UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.46834823C>A | CA2622958743 | HTR2A | c.*14G>T (n.*14G>T) | gnomAD v4 |
| 13 | g.46834823C= | CA2089283333 | HTR2A | c.*14G= (n.*14G=) | |
| 13 | g.46834823C>T | CA6977484 | HTR2A | c.*14G>A (n.*14G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 13 | g.46834824G>A | CA6977485 | HTR2A | c.*13C>T (n.*13C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834824G= | CA2089283334 | HTR2A | c.*13C= (n.*13C=) | |
| 13 | g.46834825G>A | CA609929160 | HTR2A | c.*12C>T (n.*12C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834825G= | CA2089283335 | HTR2A | c.*12C= (n.*12C=) | |
| 13 | g.46834825G>T | CA2622958744 | HTR2A | c.*12C>A (n.*12C>A) | gnomAD v4 |
| 13 | g.46834828A>G | CA2622958745 | HTR2A | c.*9T>C (n.*9T>C) | gnomAD v4 |
| 13 | g.46834828A>T | CA2622958746 | HTR2A | c.*9T>A (n.*9T>A) | gnomAD v4 |
| 13 | g.46834830T>C | CA2622958747 | HTR2A | c.*7A>G (n.*7A>G) | gnomAD v4 |
| 13 | g.46834832G>A | CA698553793 | HTR2A | c.*5C>T (n.*5C>T) | dbSNP |
| 13 | g.46834832G= | CA2089283336 | HTR2A | c.*5C= (n.*5C=) | |
| 13 | g.46834834C>T | CA2575412297 | HTR2A | c.*3G>A (n.*3G>A) | |
| 13 | g.46834835T>C | CA2622958748 | HTR2A | c.*2A>G (n.*2A>G) | gnomAD v4 |
| 13 | g.46834836A>G | CA2622958749 | HTR2A | c.*1T>C (n.*1T>C) | gnomAD v4 |
| 13 | g.46834837T>A | CA388150089 | HTR2A | c.1416A>T (p.Ter472Cys) c.927A>T (p.Ter309Cys) c.1164A>T (p.Ter388Cys) | |
| 13 | g.46834837T>C | CA388150088 | HTR2A | c.1416A>G (p.Ter472Trp) c.927A>G (p.Ter309Trp) c.1164A>G (p.Ter388Trp) | |
| 13 | g.46834837T>G | CA388150087 | HTR2A | c.1416A>C (p.Ter472Cys) c.927A>C (p.Ter309Cys) c.1164A>C (p.Ter388Cys) | |
| 13 | g.46834838C>A | CA388150091 | HTR2A | c.1415G>T (p.Ter472Leu) c.926G>T (p.Ter309Leu) c.1163G>T (p.Ter388Leu) | |
| 13 | g.46834838C>G | CA388150090 | HTR2A | c.1415G>C (p.Ter472Ser) c.926G>C (p.Ter309Ser) c.1163G>C (p.Ter388Ser) | |
| 13 | g.46834838C>T | CA483739030 | HTR2A | c.1415G>A (p.Ter472=) c.926G>A (p.Ter309=) c.1163G>A (p.Ter388=) | |
| 13 | g.46834839A>C | CA388150094 | HTR2A | c.1414T>G (p.Ter472Gly) c.925T>G (p.Ter309Gly) c.1162T>G (p.Ter388Gly) | |
| 13 | g.46834839A>G | CA388150092 | HTR2A | c.1414T>C (p.Ter472Arg) c.925T>C (p.Ter309Arg) c.1162T>C (p.Ter388Arg) | |
| 13 | g.46834839A>T | CA388150093 | HTR2A | c.1414T>A (p.Ter472Arg) c.925T>A (p.Ter309Arg) c.1162T>A (p.Ter388Arg) | |
| 13 | g.46834840C>A | CA483739031 | HTR2A | c.1413G>T (p.Val471=) c.924G>T (p.Val308=) c.1161G>T (p.Val387=) | gnomAD v4 |
| 13 | g.46834840C>G | CA483739032 | HTR2A | c.1413G>C (p.Val471=) c.924G>C (p.Val308=) c.1161G>C (p.Val387=) | |
| 13 | g.46834840C>T | CA483739034 | HTR2A | c.1413G>A (p.Val471=) c.924G>A (p.Val308=) c.1161G>A (p.Val387=) | gnomAD v4 |
| 13 | g.46834841A>C | CA388150095 | HTR2A | c.1412T>G (p.Val471Gly) c.923T>G (p.Val308Gly) c.1160T>G (p.Val387Gly) | |
| 13 | g.46834841A>G | CA388150096 | HTR2A | c.1412T>C (p.Val471Ala) c.923T>C (p.Val308Ala) c.1160T>C (p.Val387Ala) | |
| 13 | g.46834841A>T | CA388150097 | HTR2A | c.1412T>A (p.Val471Glu) c.923T>A (p.Val308Glu) c.1160T>A (p.Val387Glu) | |
| 13 | g.46834842C>A | CA388150098 | HTR2A | c.1411G>T (p.Val471Leu) c.922G>T (p.Val308Leu) c.1159G>T (p.Val387Leu) | |
| 13 | g.46834842C>G | CA388150099 | HTR2A | c.1411G>C (p.Val471Leu) c.922G>C (p.Val308Leu) c.1159G>C (p.Val387Leu) | |
| 13 | g.46834842C>T | CA388150100 | HTR2A | c.1411G>A (p.Val471Met) c.922G>A (p.Val308Met) c.1159G>A (p.Val387Met) | |
| 13 | g.46834843A= | CA2089283337 | HTR2A | c.1410T= (p.Cys470=) c.921T= (p.Cys307=) c.1158T= (p.Cys386=) | |
| 13 | g.46834843A>C | CA388150101 | HTR2A | c.1410T>G (p.Cys470Trp) c.921T>G (p.Cys307Trp) c.1158T>G (p.Cys386Trp) | dbSNP |
| 13 | g.46834843A>G | CA6977486 | HTR2A | c.1410T>C (p.Cys470=) c.921T>C (p.Cys307=) c.1158T>C (p.Cys386=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834843A>T | CA388150102 | HTR2A | c.1410T>A (p.Cys470Ter) c.921T>A (p.Cys307Ter) c.1158T>A (p.Cys386Ter) | |
| 13 | g.46834844C>A | CA388150105 | HTR2A | c.1409G>T (p.Cys470Phe) c.920G>T (p.Cys307Phe) c.1157G>T (p.Cys386Phe) | |
| 13 | g.46834844C= | CA2089283338 | HTR2A | c.1409G= (p.Cys470=) c.920G= (p.Cys307=) c.1157G= (p.Cys386=) | |
| 13 | g.46834844C>G | CA388150104 | HTR2A | c.1409G>C (p.Cys470Ser) c.920G>C (p.Cys307Ser) c.1157G>C (p.Cys386Ser) | |
| 13 | g.46834844C>T | CA388150103 | HTR2A | c.1409G>A (p.Cys470Tyr) c.920G>A (p.Cys307Tyr) c.1157G>A (p.Cys386Tyr) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.46834845A>C | CA388150106 | HTR2A | c.1408T>G (p.Cys470Gly) c.919T>G (p.Cys307Gly) c.1156T>G (p.Cys386Gly) | |
| 13 | g.46834845A>G | CA388150107 | HTR2A | c.1408T>C (p.Cys470Arg) c.919T>C (p.Cys307Arg) c.1156T>C (p.Cys386Arg) | |
| 13 | g.46834845A>T | CA388150108 | HTR2A | c.1408T>A (p.Cys470Ser) c.919T>A (p.Cys307Ser) c.1156T>A (p.Cys386Ser) | |
| 13 | g.46834846G>A | CA483739038 | HTR2A | c.1407C>T (p.Ser469=) c.918C>T (p.Ser306=) c.1155C>T (p.Ser385=) | COSMIC |
| 13 | g.46834846G>C | CA388150109 | HTR2A | c.1407C>G (p.Ser469Arg) c.918C>G (p.Ser306Arg) c.1155C>G (p.Ser385Arg) | |
| 13 | g.46834846G>T | CA388150110 | HTR2A | c.1407C>A (p.Ser469Arg) c.918C>A (p.Ser306Arg) c.1155C>A (p.Ser385Arg) | COSMIC |
| 13 | g.46834847C>A | CA388150111 | HTR2A | c.1406G>T (p.Ser469Ile) c.917G>T (p.Ser306Ile) c.1154G>T (p.Ser385Ile) | |
| 13 | g.46834847C>G | CA388150112 | HTR2A | c.1406G>C (p.Ser469Thr) c.917G>C (p.Ser306Thr) c.1154G>C (p.Ser385Thr) | |
| 13 | g.46834847C>T | CA388150113 | HTR2A | c.1406G>A (p.Ser469Asn) c.917G>A (p.Ser306Asn) c.1154G>A (p.Ser385Asn) | |
| 13 | g.46834848T>A | CA388150114 | HTR2A | c.1405A>T (p.Ser469Cys) c.916A>T (p.Ser306Cys) c.1153A>T (p.Ser385Cys) | |
| 13 | g.46834848T>C | CA388150115 | HTR2A | c.1405A>G (p.Ser469Gly) c.916A>G (p.Ser306Gly) c.1153A>G (p.Ser385Gly) | gnomAD v4 |
| 13 | g.46834848T>G | CA388150116 | HTR2A | c.1405A>C (p.Ser469Arg) c.916A>C (p.Ser306Arg) c.1153A>C (p.Ser385Arg) | |
| 13 | g.46834849C>A | CA483739042 | HTR2A | c.1404G>T (p.Val468=) c.915G>T (p.Val305=) c.1152G>T (p.Val384=) | |
| 13 | g.46834849C= | CA2089283339 | HTR2A | c.1404G= (p.Val468=) c.915G= (p.Val305=) c.1152G= (p.Val384=) | |
| 13 | g.46834849C>G | CA483739043 | HTR2A | c.1404G>C (p.Val468=) c.915G>C (p.Val305=) c.1152G>C (p.Val384=) | |
| 13 | g.46834849C>T | CA6977487 | HTR2A | c.1404G>A (p.Val468=) c.915G>A (p.Val305=) c.1152G>A (p.Val384=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.46834850A= | CA2089283341 | HTR2A | c.1403T= (p.Val468=) c.914T= (p.Val305=) c.1151T= (p.Val384=) | |
| 13 | g.46834850A>C | CA388150118 | HTR2A | c.1403T>G (p.Val468Gly) c.914T>G (p.Val305Gly) c.1151T>G (p.Val384Gly) | dbSNP |
| 13 | g.46834850A>G | CA388150119 | HTR2A | c.1403T>C (p.Val468Ala) c.914T>C (p.Val305Ala) c.1151T>C (p.Val384Ala) | |
| 13 | g.46834850A>T | CA388150117 | HTR2A | c.1403T>A (p.Val468Glu) c.914T>A (p.Val305Glu) c.1151T>A (p.Val384Glu) | |
| 13 | g.46834850dup | CA2089283340 | HTR2A | c.1403dup (p.Ser469GlufsTer7) c.914dup (p.Ser306GlufsTer7) c.1151dup (p.Ser385GlufsTer7) | dbSNP |
| 13 | g.46834851C>A | CA249253273 | HTR2A | c.1402G>T (p.Val468Leu) c.913G>T (p.Val305Leu) c.1150G>T (p.Val384Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834851C= | CA2089283342 | HTR2A | c.1402G= (p.Val468=) c.913G= (p.Val305=) c.1150G= (p.Val384=) | |
| 13 | g.46834851C>G | CA388150120 | HTR2A | c.1402G>C (p.Val468Leu) c.913G>C (p.Val305Leu) c.1150G>C (p.Val384Leu) | dbSNP |
| 13 | g.46834851C>T | CA388150121 | HTR2A | c.1402G>A (p.Val468Met) c.913G>A (p.Val305Met) c.1150G>A (p.Val384Met) | |
| 13 | g.46834852C>A | CA6977488 | HTR2A | c.1401G>T (p.Lys467Asn) c.912G>T (p.Lys304Asn) c.1149G>T (p.Lys383Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.46834852C= | CA2089283343 | HTR2A | c.1401G= (p.Lys467=) c.912G= (p.Lys304=) c.1149G= (p.Lys383=) | |
| 13 | g.46834852C>G | CA388150122 | HTR2A | c.1401G>C (p.Lys467Asn) c.912G>C (p.Lys304Asn) c.1149G>C (p.Lys383Asn) | |
| 13 | g.46834852C>T | CA483739047 | HTR2A | c.1401G>A (p.Lys467=) c.912G>A (p.Lys304=) c.1149G>A (p.Lys383=) | |
| 13 | g.46834853T>A | CA388150123 | HTR2A | c.1400A>T (p.Lys467Met) c.911A>T (p.Lys304Met) c.1148A>T (p.Lys383Met) | |
| 13 | g.46834853T>C | CA388150124 | HTR2A | c.1400A>G (p.Lys467Arg) c.911A>G (p.Lys304Arg) c.1148A>G (p.Lys383Arg) | gnomAD v4 |
| 13 | g.46834853T>G | CA388150125 | HTR2A | c.1400A>C (p.Lys467Thr) c.911A>C (p.Lys304Thr) c.1148A>C (p.Lys383Thr) | |
| 13 | g.46834854T>A | CA388150126 | HTR2A | c.1399A>T (p.Lys467Ter) c.910A>T (p.Lys304Ter) c.1147A>T (p.Lys383Ter) | |
| 13 | g.46834854T>C | CA388150127 | HTR2A | c.1399A>G (p.Lys467Glu) c.910A>G (p.Lys304Glu) c.1147A>G (p.Lys383Glu) | |
| 13 | g.46834854T>G | CA388150128 | HTR2A | c.1399A>C (p.Lys467Gln) c.910A>C (p.Lys304Gln) c.1147A>C (p.Lys383Gln) | |
| 13 | g.46834855T>A | CA388150129 | HTR2A | c.1398A>T (p.Glu466Asp) c.909A>T (p.Glu303Asp) c.1146A>T (p.Glu382Asp) | |
| 13 | g.46834855T>C | CA483739051 | HTR2A | c.1398A>G (p.Glu466=) c.909A>G (p.Glu303=) c.1146A>G (p.Glu382=) | |
| 13 | g.46834855T>G | CA388150130 | HTR2A | c.1398A>C (p.Glu466Asp) c.909A>C (p.Glu303Asp) c.1146A>C (p.Glu382Asp) | |
| 13 | g.46834856T>A | CA388150133 | HTR2A | c.1397A>T (p.Glu466Val) c.908A>T (p.Glu303Val) c.1145A>T (p.Glu382Val) | |
| 13 | g.46834856T>C | CA388150132 | HTR2A | c.1397A>G (p.Glu466Gly) c.908A>G (p.Glu303Gly) c.1145A>G (p.Glu382Gly) | COSMIC COSMIC |
| 13 | g.46834856T>G | CA388150131 | HTR2A | c.1397A>C (p.Glu466Ala) c.908A>C (p.Glu303Ala) c.1145A>C (p.Glu382Ala) | |
| 13 | g.46834857C>A | CA388150134 | HTR2A | c.1396G>T (p.Glu466Ter) c.907G>T (p.Glu303Ter) c.1144G>T (p.Glu382Ter) | |
| 13 | g.46834857C>G | CA388150135 | HTR2A | c.1396G>C (p.Glu466Gln) c.907G>C (p.Glu303Gln) c.1144G>C (p.Glu382Gln) | |
| 13 | g.46834857C>T | CA388150136 | HTR2A | c.1396G>A (p.Glu466Lys) c.907G>A (p.Glu303Lys) c.1144G>A (p.Glu382Lys) | COSMIC COSMIC |
| 13 | g.46834858A>C | CA388150137 | HTR2A | c.1395T>G (p.Asn465Lys) c.906T>G (p.Asn302Lys) c.1143T>G (p.Asn381Lys) | |
| 13 | g.46834858A>G | CA483739052 | HTR2A | c.1395T>C (p.Asn465=) c.906T>C (p.Asn302=) c.1143T>C (p.Asn381=) | |
| 13 | g.46834858A>T | CA388150138 | HTR2A | c.1395T>A (p.Asn465Lys) c.906T>A (p.Asn302Lys) c.1143T>A (p.Asn381Lys) | |
| 13 | g.46834859T>A | CA388150139 | HTR2A | c.1394A>T (p.Asn465Ile) c.905A>T (p.Asn302Ile) c.1142A>T (p.Asn381Ile) | |
| 13 | g.46834859T>C | CA388150140 | HTR2A | c.1394A>G (p.Asn465Ser) c.905A>G (p.Asn302Ser) c.1142A>G (p.Asn381Ser) | |
| 13 | g.46834859T>G | CA388150141 | HTR2A | c.1394A>C (p.Asn465Thr) c.905A>C (p.Asn302Thr) c.1142A>C (p.Asn381Thr) | |
| 13 | g.46834860T>A | CA388150142 | HTR2A | c.1393A>T (p.Asn465Tyr) c.904A>T (p.Asn302Tyr) c.1141A>T (p.Asn381Tyr) | |
| 13 | g.46834860T>C | CA6977489 | HTR2A | c.1393A>G (p.Asn465Asp) c.904A>G (p.Asn302Asp) c.1141A>G (p.Asn381Asp) | dbSNP ExAC gnomAD v4 |
| 13 | g.46834860T>G | CA388150143 | HTR2A | c.1393A>C (p.Asn465His) c.904A>C (p.Asn302His) c.1141A>C (p.Asn381His) | |
| 13 | g.46834860T= | CA2089283344 | HTR2A | c.1393A= (p.Asn465=) c.904A= (p.Asn302=) c.1141A= (p.Asn381=) | |
| 13 | g.46834861C>A | CA483739053 | HTR2A | c.1392G>T (p.Val464=) c.903G>T (p.Val301=) c.1140G>T (p.Val380=) | |
| 13 | g.46834861C>G | CA483739055 | HTR2A | c.1392G>C (p.Val464=) c.903G>C (p.Val301=) c.1140G>C (p.Val380=) | |
| 13 | g.46834861C>T | CA483739057 | HTR2A | c.1392G>A (p.Val464=) c.903G>A (p.Val301=) c.1140G>A (p.Val380=) | |
| 13 | g.46834862A= | CA2089283345 | HTR2A | c.1391T= (p.Val464=) c.902T= (p.Val301=) c.1139T= (p.Val380=) | |
| 13 | g.46834862A>C | CA388150144 | HTR2A | c.1391T>G (p.Val464Gly) c.902T>G (p.Val301Gly) c.1139T>G (p.Val380Gly) | dbSNP |
| 13 | g.46834862A>G | CA388150145 | HTR2A | c.1391T>C (p.Val464Ala) c.902T>C (p.Val301Ala) c.1139T>C (p.Val380Ala) | |
| 13 | g.46834862A>T | CA388150146 | HTR2A | c.1391T>A (p.Val464Glu) c.902T>A (p.Val301Glu) c.1139T>A (p.Val380Glu) | |
| 13 | g.46834863C>A | CA388150148 | HTR2A | c.1390G>T (p.Val464Leu) c.901G>T (p.Val301Leu) c.1138G>T (p.Val380Leu) | |
| 13 | g.46834863C>G | CA388150149 | HTR2A | c.1390G>C (p.Val464Leu) c.901G>C (p.Val301Leu) c.1138G>C (p.Val380Leu) | |
| 13 | g.46834863C>T | CA388150147 | HTR2A | c.1390G>A (p.Val464Met) c.901G>A (p.Val301Met) c.1138G>A (p.Val380Met) | |
| 13 | g.46834864T>A | CA483739059 | HTR2A | c.1389A>T (p.Gly463=) c.900A>T (p.Gly300=) c.1137A>T (p.Gly379=) | |
| 13 | g.46834864T>C | CA483739060 | HTR2A | c.1389A>G (p.Gly463=) c.900A>G (p.Gly300=) c.1137A>G (p.Gly379=) | |
| 13 | g.46834864T>G | CA483739061 | HTR2A | c.1389A>C (p.Gly463=) c.900A>C (p.Gly300=) c.1137A>C (p.Gly379=) | |
| 13 | g.46834865C>A | CA388150150 | HTR2A | c.1388G>T (p.Gly463Val) c.899G>T (p.Gly300Val) c.1136G>T (p.Gly379Val) | |
| 13 | g.46834865C>G | CA388150152 | HTR2A | c.1388G>C (p.Gly463Ala) c.899G>C (p.Gly300Ala) c.1136G>C (p.Gly379Ala) | |
| 13 | g.46834865C>T | CA388150151 | HTR2A | c.1388G>A (p.Gly463Glu) c.899G>A (p.Gly300Glu) c.1136G>A (p.Gly379Glu) | |
| 13 | g.46834866C>A | CA388150153 | HTR2A | c.1387G>T (p.Gly463Ter) c.898G>T (p.Gly300Ter) c.1135G>T (p.Gly379Ter) | COSMIC |
| 13 | g.46834866C= | CA2089283346 | HTR2A | c.1387G= (p.Gly463=) c.898G= (p.Gly300=) c.1135G= (p.Gly379=) | |
| 13 | g.46834866C>G | CA388150154 | HTR2A | c.1387G>C (p.Gly463Arg) c.898G>C (p.Gly300Arg) c.1135G>C (p.Gly379Arg) | |
| 13 | g.46834866C>T | CA6977490 | HTR2A | c.1387G>A (p.Gly463Arg) c.898G>A (p.Gly300Arg) c.1135G>A (p.Gly379Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.46834867G>A | CA6977491 | HTR2A | c.1386C>T (p.Asp462=) c.897C>T (p.Asp299=) c.1134C>T (p.Asp378=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.46834867G>C | CA388150155 | HTR2A | c.1386C>G (p.Asp462Glu) c.897C>G (p.Asp299Glu) c.1134C>G (p.Asp378Glu) | dbSNP gnomAD v4 |
| 13 | g.46834867G= | CA2089283347 | HTR2A | c.1386C= (p.Asp462=) c.897C= (p.Asp299=) c.1134C= (p.Asp378=) | |
| 13 | g.46834867G>T | CA249253322 | HTR2A | c.1386C>A (p.Asp462Glu) c.897C>A (p.Asp299Glu) c.1134C>A (p.Asp378Glu) | dbSNP |
| 13 | g.46834868T>A | CA388150156 | HTR2A | c.1385A>T (p.Asp462Val) c.896A>T (p.Asp299Val) c.1133A>T (p.Asp378Val) | gnomAD v4 |
| 13 | g.46834868T>C | CA388150157 | HTR2A | c.1385A>G (p.Asp462Gly) c.896A>G (p.Asp299Gly) c.1133A>G (p.Asp378Gly) | |
| 13 | g.46834868T>G | CA388150158 | HTR2A | c.1385A>C (p.Asp462Ala) c.896A>C (p.Asp299Ala) c.1133A>C (p.Asp378Ala) | COSMIC |
| 13 | g.46834869C>A | CA388150159 | HTR2A | c.1384G>T (p.Asp462Tyr) c.895G>T (p.Asp299Tyr) c.1132G>T (p.Asp378Tyr) | dbSNP |
| 13 | g.46834869C= | CA2089283348 | HTR2A | c.1384G= (p.Asp462=) c.895G= (p.Asp299=) c.1132G= (p.Asp378=) | |
| 13 | g.46834869C>G | CA388150160 | HTR2A | c.1384G>C (p.Asp462His) c.895G>C (p.Asp299His) c.1132G>C (p.Asp378His) | gnomAD v4 |
| 13 | g.46834869C>T | CA6977492 | HTR2A | c.1384G>A (p.Asp462Asn) c.895G>A (p.Asp299Asn) c.1132G>A (p.Asp378Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 13 | g.46834870G>A | CA6977493 | HTR2A | c.1383C>T (p.Ser461=) c.894C>T (p.Ser298=) c.1131C>T (p.Ser377=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834870G>C | CA388150161 | HTR2A | c.1383C>G (p.Ser461Arg) c.894C>G (p.Ser298Arg) c.1131C>G (p.Ser377Arg) | |
| 13 | g.46834870G= | CA2089283349 | HTR2A | c.1383C= (p.Ser461=) c.894C= (p.Ser298=) c.1131C= (p.Ser377=) | |
| 13 | g.46834870G>T | CA388150162 | HTR2A | c.1383C>A (p.Ser461Arg) c.894C>A (p.Ser298Arg) c.1131C>A (p.Ser377Arg) | |
| 13 | g.46834871C>A | CA388150165 | HTR2A | c.1382G>T (p.Ser461Ile) c.893G>T (p.Ser298Ile) c.1130G>T (p.Ser377Ile) | |
| 13 | g.46834871C>G | CA388150163 | HTR2A | c.1382G>C (p.Ser461Thr) c.893G>C (p.Ser298Thr) c.1130G>C (p.Ser377Thr) | |
| 13 | g.46834871C>T | CA388150164 | HTR2A | c.1382G>A (p.Ser461Asn) c.893G>A (p.Ser298Asn) c.1130G>A (p.Ser377Asn) | |
| 13 | g.46834872T>A | CA388150166 | HTR2A | c.1381A>T (p.Ser461Cys) c.892A>T (p.Ser298Cys) c.1129A>T (p.Ser377Cys) | |
| 13 | g.46834872T>C | CA388150167 | HTR2A | c.1381A>G (p.Ser461Gly) c.892A>G (p.Ser298Gly) c.1129A>G (p.Ser377Gly) | gnomAD v4 |
| 13 | g.46834872T>G | CA388150168 | HTR2A | c.1381A>C (p.Ser461Arg) c.892A>C (p.Ser298Arg) c.1129A>C (p.Ser377Arg) | |
| 13 | g.46834873A= | CA2089283350 | HTR2A | c.1380T= (p.Asn460=) c.891T= (p.Asn297=) c.1128T= (p.Asn376=) | |
| 13 | g.46834873A>C | CA388150169 | HTR2A | c.1380T>G (p.Asn460Lys) c.891T>G (p.Asn297Lys) c.1128T>G (p.Asn376Lys) | |
| 13 | g.46834873A>G | CA483739068 | HTR2A | c.1380T>C (p.Asn460=) c.891T>C (p.Asn297=) c.1128T>C (p.Asn376=) | dbSNP |
| 13 | g.46834873A>T | CA388150170 | HTR2A | c.1380T>A (p.Asn460Lys) c.891T>A (p.Asn297Lys) c.1128T>A (p.Asn376Lys) | |
| 13 | g.46834874T>A | CA388150172 | HTR2A | c.1379A>T (p.Asn460Ile) c.890A>T (p.Asn297Ile) c.1127A>T (p.Asn376Ile) | |
| 13 | g.46834874T>C | CA6977494 | HTR2A | c.1379A>G (p.Asn460Ser) c.890A>G (p.Asn297Ser) c.1127A>G (p.Asn376Ser) | dbSNP ExAC |
| 13 | g.46834874T>G | CA388150174 | HTR2A | c.1379A>C (p.Asn460Thr) c.890A>C (p.Asn297Thr) c.1127A>C (p.Asn376Thr) | |
| 13 | g.46834874T= | CA2089283351 | HTR2A | c.1379A= (p.Asn460=) c.890A= (p.Asn297=) c.1127A= (p.Asn376=) | |
| 13 | g.46834875T>A | CA388150176 | HTR2A | c.1378A>T (p.Asn460Tyr) c.889A>T (p.Asn297Tyr) c.1126A>T (p.Asn376Tyr) | |
| 13 | g.46834875T>C | CA388150177 | HTR2A | c.1378A>G (p.Asn460Asp) c.889A>G (p.Asn297Asp) c.1126A>G (p.Asn376Asp) | |
| 13 | g.46834875T>G | CA388150178 | HTR2A | c.1378A>C (p.Asn460His) c.889A>C (p.Asn297His) c.1126A>C (p.Asn376His) | |
| 13 | g.46834876G>A | CA483739069 | HTR2A | c.1377C>T (p.Asp459=) c.888C>T (p.Asp296=) c.1125C>T (p.Asp375=) | gnomAD v4 |
| 13 | g.46834876G>C | CA388150180 | HTR2A | c.1377C>G (p.Asp459Glu) c.888C>G (p.Asp296Glu) c.1125C>G (p.Asp375Glu) | |
| 13 | g.46834876G>T | CA388150182 | HTR2A | c.1377C>A (p.Asp459Glu) c.888C>A (p.Asp296Glu) c.1125C>A (p.Asp375Glu) | gnomAD v4 |
| 13 | g.46834877T>A | CA388150184 | HTR2A | c.1376A>T (p.Asp459Val) c.887A>T (p.Asp296Val) c.1124A>T (p.Asp375Val) | |
| 13 | g.46834877T>C | CA388150186 | HTR2A | c.1376A>G (p.Asp459Gly) c.887A>G (p.Asp296Gly) c.1124A>G (p.Asp375Gly) | |
| 13 | g.46834877T>G | CA388150187 | HTR2A | c.1376A>C (p.Asp459Ala) c.887A>C (p.Asp296Ala) c.1124A>C (p.Asp375Ala) | |
| 13 | g.46834878C>A | CA388150190 | HTR2A | c.1375G>T (p.Asp459Tyr) c.886G>T (p.Asp296Tyr) c.1123G>T (p.Asp375Tyr) | |
| 13 | g.46834878C>G | CA388150191 | HTR2A | c.1375G>C (p.Asp459His) c.886G>C (p.Asp296His) c.1123G>C (p.Asp375His) | |
| 13 | g.46834878C>T | CA388150193 | HTR2A | c.1375G>A (p.Asp459Asn) c.886G>A (p.Asp296Asn) c.1123G>A (p.Asp375Asn) | |
| 13 | g.46834879T>A | CA388150195 | HTR2A | c.1374A>T (p.Lys458Asn) c.885A>T (p.Lys295Asn) c.1122A>T (p.Lys374Asn) | |
| 13 | g.46834879T>C | CA483739073 | HTR2A | c.1374A>G (p.Lys458=) c.885A>G (p.Lys295=) c.1122A>G (p.Lys374=) | dbSNP |
| 13 | g.46834879T>G | CA388150196 | HTR2A | c.1374A>C (p.Lys458Asn) c.885A>C (p.Lys295Asn) c.1122A>C (p.Lys374Asn) | |
| 13 | g.46834879T= | CA2089283352 | HTR2A | c.1374A= (p.Lys458=) c.885A= (p.Lys295=) c.1122A= (p.Lys374=) | |
| 13 | g.46834880T>A | CA388150199 | HTR2A | c.1373A>T (p.Lys458Ile) c.884A>T (p.Lys295Ile) c.1121A>T (p.Lys374Ile) | |
| 13 | g.46834880T>C | CA388150200 | HTR2A | c.1373A>G (p.Lys458Arg) c.884A>G (p.Lys295Arg) c.1121A>G (p.Lys374Arg) | |
| 13 | g.46834880T>G | CA388150202 | HTR2A | c.1373A>C (p.Lys458Thr) c.884A>C (p.Lys295Thr) c.1121A>C (p.Lys374Thr) | |
| 13 | g.46834881T>A | CA388150208 | HTR2A | c.1372A>T (p.Lys458Ter) c.883A>T (p.Lys295Ter) c.1120A>T (p.Lys374Ter) | |
| 13 | g.46834881T>C | CA388150206 | HTR2A | c.1372A>G (p.Lys458Glu) c.883A>G (p.Lys295Glu) c.1120A>G (p.Lys374Glu) | |
| 13 | g.46834881T>G | CA388150204 | HTR2A | c.1372A>C (p.Lys458Gln) c.883A>C (p.Lys295Gln) c.1120A>C (p.Lys374Gln) | |
| 13 | g.46834882A>C | CA483739077 | HTR2A | c.1371T>G (p.Ser457=) c.882T>G (p.Ser294=) c.1119T>G (p.Ser373=) | |
| 13 | g.46834882A>G | CA483739078 | HTR2A | c.1371T>C (p.Ser457=) c.882T>C (p.Ser294=) c.1119T>C (p.Ser373=) | gnomAD v4 |
| 13 | g.46834882A>T | CA483739079 | HTR2A | c.1371T>A (p.Ser457=) c.882T>A (p.Ser294=) c.1119T>A (p.Ser373=) | |
| 13 | g.46834883G>A | CA388150210 | HTR2A | c.1370C>T (p.Ser457Phe) c.881C>T (p.Ser294Phe) c.1118C>T (p.Ser373Phe) | |
| 13 | g.46834883G>C | CA388150211 | HTR2A | c.1370C>G (p.Ser457Cys) c.881C>G (p.Ser294Cys) c.1118C>G (p.Ser373Cys) | |
| 13 | g.46834883G>T | CA388150213 | HTR2A | c.1370C>A (p.Ser457Tyr) c.881C>A (p.Ser294Tyr) c.1118C>A (p.Ser373Tyr) | |
| 13 | g.46834884A>C | CA388150216 | HTR2A | c.1369T>G (p.Ser457Ala) c.880T>G (p.Ser294Ala) c.1117T>G (p.Ser373Ala) | |
| 13 | g.46834884A>G | CA388150217 | HTR2A | c.1369T>C (p.Ser457Pro) c.880T>C (p.Ser294Pro) c.1117T>C (p.Ser373Pro) | |
| 13 | g.46834884A>T | CA388150218 | HTR2A | c.1369T>A (p.Ser457Thr) c.880T>A (p.Ser294Thr) c.1117T>A (p.Ser373Thr) | |
| 13 | g.46834885_46834886insCTAAA | CA2622958750 | HTR2A | c.1369_1370insTAGTT (p.Ser457LeufsTer10) c.880_881insTAGTT (p.Ser294LeufsTer10) c.1117_1118insTAGTT (p.Ser373LeufsTer10) | gnomAD v4 |
| 13 | g.46834885A>C | CA483739081 | HTR2A | c.1368T>G (p.Ala456=) c.879T>G (p.Ala293=) c.1116T>G (p.Ala372=) | |
| 13 | g.46834885A>G | CA483739082 | HTR2A | c.1368T>C (p.Ala456=) c.879T>C (p.Ala293=) c.1116T>C (p.Ala372=) | |
| 13 | g.46834885A>T | CA483739083 | HTR2A | c.1368T>A (p.Ala456=) c.879T>A (p.Ala293=) c.1116T>A (p.Ala372=) | |
| 13 | g.46834886G>A | CA388150219 | HTR2A | c.1367C>T (p.Ala456Val) c.878C>T (p.Ala293Val) c.1115C>T (p.Ala372Val) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.46834886G>C | CA388150221 | HTR2A | c.1367C>G (p.Ala456Gly) c.878C>G (p.Ala293Gly) c.1115C>G (p.Ala372Gly) | |
| 13 | g.46834886G= | CA2089283353 | HTR2A | c.1367C= (p.Ala456=) c.878C= (p.Ala293=) c.1115C= (p.Ala372=) | |
| 13 | g.46834886G>T | CA388150223 | HTR2A | c.1367C>A (p.Ala456Asp) c.878C>A (p.Ala293Asp) c.1115C>A (p.Ala372Asp) | |
| 13 | g.46834887C>A | CA249253342 | HTR2A | c.1366G>T (p.Ala456Ser) c.877G>T (p.Ala293Ser) c.1114G>T (p.Ala372Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834887C= | CA2089283354 | HTR2A | c.1366G= (p.Ala456=) c.877G= (p.Ala293=) c.1114G= (p.Ala372=) | |
| 13 | g.46834887C>G | CA388150225 | HTR2A | c.1366G>C (p.Ala456Pro) c.877G>C (p.Ala293Pro) c.1114G>C (p.Ala372Pro) | dbSNP |
| 13 | g.46834887C>T | CA388150227 | HTR2A | c.1366G>A (p.Ala456Thr) c.877G>A (p.Ala293Thr) c.1114G>A (p.Ala372Thr) | gnomAD v4 |
| 13 | g.46834888C>A | CA388150232 | HTR2A | c.1365G>T (p.Glu455Asp) c.876G>T (p.Glu292Asp) c.1113G>T (p.Glu371Asp) | |
| 13 | g.46834888C= | CA2089283355 | HTR2A | c.1365G= (p.Glu455=) c.876G= (p.Glu292=) c.1113G= (p.Glu371=) | |
| 13 | g.46834888C>G | CA388150231 | HTR2A | c.1365G>C (p.Glu455Asp) c.876G>C (p.Glu292Asp) c.1113G>C (p.Glu371Asp) | COSMIC |
| 13 | g.46834888C>T | CA6977495 | HTR2A | c.1365G>A (p.Glu455=) c.876G>A (p.Glu292=) c.1113G>A (p.Glu371=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834889T>A | CA388150234 | HTR2A | c.1364A>T (p.Glu455Val) c.875A>T (p.Glu292Val) c.1112A>T (p.Glu371Val) | |
| 13 | g.46834889T>C | CA388150235 | HTR2A | c.1364A>G (p.Glu455Gly) c.875A>G (p.Glu292Gly) c.1112A>G (p.Glu371Gly) | |
| 13 | g.46834889T>G | CA388150237 | HTR2A | c.1364A>C (p.Glu455Ala) c.875A>C (p.Glu292Ala) c.1112A>C (p.Glu371Ala) | |
| 13 | g.46834890C>A | CA388150239 | HTR2A | c.1363G>T (p.Glu455Ter) c.874G>T (p.Glu292Ter) c.1111G>T (p.Glu371Ter) | |
| 13 | g.46834890C>G | CA388150241 | HTR2A | c.1363G>C (p.Glu455Gln) c.874G>C (p.Glu292Gln) c.1111G>C (p.Glu371Gln) | |
| 13 | g.46834890C>T | CA388150242 | HTR2A | c.1363G>A (p.Glu455Lys) c.874G>A (p.Glu292Lys) c.1111G>A (p.Glu371Lys) | |
| 13 | g.46834891T>A | CA388150246 | HTR2A | c.1362A>T (p.Glu454Asp) c.873A>T (p.Glu291Asp) c.1110A>T (p.Glu370Asp) | |
| 13 | g.46834891T>C | CA483739088 | HTR2A | c.1362A>G (p.Glu454=) c.873A>G (p.Glu291=) c.1110A>G (p.Glu370=) | |
| 13 | g.46834891T>G | CA388150245 | HTR2A | c.1362A>C (p.Glu454Asp) c.873A>C (p.Glu291Asp) c.1110A>C (p.Glu370Asp) | COSMIC |
| 13 | g.46834892T>A | CA388150248 | HTR2A | c.1361A>T (p.Glu454Val) c.872A>T (p.Glu291Val) c.1109A>T (p.Glu370Val) | gnomAD v4 |
| 13 | g.46834892T>C | CA388150250 | HTR2A | c.1361A>G (p.Glu454Gly) c.872A>G (p.Glu291Gly) c.1109A>G (p.Glu370Gly) | |
| 13 | g.46834892T>G | CA388150251 | HTR2A | c.1361A>C (p.Glu454Ala) c.872A>C (p.Glu291Ala) c.1109A>C (p.Glu370Ala) | |
| 13 | g.46834893C>A | CA388150253 | HTR2A | c.1360G>T (p.Glu454Ter) c.871G>T (p.Glu291Ter) c.1108G>T (p.Glu370Ter) | COSMIC COSMIC |
| 13 | g.46834893C= | CA2089283356 | HTR2A | c.1360G= (p.Glu454=) c.871G= (p.Glu291=) c.1108G= (p.Glu370=) | |
| 13 | g.46834893C>G | CA6977496 | HTR2A | c.1360G>C (p.Glu454Gln) c.871G>C (p.Glu291Gln) c.1108G>C (p.Glu370Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834893C>T | CA388150256 | HTR2A | c.1360G>A (p.Glu454Lys) c.871G>A (p.Glu291Lys) c.1108G>A (p.Glu370Lys) | |
| 13 | g.46834894A>C | CA483739092 | HTR2A | c.1359T>G (p.Ser453=) c.870T>G (p.Ser290=) c.1107T>G (p.Ser369=) | |
| 13 | g.46834894A>G | CA483739094 | HTR2A | c.1359T>C (p.Ser453=) c.870T>C (p.Ser290=) c.1107T>C (p.Ser369=) | |
| 13 | g.46834894A>T | CA483739093 | HTR2A | c.1359T>A (p.Ser453=) c.870T>A (p.Ser290=) c.1107T>A (p.Ser369=) | |
| 13 | g.46834895G>A | CA249253349 | HTR2A | c.1358C>T (p.Ser453Phe) c.869C>T (p.Ser290Phe) c.1106C>T (p.Ser369Phe) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.46834895G>C | CA6977497 | HTR2A | c.1358C>G (p.Ser453Cys) c.869C>G (p.Ser290Cys) c.1106C>G (p.Ser369Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834895G= | CA2089283357 | HTR2A | c.1358C= (p.Ser453=) c.869C= (p.Ser290=) c.1106C= (p.Ser369=) | |
| 13 | g.46834895G>T | CA388150258 | HTR2A | c.1358C>A (p.Ser453Tyr) c.869C>A (p.Ser290Tyr) c.1106C>A (p.Ser369Tyr) | |
| 13 | g.46834896A= | CA2089283358 | HTR2A | c.1357T= (p.Ser453=) c.868T= (p.Ser290=) c.1105T= (p.Ser369=) | |
| 13 | g.46834896A>C | CA388150261 | HTR2A | c.1357T>G (p.Ser453Ala) c.868T>G (p.Ser290Ala) c.1105T>G (p.Ser369Ala) | |
| 13 | g.46834896A>G | CA388150262 | HTR2A | c.1357T>C (p.Ser453Pro) c.868T>C (p.Ser290Pro) c.1105T>C (p.Ser369Pro) | |
| 13 | g.46834896A>T | CA6977498 | HTR2A | c.1357T>A (p.Ser453Thr) c.868T>A (p.Ser290Thr) c.1105T>A (p.Ser369Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.46834897A>C | CA388150265 | HTR2A | c.1356T>G (p.His452Gln) c.867T>G (p.His289Gln) c.1104T>G (p.His368Gln) | |
| 13 | g.46834897A>G | CA483739096 | HTR2A | c.1356T>C (p.His452=) c.867T>C (p.His289=) c.1104T>C (p.His368=) | |
| 13 | g.46834897A>T | CA388150266 | HTR2A | c.1356T>A (p.His452Gln) c.867T>A (p.His289Gln) c.1104T>A (p.His368Gln) | gnomAD v4 |
| 13 | g.46834898T>A | CA6977499 | HTR2A | c.1355A>T (p.His452Leu) c.866A>T (p.His289Leu) c.1103A>T (p.His368Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.46834898T>C | CA249253350 | HTR2A | c.1355A>G (p.His452Arg) c.866A>G (p.His289Arg) c.1103A>G (p.His368Arg) | dbSNP gnomAD v4 |
| 13 | g.46834898T>G | CA388150270 | HTR2A | c.1355A>C (p.His452Pro) c.866A>C (p.His289Pro) c.1103A>C (p.His368Pro) | dbSNP gnomAD v4 |
| 13 | g.46834898T= | CA2089283359 | HTR2A | c.1355A= (p.His452=) c.866A= (p.His289=) c.1103A= (p.His368=) | |
| 13 | g.46834899G>A | CA6977500 | HTR2A | c.1354C>T (p.His452Tyr) c.865C>T (p.His289Tyr) c.1102C>T (p.His368Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834899G>C | CA388150272 | HTR2A | c.1354C>G (p.His452Asp) c.865C>G (p.His289Asp) c.1102C>G (p.His368Asp) | |
| 13 | g.46834899G= | CA1630855946 | HTR2A | c.1354C= (p.His452=) c.865C= (p.His289=) c.1102C= (p.His368=) | |
| 13 | g.46834899G>T | CA388150274 | HTR2A | c.1354C>A (p.His452Asn) c.865C>A (p.His289Asn) c.1102C>A (p.His368Asn) | |
| 13 | g.46834900C>A | CA388150275 | HTR2A | c.1353G>T (p.Gln451His) c.864G>T (p.Gln288His) c.1101G>T (p.Gln367His) | |
| 13 | g.46834900C>G | CA388150277 | HTR2A | c.1353G>C (p.Gln451His) c.864G>C (p.Gln288His) c.1101G>C (p.Gln367His) | |
| 13 | g.46834900C>T | CA483739098 | HTR2A | c.1353G>A (p.Gln451=) c.864G>A (p.Gln288=) c.1101G>A (p.Gln367=) | |
| 13 | g.46834901T>A | CA388150279 | HTR2A | c.1352A>T (p.Gln451Leu) c.863A>T (p.Gln288Leu) c.1100A>T (p.Gln367Leu) | |
| 13 | g.46834901T>C | CA388150282 | HTR2A | c.1352A>G (p.Gln451Arg) c.863A>G (p.Gln288Arg) c.1100A>G (p.Gln367Arg) | |
| 13 | g.46834901T>G | CA388150280 | HTR2A | c.1352A>C (p.Gln451Pro) c.863A>C (p.Gln288Pro) c.1100A>C (p.Gln367Pro) | |
| 13 | g.46834902G>A | CA388150284 | HTR2A | c.1351C>T (p.Gln451Ter) c.862C>T (p.Gln288Ter) c.1099C>T (p.Gln367Ter) | |
| 13 | g.46834902G>C | CA388150286 | HTR2A | c.1351C>G (p.Gln451Glu) c.862C>G (p.Gln288Glu) c.1099C>G (p.Gln367Glu) | |
| 13 | g.46834902G>T | CA388150287 | HTR2A | c.1351C>A (p.Gln451Lys) c.862C>A (p.Gln288Lys) c.1099C>A (p.Gln367Lys) | |
| 13 | g.46834903C>A | CA388150289 | HTR2A | c.1350G>T (p.Lys450Asn) c.861G>T (p.Lys287Asn) c.1098G>T (p.Lys366Asn) | |
| 13 | g.46834903C= | CA2089283360 | HTR2A | c.1350G= (p.Lys450=) c.861G= (p.Lys287=) c.1098G= (p.Lys366=) | |
| 13 | g.46834903C>G | CA388150291 | HTR2A | c.1350G>C (p.Lys450Asn) c.861G>C (p.Lys287Asn) c.1098G>C (p.Lys366Asn) | |
| 13 | g.46834903C>T | CA6977501 | HTR2A | c.1350G>A (p.Lys450=) c.861G>A (p.Lys287=) c.1098G>A (p.Lys366=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834904T>A | CA388150293 | HTR2A | c.1349A>T (p.Lys450Met) c.860A>T (p.Lys287Met) c.1097A>T (p.Lys366Met) | |
| 13 | g.46834904T>C | CA388150295 | HTR2A | c.1349A>G (p.Lys450Arg) c.860A>G (p.Lys287Arg) c.1097A>G (p.Lys366Arg) | |
| 13 | g.46834904T>G | CA388150297 | HTR2A | c.1349A>C (p.Lys450Thr) c.860A>C (p.Lys287Thr) c.1097A>C (p.Lys366Thr) | |
| 13 | g.46834905T>A | CA388150299 | HTR2A | c.1348A>T (p.Lys450Ter) c.859A>T (p.Lys287Ter) c.1096A>T (p.Lys366Ter) | |
| 13 | g.46834905T>C | CA6977502 | HTR2A | c.1348A>G (p.Lys450Glu) c.859A>G (p.Lys287Glu) c.1096A>G (p.Lys366Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.46834905T>G | CA388150302 | HTR2A | c.1348A>C (p.Lys450Gln) c.859A>C (p.Lys287Gln) c.1096A>C (p.Lys366Gln) | |
| 13 | g.46834905T= | CA2089283361 | HTR2A | c.1348A= (p.Lys450=) c.859A= (p.Lys287=) c.1096A= (p.Lys366=) | |
| 13 | g.46834906T>A | CA483739105 | HTR2A | c.1347A>T (p.Gly449=) c.858A>T (p.Gly286=) c.1095A>T (p.Gly365=) | |
| 13 | g.46834906T>C | CA483739106 | HTR2A | c.1347A>G (p.Gly449=) c.858A>G (p.Gly286=) c.1095A>G (p.Gly365=) | |
| 13 | g.46834906T>G | CA483739107 | HTR2A | c.1347A>C (p.Gly449=) c.858A>C (p.Gly286=) c.1095A>C (p.Gly365=) | |
| 13 | g.46834907C>A | CA388150306 | HTR2A | c.1346G>T (p.Gly449Val) c.857G>T (p.Gly286Val) c.1094G>T (p.Gly365Val) | gnomAD v4 |
| 13 | g.46834907C>G | CA388150303 | HTR2A | c.1346G>C (p.Gly449Ala) c.857G>C (p.Gly286Ala) c.1094G>C (p.Gly365Ala) | |
| 13 | g.46834907C>T | CA388150305 | HTR2A | c.1346G>A (p.Gly449Glu) c.857G>A (p.Gly286Glu) c.1094G>A (p.Gly365Glu) | COSMIC COSMIC |
| 13 | g.46834908C>A | CA388150307 | HTR2A | c.1345G>T (p.Gly449Ter) c.856G>T (p.Gly286Ter) c.1093G>T (p.Gly365Ter) | |
| 13 | g.46834908C= | CA2089283362 | HTR2A | c.1345G= (p.Gly449=) c.856G= (p.Gly286=) c.1093G= (p.Gly365=) | |
| 13 | g.46834908C>G | CA388150308 | HTR2A | c.1345G>C (p.Gly449Arg) c.856G>C (p.Gly286Arg) c.1093G>C (p.Gly365Arg) | dbSNP |
| 13 | g.46834908C>T | CA388150309 | HTR2A | c.1345G>A (p.Gly449Arg) c.856G>A (p.Gly286Arg) c.1093G>A (p.Gly365Arg) | |
| 13 | g.46834909T>A | CA483739112 | HTR2A | c.1344A>T (p.Leu448=) c.855A>T (p.Leu285=) c.1092A>T (p.Leu364=) | |
| 13 | g.46834909T>C | CA483739113 | HTR2A | c.1344A>G (p.Leu448=) c.855A>G (p.Leu285=) c.1092A>G (p.Leu364=) | |
| 13 | g.46834909T>G | CA483739114 | HTR2A | c.1344A>C (p.Leu448=) c.855A>C (p.Leu285=) c.1092A>C (p.Leu364=) | |
| 13 | g.46834910A>C | CA388150311 | HTR2A | c.1343T>G (p.Leu448Arg) c.854T>G (p.Leu285Arg) c.1091T>G (p.Leu364Arg) | |
| 13 | g.46834910A>G | CA388150312 | HTR2A | c.1343T>C (p.Leu448Pro) c.854T>C (p.Leu285Pro) c.1091T>C (p.Leu364Pro) | |
| 13 | g.46834910A>T | CA388150313 | HTR2A | c.1343T>A (p.Leu448Gln) c.854T>A (p.Leu285Gln) c.1091T>A (p.Leu364Gln) | |
| 13 | g.46834911G>A | CA483739115 | HTR2A | c.1342C>T (p.Leu448=) c.853C>T (p.Leu285=) c.1090C>T (p.Leu364=) | |
| 13 | g.46834911G>C | CA388150314 | HTR2A | c.1342C>G (p.Leu448Val) c.853C>G (p.Leu285Val) c.1090C>G (p.Leu364Val) | gnomAD v4 |
| 13 | g.46834911G>T | CA388150316 | HTR2A | c.1342C>A (p.Leu448Ile) c.853C>A (p.Leu285Ile) c.1090C>A (p.Leu364Ile) | |
| 13 | g.46834912A>C | CA483739119 | HTR2A | c.1341T>G (p.Ala447=) c.852T>G (p.Ala284=) c.1089T>G (p.Ala363=) | |
| 13 | g.46834912A>G | CA483739117 | HTR2A | c.1341T>C (p.Ala447=) c.852T>C (p.Ala284=) c.1089T>C (p.Ala363=) | |
| 13 | g.46834912A>T | CA483739118 | HTR2A | c.1341T>A (p.Ala447=) c.852T>A (p.Ala284=) c.1089T>A (p.Ala363=) | |
| 13 | g.46834913G>A | CA6977503 | HTR2A | c.1340C>T (p.Ala447Val) c.851C>T (p.Ala284Val) c.1088C>T (p.Ala363Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834913G>C | CA388150319 | HTR2A | c.1340C>G (p.Ala447Gly) c.851C>G (p.Ala284Gly) c.1088C>G (p.Ala363Gly) | |
| 13 | g.46834913G= | CA2018007891 | HTR2A | c.1340C= (p.Ala447=) c.851C= (p.Ala284=) c.1088C= (p.Ala363=) | |
| 13 | g.46834913G>T | CA388150321 | HTR2A | c.1340C>A (p.Ala447Asp) c.851C>A (p.Ala284Asp) c.1088C>A (p.Ala363Asp) | |
| 13 | g.46834914C>A | CA388150325 | HTR2A | c.1339G>T (p.Ala447Ser) c.850G>T (p.Ala284Ser) c.1087G>T (p.Ala363Ser) | |
| 13 | g.46834914C= | CA2089283363 | HTR2A | c.1339G= (p.Ala447=) c.850G= (p.Ala284=) c.1087G= (p.Ala363=) | |
| 13 | g.46834914C>G | CA388150323 | HTR2A | c.1339G>C (p.Ala447Pro) c.850G>C (p.Ala284Pro) c.1087G>C (p.Ala363Pro) | |
| 13 | g.46834914C>T | CA6977504 | HTR2A | c.1339G>A (p.Ala447Thr) c.850G>A (p.Ala284Thr) c.1087G>A (p.Ala363Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.46834915A>C | CA483739121 | HTR2A | c.1338T>G (p.Val446=) c.849T>G (p.Val283=) c.1086T>G (p.Val362=) | |
| 13 | g.46834915A>G | CA483739123 | HTR2A | c.1338T>C (p.Val446=) c.849T>C (p.Val283=) c.1086T>C (p.Val362=) | |
| 13 | g.46834915A>T | CA483739125 | HTR2A | c.1338T>A (p.Val446=) c.849T>A (p.Val283=) c.1086T>A (p.Val362=) | |
| 13 | g.46834916A= | CA2089283364 | HTR2A | c.1337T= (p.Val446=) c.848T= (p.Val283=) c.1085T= (p.Val362=) | |
| 13 | g.46834916A>C | CA388150327 | HTR2A | c.1337T>G (p.Val446Gly) c.848T>G (p.Val283Gly) c.1085T>G (p.Val362Gly) | |
| 13 | g.46834916A>G | CA6977505 | HTR2A | c.1337T>C (p.Val446Ala) c.848T>C (p.Val283Ala) c.1085T>C (p.Val362Ala) | dbSNP ExAC gnomAD v2 |
| 13 | g.46834916A>T | CA388150329 | HTR2A | c.1337T>A (p.Val446Asp) c.848T>A (p.Val283Asp) c.1085T>A (p.Val362Asp) | |
| 13 | g.46834917C>A | CA388150332 | HTR2A | c.1336G>T (p.Val446Phe) c.847G>T (p.Val283Phe) c.1084G>T (p.Val362Phe) | |
| 13 | g.46834917C>G | CA388150336 | HTR2A | c.1336G>C (p.Val446Leu) c.847G>C (p.Val283Leu) c.1084G>C (p.Val362Leu) | |
| 13 | g.46834917C>T | CA388150334 | HTR2A | c.1336G>A (p.Val446Ile) c.847G>A (p.Val283Ile) c.1084G>A (p.Val362Ile) | gnomAD v4 |
| 13 | g.46834918C>A | CA388150338 | HTR2A | c.1335G>T (p.Met445Ile) c.846G>T (p.Met282Ile) c.1083G>T (p.Met361Ile) | |
| 13 | g.46834918C= | CA2089283365 | HTR2A | c.1335G= (p.Met445=) c.846G= (p.Met282=) c.1083G= (p.Met361=) | |
| 13 | g.46834918C>G | CA388150340 | HTR2A | c.1335G>C (p.Met445Ile) c.846G>C (p.Met282Ile) c.1083G>C (p.Met361Ile) | dbSNP |
| 13 | g.46834918C>T | CA388150342 | HTR2A | c.1335G>A (p.Met445Ile) c.846G>A (p.Met282Ile) c.1083G>A (p.Met361Ile) | |
| 13 | g.46834919A= | CA2089283366 | HTR2A | c.1334T= (p.Met445=) c.845T= (p.Met282=) c.1082T= (p.Met361=) | |
| 13 | g.46834919A>C | CA388150344 | HTR2A | c.1334T>G (p.Met445Arg) c.845T>G (p.Met282Arg) c.1082T>G (p.Met361Arg) | |
| 13 | g.46834919A>G | CA388150346 | HTR2A | c.1334T>C (p.Met445Thr) c.845T>C (p.Met282Thr) c.1082T>C (p.Met361Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.46834919A>T | CA388150349 | HTR2A | c.1334T>A (p.Met445Lys) c.845T>A (p.Met282Lys) c.1082T>A (p.Met361Lys) | |
| 13 | g.46834920T>A | CA388150351 | HTR2A | c.1333A>T (p.Met445Leu) c.844A>T (p.Met282Leu) c.1081A>T (p.Met361Leu) | |
| 13 | g.46834920T>C | CA388150353 | HTR2A | c.1333A>G (p.Met445Val) c.844A>G (p.Met282Val) c.1081A>G (p.Met361Val) | gnomAD v4 |
| 13 | g.46834920T>G | CA388150354 | HTR2A | c.1333A>C (p.Met445Leu) c.844A>C (p.Met282Leu) c.1081A>C (p.Met361Leu) | |
| 13 | g.46834921T>A | CA483739129 | HTR2A | c.1332A>T (p.Ser444=) c.843A>T (p.Ser281=) c.1080A>T (p.Ser360=) | |
| 13 | g.46834921T>C | CA483739130 | HTR2A | c.1332A>G (p.Ser444=) c.843A>G (p.Ser281=) c.1080A>G (p.Ser360=) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.46834921T>G | CA483739131 | HTR2A | c.1332A>C (p.Ser444=) c.843A>C (p.Ser281=) c.1080A>C (p.Ser360=) | |
| 13 | g.46834921T= | CA2089283367 | HTR2A | c.1332A= (p.Ser444=) c.843A= (p.Ser281=) c.1080A= (p.Ser360=) | |
| 13 | g.46834922G>A | CA388150356 | HTR2A | c.1331C>T (p.Ser444Leu) c.842C>T (p.Ser281Leu) c.1079C>T (p.Ser360Leu) | |
| 13 | g.46834922G>C | CA388150358 | HTR2A | c.1331C>G (p.Ser444Ter) c.842C>G (p.Ser281Ter) c.1079C>G (p.Ser360Ter) | |
| 13 | g.46834922G>T | CA388150360 | HTR2A | c.1331C>A (p.Ser444Ter) c.842C>A (p.Ser281Ter) c.1079C>A (p.Ser360Ter) | |
| 13 | g.46834923A>C | CA388150361 | HTR2A | c.1330T>G (p.Ser444Ala) c.841T>G (p.Ser281Ala) c.1078T>G (p.Ser360Ala) | |
| 13 | g.46834923A>G | CA388150365 | HTR2A | c.1330T>C (p.Ser444Pro) c.841T>C (p.Ser281Pro) c.1078T>C (p.Ser360Pro) | |
| 13 | g.46834923A>T | CA388150363 | HTR2A | c.1330T>A (p.Ser444Thr) c.841T>A (p.Ser281Thr) c.1078T>A (p.Ser360Thr) |