Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.46834975C>ACA388150569HTR2Ac.1278G>T (p.Met426Ile)
c.789G>T (p.Met263Ile)
c.1026G>T (p.Met342Ile)
13g.46834975C>GCA388150570HTR2Ac.1278G>C (p.Met426Ile)
c.789G>C (p.Met263Ile)
c.1026G>C (p.Met342Ile)
13g.46834975C>TCA388150572HTR2Ac.1278G>A (p.Met426Ile)
c.789G>A (p.Met263Ile)
c.1026G>A (p.Met342Ile)
 gnomAD v4
13g.46834976A>CCA388150575HTR2Ac.1277T>G (p.Met426Arg)
c.788T>G (p.Met263Arg)
c.1025T>G (p.Met342Arg)
13g.46834976A>GCA388150576HTR2Ac.1277T>C (p.Met426Thr)
c.788T>C (p.Met263Thr)
c.1025T>C (p.Met342Thr)
13g.46834976A>TCA388150578HTR2Ac.1277T>A (p.Met426Lys)
c.788T>A (p.Met263Lys)
c.1025T>A (p.Met342Lys)
 gnomAD v4
13g.46834977T>ACA388150583HTR2Ac.1276A>T (p.Met426Leu)
c.787A>T (p.Met263Leu)
c.1024A>T (p.Met342Leu)
13g.46834977T>CCA388150581HTR2Ac.1276A>G (p.Met426Val)
c.787A>G (p.Met263Val)
c.1024A>G (p.Met342Val)
 dbSNP gnomAD v2 gnomAD v4
13g.46834977T>GCA388150580HTR2Ac.1276A>C (p.Met426Leu)
c.787A>C (p.Met263Leu)
c.1024A>C (p.Met342Leu)
13g.46834977T=CA2089283392HTR2Ac.1276A= (p.Met426=)
c.787A= (p.Met263=)
c.1024A= (p.Met342=)
13g.46834978T>ACA388150587HTR2Ac.1275A>T (p.Gln425His)
c.786A>T (p.Gln262His)
c.1023A>T (p.Gln341His)
 dbSNP
13g.46834978T>CCA483739195HTR2Ac.1275A>G (p.Gln425=)
c.786A>G (p.Gln262=)
c.1023A>G (p.Gln341=)
13g.46834978T>GCA388150585HTR2Ac.1275A>C (p.Gln425His)
c.786A>C (p.Gln262His)
c.1023A>C (p.Gln341His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46834978T=CA2089283393HTR2Ac.1275A= (p.Gln425=)
c.786A= (p.Gln262=)
c.1023A= (p.Gln341=)
13g.46834979T>ACA388150589HTR2Ac.1274A>T (p.Gln425Leu)
c.785A>T (p.Gln262Leu)
c.1022A>T (p.Gln341Leu)
13g.46834979T>CCA388150591HTR2Ac.1274A>G (p.Gln425Arg)
c.785A>G (p.Gln262Arg)
c.1022A>G (p.Gln341Arg)
 dbSNP
13g.46834979T>GCA388150592HTR2Ac.1274A>C (p.Gln425Pro)
c.785A>C (p.Gln262Pro)
c.1022A>C (p.Gln341Pro)
13g.46834979T=CA2089283394HTR2Ac.1274A= (p.Gln425=)
c.785A= (p.Gln262=)
c.1022A= (p.Gln341=)
13g.46834980G>ACA388150593HTR2Ac.1273C>T (p.Gln425Ter)
c.784C>T (p.Gln262Ter)
c.1021C>T (p.Gln341Ter)
13g.46834980G>CCA388150594HTR2Ac.1273C>G (p.Gln425Glu)
c.784C>G (p.Gln262Glu)
c.1021C>G (p.Gln341Glu)
13g.46834980G>TCA388150596HTR2Ac.1273C>A (p.Gln425Lys)
c.784C>A (p.Gln262Lys)
c.1021C>A (p.Gln341Lys)
13g.46834981A>CCA483739201HTR2Ac.1272T>G (p.Leu424=)
c.783T>G (p.Leu261=)
c.1020T>G (p.Leu340=)
13g.46834981A>GCA483739199HTR2Ac.1272T>C (p.Leu424=)
c.783T>C (p.Leu261=)
c.1020T>C (p.Leu340=)
13g.46834981A>TCA483739198HTR2Ac.1272T>A (p.Leu424=)
c.783T>A (p.Leu261=)
c.1020T>A (p.Leu340=)
13g.46834982A>CCA388150598HTR2Ac.1271T>G (p.Leu424Arg)
c.782T>G (p.Leu261Arg)
c.1019T>G (p.Leu340Arg)
13g.46834982A>GCA388150600HTR2Ac.1271T>C (p.Leu424Pro)
c.782T>C (p.Leu261Pro)
c.1019T>C (p.Leu340Pro)
13g.46834982A>TCA388150601HTR2Ac.1271T>A (p.Leu424His)
c.782T>A (p.Leu261His)
c.1019T>A (p.Leu340His)
13g.46834983G>ACA6977511HTR2Ac.1270C>T (p.Leu424Phe)
c.781C>T (p.Leu261Phe)
c.1018C>T (p.Leu340Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834983G>CCA388150604HTR2Ac.1270C>G (p.Leu424Val)
c.781C>G (p.Leu261Val)
c.1018C>G (p.Leu340Val)
 gnomAD v4
13g.46834983G=CA2089283395HTR2Ac.1270C= (p.Leu424=)
c.781C= (p.Leu261=)
c.1018C= (p.Leu340=)
13g.46834983G>TCA388150606HTR2Ac.1270C>A (p.Leu424Ile)
c.781C>A (p.Leu261Ile)
c.1018C>A (p.Leu340Ile)
13g.46834984T>ACA388150611HTR2Ac.1269A>T (p.Gln423His)
c.780A>T (p.Gln260His)
c.1017A>T (p.Gln339His)
13g.46834984T>CCA483739204HTR2Ac.1269A>G (p.Gln423=)
c.780A>G (p.Gln260=)
c.1017A>G (p.Gln339=)
13g.46834984T>GCA388150609HTR2Ac.1269A>C (p.Gln423His)
c.780A>C (p.Gln260His)
c.1017A>C (p.Gln339His)
13g.46834985T>ACA388150613HTR2Ac.1268A>T (p.Gln423Leu)
c.779A>T (p.Gln260Leu)
c.1016A>T (p.Gln339Leu)
13g.46834985T>CCA388150614HTR2Ac.1268A>G (p.Gln423Arg)
c.779A>G (p.Gln260Arg)
c.1016A>G (p.Gln339Arg)
 gnomAD v4
13g.46834985T>GCA388150617HTR2Ac.1268A>C (p.Gln423Pro)
c.779A>C (p.Gln260Pro)
c.1016A>C (p.Gln339Pro)
13g.46834986G>ACA388150618HTR2Ac.1267C>T (p.Gln423Ter)
c.778C>T (p.Gln260Ter)
c.1015C>T (p.Gln339Ter)
13g.46834986G>CCA388150620HTR2Ac.1267C>G (p.Gln423Glu)
c.778C>G (p.Gln260Glu)
c.1015C>G (p.Gln339Glu)
13g.46834986G>TCA388150622HTR2Ac.1267C>A (p.Gln423Lys)
c.778C>A (p.Gln260Lys)
c.1015C>A (p.Gln339Lys)
13g.46834987G>ACA483739209HTR2Ac.1266C>T (p.Ser422=)
c.777C>T (p.Ser259=)
c.1014C>T (p.Ser338=)
13g.46834987G>CCA388150623HTR2Ac.1266C>G (p.Ser422Arg)
c.777C>G (p.Ser259Arg)
c.1014C>G (p.Ser338Arg)
13g.46834987G>TCA388150625HTR2Ac.1266C>A (p.Ser422Arg)
c.777C>A (p.Ser259Arg)
c.1014C>A (p.Ser338Arg)
13g.46834988C>ACA388150627HTR2Ac.1265G>T (p.Ser422Ile)
c.776G>T (p.Ser259Ile)
c.1013G>T (p.Ser338Ile)
13g.46834988C>GCA388150629HTR2Ac.1265G>C (p.Ser422Thr)
c.776G>C (p.Ser259Thr)
c.1013G>C (p.Ser338Thr)
13g.46834988C>TCA388150632HTR2Ac.1265G>A (p.Ser422Asn)
c.776G>A (p.Ser259Asn)
c.1013G>A (p.Ser338Asn)
13g.46834989T>ACA388150633HTR2Ac.1264A>T (p.Ser422Cys)
c.775A>T (p.Ser259Cys)
c.1012A>T (p.Ser338Cys)
13g.46834989T>CCA388150634HTR2Ac.1264A>G (p.Ser422Gly)
c.775A>G (p.Ser259Gly)
c.1012A>G (p.Ser338Gly)
13g.46834989T>GCA388150636HTR2Ac.1264A>C (p.Ser422Arg)
c.775A>C (p.Ser259Arg)
c.1012A>C (p.Ser338Arg)
13g.46834990A>CCA483739211HTR2Ac.1263T>G (p.Ser421=)
c.774T>G (p.Ser258=)
c.1011T>G (p.Ser337=)
13g.46834990A>GCA483739213HTR2Ac.1263T>C (p.Ser421=)
c.774T>C (p.Ser258=)
c.1011T>C (p.Ser337=)
13g.46834990A>TCA483739215HTR2Ac.1263T>A (p.Ser421=)
c.774T>A (p.Ser258=)
c.1011T>A (p.Ser337=)
13g.46834991G>ACA249253446HTR2Ac.1262C>T (p.Ser421Phe)
c.773C>T (p.Ser258Phe)
c.1010C>T (p.Ser337Phe)
 dbSNP
13g.46834991G>CCA388150638HTR2Ac.1262C>G (p.Ser421Cys)
c.773C>G (p.Ser258Cys)
c.1010C>G (p.Ser337Cys)
13g.46834991G=CA2089283396HTR2Ac.1262C= (p.Ser421=)
c.773C= (p.Ser258=)
c.1010C= (p.Ser337=)
13g.46834991G>TCA6977512HTR2Ac.1262C>A (p.Ser421Tyr)
c.773C>A (p.Ser258Tyr)
c.1010C>A (p.Ser337Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834992A>CCA388150639HTR2Ac.1261T>G (p.Ser421Ala)
c.772T>G (p.Ser258Ala)
c.1009T>G (p.Ser337Ala)
13g.46834992A>GCA388150641HTR2Ac.1261T>C (p.Ser421Pro)
c.772T>C (p.Ser258Pro)
c.1009T>C (p.Ser337Pro)
13g.46834992A>TCA388150640HTR2Ac.1261T>A (p.Ser421Thr)
c.772T>A (p.Ser258Thr)
c.1009T>A (p.Ser337Thr)
13g.46834993C>ACA388150642HTR2Ac.1260G>T (p.Lys420Asn)
c.771G>T (p.Lys257Asn)
c.1008G>T (p.Lys336Asn)
13g.46834993C=CA2089283397HTR2Ac.1260G= (p.Lys420=)
c.771G= (p.Lys257=)
c.1008G= (p.Lys336=)
13g.46834993C>GCA388150643HTR2Ac.1260G>C (p.Lys420Asn)
c.771G>C (p.Lys257Asn)
c.1008G>C (p.Lys336Asn)
 dbSNP
13g.46834993C>TCA483739217HTR2Ac.1260G>A (p.Lys420=)
c.771G>A (p.Lys257=)
c.1008G>A (p.Lys336=)
 ClinVar dbSNP
13g.46834994T>ACA388150645HTR2Ac.1259A>T (p.Lys420Met)
c.770A>T (p.Lys257Met)
c.1007A>T (p.Lys336Met)
13g.46834994T>CCA388150647HTR2Ac.1259A>G (p.Lys420Arg)
c.770A>G (p.Lys257Arg)
c.1007A>G (p.Lys336Arg)
13g.46834994T>GCA388150648HTR2Ac.1259A>C (p.Lys420Thr)
c.770A>C (p.Lys257Thr)
c.1007A>C (p.Lys336Thr)
13g.46834995T>ACA388150650HTR2Ac.1258A>T (p.Lys420Ter)
c.769A>T (p.Lys257Ter)
c.1006A>T (p.Lys336Ter)
13g.46834995T>CCA388150652HTR2Ac.1258A>G (p.Lys420Glu)
c.769A>G (p.Lys257Glu)
c.1006A>G (p.Lys336Glu)
13g.46834995T>GCA388150654HTR2Ac.1258A>C (p.Lys420Gln)
c.769A>C (p.Lys257Gln)
c.1006A>C (p.Lys336Gln)
13g.46834996G>ACA483739221HTR2Ac.1257C>T (p.Tyr419=)
c.768C>T (p.Tyr256=)
c.1005C>T (p.Tyr335=)
 dbSNP gnomAD v4
13g.46834996G>CCA388150657HTR2Ac.1257C>G (p.Tyr419Ter)
c.768C>G (p.Tyr256Ter)
c.1005C>G (p.Tyr335Ter)
13g.46834996G>TCA388150658HTR2Ac.1257C>A (p.Tyr419Ter)
c.768C>A (p.Tyr256Ter)
c.1005C>A (p.Tyr335Ter)
13g.46834997T>ACA388150665HTR2Ac.1256A>T (p.Tyr419Phe)
c.767A>T (p.Tyr256Phe)
c.1004A>T (p.Tyr335Phe)
13g.46834997T>CCA6977513HTR2Ac.1256A>G (p.Tyr419Cys)
c.767A>G (p.Tyr256Cys)
c.1004A>G (p.Tyr335Cys)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46834997T>GCA388150662HTR2Ac.1256A>C (p.Tyr419Ser)
c.767A>C (p.Tyr256Ser)
c.1004A>C (p.Tyr335Ser)
13g.46834997T=CA2089283398HTR2Ac.1256A= (p.Tyr419=)
c.767A= (p.Tyr256=)
c.1004A= (p.Tyr335=)
13g.46834998A>CCA388150667HTR2Ac.1255T>G (p.Tyr419Asp)
c.766T>G (p.Tyr256Asp)
c.1003T>G (p.Tyr335Asp)
13g.46834998A>GCA388150668HTR2Ac.1255T>C (p.Tyr419His)
c.766T>C (p.Tyr256His)
c.1003T>C (p.Tyr335His)
 gnomAD v4
13g.46834998A>TCA388150670HTR2Ac.1255T>A (p.Tyr419Asn)
c.766T>A (p.Tyr256Asn)
c.1003T>A (p.Tyr335Asn)
13g.46834999G>ACA483739223HTR2Ac.1254C>T (p.Ala418=)
c.765C>T (p.Ala255=)
c.1002C>T (p.Ala334=)
13g.46834999G>CCA483739224HTR2Ac.1254C>G (p.Ala418=)
c.765C>G (p.Ala255=)
c.1002C>G (p.Ala334=)
13g.46834999G=CA2089283399HTR2Ac.1254C= (p.Ala418=)
c.765C= (p.Ala255=)
c.1002C= (p.Ala334=)
13g.46834999G>TCA483739225HTR2Ac.1254C>A (p.Ala418=)
c.765C>A (p.Ala255=)
c.1002C>A (p.Ala334=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46835000G>ACA388150673HTR2Ac.1253C>T (p.Ala418Val)
c.764C>T (p.Ala255Val)
c.1001C>T (p.Ala334Val)
13g.46835000G>CCA388150675HTR2Ac.1253C>G (p.Ala418Gly)
c.764C>G (p.Ala255Gly)
c.1001C>G (p.Ala334Gly)
13g.46835000G>TCA388150677HTR2Ac.1253C>A (p.Ala418Asp)
c.764C>A (p.Ala255Asp)
c.1001C>A (p.Ala334Asp)
13g.46835001C>ACA388150680HTR2Ac.1252G>T (p.Ala418Ser)
c.763G>T (p.Ala255Ser)
c.1000G>T (p.Ala334Ser)
13g.46835001C>GCA388150682HTR2Ac.1252G>C (p.Ala418Pro)
c.763G>C (p.Ala255Pro)
c.1000G>C (p.Ala334Pro)
13g.46835001C>TCA388150684HTR2Ac.1252G>A (p.Ala418Thr)
c.763G>A (p.Ala255Thr)
c.1000G>A (p.Ala334Thr)
13g.46835002C>ACA388150687HTR2Ac.1251G>T (p.Leu417Phe)
c.762G>T (p.Leu254Phe)
c.999G>T (p.Leu333Phe)
13g.46835002C=CA2089283400HTR2Ac.1251G= (p.Leu417=)
c.762G= (p.Leu254=)
c.999G= (p.Leu333=)
13g.46835002C>GCA249253470HTR2Ac.1251G>C (p.Leu417Phe)
c.762G>C (p.Leu254Phe)
c.999G>C (p.Leu333Phe)
 dbSNP gnomAD v2 gnomAD v4
13g.46835002C>TCA6977514HTR2Ac.1251G>A (p.Leu417=)
c.762G>A (p.Leu254=)
c.999G>A (p.Leu333=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835003A=CA2089283401HTR2Ac.1250T= (p.Leu417=)
c.761T= (p.Leu254=)
c.998T= (p.Leu333=)
13g.46835003A>CCA388150692HTR2Ac.1250T>G (p.Leu417Trp)
c.761T>G (p.Leu254Trp)
c.998T>G (p.Leu333Trp)
13g.46835003A>GCA249253480HTR2Ac.1250T>C (p.Leu417Ser)
c.761T>C (p.Leu254Ser)
c.998T>C (p.Leu333Ser)
 dbSNP gnomAD v4
13g.46835003A>TCA388150690HTR2Ac.1250T>A (p.Leu417Ter)
c.761T>A (p.Leu254Ter)
c.998T>A (p.Leu333Ter)
13g.46835004A>CCA388150695HTR2Ac.1249T>G (p.Leu417Val)
c.760T>G (p.Leu254Val)
c.997T>G (p.Leu333Val)
13g.46835004A>GCA483739228HTR2Ac.1249T>C (p.Leu417=)
c.760T>C (p.Leu254=)
c.997T>C (p.Leu333=)
13g.46835004A>TCA388150697HTR2Ac.1249T>A (p.Leu417Met)
c.760T>A (p.Leu254Met)
c.997T>A (p.Leu333Met)
13g.46835005A=CA2089283402HTR2Ac.1248T= (p.Ala416=)
c.759T= (p.Ala253=)
c.996T= (p.Ala332=)
13g.46835005A>CCA483739229HTR2Ac.1248T>G (p.Ala416=)
c.759T>G (p.Ala253=)
c.996T>G (p.Ala332=)
 dbSNP gnomAD v3 gnomAD v4
13g.46835005A>GCA483739230HTR2Ac.1248T>C (p.Ala416=)
c.759T>C (p.Ala253=)
c.996T>C (p.Ala332=)
13g.46835005A>TCA483739231HTR2Ac.1248T>A (p.Ala416=)
c.759T>A (p.Ala253=)
c.996T>A (p.Ala332=)
13g.46835006G>ACA388150698HTR2Ac.1247C>T (p.Ala416Val)
c.758C>T (p.Ala253Val)
c.995C>T (p.Ala332Val)
13g.46835006G>CCA388150699HTR2Ac.1247C>G (p.Ala416Gly)
c.758C>G (p.Ala253Gly)
c.995C>G (p.Ala332Gly)
13g.46835006G>TCA388150700HTR2Ac.1247C>A (p.Ala416Asp)
c.758C>A (p.Ala253Asp)
c.995C>A (p.Ala332Asp)
 gnomAD v4
13g.46835007C>ACA388150701HTR2Ac.1246G>T (p.Ala416Ser)
c.757G>T (p.Ala253Ser)
c.994G>T (p.Ala332Ser)
13g.46835007C>GCA388150702HTR2Ac.1246G>C (p.Ala416Pro)
c.757G>C (p.Ala253Pro)
c.994G>C (p.Ala332Pro)
13g.46835007C>TCA388150703HTR2Ac.1246G>A (p.Ala416Thr)
c.757G>A (p.Ala253Thr)
c.994G>A (p.Ala332Thr)
13g.46835008C>ACA483739233HTR2Ac.1245G>T (p.Pro415=)
c.756G>T (p.Pro252=)
c.993G>T (p.Pro331=)
13g.46835008C=CA2089283403HTR2Ac.1245G= (p.Pro415=)
c.756G= (p.Pro252=)
c.993G= (p.Pro331=)
13g.46835008C>GCA483739234HTR2Ac.1245G>C (p.Pro415=)
c.756G>C (p.Pro252=)
c.993G>C (p.Pro331=)
13g.46835008C>TCA6977515HTR2Ac.1245G>A (p.Pro415=)
c.756G>A (p.Pro252=)
c.993G>A (p.Pro331=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835009G>ACA6977516HTR2Ac.1244C>T (p.Pro415Leu)
c.755C>T (p.Pro252Leu)
c.992C>T (p.Pro331Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46835009G>CCA388150708HTR2Ac.1244C>G (p.Pro415Arg)
c.755C>G (p.Pro252Arg)
c.992C>G (p.Pro331Arg)
13g.46835009G=CA2089283404HTR2Ac.1244C= (p.Pro415=)
c.755C= (p.Pro252=)
c.992C= (p.Pro331=)
13g.46835009G>TCA388150709HTR2Ac.1244C>A (p.Pro415Gln)
c.755C>A (p.Pro252Gln)
c.992C>A (p.Pro331Gln)
13g.46835010G>ACA388150716HTR2Ac.1243C>T (p.Pro415Ser)
c.754C>T (p.Pro252Ser)
c.991C>T (p.Pro331Ser)
 gnomAD v4
13g.46835010G>CCA388150718HTR2Ac.1243C>G (p.Pro415Ala)
c.754C>G (p.Pro252Ala)
c.991C>G (p.Pro331Ala)
13g.46835010G>TCA388150714HTR2Ac.1243C>A (p.Pro415Thr)
c.754C>A (p.Pro252Thr)
c.991C>A (p.Pro331Thr)
13g.46835011T>ACA483739252HTR2Ac.1242A>T (p.Ile414=)
c.753A>T (p.Ile251=)
c.990A>T (p.Ile330=)
13g.46835011T>CCA388150720HTR2Ac.1242A>G (p.Ile414Met)
c.753A>G (p.Ile251Met)
c.990A>G (p.Ile330Met)
 dbSNP gnomAD v4
13g.46835011T>GCA483739253HTR2Ac.1242A>C (p.Ile414=)
c.753A>C (p.Ile251=)
c.990A>C (p.Ile330=)
13g.46835011T=CA2089283405HTR2Ac.1242A= (p.Ile414=)
c.753A= (p.Ile251=)
c.990A= (p.Ile330=)
13g.46835012A=CA2089283406HTR2Ac.1241T= (p.Ile414=)
c.752T= (p.Ile251=)
c.989T= (p.Ile330=)
13g.46835012A>CCA249253499HTR2Ac.1241T>G (p.Ile414Arg)
c.752T>G (p.Ile251Arg)
c.989T>G (p.Ile330Arg)
 dbSNP
13g.46835012A>GCA388150723HTR2Ac.1241T>C (p.Ile414Thr)
c.752T>C (p.Ile251Thr)
c.989T>C (p.Ile330Thr)
 COSMIC
13g.46835012A>TCA388150726HTR2Ac.1241T>A (p.Ile414Lys)
c.752T>A (p.Ile251Lys)
c.989T>A (p.Ile330Lys)
13g.46835013T>ACA388150734HTR2Ac.1240A>T (p.Ile414Leu)
c.751A>T (p.Ile251Leu)
c.988A>T (p.Ile330Leu)
13g.46835013T>CCA388150732HTR2Ac.1240A>G (p.Ile414Val)
c.751A>G (p.Ile251Val)
c.988A>G (p.Ile330Val)
 dbSNP gnomAD v3 gnomAD v4
13g.46835013T>GCA388150730HTR2Ac.1240A>C (p.Ile414Leu)
c.751A>C (p.Ile251Leu)
c.988A>C (p.Ile330Leu)
13g.46835013T=CA2089283407HTR2Ac.1240A= (p.Ile414=)
c.751A= (p.Ile251=)
c.988A= (p.Ile330=)
13g.46835014T>ACA6977517HTR2Ac.1239A>T (p.Thr413=)
c.750A>T (p.Thr250=)
c.987A>T (p.Thr329=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835014T>CCA483739259HTR2Ac.1239A>G (p.Thr413=)
c.750A>G (p.Thr250=)
c.987A>G (p.Thr329=)
13g.46835014T>GCA483739258HTR2Ac.1239A>C (p.Thr413=)
c.750A>C (p.Thr250=)
c.987A>C (p.Thr329=)
13g.46835014T=CA2089283408HTR2Ac.1239A= (p.Thr413=)
c.750A= (p.Thr250=)
c.987A= (p.Thr329=)
13g.46835015G>ACA388150738HTR2Ac.1238C>T (p.Thr413Ile)
c.749C>T (p.Thr250Ile)
c.986C>T (p.Thr329Ile)
13g.46835015G>CCA388150739HTR2Ac.1238C>G (p.Thr413Arg)
c.749C>G (p.Thr250Arg)
c.986C>G (p.Thr329Arg)
 gnomAD v4
13g.46835015G>TCA388150740HTR2Ac.1238C>A (p.Thr413Lys)
c.749C>A (p.Thr250Lys)
c.986C>A (p.Thr329Lys)
13g.46835016T>ACA388150741HTR2Ac.1237A>T (p.Thr413Ser)
c.748A>T (p.Thr250Ser)
c.985A>T (p.Thr329Ser)
13g.46835016T>CCA388150742HTR2Ac.1237A>G (p.Thr413Ala)
c.748A>G (p.Thr250Ala)
c.985A>G (p.Thr329Ala)
 gnomAD v4
13g.46835016T>GCA388150743HTR2Ac.1237A>C (p.Thr413Pro)
c.748A>C (p.Thr250Pro)
c.985A>C (p.Thr329Pro)
13g.46835017G>ACA483739261HTR2Ac.1236C>T (p.Asn412=)
c.747C>T (p.Asn249=)
c.984C>T (p.Asn328=)
13g.46835017G>CCA388150746HTR2Ac.1236C>G (p.Asn412Lys)
c.747C>G (p.Asn249Lys)
c.984C>G (p.Asn328Lys)
 gnomAD v4
13g.46835017G>TCA388150745HTR2Ac.1236C>A (p.Asn412Lys)
c.747C>A (p.Asn249Lys)
c.984C>A (p.Asn328Lys)
13g.46835018T>ACA388150747HTR2Ac.1235A>T (p.Asn412Ile)
c.746A>T (p.Asn249Ile)
c.983A>T (p.Asn328Ile)
13g.46835018T>CCA388150751HTR2Ac.1235A>G (p.Asn412Ser)
c.746A>G (p.Asn249Ser)
c.983A>G (p.Asn328Ser)
13g.46835018T>GCA388150749HTR2Ac.1235A>C (p.Asn412Thr)
c.746A>C (p.Asn249Thr)
c.983A>C (p.Asn328Thr)
13g.46835019T>ACA388150759HTR2Ac.1234A>T (p.Asn412Tyr)
c.745A>T (p.Asn249Tyr)
c.982A>T (p.Asn328Tyr)
13g.46835019T>CCA388150763HTR2Ac.1234A>G (p.Asn412Asp)
c.745A>G (p.Asn249Asp)
c.982A>G (p.Asn328Asp)
13g.46835019T>GCA388150762HTR2Ac.1234A>C (p.Asn412His)
c.745A>C (p.Asn249His)
c.982A>C (p.Asn328His)
13g.46835020C>ACA483739263HTR2Ac.1233G>T (p.Val411=)
c.744G>T (p.Val248=)
c.981G>T (p.Val327=)
13g.46835020C>GCA483739264HTR2Ac.1233G>C (p.Val411=)
c.744G>C (p.Val248=)
c.981G>C (p.Val327=)
13g.46835020C>TCA483739265HTR2Ac.1233G>A (p.Val411=)
c.744G>A (p.Val248=)
c.981G>A (p.Val327=)
13g.46835021A=CA2089283409HTR2Ac.1232T= (p.Val411=)
c.743T= (p.Val248=)
c.980T= (p.Val327=)
13g.46835021A>CCA388150766HTR2Ac.1232T>G (p.Val411Gly)
c.743T>G (p.Val248Gly)
c.980T>G (p.Val327Gly)
 dbSNP gnomAD v2 gnomAD v4
13g.46835021A>GCA388150771HTR2Ac.1232T>C (p.Val411Ala)
c.743T>C (p.Val248Ala)
c.980T>C (p.Val327Ala)
13g.46835021A>TCA388150769HTR2Ac.1232T>A (p.Val411Glu)
c.743T>A (p.Val248Glu)
c.980T>A (p.Val327Glu)
13g.46835022C>ACA388150773HTR2Ac.1231G>T (p.Val411Leu)
c.742G>T (p.Val248Leu)
c.979G>T (p.Val327Leu)
 gnomAD v4
13g.46835022C>GCA388150777HTR2Ac.1231G>C (p.Val411Leu)
c.742G>C (p.Val248Leu)
c.979G>C (p.Val327Leu)
13g.46835022C>TCA388150778HTR2Ac.1231G>A (p.Val411Met)
c.742G>A (p.Val248Met)
c.979G>A (p.Val327Met)
13g.46835023T>ACA388150781HTR2Ac.1230A>T (p.Leu410Phe)
c.741A>T (p.Leu247Phe)
c.978A>T (p.Leu326Phe)
13g.46835023T>CCA483739267HTR2Ac.1230A>G (p.Leu410=)
c.741A>G (p.Leu247=)
c.978A>G (p.Leu326=)
 gnomAD v4
13g.46835023T>GCA388150784HTR2Ac.1230A>C (p.Leu410Phe)
c.741A>C (p.Leu247Phe)
c.978A>C (p.Leu326Phe)
13g.46835024A>CCA388150786HTR2Ac.1229T>G (p.Leu410Ter)
c.740T>G (p.Leu247Ter)
c.977T>G (p.Leu326Ter)
13g.46835024A>GCA388150788HTR2Ac.1229T>C (p.Leu410Ser)
c.740T>C (p.Leu247Ser)
c.977T>C (p.Leu326Ser)
 gnomAD v4
13g.46835024A>TCA388150790HTR2Ac.1229T>A (p.Leu410Ter)
c.740T>A (p.Leu247Ter)
c.977T>A (p.Leu326Ter)
13g.46835025A=CA2089283410HTR2Ac.1228T= (p.Leu410=)
c.739T= (p.Leu247=)
c.976T= (p.Leu326=)
13g.46835025A>CCA388150793HTR2Ac.1228T>G (p.Leu410Val)
c.739T>G (p.Leu247Val)
c.976T>G (p.Leu326Val)
13g.46835025A>GCA6977519HTR2Ac.1228T>C (p.Leu410=)
c.739T>C (p.Leu247=)
c.976T>C (p.Leu326=)
 dbSNP ExAC gnomAD v2 gnomAD v4
13g.46835025A>TCA6977518HTR2Ac.1228T>A (p.Leu410Ile)
c.739T>A (p.Leu247Ile)
c.976T>A (p.Leu326Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835026A>CCA388150794HTR2Ac.1227T>G (p.Ile409Met)
c.738T>G (p.Ile246Met)
c.975T>G (p.Ile325Met)
13g.46835026A>GCA483739272HTR2Ac.1227T>C (p.Ile409=)
c.738T>C (p.Ile246=)
c.975T>C (p.Ile325=)
13g.46835026A>TCA483739273HTR2Ac.1227T>A (p.Ile409=)
c.738T>A (p.Ile246=)
c.975T>A (p.Ile325=)
13g.46835027A>CCA388150797HTR2Ac.1226T>G (p.Ile409Ser)
c.737T>G (p.Ile246Ser)
c.974T>G (p.Ile325Ser)
13g.46835027A>GCA388150795HTR2Ac.1226T>C (p.Ile409Thr)
c.737T>C (p.Ile246Thr)
c.974T>C (p.Ile325Thr)
 gnomAD v4
13g.46835027A>TCA388150796HTR2Ac.1226T>A (p.Ile409Asn)
c.737T>A (p.Ile246Asn)
c.974T>A (p.Ile325Asn)
13g.46835028T>ACA6977520HTR2Ac.1225A>T (p.Ile409Phe)
c.736A>T (p.Ile246Phe)
c.973A>T (p.Ile325Phe)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835028T>CCA388150798HTR2Ac.1225A>G (p.Ile409Val)
c.736A>G (p.Ile246Val)
c.973A>G (p.Ile325Val)
13g.46835028T>GCA388150799HTR2Ac.1225A>C (p.Ile409Leu)
c.736A>C (p.Ile246Leu)
c.973A>C (p.Ile325Leu)
13g.46835028T=CA2089283411HTR2Ac.1225A= (p.Ile409=)
c.736A= (p.Ile246=)
c.973A= (p.Ile325=)
13g.46835029T>ACA388150802HTR2Ac.1224A>T (p.Leu408Phe)
c.735A>T (p.Leu245Phe)
c.972A>T (p.Leu324Phe)
13g.46835029T>CCA483739277HTR2Ac.1224A>G (p.Leu408=)
c.735A>G (p.Leu245=)
c.972A>G (p.Leu324=)
13g.46835029T>GCA388150803HTR2Ac.1224A>C (p.Leu408Phe)
c.735A>C (p.Leu245Phe)
c.972A>C (p.Leu324Phe)
13g.46835030A>CCA388150805HTR2Ac.1223T>G (p.Leu408Ter)
c.734T>G (p.Leu245Ter)
c.971T>G (p.Leu324Ter)
13g.46835030A>GCA388150807HTR2Ac.1223T>C (p.Leu408Ser)
c.734T>C (p.Leu245Ser)
c.971T>C (p.Leu324Ser)
13g.46835030A>TCA388150808HTR2Ac.1223T>A (p.Leu408Ter)
c.734T>A (p.Leu245Ter)
c.971T>A (p.Leu324Ter)
13g.46835031A>CCA388150812HTR2Ac.1222T>G (p.Leu408Val)
c.733T>G (p.Leu245Val)
c.970T>G (p.Leu324Val)
13g.46835031A>GCA483739279HTR2Ac.1222T>C (p.Leu408=)
c.733T>C (p.Leu245=)
c.970T>C (p.Leu324=)
13g.46835031A>TCA388150815HTR2Ac.1222T>A (p.Leu408Ile)
c.733T>A (p.Leu245Ile)
c.970T>A (p.Leu324Ile)
13g.46835032C>ACA388150817HTR2Ac.1221G>T (p.Gln407His)
c.732G>T (p.Gln244His)
c.969G>T (p.Gln323His)
13g.46835032C>GCA388150820HTR2Ac.1221G>C (p.Gln407His)
c.732G>C (p.Gln244His)
c.969G>C (p.Gln323His)
13g.46835032C>TCA483739281HTR2Ac.1221G>A (p.Gln407=)
c.732G>A (p.Gln244=)
c.969G>A (p.Gln323=)
 COSMIC
13g.46835033T>ACA388150829HTR2Ac.1220A>T (p.Gln407Leu)
c.731A>T (p.Gln244Leu)
c.968A>T (p.Gln323Leu)
13g.46835033T>CCA388150824HTR2Ac.1220A>G (p.Gln407Arg)
c.731A>G (p.Gln244Arg)
c.968A>G (p.Gln323Arg)
13g.46835033T>GCA388150822HTR2Ac.1220A>C (p.Gln407Pro)
c.731A>C (p.Gln244Pro)
c.968A>C (p.Gln323Pro)
13g.46835034G>ACA388150838HTR2Ac.1219C>T (p.Gln407Ter)
c.730C>T (p.Gln244Ter)
c.967C>T (p.Gln323Ter)
13g.46835034G>CCA388150831HTR2Ac.1219C>G (p.Gln407Glu)
c.730C>G (p.Gln244Glu)
c.967C>G (p.Gln323Glu)
13g.46835034G>TCA388150833HTR2Ac.1219C>A (p.Gln407Lys)
c.730C>A (p.Gln244Lys)
c.967C>A (p.Gln323Lys)
 gnomAD v4
13g.46835035C>ACA388150840HTR2Ac.1218G>T (p.Leu406Phe)
c.729G>T (p.Leu243Phe)
c.966G>T (p.Leu322Phe)
13g.46835035C>GCA388150843HTR2Ac.1218G>C (p.Leu406Phe)
c.729G>C (p.Leu243Phe)
c.966G>C (p.Leu322Phe)
13g.46835035C>TCA483739284HTR2Ac.1218G>A (p.Leu406=)
c.729G>A (p.Leu243=)
c.966G>A (p.Leu322=)
 gnomAD v4
13g.46835036A>CCA388150844HTR2Ac.1217T>G (p.Leu406Trp)
c.728T>G (p.Leu243Trp)
c.965T>G (p.Leu322Trp)
13g.46835036A>GCA388150846HTR2Ac.1217T>C (p.Leu406Ser)
c.728T>C (p.Leu243Ser)
c.965T>C (p.Leu322Ser)
 gnomAD v4
13g.46835036A>TCA388150849HTR2Ac.1217T>A (p.Leu406Ter)
c.728T>A (p.Leu243Ter)
c.965T>A (p.Leu322Ter)
13g.46835037A=CA2089283412HTR2Ac.1216T= (p.Leu406=)
c.727T= (p.Leu243=)
c.964T= (p.Leu322=)
13g.46835037A>CCA388150852HTR2Ac.1216T>G (p.Leu406Val)
c.727T>G (p.Leu243Val)
c.964T>G (p.Leu322Val)
13g.46835037A>GCA483739286HTR2Ac.1216T>C (p.Leu406=)
c.727T>C (p.Leu243=)
c.964T>C (p.Leu322=)
 dbSNP gnomAD v2 gnomAD v4
13g.46835037A>TCA388150856HTR2Ac.1216T>A (p.Leu406Met)
c.727T>A (p.Leu243Met)
c.964T>A (p.Leu322Met)
13g.46835038T>ACA483739290HTR2Ac.1215A>T (p.Pro405=)
c.726A>T (p.Pro242=)
c.963A>T (p.Pro321=)
13g.46835038T>CCA6977521HTR2Ac.1215A>G (p.Pro405=)
c.726A>G (p.Pro242=)
c.963A>G (p.Pro321=)
 dbSNP ExAC gnomAD v2
13g.46835038T>GCA483739291HTR2Ac.1215A>C (p.Pro405=)
c.726A>C (p.Pro242=)
c.963A>C (p.Pro321=)
13g.46835038T=CA2089283413HTR2Ac.1215A= (p.Pro405=)
c.726A= (p.Pro242=)
c.963A= (p.Pro321=)
13g.46835039G>ACA388150860HTR2Ac.1214C>T (p.Pro405Leu)
c.725C>T (p.Pro242Leu)
c.962C>T (p.Pro321Leu)
13g.46835039G>CCA388150861HTR2Ac.1214C>G (p.Pro405Arg)
c.725C>G (p.Pro242Arg)
c.962C>G (p.Pro321Arg)
13g.46835039G>TCA388150863HTR2Ac.1214C>A (p.Pro405Gln)
c.725C>A (p.Pro242Gln)
c.962C>A (p.Pro321Gln)
13g.46835040G>ACA388150868HTR2Ac.1213C>T (p.Pro405Ser)
c.724C>T (p.Pro242Ser)
c.961C>T (p.Pro321Ser)
13g.46835040G>CCA388150869HTR2Ac.1213C>G (p.Pro405Ala)
c.724C>G (p.Pro242Ala)
c.961C>G (p.Pro321Ala)
 gnomAD v4
13g.46835040G=CA2089283414HTR2Ac.1213C= (p.Pro405=)
c.724C= (p.Pro242=)
c.961C= (p.Pro321=)
13g.46835040G>TCA6977523HTR2Ac.1213C>A (p.Pro405Thr)
c.724C>A (p.Pro242Thr)
c.961C>A (p.Pro321Thr)
 dbSNP ExAC gnomAD v4
13g.46835041T>ACA388150874HTR2Ac.1212A>T (p.Lys404Asn)
c.723A>T (p.Lys241Asn)
c.960A>T (p.Lys320Asn)
13g.46835041T>CCA483739300HTR2Ac.1212A>G (p.Lys404=)
c.723A>G (p.Lys241=)
c.960A>G (p.Lys320=)
 gnomAD v4
13g.46835041T>GCA388150879HTR2Ac.1212A>C (p.Lys404Asn)
c.723A>C (p.Lys241Asn)
c.960A>C (p.Lys320Asn)
 COSMIC
13g.46835046dupCA6977522HTR2Ac.1212dup (p.Pro405ThrfsTer18)
c.723dup (p.Pro242ThrfsTer18)
c.960dup (p.Pro321ThrfsTer18)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
13g.46835042T>ACA388150881HTR2Ac.1211A>T (p.Lys404Ile)
c.722A>T (p.Lys241Ile)
c.959A>T (p.Lys320Ile)
13g.46835042T>CCA388150884HTR2Ac.1211A>G (p.Lys404Arg)
c.722A>G (p.Lys241Arg)
c.959A>G (p.Lys320Arg)
13g.46835042T>GCA388150885HTR2Ac.1211A>C (p.Lys404Thr)
c.722A>C (p.Lys241Thr)
c.959A>C (p.Lys320Thr)
 dbSNP
13g.46835042T=CA2089283415HTR2Ac.1211A= (p.Lys404=)
c.722A= (p.Lys241=)
c.959A= (p.Lys320=)
13g.46835043T>ACA388150887HTR2Ac.1210A>T (p.Lys404Ter)
c.721A>T (p.Lys241Ter)
c.958A>T (p.Lys320Ter)
13g.46835043T>CCA388150891HTR2Ac.1210A>G (p.Lys404Glu)
c.721A>G (p.Lys241Glu)
c.958A>G (p.Lys320Glu)
13g.46835043T>GCA388150889HTR2Ac.1210A>C (p.Lys404Gln)
c.721A>C (p.Lys241Gln)
c.958A>C (p.Lys320Gln)
13g.46835044T>ACA388150894HTR2Ac.1209A>T (p.Lys403Asn)
c.720A>T (p.Lys240Asn)
c.957A>T (p.Lys319Asn)
13g.46835044T>CCA483739304HTR2Ac.1209A>G (p.Lys403=)
c.720A>G (p.Lys240=)
c.957A>G (p.Lys319=)
13g.46835044T>GCA388150909HTR2Ac.1209A>C (p.Lys403Asn)
c.720A>C (p.Lys240Asn)
c.957A>C (p.Lys319Asn)
13g.46835045T>ACA388150911HTR2Ac.1208A>T (p.Lys403Ile)
c.719A>T (p.Lys240Ile)
c.956A>T (p.Lys319Ile)
13g.46835045T>CCA388150912HTR2Ac.1208A>G (p.Lys403Arg)
c.719A>G (p.Lys240Arg)
c.956A>G (p.Lys319Arg)
13g.46835045T>GCA388150913HTR2Ac.1208A>C (p.Lys403Thr)
c.719A>C (p.Lys240Thr)
c.956A>C (p.Lys319Thr)
13g.46835046T>ACA388150918HTR2Ac.1207A>T (p.Lys403Ter)
c.718A>T (p.Lys240Ter)
c.955A>T (p.Lys319Ter)
13g.46835046T>CCA388150920HTR2Ac.1207A>G (p.Lys403Glu)
c.718A>G (p.Lys240Glu)
c.955A>G (p.Lys319Glu)
 dbSNP gnomAD v4
13g.46835046T>GCA388150915HTR2Ac.1207A>C (p.Lys403Gln)
c.718A>C (p.Lys240Gln)
c.955A>C (p.Lys319Gln)
13g.46835047G>ACA483739311HTR2Ac.1206C>T (p.Asn402=)
c.717C>T (p.Asn239=)
c.954C>T (p.Asn318=)
13g.46835047G>CCA388150922HTR2Ac.1206C>G (p.Asn402Lys)
c.717C>G (p.Asn239Lys)
c.954C>G (p.Asn318Lys)
13g.46835047G=CA2089283416HTR2Ac.1206C= (p.Asn402=)
c.717C= (p.Asn239=)
c.954C= (p.Asn318=)
13g.46835047G>TCA388150924HTR2Ac.1206C>A (p.Asn402Lys)
c.717C>A (p.Asn239Lys)
c.954C>A (p.Asn318Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46835048T>ACA388150926HTR2Ac.1205A>T (p.Asn402Ile)
c.716A>T (p.Asn239Ile)
c.953A>T (p.Asn318Ile)
13g.46835048T>CCA388150929HTR2Ac.1205A>G (p.Asn402Ser)
c.716A>G (p.Asn239Ser)
c.953A>G (p.Asn318Ser)
 gnomAD v4
13g.46835048T>GCA388150932HTR2Ac.1205A>C (p.Asn402Thr)
c.716A>C (p.Asn239Thr)
c.953A>C (p.Asn318Thr)
13g.46835049T>ACA388150934HTR2Ac.1204A>T (p.Asn402Tyr)
c.715A>T (p.Asn239Tyr)
c.952A>T (p.Asn318Tyr)
13g.46835049T>CCA388150936HTR2Ac.1204A>G (p.Asn402Asp)
c.715A>G (p.Asn239Asp)
c.952A>G (p.Asn318Asp)
13g.46835049T>GCA388150938HTR2Ac.1204A>C (p.Asn402His)
c.715A>C (p.Asn239His)
c.952A>C (p.Asn318His)
13g.46835050T>ACA388150941HTR2Ac.1203A>T (p.Glu401Asp)
c.714A>T (p.Glu238Asp)
c.951A>T (p.Glu317Asp)
13g.46835050T>CCA483739317HTR2Ac.1203A>G (p.Glu401=)
c.714A>G (p.Glu238=)
c.951A>G (p.Glu317=)
13g.46835050T>GCA388150944HTR2Ac.1203A>C (p.Glu401Asp)
c.714A>C (p.Glu238Asp)
c.951A>C (p.Glu317Asp)
13g.46835051T>ACA388150946HTR2Ac.1202A>T (p.Glu401Val)
c.713A>T (p.Glu238Val)
c.950A>T (p.Glu317Val)
13g.46835051T>CCA388150948HTR2Ac.1202A>G (p.Glu401Gly)
c.713A>G (p.Glu238Gly)
c.950A>G (p.Glu317Gly)
 dbSNP gnomAD v3 gnomAD v4
13g.46835051T>GCA388150951HTR2Ac.1202A>C (p.Glu401Ala)
c.713A>C (p.Glu238Ala)
c.950A>C (p.Glu317Ala)
13g.46835051T=CA2089283417HTR2Ac.1202A= (p.Glu401=)
c.713A= (p.Glu238=)
c.950A= (p.Glu317=)
13g.46835052C>ACA388150953HTR2Ac.1201G>T (p.Glu401Ter)
c.712G>T (p.Glu238Ter)
c.949G>T (p.Glu317Ter)
13g.46835052C=CA2089283418HTR2Ac.1201G= (p.Glu401=)
c.712G= (p.Glu238=)
c.949G= (p.Glu317=)
13g.46835052C>GCA6977524HTR2Ac.1201G>C (p.Glu401Gln)
c.712G>C (p.Glu238Gln)
c.949G>C (p.Glu317Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
13g.46835052C>TCA388150956HTR2Ac.1201G>A (p.Glu401Lys)
c.712G>A (p.Glu238Lys)
c.949G>A (p.Glu317Lys)
 dbSNP gnomAD v2 COSMIC COSMIC
13g.46835053C>ACA388150959HTR2Ac.1200G>T (p.Lys400Asn)
c.711G>T (p.Lys237Asn)
c.948G>T (p.Lys316Asn)
13g.46835053C=CA2089283419HTR2Ac.1200G= (p.Lys400=)
c.711G= (p.Lys237=)
c.948G= (p.Lys316=)
13g.46835053C>GCA388150961HTR2Ac.1200G>C (p.Lys400Asn)
c.711G>C (p.Lys237Asn)
c.948G>C (p.Lys316Asn)
 dbSNP gnomAD v2 gnomAD v4
13g.46835053C>TCA483739324HTR2Ac.1200G>A (p.Lys400=)
c.711G>A (p.Lys237=)
c.948G>A (p.Lys316=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
13g.46835054T>ACA388150965HTR2Ac.1199A>T (p.Lys400Met)
c.710A>T (p.Lys237Met)
c.947A>T (p.Lys316Met)
13g.46835054T>CCA388150968HTR2Ac.1199A>G (p.Lys400Arg)
c.710A>G (p.Lys237Arg)
c.947A>G (p.Lys316Arg)
 gnomAD v4
13g.46835054T>GCA388150971HTR2Ac.1199A>C (p.Lys400Thr)
c.710A>C (p.Lys237Thr)
c.947A>C (p.Lys316Thr)
13g.46835055T>ACA388150973HTR2Ac.1198A>T (p.Lys400Ter)
c.709A>T (p.Lys237Ter)
c.946A>T (p.Lys316Ter)
13g.46835055T>CCA388150975HTR2Ac.1198A>G (p.Lys400Glu)
c.709A>G (p.Lys237Glu)
c.946A>G (p.Lys316Glu)
13g.46835055T>GCA6977525HTR2Ac.1198A>C (p.Lys400Gln)
c.709A>C (p.Lys237Gln)
c.946A>C (p.Lys316Gln)
 dbSNP ExAC gnomAD v4
13g.46835055T=CA2089283420HTR2Ac.1198A= (p.Lys400=)
c.709A= (p.Lys237=)
c.946A= (p.Lys316=)
13g.46835056G>ACA483739330HTR2Ac.1197C>T (p.Tyr399=)
c.708C>T (p.Tyr236=)
c.945C>T (p.Tyr315=)
13g.46835056G>CCA388150979HTR2Ac.1197C>G (p.Tyr399Ter)
c.708C>G (p.Tyr236Ter)
c.945C>G (p.Tyr315Ter)
13g.46835056G=CA2089283421HTR2Ac.1197C= (p.Tyr399=)
c.708C= (p.Tyr236=)
c.945C= (p.Tyr315=)
13g.46835056G>TCA388150983HTR2Ac.1197C>A (p.Tyr399Ter)
c.708C>A (p.Tyr236Ter)
c.945C>A (p.Tyr315Ter)
 dbSNP gnomAD v2
13g.46835057T>ACA388150986HTR2Ac.1196A>T (p.Tyr399Phe)
c.707A>T (p.Tyr236Phe)
c.944A>T (p.Tyr315Phe)
13g.46835057T>CCA388150988HTR2Ac.1196A>G (p.Tyr399Cys)
c.707A>G (p.Tyr236Cys)
c.944A>G (p.Tyr315Cys)
 gnomAD v4
13g.46835057T>GCA388150990HTR2Ac.1196A>C (p.Tyr399Ser)
c.707A>C (p.Tyr236Ser)
c.944A>C (p.Tyr315Ser)
13g.46835058A>CCA388150996HTR2Ac.1195T>G (p.Tyr399Asp)
c.706T>G (p.Tyr236Asp)
c.943T>G (p.Tyr315Asp)
13g.46835058A>GCA388150995HTR2Ac.1195T>C (p.Tyr399His)
c.706T>C (p.Tyr236His)
c.943T>C (p.Tyr315His)
13g.46835058A>TCA388150993HTR2Ac.1195T>A (p.Tyr399Asn)
c.706T>A (p.Tyr236Asn)
c.943T>A (p.Tyr315Asn)
13g.46835059C>ACA388150999HTR2Ac.1194G>T (p.Gln398His)
c.705G>T (p.Gln235His)
c.942G>T (p.Gln314His)
13g.46835059C>GCA388151001HTR2Ac.1194G>C (p.Gln398His)
c.705G>C (p.Gln235His)
c.942G>C (p.Gln314His)
13g.46835059C>TCA483739336HTR2Ac.1194G>A (p.Gln398=)
c.705G>A (p.Gln235=)
c.942G>A (p.Gln314=)
13g.46835060T>ACA388151004HTR2Ac.1193A>T (p.Gln398Leu)
c.704A>T (p.Gln235Leu)
c.941A>T (p.Gln314Leu)
13g.46835060T>CCA388151005HTR2Ac.1193A>G (p.Gln398Arg)
c.704A>G (p.Gln235Arg)
c.941A>G (p.Gln314Arg)
13g.46835060T>GCA388151008HTR2Ac.1193A>C (p.Gln398Pro)
c.704A>C (p.Gln235Pro)
c.941A>C (p.Gln314Pro)
13g.46835061G>ACA388151010HTR2Ac.1192C>T (p.Gln398Ter)
c.703C>T (p.Gln235Ter)
c.940C>T (p.Gln314Ter)
13g.46835061G>CCA388151013HTR2Ac.1192C>G (p.Gln398Glu)
c.703C>G (p.Gln235Glu)
c.940C>G (p.Gln314Glu)
 COSMIC
13g.46835061G>TCA388151014HTR2Ac.1192C>A (p.Gln398Lys)
c.703C>A (p.Gln235Lys)
c.940C>A (p.Gln314Lys)
13g.46835062A>CCA388151017HTR2Ac.1191T>G (p.Cys397Trp)
c.702T>G (p.Cys234Trp)
c.939T>G (p.Cys313Trp)
13g.46835062A>GCA483739343HTR2Ac.1191T>C (p.Cys397=)
c.702T>C (p.Cys234=)
c.939T>C (p.Cys313=)
13g.46835062A>TCA388151019HTR2Ac.1191T>A (p.Cys397Ter)
c.702T>A (p.Cys234Ter)
c.939T>A (p.Cys313Ter)
13g.46835063C>ACA388151021HTR2Ac.1190G>T (p.Cys397Phe)
c.701G>T (p.Cys234Phe)
c.938G>T (p.Cys313Phe)
13g.46835063C>GCA388151023HTR2Ac.1190G>C (p.Cys397Ser)
c.701G>C (p.Cys234Ser)
c.938G>C (p.Cys313Ser)
13g.46835063C>TCA388151026HTR2Ac.1190G>A (p.Cys397Tyr)
c.701G>A (p.Cys234Tyr)
c.938G>A (p.Cys313Tyr)
13g.46835064A>CCA388151033HTR2Ac.1189T>G (p.Cys397Gly)
c.700T>G (p.Cys234Gly)
c.937T>G (p.Cys313Gly)
13g.46835064A>GCA388151029HTR2Ac.1189T>C (p.Cys397Arg)
c.700T>C (p.Cys234Arg)
c.937T>C (p.Cys313Arg)
 gnomAD v4
13g.46835064A>TCA388151030HTR2Ac.1189T>A (p.Cys397Ser)
c.700T>A (p.Cys234Ser)
c.937T>A (p.Cys313Ser)
13g.46835065C>ACA388151035HTR2Ac.1188G>T (p.Gln396His)
c.699G>T (p.Gln233His)
c.936G>T (p.Gln312His)
13g.46835065C=CA2089283422HTR2Ac.1188G= (p.Gln396=)
c.699G= (p.Gln233=)
c.936G= (p.Gln312=)
13g.46835065C>GCA388151038HTR2Ac.1188G>C (p.Gln396His)
c.699G>C (p.Gln233His)
c.936G>C (p.Gln312His)
13g.46835065C>TCA483739348HTR2Ac.1188G>A (p.Gln396=)
c.699G>A (p.Gln233=)
c.936G>A (p.Gln312=)
 dbSNP
13g.46835066T>ACA388151039HTR2Ac.1187A>T (p.Gln396Leu)
c.698A>T (p.Gln233Leu)
c.935A>T (p.Gln312Leu)
13g.46835066T>CCA388151040HTR2Ac.1187A>G (p.Gln396Arg)
c.698A>G (p.Gln233Arg)
c.935A>G (p.Gln312Arg)
13g.46835066T>GCA388151043HTR2Ac.1187A>C (p.Gln396Pro)
c.698A>C (p.Gln233Pro)
c.935A>C (p.Gln312Pro)
13g.46835067G>ACA388151045HTR2Ac.1186C>T (p.Gln396Ter)
c.697C>T (p.Gln233Ter)
c.934C>T (p.Gln312Ter)
 COSMIC
13g.46835067G>CCA388151047HTR2Ac.1186C>G (p.Gln396Glu)
c.697C>G (p.Gln233Glu)
c.934C>G (p.Gln312Glu)
13g.46835067G>TCA388151049HTR2Ac.1186C>A (p.Gln396Lys)
c.697C>A (p.Gln233Lys)
c.934C>A (p.Gln312Lys)
13g.46835068A>CCA388151052HTR2Ac.1185T>G (p.Ile395Met)
c.696T>G (p.Ile232Met)
c.933T>G (p.Ile311Met)
13g.46835068A>GCA483739352HTR2Ac.1185T>C (p.Ile395=)
c.696T>C (p.Ile232=)
c.933T>C (p.Ile311=)
13g.46835068A>TCA483739350HTR2Ac.1185T>A (p.Ile395=)
c.696T>A (p.Ile232=)
c.933T>A (p.Ile311=)
13g.46835069A>CCA388151056HTR2Ac.1184T>G (p.Ile395Ser)
c.695T>G (p.Ile232Ser)
c.932T>G (p.Ile311Ser)
13g.46835069A>GCA388151058HTR2Ac.1184T>C (p.Ile395Thr)
c.695T>C (p.Ile232Thr)
c.932T>C (p.Ile311Thr)
13g.46835069A>TCA388151061HTR2Ac.1184T>A (p.Ile395Asn)
c.695T>A (p.Ile232Asn)
c.932T>A (p.Ile311Asn)
13g.46835070T>ACA388151064HTR2Ac.1183A>T (p.Ile395Phe)
c.694A>T (p.Ile232Phe)
c.931A>T (p.Ile311Phe)
13g.46835070T>CCA388151068HTR2Ac.1183A>G (p.Ile395Val)
c.694A>G (p.Ile232Val)
c.931A>G (p.Ile311Val)
13g.46835070T>GCA388151066HTR2Ac.1183A>C (p.Ile395Leu)
c.694A>C (p.Ile232Leu)
c.931A>C (p.Ile311Leu)
13g.46835071A>CCA388151070HTR2Ac.1182T>G (p.Tyr394Ter)
c.693T>G (p.Tyr231Ter)
c.930T>G (p.Tyr310Ter)
13g.46835071A>GCA483739355HTR2Ac.1182T>C (p.Tyr394=)
c.693T>C (p.Tyr231=)
c.930T>C (p.Tyr310=)
13g.46835071A>TCA388151072HTR2Ac.1182T>A (p.Tyr394Ter)
c.693T>A (p.Tyr231Ter)
c.930T>A (p.Tyr310Ter)
 gnomAD v4
13g.46835072T>ACA388151074HTR2Ac.1181A>T (p.Tyr394Phe)
c.692A>T (p.Tyr231Phe)
c.929A>T (p.Tyr310Phe)
13g.46835072T>CCA388151087HTR2Ac.1181A>G (p.Tyr394Cys)
c.692A>G (p.Tyr231Cys)
c.929A>G (p.Tyr310Cys)
13g.46835072T>GCA388151090HTR2Ac.1181A>C (p.Tyr394Ser)
c.692A>C (p.Tyr231Ser)
c.929A>C (p.Tyr310Ser)
13g.46835073A>CCA388151094HTR2Ac.1180T>G (p.Tyr394Asp)
c.691T>G (p.Tyr231Asp)
c.928T>G (p.Tyr310Asp)
13g.46835073A>GCA388151096HTR2Ac.1180T>C (p.Tyr394His)
c.691T>C (p.Tyr231His)
c.928T>C (p.Tyr310His)
 COSMIC
13g.46835073A>TCA388151098HTR2Ac.1180T>A (p.Tyr394Asn)
c.691T>A (p.Tyr231Asn)
c.928T>A (p.Tyr310Asn)
13g.46835074C>ACA483739360HTR2Ac.1179G>T (p.Arg393=)
c.690G>T (p.Arg230=)
c.927G>T (p.Arg309=)
 gnomAD v4
13g.46835074C>GCA483739365HTR2Ac.1179G>C (p.Arg393=)
c.690G>C (p.Arg230=)
c.927G>C (p.Arg309=)
13g.46835074C>TCA483739363HTR2Ac.1179G>A (p.Arg393=)
c.690G>A (p.Arg230=)
c.927G>A (p.Arg309=)
13g.46835075C>ACA388151100HTR2Ac.1178G>T (p.Arg393Leu)
c.689G>T (p.Arg230Leu)
c.926G>T (p.Arg309Leu)
 COSMIC
13g.46835075C=CA2089283423HTR2Ac.1178G= (p.Arg393=)
c.689G= (p.Arg230=)
c.926G= (p.Arg309=)
13g.46835075C>GCA388151102HTR2Ac.1178G>C (p.Arg393Pro)
c.689G>C (p.Arg230Pro)
c.926G>C (p.Arg309Pro)
13g.46835075C>TCA6977526HTR2Ac.1178G>A (p.Arg393Gln)
c.689G>A (p.Arg230Gln)
c.926G>A (p.Arg309Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched