (p.His452Asp)
c.865C>G (p.His289Asp)
c.1102C>G (p.His368Asp)
13g.46834899G=CA1630855946HTR2Ac.1354C= (p.His452=)
c.865C= (p.His289=)
c.1102C= (p.His368=)
13g.46834899G>TCA388150274HTR2Ac.1354C>A (p.His452Asn)
c.865C>A (p.His289Asn)
c.1102C>A (p.His368Asn)
13g.46834900C>ACA388150275HTR2Ac.1353G>T (p.Gln451His)
c.864G>T (p.Gln288His)
c.1101G>T (p.Gln367His)
13g.46834900C>GCA388150277HTR2Ac.1353G>C (p.Gln451His)
c.864G>C (p.Gln288His)
c.1101G>C (p.Gln367His)
13g.46834900C>TCA483739098HTR2Ac.1353G>A (p.Gln451=)
c.864G>A (p.Gln288=)
c.1101G>A (p.Gln367=)
13g.46834901T>ACA388150279HTR2Ac.1352A>T (p.Gln451Leu)
c.863A>T (p.Gln288Leu)
c.1100A>T (p.Gln367Leu)
13g.46834901T>CCA388150282HTR2Ac.1352A>G (p.Gln451Arg)
c.863A>G (p.Gln288Arg)
c.1100A>G (p.Gln367Arg)
13g.46834901T>GCA388150280HTR2Ac.1352A>C (p.Gln451Pro)
c.863A>C (p.Gln288Pro)
c.1100A>C (p.Gln367Pro)
13g.46834902G>ACA388150284HTR2Ac.1351C>T (p.Gln451Ter)
c.862C>T (p.Gln288Ter)
c.1099C>T (p.Gln367Ter)
13g.46834902G>CCA388150286HTR2Ac.1351C>G (p.Gln451Glu)
c.862C>G (p.Gln288Glu)
c.1099C>G (p.Gln367Glu)
13g.46834902G>TCA388150287HTR2Ac.1351C>A (p.Gln451Lys)
c.862C>A (p.Gln288Lys)
c.1099C>A (p.Gln367Lys)
13g.46834903C>ACA388150289HTR2Ac.1350G>T (p.Lys450Asn)
c.861G>T (p.Lys287Asn)
c.1098G>T (p.Lys366Asn)
13g.46834903C=CA2089283360HTR2Ac.1350G= (p.Lys450=)
c.861G= (p.Lys287=)
c.1098G= (p.Lys366=)
13g.46834903C>GCA388150291HTR2Ac.1350G>C (p.Lys450Asn)
c.861G>C (p.Lys287Asn)
c.1098G>C (p.Lys366Asn)
13g.46834903C>TCA6977501HTR2Ac.1350G>A (p.Lys450=)
c.861G>A (p.Lys287=)
c.1098G>A (p.Lys366=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834904T>ACA388150293HTR2Ac.1349A>T (p.Lys450Met)
c.860A>T (p.Lys287Met)
c.1097A>T (p.Lys366Met)
13g.46834904T>CCA388150295HTR2Ac.1349A>G (p.Lys450Arg)
c.860A>G (p.Lys287Arg)
c.1097A>G (p.Lys366Arg)
13g.46834904T>GCA388150297HTR2Ac.1349A>C (p.Lys450Thr)
c.860A>C (p.Lys287Thr)
c.1097A>C (p.Lys366Thr)
13g.46834905T>ACA388150299HTR2Ac.1348A>T (p.Lys450Ter)
c.859A>T (p.Lys287Ter)
c.1096A>T (p.Lys366Ter)
13g.46834905T>CCA6977502HTR2Ac.1348A>G (p.Lys450Glu)
c.859A>G (p.Lys287Glu)
c.1096A>G (p.Lys366Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834905T>GCA388150302HTR2Ac.1348A>C (p.Lys450Gln)
c.859A>C (p.Lys287Gln)
c.1096A>C (p.Lys366Gln)
13g.46834905T=CA2089283361HTR2Ac.1348A= (p.Lys450=)
c.859A= (p.Lys287=)
c.1096A= (p.Lys366=)
13g.46834906T>ACA483739105HTR2Ac.1347A>T (p.Gly449=)
c.858A>T (p.Gly286=)
c.1095A>T (p.Gly365=)
13g.46834906T>CCA483739106HTR2Ac.1347A>G (p.Gly449=)
c.858A>G (p.Gly286=)
c.1095A>G (p.Gly365=)
13g.46834906T>GCA483739107HTR2Ac.1347A>C (p.Gly449=)
c.858A>C (p.Gly286=)
c.1095A>C (p.Gly365=)
13g.46834907C>ACA388150306HTR2Ac.1346G>T (p.Gly449Val)
c.857G>T (p.Gly286Val)
c.1094G>T (p.Gly365Val)
 gnomAD v4
13g.46834907C>GCA388150303HTR2Ac.1346G>C (p.Gly449Ala)
c.857G>C (p.Gly286Ala)
c.1094G>C (p.Gly365Ala)
13g.46834907C>TCA388150305HTR2Ac.1346G>A (p.Gly449Glu)
c.857G>A (p.Gly286Glu)
c.1094G>A (p.Gly365Glu)
 COSMIC COSMIC
13g.46834908C>ACA388150307HTR2Ac.1345G>T (p.Gly449Ter)
c.856G>T (p.Gly286Ter)
c.1093G>T (p.Gly365Ter)
13g.46834908C=CA2089283362HTR2Ac.1345G= (p.Gly449=)
c.856G= (p.Gly286=)
c.1093G= (p.Gly365=)
13g.46834908C>GCA388150308HTR2Ac.1345G>C (p.Gly449Arg)
c.856G>C (p.Gly286Arg)
c.1093G>C (p.Gly365Arg)
 dbSNP
13g.46834908C>TCA388150309HTR2Ac.1345G>A (p.Gly449Arg)
c.856G>A (p.Gly286Arg)
c.1093G>A (p.Gly365Arg)
13g.46834909T>ACA483739112HTR2Ac.1344A>T (p.Leu448=)
c.855A>T (p.Leu285=)
c.1092A>T (p.Leu364=)
13g.46834909T>CCA483739113HTR2Ac.1344A>G (p.Leu448=)
c.855A>G (p.Leu285=)
c.1092A>G (p.Leu364=)
13g.46834909T>GCA483739114HTR2Ac.1344A>C (p.Leu448=)
c.855A>C (p.Leu285=)
c.1092A>C (p.Leu364=)
13g.46834910A>CCA388150311HTR2Ac.1343T>G (p.Leu448Arg)
c.854T>G (p.Leu285Arg)
c.1091T>G (p.Leu364Arg)
13g.46834910A>GCA388150312HTR2Ac.1343T>C (p.Leu448Pro)
c.854T>C (p.Leu285Pro)
c.1091T>C (p.Leu364Pro)
13g.46834910A>TCA388150313HTR2Ac.1343T>A (p.Leu448Gln)
c.854T>A (p.Leu285Gln)
c.1091T>A (p.Leu364Gln)
13g.46834911G>ACA483739115HTR2Ac.1342C>T (p.Leu448=)
c.853C>T (p.Leu285=)
c.1090C>T (p.Leu364=)
13g.46834911G>CCA388150314HTR2Ac.1342C>G (p.Leu448Val)
c.853C>G (p.Leu285Val)
c.1090C>G (p.Leu364Val)
 gnomAD v4
13g.46834911G>TCA388150316HTR2Ac.1342C>A (p.Leu448Ile)
c.853C>A (p.Leu285Ile)
c.1090C>A (p.Leu364Ile)
13g.46834912A>CCA483739119HTR2Ac.1341T>G (p.Ala447=)
c.852T>G (p.Ala284=)
c.1089T>G (p.Ala363=)
13g.46834912A>GCA483739117HTR2Ac.1341T>C (p.Ala447=)
c.852T>C (p.Ala284=)
c.1089T>C (p.Ala363=)
13g.46834912A>TCA483739118HTR2Ac.1341T>A (p.Ala447=)
c.852T>A (p.Ala284=)
c.1089T>A (p.Ala363=)
13g.46834913G>ACA6977503HTR2Ac.1340C>T (p.Ala447Val)
c.851C>T (p.Ala284Val)
c.1088C>T (p.Ala363Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834913G>CCA388150319HTR2Ac.1340C>G (p.Ala447Gly)
c.851C>G (p.Ala284Gly)
c.1088C>G (p.Ala363Gly)
13g.46834913G=CA2018007891HTR2Ac.1340C= (p.Ala447=)
c.851C= (p.Ala284=)
c.1088C= (p.Ala363=)
13g.46834913G>TCA388150321HTR2Ac.1340C>A (p.Ala447Asp)
c.851C>A (p.Ala284Asp)
c.1088C>A (p.Ala363Asp)
13g.46834914C>ACA388150325HTR2Ac.1339G>T (p.Ala447Ser)
c.850G>T (p.Ala284Ser)
c.1087G>T (p.Ala363Ser)
13g.46834914C=CA2089283363HTR2Ac.1339G= (p.Ala447=)
c.850G= (p.Ala284=)
c.1087G= (p.Ala363=)
13g.46834914C>GCA388150323HTR2Ac.1339G>C (p.Ala447Pro)
c.850G>C (p.Ala284Pro)
c.1087G>C (p.Ala363Pro)
13g.46834914C>TCA6977504HTR2Ac.1339G>A (p.Ala447Thr)
c.850G>A (p.Ala284Thr)
c.1087G>A (p.Ala363Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834915A>CCA483739121HTR2Ac.1338T>G (p.Val446=)
c.849T>G (p.Val283=)
c.1086T>G (p.Val362=)
13g.46834915A>GCA483739123HTR2Ac.1338T>C (p.Val446=)
c.849T>C (p.Val283=)
c.1086T>C (p.Val362=)
13g.46834915A>TCA483739125HTR2Ac.1338T>A (p.Val446=)
c.849T>A (p.Val283=)
c.1086T>A (p.Val362=)
13g.46834916A=CA2089283364HTR2Ac.1337T= (p.Val446=)
c.848T= (p.Val283=)
c.1085T= (p.Val362=)
13g.46834916A>CCA388150327HTR2Ac.1337T>G (p.Val446Gly)
c.848T>G (p.Val283Gly)
c.1085T>G (p.Val362Gly)
13g.46834916A>GCA6977505HTR2Ac.1337T>C (p.Val446Ala)
c.848T>C (p.Val283Ala)
c.1085T>C (p.Val362Ala)
 dbSNP ExAC gnomAD v2
13g.46834916A>TCA388150329HTR2Ac.1337T>A (p.Val446Asp)
c.848T>A (p.Val283Asp)
c.1085T>A (p.Val362Asp)
13g.46834917C>ACA388150332HTR2Ac.1336G>T (p.Val446Phe)
c.847G>T (p.Val283Phe)
c.1084G>T (p.Val362Phe)
13g.46834917C>GCA388150336HTR2Ac.1336G>C (p.Val446Leu)
c.847G>C (p.Val283Leu)
c.1084G>C (p.Val362Leu)
13g.46834917C>TCA388150334HTR2Ac.1336G>A (p.Val446Ile)
c.847G>A (p.Val283Ile)
c.1084G>A (p.Val362Ile)
 gnomAD v4
13g.46834918C>ACA388150338HTR2Ac.1335G>T (p.Met445Ile)
c.846G>T (p.Met282Ile)
c.1083G>T (p.Met361Ile)
13g.46834918C=CA2089283365HTR2Ac.1335G= (p.Met445=)
c.846G= (p.Met282=)
c.1083G= (p.Met361=)
13g.46834918C>GCA388150340HTR2Ac.1335G>C (p.Met445Ile)
c.846G>C (p.Met282Ile)
c.1083G>C (p.Met361Ile)
 dbSNP
13g.46834918C>TCA388150342HTR2Ac.1335G>A (p.Met445Ile)
c.846G>A (p.Met282Ile)
c.1083G>A (p.Met361Ile)
13g.46834919A=CA2089283366HTR2Ac.1334T= (p.Met445=)
c.845T= (p.Met282=)
c.1082T= (p.Met361=)
13g.46834919A>CCA388150344HTR2Ac.1334T>G (p.Met445Arg)
c.845T>G (p.Met282Arg)
c.1082T>G (p.Met361Arg)
13g.46834919A>GCA388150346HTR2Ac.1334T>C (p.Met445Thr)
c.845T>C (p.Met282Thr)
c.1082T>C (p.Met361Thr)
 dbSNP gnomAD v2 gnomAD v4
13g.46834919A>TCA388150349HTR2Ac.1334T>A (p.Met445Lys)
c.845T>A (p.Met282Lys)
c.1082T>A (p.Met361Lys)
13g.46834920T>ACA388150351HTR2Ac.1333A>T (p.Met445Leu)
c.844A>T (p.Met282Leu)
c.1081A>T (p.Met361Leu)
13g.46834920T>CCA388150353HTR2Ac.1333A>G (p.Met445Val)
c.844A>G (p.Met282Val)
c.1081A>G (p.Met361Val)
 gnomAD v4
13g.46834920T>GCA388150354HTR2Ac.1333A>C (p.Met445Leu)
c.844A>C (p.Met282Leu)
c.1081A>C (p.Met361Leu)
13g.46834921T>ACA483739129HTR2Ac.1332A>T (p.Ser444=)
c.843A>T (p.Ser281=)
c.1080A>T (p.Ser360=)
13g.46834921T>CCA483739130HTR2Ac.1332A>G (p.Ser444=)
c.843A>G (p.Ser281=)
c.1080A>G (p.Ser360=)
 dbSNP gnomAD v2 gnomAD v4
13g.46834921T>GCA483739131HTR2Ac.1332A>C (p.Ser444=)
c.843A>C (p.Ser281=)
c.1080A>C (p.Ser360=)
13g.46834921T=CA2089283367HTR2Ac.1332A= (p.Ser444=)
c.843A= (p.Ser281=)
c.1080A= (p.Ser360=)
13g.46834922G>ACA388150356HTR2Ac.1331C>T (p.Ser444Leu)
c.842C>T (p.Ser281Leu)
c.1079C>T (p.Ser360Leu)
13g.46834922G>CCA388150358HTR2Ac.1331C>G (p.Ser444Ter)
c.842C>G (p.Ser281Ter)
c.1079C>G (p.Ser360Ter)
13g.46834922G>TCA388150360HTR2Ac.1331C>A (p.Ser444Ter)
c.842C>A (p.Ser281Ter)
c.1079C>A (p.Ser360Ter)
13g.46834923A>CCA388150361HTR2Ac.1330T>G (p.Ser444Ala)
c.841T>G (p.Ser281Ala)
c.1078T>G (p.Ser360Ala)
13g.46834923A>GCA388150365HTR2Ac.1330T>C (p.Ser444Pro)
c.841T>C (p.Ser281Pro)
c.1078T>C (p.Ser360Pro)
13g.46834923A>TCA388150363HTR2Ac.1330T>A (p.Ser444Thr)
c.841T>A (p.Ser281Thr)
c.1078T>A (p.Ser360Thr)
13g.46834924G>ACA483739133HTR2Ac.1329C>T (p.Cys443=)
c.840C>T (p.Cys280=)
c.1077C>T (p.Cys359=)
13g.46834924G>CCA388150367HTR2Ac.1329C>G (p.Cys443Trp)
c.840C>G (p.Cys280Trp)
c.1077C>G (p.Cys359Trp)
13g.46834924G>TCA388150369HTR2Ac.1329C>A (p.Cys443Ter)
c.840C>A (p.Cys280Ter)
c.1077C>A (p.Cys359Ter)
13g.46834925C>ACA388150371HTR2Ac.1328G>T (p.Cys443Phe)
c.839G>T (p.Cys280Phe)
c.1076G>T (p.Cys359Phe)
13g.46834925C=CA2089283368HTR2Ac.1328G= (p.Cys443=)
c.839G= (p.Cys280=)
c.1076G= (p.Cys359=)
13g.46834925C>GCA388150373HTR2Ac.1328G>C (p.Cys443Ser)
c.839G>C (p.Cys280Ser)
c.1076G>C (p.Cys359Ser)
13g.46834925C>TCA388150375HTR2Ac.1328G>A (p.Cys443Tyr)
c.839G>A (p.Cys280Tyr)
c.1076G>A (p.Cys359Tyr)
 dbSNP
13g.46834926A=CA2089283369HTR2Ac.1327T= (p.Cys443=)
c.838T= (p.Cys280=)
c.1075T= (p.Cys359=)
13g.46834926A>CCA6977506HTR2Ac.1327T>G (p.Cys443Gly)
c.838T>G (p.Cys280Gly)
c.1075T>G (p.Cys359Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834926A>GCA388150378HTR2Ac.1327T>C (p.Cys443Arg)
c.838T>C (p.Cys280Arg)
c.1075T>C (p.Cys359Arg)
13g.46834926A>TCA388150380HTR2Ac.1327T>A (p.Cys443Ser)
c.838T>A (p.Cys280Ser)
c.1075T>A (p.Cys359Ser)
13g.46834927G>ACA483739136HTR2Ac.1326C>T (p.Asp442=)
c.837C>T (p.Asp279=)
c.1074C>T (p.Asp358=)
13g.46834927G>CCA388150382HTR2Ac.1326C>G (p.Asp442Glu)
c.837C>G (p.Asp279Glu)
c.1074C>G (p.Asp358Glu)
13g.46834927G>TCA388150383HTR2Ac.1326C>A (p.Asp442Glu)
c.837C>A (p.Asp279Glu)
c.1074C>A (p.Asp358Glu)
13g.46834928T>ACA388150388HTR2Ac.1325A>T (p.Asp442Val)
c.836A>T (p.Asp279Val)
c.1073A>T (p.Asp358Val)
13g.46834928T>CCA249253376HTR2Ac.1325A>G (p.Asp442Gly)
c.836A>G (p.Asp279Gly)
c.1073A>G (p.Asp358Gly)
 dbSNP gnomAD v4
13g.46834928T>GCA388150386HTR2Ac.1325A>C (p.Asp442Ala)
c.836A>C (p.Asp279Ala)
c.1073A>C (p.Asp358Ala)
13g.46834928T=CA2089283370HTR2Ac.1325A= (p.Asp442=)
c.836A= (p.Asp279=)
c.1073A= (p.Asp358=)
13g.46834930_46834935delCA2799080101HTR2Ac.1320_1325del (p.Asn441_Asp442del)
c.831_836del (p.Asn278_Asp279del)
c.1068_1073del (p.Asn357_Asp358del)
13g.46834929C>ACA388150394HTR2Ac.1324G>T (p.Asp442Tyr)
c.835G>T (p.Asp279Tyr)
c.1072G>T (p.Asp358Tyr)
 gnomAD v4
13g.46834929C>GCA388150390HTR2Ac.1324G>C (p.Asp442His)
c.835G>C (p.Asp279His)
c.1072G>C (p.Asp358His)
13g.46834929C>TCA388150392HTR2Ac.1324G>A (p.Asp442Asn)
c.835G>A (p.Asp279Asn)
c.1072G>A (p.Asp358Asn)
13g.46834930A=CA2089283371HTR2Ac.1323T= (p.Asn441=)
c.834T= (p.Asn278=)
c.1071T= (p.Asn357=)
13g.46834930A>CCA388150396HTR2Ac.1323T>G (p.Asn441Lys)
c.834T>G (p.Asn278Lys)
c.1071T>G (p.Asn357Lys)
13g.46834930A>GCA6977507HTR2Ac.1323T>C (p.Asn441=)
c.834T>C (p.Asn278=)
c.1071T>C (p.Asn357=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834930A>TCA249253377HTR2Ac.1323T>A (p.Asn441Lys)
c.834T>A (p.Asn278Lys)
c.1071T>A (p.Asn357Lys)
 dbSNP gnomAD v3 gnomAD v4
13g.46834931T>ACA388150399HTR2Ac.1322A>T (p.Asn441Ile)
c.833A>T (p.Asn278Ile)
c.1070A>T (p.Asn357Ile)
13g.46834931T>CCA388150404HTR2Ac.1322A>G (p.Asn441Ser)
c.833A>G (p.Asn278Ser)
c.1070A>G (p.Asn357Ser)
13g.46834931T>GCA388150406HTR2Ac.1322A>C (p.Asn441Thr)
c.833A>C (p.Asn278Thr)
c.1070A>C (p.Asn357Thr)
13g.46834932T>ACA388150408HTR2Ac.1321A>T (p.Asn441Tyr)
c.832A>T (p.Asn278Tyr)
c.1069A>T (p.Asn357Tyr)
13g.46834932T>CCA388150410HTR2Ac.1321A>G (p.Asn441Asp)
c.832A>G (p.Asn278Asp)
c.1069A>G (p.Asn357Asp)
13g.46834932T>GCA388150411HTR2Ac.1321A>C (p.Asn441His)
c.832A>C (p.Asn278His)
c.1069A>C (p.Asn357His)
13g.46834932T=CA2089283372HTR2Ac.1321A= (p.Asn441=)
c.832A= (p.Asn278=)
c.1069A= (p.Asn357=)
13g.46834932_46834933insTGCA609929161HTR2Ac.1320_1321insCA (p.Asn441GlnfsTer9)
c.831_832insCA (p.Asn278GlnfsTer9)
c.1068_1069insCA (p.Asn357GlnfsTer9)
 dbSNP gnomAD v2 gnomAD v4
13g.46834933A=CA2089283373HTR2Ac.1320T= (p.Asp440=)
c.831T= (p.Asp277=)
c.1068T= (p.Asp356=)
13g.46834933A>CCA388150413HTR2Ac.1320T>G (p.Asp440Glu)
c.831T>G (p.Asp277Glu)
c.1068T>G (p.Asp356Glu)
13g.46834933A>GCA483739143HTR2Ac.1320T>C (p.Asp440=)
c.831T>C (p.Asp277=)
c.1068T>C (p.Asp356=)
 dbSNP
13g.46834933A>TCA388150415HTR2Ac.1320T>A (p.Asp440Glu)
c.831T>A (p.Asp277Glu)
c.1068T>A (p.Asp356Glu)
13g.46834934T>ACA388150421HTR2Ac.1319A>T (p.Asp440Val)
c.830A>T (p.Asp277Val)
c.1067A>T (p.Asp356Val)
13g.46834934T>CCA388150417HTR2Ac.1319A>G (p.Asp440Gly)
c.830A>G (p.Asp277Gly)
c.1067A>G (p.Asp356Gly)
13g.46834934T>GCA388150419HTR2Ac.1319A>C (p.Asp440Ala)
c.830A>C (p.Asp277Ala)
c.1067A>C (p.Asp356Ala)
13g.46834935C>ACA388150422HTR2Ac.1318G>T (p.Asp440Tyr)
c.829G>T (p.Asp277Tyr)
c.1066G>T (p.Asp356Tyr)
13g.46834935C>GCA388150423HTR2Ac.1318G>C (p.Asp440His)
c.829G>C (p.Asp277His)
c.1066G>C (p.Asp356His)
13g.46834935C>TCA388150424HTR2Ac.1318G>A (p.Asp440Asn)
c.829G>A (p.Asp277Asn)
c.1066G>A (p.Asp356Asn)
13g.46834936T>ACA483739147HTR2Ac.1317A>T (p.Thr439=)
c.828A>T (p.Thr276=)
c.1065A>T (p.Thr355=)
13g.46834936T>CCA483739148HTR2Ac.1317A>G (p.Thr439=)
c.828A>G (p.Thr276=)
c.1065A>G (p.Thr355=)
13g.46834936T>GCA249253382HTR2Ac.1317A>C (p.Thr439=)
c.828A>C (p.Thr276=)
c.1065A>C (p.Thr355=)
 dbSNP gnomAD v3 gnomAD v4
13g.46834936T=CA2089283374HTR2Ac.1317A= (p.Thr439=)
c.828A= (p.Thr276=)
c.1065A= (p.Thr355=)
13g.46834937G>ACA388150425HTR2Ac.1316C>T (p.Thr439Ile)
c.827C>T (p.Thr276Ile)
c.1064C>T (p.Thr355Ile)
13g.46834937G>CCA388150426HTR2Ac.1316C>G (p.Thr439Arg)
c.827C>G (p.Thr276Arg)
c.1064C>G (p.Thr355Arg)
13g.46834937G>TCA388150427HTR2Ac.1316C>A (p.Thr439Lys)
c.827C>A (p.Thr276Lys)
c.1064C>A (p.Thr355Lys)
13g.46834938T>ACA388150428HTR2Ac.1315A>T (p.Thr439Ser)
c.826A>T (p.Thr276Ser)
c.1063A>T (p.Thr355Ser)
13g.46834938T>CCA388150429HTR2Ac.1315A>G (p.Thr439Ala)
c.826A>G (p.Thr276Ala)
c.1063A>G (p.Thr355Ala)
 gnomAD v4
13g.46834938T>GCA388150430HTR2Ac.1315A>C (p.Thr439Pro)
c.826A>C (p.Thr276Pro)
c.1063A>C (p.Thr355Pro)
13g.46834939T>ACA483739153HTR2Ac.1314A>T (p.Thr438=)
c.825A>T (p.Thr275=)
c.1062A>T (p.Thr354=)
13g.46834939T>CCA483739152HTR2Ac.1314A>G (p.Thr438=)
c.825A>G (p.Thr275=)
c.1062A>G (p.Thr354=)
 dbSNP
13g.46834939T>GCA483739154HTR2Ac.1314A>C (p.Thr438=)
c.825A>C (p.Thr275=)
c.1062A>C (p.Thr354=)
13g.46834939T=CA2089283375HTR2Ac.1314A= (p.Thr438=)
c.825A= (p.Thr275=)
c.1062A= (p.Thr354=)
13g.46834940G>ACA388150431HTR2Ac.1313C>T (p.Thr438Ile)
c.824C>T (p.Thr275Ile)
c.1061C>T (p.Thr354Ile)
 dbSNP gnomAD v4
13g.46834940G>CCA388150432HTR2Ac.1313C>G (p.Thr438Arg)
c.824C>G (p.Thr275Arg)
c.1061C>G (p.Thr354Arg)
13g.46834940G=CA2089283376HTR2Ac.1313C= (p.Thr438=)
c.824C= (p.Thr275=)
c.1061C= (p.Thr354=)
13g.46834940G>TCA388150433HTR2Ac.1313C>A (p.Thr438Lys)
c.824C>A (p.Thr275Lys)
c.1061C>A (p.Thr354Lys)
 dbSNP
13g.46834941T>ACA388150435HTR2Ac.1312A>T (p.Thr438Ser)
c.823A>T (p.Thr275Ser)
c.1060A>T (p.Thr354Ser)
13g.46834941T>CCA388150436HTR2Ac.1312A>G (p.Thr438Ala)
c.823A>G (p.Thr275Ala)
c.1060A>G (p.Thr354Ala)
 gnomAD v4
13g.46834941T>GCA388150434HTR2Ac.1312A>C (p.Thr438Pro)
c.823A>C (p.Thr275Pro)
c.1060A>C (p.Thr354Pro)
13g.46834942C>ACA388150437HTR2Ac.1311G>T (p.Lys437Asn)
c.822G>T (p.Lys274Asn)
c.1059G>T (p.Lys353Asn)
13g.46834942C=CA2089283377HTR2Ac.1311G= (p.Lys437=)
c.822G= (p.Lys274=)
c.1059G= (p.Lys353=)
13g.46834942C>GCA388150438HTR2Ac.1311G>C (p.Lys437Asn)
c.822G>C (p.Lys274Asn)
c.1059G>C (p.Lys353Asn)
13g.46834942C>TCA249253394HTR2Ac.1311G>A (p.Lys437=)
c.822G>A (p.Lys274=)
c.1059G>A (p.Lys353=)
 dbSNP
13g.46834943T>ACA388150439HTR2Ac.1310A>T (p.Lys437Met)
c.821A>T (p.Lys274Met)
c.1058A>T (p.Lys353Met)
13g.46834943T>CCA388150440HTR2Ac.1310A>G (p.Lys437Arg)
c.821A>G (p.Lys274Arg)
c.1058A>G (p.Lys353Arg)
 dbSNP gnomAD v2 gnomAD v4
13g.46834943T>GCA388150441HTR2Ac.1310A>C (p.Lys437Thr)
c.821A>C (p.Lys274Thr)
c.1058A>C (p.Lys353Thr)
13g.46834943T=CA2089283378HTR2Ac.1310A= (p.Lys437=)
c.821A= (p.Lys274=)
c.1058A= (p.Lys353=)
13g.46834944T>ACA388150442HTR2Ac.1309A>T (p.Lys437Ter)
c.820A>T (p.Lys274Ter)
c.1057A>T (p.Lys353Ter)
13g.46834944T>CCA388150443HTR2Ac.1309A>G (p.Lys437Glu)
c.820A>G (p.Lys274Glu)
c.1057A>G (p.Lys353Glu)
13g.46834944T>GCA388150444HTR2Ac.1309A>C (p.Lys437Gln)
c.820A>C (p.Lys274Gln)
c.1057A>C (p.Lys353Gln)
 gnomAD v4
13g.46834945G>ACA483739161HTR2Ac.1308C>T (p.Ala436=)
c.819C>T (p.Ala273=)
c.1056C>T (p.Ala352=)
13g.46834945G>CCA483739162HTR2Ac.1308C>G (p.Ala436=)
c.819C>G (p.Ala273=)
c.1056C>G (p.Ala352=)
13g.46834945G>TCA483739163HTR2Ac.1308C>A (p.Ala436=)
c.819C>A (p.Ala273=)
c.1056C>A (p.Ala352=)
13g.46834946G>ACA388150445HTR2Ac.1307C>T (p.Ala436Val)
c.818C>T (p.Ala273Val)
c.1055C>T (p.Ala352Val)
 dbSNP gnomAD v3 gnomAD v4
13g.46834946G>CCA6977508HTR2Ac.1307C>G (p.Ala436Gly)
c.818C>G (p.Ala273Gly)
c.1055C>G (p.Ala352Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46834946G=CA2089283379HTR2Ac.1307C= (p.Ala436=)
c.818C= (p.Ala273=)
c.1055C= (p.Ala352=)
13g.46834946G>TCA388150446HTR2Ac.1307C>A (p.Ala436Asp)
c.818C>A (p.Ala273Asp)
c.1055C>A (p.Ala352Asp)
 dbSNP gnomAD v2 gnomAD v4
13g.46834947C>ACA388150447HTR2Ac.1306G>T (p.Ala436Ser)
c.817G>T (p.Ala273Ser)
c.1054G>T (p.Ala352Ser)
13g.46834947C=CA2089283380HTR2Ac.1306G= (p.Ala436=)
c.817G= (p.Ala273=)
c.1054G= (p.Ala352=)
13g.46834947C>GCA388150448HTR2Ac.1306G>C (p.Ala436Pro)
c.817G>C (p.Ala273Pro)
c.1054G>C (p.Ala352Pro)
13g.46834947C>TCA388150449HTR2Ac.1306G>A (p.Ala436Thr)
c.817G>A (p.Ala273Thr)
c.1054G>A (p.Ala352Thr)
 dbSNP
13g.46834948A=CA2089283381HTR2Ac.1305T= (p.Asp435=)
c.816T= (p.Asp272=)
c.1053T= (p.Asp351=)
13g.46834948A>CCA388150451HTR2Ac.1305T>G (p.Asp435Glu)
c.816T>G (p.Asp272Glu)
c.1053T>G (p.Asp351Glu)
13g.46834948A>GCA483739166HTR2Ac.1305T>C (p.Asp435=)
c.816T>C (p.Asp272=)
c.1053T>C (p.Asp351=)
 dbSNP
13g.46834948A>TCA388150450HTR2Ac.1305T>A (p.Asp435Glu)
c.816T>A (p.Asp272Glu)
c.1053T>A (p.Asp351Glu)
13g.46834949T>ACA388150452HTR2Ac.1304A>T (p.Asp435Val)
c.815A>T (p.Asp272Val)
c.1052A>T (p.Asp351Val)
13g.46834949T>CCA388150453HTR2Ac.1304A>G (p.Asp435Gly)
c.815A>G (p.Asp272Gly)
c.1052A>G (p.Asp351Gly)
 gnomAD v4
13g.46834949T>GCA388150454HTR2Ac.1304A>C (p.Asp435Ala)
c.815A>C (p.Asp272Ala)
c.1052A>C (p.Asp351Ala)
13g.46834950C>ACA388150455HTR2Ac.1303G>T (p.Asp435Tyr)
c.814G>T (p.Asp272Tyr)
c.1051G>T (p.Asp351Tyr)
13g.46834950C=CA2089283382HTR2Ac.1303G= (p.Asp435=)
c.814G= (p.Asp272=)
c.1051G= (p.Asp351=)
13g.46834950C>GCA388150456HTR2Ac.1303G>C (p.Asp435His)
c.814G>C (p.Asp272His)
c.1051G>C (p.Asp351His)
 dbSNP gnomAD v3 gnomAD v4
13g.46834950C>TCA388150457HTR2Ac.1303G>A (p.Asp435Asn)
c.814G>A (p.Asp272Asn)
c.1051G>A (p.Asp351Asn)
 dbSNP gnomAD v4
13g.46834951T>ACA388150460HTR2Ac.1302A>T (p.Gln434His)
c.813A>T (p.Gln271His)
c.1050A>T (p.Gln350His)
13g.46834951T>CCA483739170HTR2Ac.1302A>G (p.Gln434=)
c.813A>G (p.Gln271=)
c.1050A>G (p.Gln350=)
 gnomAD v4
13g.46834951T>GCA388150462HTR2Ac.1302A>C (p.Gln434His)
c.813A>C (p.Gln271His)
c.1050A>C (p.Gln350His)
13g.46834952T>ACA388150464HTR2Ac.1301A>T (p.Gln434Leu)
c.812A>T (p.Gln271Leu)
c.1049A>T (p.Gln350Leu)
13g.46834952T>CCA6977509HTR2Ac.1301A>G (p.Gln434Arg)
c.812A>G (p.Gln271Arg)
c.1049A>G (p.Gln350Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834952T>GCA388150467HTR2Ac.1301A>C (p.Gln434Pro)
c.812A>C (p.Gln271Pro)
c.1049A>C (p.Gln350Pro)
13g.46834952T=CA2089283383HTR2Ac.1301A= (p.Gln434=)
c.812A= (p.Gln271=)
c.1049A= (p.Gln350=)
13g.46834953G>ACA388150472HTR2Ac.1300C>T (p.Gln434Ter)
c.811C>T (p.Gln271Ter)
c.1048C>T (p.Gln350Ter)
 gnomAD v4
13g.46834953G>CCA388150471HTR2Ac.1300C>G (p.Gln434Glu)
c.811C>G (p.Gln271Glu)
c.1048C>G (p.Gln350Glu)
13g.46834953G>TCA388150470HTR2Ac.1300C>A (p.Gln434Lys)
c.811C>A (p.Gln271Lys)
c.1048C>A (p.Gln350Lys)
13g.46834954C>ACA388150475HTR2Ac.1299G>T (p.Lys433Asn)
c.810G>T (p.Lys270Asn)
c.1047G>T (p.Lys349Asn)
 dbSNP gnomAD v2 gnomAD v4
13g.46834954C=CA2089283384HTR2Ac.1299G= (p.Lys433=)
c.810G= (p.Lys270=)
c.1047G= (p.Lys349=)
13g.46834954C>GCA388150477HTR2Ac.1299G>C (p.Lys433Asn)
c.810G>C (p.Lys270Asn)
c.1047G>C (p.Lys349Asn)
13g.46834954C>TCA483739171HTR2Ac.1299G>A (p.Lys433=)
c.810G>A (p.Lys270=)
c.1047G>A (p.Lys349=)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched