Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
13 | g.46834924G>A | CA483739133 | HTR2A | c.1329C>T (p.Cys443=) c.840C>T (p.Cys280=) c.1077C>T (p.Cys359=) | |
13 | g.46834924G>C | CA388150367 | HTR2A | c.1329C>G (p.Cys443Trp) c.840C>G (p.Cys280Trp) c.1077C>G (p.Cys359Trp) | |
13 | g.46834924G>T | CA388150369 | HTR2A | c.1329C>A (p.Cys443Ter) c.840C>A (p.Cys280Ter) c.1077C>A (p.Cys359Ter) | |
13 | g.46834925C>A | CA388150371 | HTR2A | c.1328G>T (p.Cys443Phe) c.839G>T (p.Cys280Phe) c.1076G>T (p.Cys359Phe) | |
13 | g.46834925C= | CA2089283368 | HTR2A | c.1328G= (p.Cys443=) c.839G= (p.Cys280=) c.1076G= (p.Cys359=) | |
13 | g.46834925C>G | CA388150373 | HTR2A | c.1328G>C (p.Cys443Ser) c.839G>C (p.Cys280Ser) c.1076G>C (p.Cys359Ser) | |
13 | g.46834925C>T | CA388150375 | HTR2A | c.1328G>A (p.Cys443Tyr) c.839G>A (p.Cys280Tyr) c.1076G>A (p.Cys359Tyr) | dbSNP |
13 | g.46834926A= | CA2089283369 | HTR2A | c.1327T= (p.Cys443=) c.838T= (p.Cys280=) c.1075T= (p.Cys359=) | |
13 | g.46834926A>C | CA6977506 | HTR2A | c.1327T>G (p.Cys443Gly) c.838T>G (p.Cys280Gly) c.1075T>G (p.Cys359Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.46834926A>G | CA388150378 | HTR2A | c.1327T>C (p.Cys443Arg) c.838T>C (p.Cys280Arg) c.1075T>C (p.Cys359Arg) | |
13 | g.46834926A>T | CA388150380 | HTR2A | c.1327T>A (p.Cys443Ser) c.838T>A (p.Cys280Ser) c.1075T>A (p.Cys359Ser) | |
13 | g.46834927G>A | CA483739136 | HTR2A | c.1326C>T (p.Asp442=) c.837C>T (p.Asp279=) c.1074C>T (p.Asp358=) | |
13 | g.46834927G>C | CA388150382 | HTR2A | c.1326C>G (p.Asp442Glu) c.837C>G (p.Asp279Glu) c.1074C>G (p.Asp358Glu) | |
13 | g.46834927G>T | CA388150383 | HTR2A | c.1326C>A (p.Asp442Glu) c.837C>A (p.Asp279Glu) c.1074C>A (p.Asp358Glu) | |
13 | g.46834928T>A | CA388150388 | HTR2A | c.1325A>T (p.Asp442Val) c.836A>T (p.Asp279Val) c.1073A>T (p.Asp358Val) | |
13 | g.46834928T>C | CA249253376 | HTR2A | c.1325A>G (p.Asp442Gly) c.836A>G (p.Asp279Gly) c.1073A>G (p.Asp358Gly) | dbSNP gnomAD v4 |
13 | g.46834928T>G | CA388150386 | HTR2A | c.1325A>C (p.Asp442Ala) c.836A>C (p.Asp279Ala) c.1073A>C (p.Asp358Ala) | |
13 | g.46834928T= | CA2089283370 | HTR2A | c.1325A= (p.Asp442=) c.836A= (p.Asp279=) c.1073A= (p.Asp358=) | |
13 | g.46834930_46834935del | CA2799080101 | HTR2A | c.1320_1325del (p.Asn441_Asp442del) c.831_836del (p.Asn278_Asp279del) c.1068_1073del (p.Asn357_Asp358del) | |
13 | g.46834929C>A | CA388150394 | HTR2A | c.1324G>T (p.Asp442Tyr) c.835G>T (p.Asp279Tyr) c.1072G>T (p.Asp358Tyr) | gnomAD v4 |
13 | g.46834929C>G | CA388150390 | HTR2A | c.1324G>C (p.Asp442His) c.835G>C (p.Asp279His) c.1072G>C (p.Asp358His) | |
13 | g.46834929C>T | CA388150392 | HTR2A | c.1324G>A (p.Asp442Asn) c.835G>A (p.Asp279Asn) c.1072G>A (p.Asp358Asn) | |
13 | g.46834930A= | CA2089283371 | HTR2A | c.1323T= (p.Asn441=) c.834T= (p.Asn278=) c.1071T= (p.Asn357=) | |
13 | g.46834930A>C | CA388150396 | HTR2A | c.1323T>G (p.Asn441Lys) c.834T>G (p.Asn278Lys) c.1071T>G (p.Asn357Lys) | |
13 | g.46834930A>G | CA6977507 | HTR2A | c.1323T>C (p.Asn441=) c.834T>C (p.Asn278=) c.1071T>C (p.Asn357=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.46834930A>T | CA249253377 | HTR2A | c.1323T>A (p.Asn441Lys) c.834T>A (p.Asn278Lys) c.1071T>A (p.Asn357Lys) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.46834931T>A | CA388150399 | HTR2A | c.1322A>T (p.Asn441Ile) c.833A>T (p.Asn278Ile) c.1070A>T (p.Asn357Ile) | |
13 | g.46834931T>C | CA388150404 | HTR2A | c.1322A>G (p.Asn441Ser) c.833A>G (p.Asn278Ser) c.1070A>G (p.Asn357Ser) | |
13 | g.46834931T>G | CA388150406 | HTR2A | c.1322A>C (p.Asn441Thr) c.833A>C (p.Asn278Thr) c.1070A>C (p.Asn357Thr) | |
13 | g.46834932T>A | CA388150408 | HTR2A | c.1321A>T (p.Asn441Tyr) c.832A>T (p.Asn278Tyr) c.1069A>T (p.Asn357Tyr) | |
13 | g.46834932T>C | CA388150410 | HTR2A | c.1321A>G (p.Asn441Asp) c.832A>G (p.Asn278Asp) c.1069A>G (p.Asn357Asp) | |
13 | g.46834932T>G | CA388150411 | HTR2A | c.1321A>C (p.Asn441His) c.832A>C (p.Asn278His) c.1069A>C (p.Asn357His) | |
13 | g.46834932T= | CA2089283372 | HTR2A | c.1321A= (p.Asn441=) c.832A= (p.Asn278=) c.1069A= (p.Asn357=) | |
13 | g.46834932_46834933insTG | CA609929161 | HTR2A | c.1320_1321insCA (p.Asn441GlnfsTer9) c.831_832insCA (p.Asn278GlnfsTer9) c.1068_1069insCA (p.Asn357GlnfsTer9) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834933A= | CA2089283373 | HTR2A | c.1320T= (p.Asp440=) c.831T= (p.Asp277=) c.1068T= (p.Asp356=) | |
13 | g.46834933A>C | CA388150413 | HTR2A | c.1320T>G (p.Asp440Glu) c.831T>G (p.Asp277Glu) c.1068T>G (p.Asp356Glu) | |
13 | g.46834933A>G | CA483739143 | HTR2A | c.1320T>C (p.Asp440=) c.831T>C (p.Asp277=) c.1068T>C (p.Asp356=) | dbSNP |
13 | g.46834933A>T | CA388150415 | HTR2A | c.1320T>A (p.Asp440Glu) c.831T>A (p.Asp277Glu) c.1068T>A (p.Asp356Glu) | |
13 | g.46834934T>A | CA388150421 | HTR2A | c.1319A>T (p.Asp440Val) c.830A>T (p.Asp277Val) c.1067A>T (p.Asp356Val) | |
13 | g.46834934T>C | CA388150417 | HTR2A | c.1319A>G (p.Asp440Gly) c.830A>G (p.Asp277Gly) c.1067A>G (p.Asp356Gly) | |
13 | g.46834934T>G | CA388150419 | HTR2A | c.1319A>C (p.Asp440Ala) c.830A>C (p.Asp277Ala) c.1067A>C (p.Asp356Ala) | |
13 | g.46834935C>A | CA388150422 | HTR2A | c.1318G>T (p.Asp440Tyr) c.829G>T (p.Asp277Tyr) c.1066G>T (p.Asp356Tyr) | |
13 | g.46834935C>G | CA388150423 | HTR2A | c.1318G>C (p.Asp440His) c.829G>C (p.Asp277His) c.1066G>C (p.Asp356His) | |
13 | g.46834935C>T | CA388150424 | HTR2A | c.1318G>A (p.Asp440Asn) c.829G>A (p.Asp277Asn) c.1066G>A (p.Asp356Asn) | |
13 | g.46834936T>A | CA483739147 | HTR2A | c.1317A>T (p.Thr439=) c.828A>T (p.Thr276=) c.1065A>T (p.Thr355=) | |
13 | g.46834936T>C | CA483739148 | HTR2A | c.1317A>G (p.Thr439=) c.828A>G (p.Thr276=) c.1065A>G (p.Thr355=) | |
13 | g.46834936T>G | CA249253382 | HTR2A | c.1317A>C (p.Thr439=) c.828A>C (p.Thr276=) c.1065A>C (p.Thr355=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.46834936T= | CA2089283374 | HTR2A | c.1317A= (p.Thr439=) c.828A= (p.Thr276=) c.1065A= (p.Thr355=) | |
13 | g.46834937G>A | CA388150425 | HTR2A | c.1316C>T (p.Thr439Ile) c.827C>T (p.Thr276Ile) c.1064C>T (p.Thr355Ile) | |
13 | g.46834937G>C | CA388150426 | HTR2A | c.1316C>G (p.Thr439Arg) c.827C>G (p.Thr276Arg) c.1064C>G (p.Thr355Arg) | |
13 | g.46834937G>T | CA388150427 | HTR2A | c.1316C>A (p.Thr439Lys) c.827C>A (p.Thr276Lys) c.1064C>A (p.Thr355Lys) | |
13 | g.46834938T>A | CA388150428 | HTR2A | c.1315A>T (p.Thr439Ser) c.826A>T (p.Thr276Ser) c.1063A>T (p.Thr355Ser) | |
13 | g.46834938T>C | CA388150429 | HTR2A | c.1315A>G (p.Thr439Ala) c.826A>G (p.Thr276Ala) c.1063A>G (p.Thr355Ala) | gnomAD v4 |
13 | g.46834938T>G | CA388150430 | HTR2A | c.1315A>C (p.Thr439Pro) c.826A>C (p.Thr276Pro) c.1063A>C (p.Thr355Pro) | |
13 | g.46834939T>A | CA483739153 | HTR2A | c.1314A>T (p.Thr438=) c.825A>T (p.Thr275=) c.1062A>T (p.Thr354=) | |
13 | g.46834939T>C | CA483739152 | HTR2A | c.1314A>G (p.Thr438=) c.825A>G (p.Thr275=) c.1062A>G (p.Thr354=) | dbSNP |
13 | g.46834939T>G | CA483739154 | HTR2A | c.1314A>C (p.Thr438=) c.825A>C (p.Thr275=) c.1062A>C (p.Thr354=) | |
13 | g.46834939T= | CA2089283375 | HTR2A | c.1314A= (p.Thr438=) c.825A= (p.Thr275=) c.1062A= (p.Thr354=) | |
13 | g.46834940G>A | CA388150431 | HTR2A | c.1313C>T (p.Thr438Ile) c.824C>T (p.Thr275Ile) c.1061C>T (p.Thr354Ile) | dbSNP gnomAD v4 |
13 | g.46834940G>C | CA388150432 | HTR2A | c.1313C>G (p.Thr438Arg) c.824C>G (p.Thr275Arg) c.1061C>G (p.Thr354Arg) | |
13 | g.46834940G= | CA2089283376 | HTR2A | c.1313C= (p.Thr438=) c.824C= (p.Thr275=) c.1061C= (p.Thr354=) | |
13 | g.46834940G>T | CA388150433 | HTR2A | c.1313C>A (p.Thr438Lys) c.824C>A (p.Thr275Lys) c.1061C>A (p.Thr354Lys) | dbSNP |
13 | g.46834941T>A | CA388150435 | HTR2A | c.1312A>T (p.Thr438Ser) c.823A>T (p.Thr275Ser) c.1060A>T (p.Thr354Ser) | |
13 | g.46834941T>C | CA388150436 | HTR2A | c.1312A>G (p.Thr438Ala) c.823A>G (p.Thr275Ala) c.1060A>G (p.Thr354Ala) | gnomAD v4 |
13 | g.46834941T>G | CA388150434 | HTR2A | c.1312A>C (p.Thr438Pro) c.823A>C (p.Thr275Pro) c.1060A>C (p.Thr354Pro) | |
13 | g.46834942C>A | CA388150437 | HTR2A | c.1311G>T (p.Lys437Asn) c.822G>T (p.Lys274Asn) c.1059G>T (p.Lys353Asn) | |
13 | g.46834942C= | CA2089283377 | HTR2A | c.1311G= (p.Lys437=) c.822G= (p.Lys274=) c.1059G= (p.Lys353=) | |
13 | g.46834942C>G | CA388150438 | HTR2A | c.1311G>C (p.Lys437Asn) c.822G>C (p.Lys274Asn) c.1059G>C (p.Lys353Asn) | |
13 | g.46834942C>T | CA249253394 | HTR2A | c.1311G>A (p.Lys437=) c.822G>A (p.Lys274=) c.1059G>A (p.Lys353=) | dbSNP |
13 | g.46834943T>A | CA388150439 | HTR2A | c.1310A>T (p.Lys437Met) c.821A>T (p.Lys274Met) c.1058A>T (p.Lys353Met) | |
13 | g.46834943T>C | CA388150440 | HTR2A | c.1310A>G (p.Lys437Arg) c.821A>G (p.Lys274Arg) c.1058A>G (p.Lys353Arg) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834943T>G | CA388150441 | HTR2A | c.1310A>C (p.Lys437Thr) c.821A>C (p.Lys274Thr) c.1058A>C (p.Lys353Thr) | |
13 | g.46834943T= | CA2089283378 | HTR2A | c.1310A= (p.Lys437=) c.821A= (p.Lys274=) c.1058A= (p.Lys353=) | |
13 | g.46834944T>A | CA388150442 | HTR2A | c.1309A>T (p.Lys437Ter) c.820A>T (p.Lys274Ter) c.1057A>T (p.Lys353Ter) | |
13 | g.46834944T>C | CA388150443 | HTR2A | c.1309A>G (p.Lys437Glu) c.820A>G (p.Lys274Glu) c.1057A>G (p.Lys353Glu) | |
13 | g.46834944T>G | CA388150444 | HTR2A | c.1309A>C (p.Lys437Gln) c.820A>C (p.Lys274Gln) c.1057A>C (p.Lys353Gln) | gnomAD v4 |
13 | g.46834945G>A | CA483739161 | HTR2A | c.1308C>T (p.Ala436=) c.819C>T (p.Ala273=) c.1056C>T (p.Ala352=) | |
13 | g.46834945G>C | CA483739162 | HTR2A | c.1308C>G (p.Ala436=) c.819C>G (p.Ala273=) c.1056C>G (p.Ala352=) | |
13 | g.46834945G>T | CA483739163 | HTR2A | c.1308C>A (p.Ala436=) c.819C>A (p.Ala273=) c.1056C>A (p.Ala352=) | |
13 | g.46834946G>A | CA388150445 | HTR2A | c.1307C>T (p.Ala436Val) c.818C>T (p.Ala273Val) c.1055C>T (p.Ala352Val) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.46834946G>C | CA6977508 | HTR2A | c.1307C>G (p.Ala436Gly) c.818C>G (p.Ala273Gly) c.1055C>G (p.Ala352Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.46834946G= | CA2089283379 | HTR2A | c.1307C= (p.Ala436=) c.818C= (p.Ala273=) c.1055C= (p.Ala352=) | |
13 | g.46834946G>T | CA388150446 | HTR2A | c.1307C>A (p.Ala436Asp) c.818C>A (p.Ala273Asp) c.1055C>A (p.Ala352Asp) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834947C>A | CA388150447 | HTR2A | c.1306G>T (p.Ala436Ser) c.817G>T (p.Ala273Ser) c.1054G>T (p.Ala352Ser) | |
13 | g.46834947C= | CA2089283380 | HTR2A | c.1306G= (p.Ala436=) c.817G= (p.Ala273=) c.1054G= (p.Ala352=) | |
13 | g.46834947C>G | CA388150448 | HTR2A | c.1306G>C (p.Ala436Pro) c.817G>C (p.Ala273Pro) c.1054G>C (p.Ala352Pro) | |
13 | g.46834947C>T | CA388150449 | HTR2A | c.1306G>A (p.Ala436Thr) c.817G>A (p.Ala273Thr) c.1054G>A (p.Ala352Thr) | dbSNP |
13 | g.46834948A= | CA2089283381 | HTR2A | c.1305T= (p.Asp435=) c.816T= (p.Asp272=) c.1053T= (p.Asp351=) | |
13 | g.46834948A>C | CA388150451 | HTR2A | c.1305T>G (p.Asp435Glu) c.816T>G (p.Asp272Glu) c.1053T>G (p.Asp351Glu) | |
13 | g.46834948A>G | CA483739166 | HTR2A | c.1305T>C (p.Asp435=) c.816T>C (p.Asp272=) c.1053T>C (p.Asp351=) | dbSNP |
13 | g.46834948A>T | CA388150450 | HTR2A | c.1305T>A (p.Asp435Glu) c.816T>A (p.Asp272Glu) c.1053T>A (p.Asp351Glu) | |
13 | g.46834949T>A | CA388150452 | HTR2A | c.1304A>T (p.Asp435Val) c.815A>T (p.Asp272Val) c.1052A>T (p.Asp351Val) | |
13 | g.46834949T>C | CA388150453 | HTR2A | c.1304A>G (p.Asp435Gly) c.815A>G (p.Asp272Gly) c.1052A>G (p.Asp351Gly) | gnomAD v4 |
13 | g.46834949T>G | CA388150454 | HTR2A | c.1304A>C (p.Asp435Ala) c.815A>C (p.Asp272Ala) c.1052A>C (p.Asp351Ala) | |
13 | g.46834950C>A | CA388150455 | HTR2A | c.1303G>T (p.Asp435Tyr) c.814G>T (p.Asp272Tyr) c.1051G>T (p.Asp351Tyr) | |
13 | g.46834950C= | CA2089283382 | HTR2A | c.1303G= (p.Asp435=) c.814G= (p.Asp272=) c.1051G= (p.Asp351=) | |
13 | g.46834950C>G | CA388150456 | HTR2A | c.1303G>C (p.Asp435His) c.814G>C (p.Asp272His) c.1051G>C (p.Asp351His) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.46834950C>T | CA388150457 | HTR2A | c.1303G>A (p.Asp435Asn) c.814G>A (p.Asp272Asn) c.1051G>A (p.Asp351Asn) | dbSNP gnomAD v4 |
13 | g.46834951T>A | CA388150460 | HTR2A | c.1302A>T (p.Gln434His) c.813A>T (p.Gln271His) c.1050A>T (p.Gln350His) | |
13 | g.46834951T>C | CA483739170 | HTR2A | c.1302A>G (p.Gln434=) c.813A>G (p.Gln271=) c.1050A>G (p.Gln350=) | gnomAD v4 |
13 | g.46834951T>G | CA388150462 | HTR2A | c.1302A>C (p.Gln434His) c.813A>C (p.Gln271His) c.1050A>C (p.Gln350His) | |
13 | g.46834952T>A | CA388150464 | HTR2A | c.1301A>T (p.Gln434Leu) c.812A>T (p.Gln271Leu) c.1049A>T (p.Gln350Leu) | |
13 | g.46834952T>C | CA6977509 | HTR2A | c.1301A>G (p.Gln434Arg) c.812A>G (p.Gln271Arg) c.1049A>G (p.Gln350Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
13 | g.46834952T>G | CA388150467 | HTR2A | c.1301A>C (p.Gln434Pro) c.812A>C (p.Gln271Pro) c.1049A>C (p.Gln350Pro) | |
13 | g.46834952T= | CA2089283383 | HTR2A | c.1301A= (p.Gln434=) c.812A= (p.Gln271=) c.1049A= (p.Gln350=) | |
13 | g.46834953G>A | CA388150472 | HTR2A | c.1300C>T (p.Gln434Ter) c.811C>T (p.Gln271Ter) c.1048C>T (p.Gln350Ter) | gnomAD v4 |
13 | g.46834953G>C | CA388150471 | HTR2A | c.1300C>G (p.Gln434Glu) c.811C>G (p.Gln271Glu) c.1048C>G (p.Gln350Glu) | |
13 | g.46834953G>T | CA388150470 | HTR2A | c.1300C>A (p.Gln434Lys) c.811C>A (p.Gln271Lys) c.1048C>A (p.Gln350Lys) | |
13 | g.46834954C>A | CA388150475 | HTR2A | c.1299G>T (p.Lys433Asn) c.810G>T (p.Lys270Asn) c.1047G>T (p.Lys349Asn) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834954C= | CA2089283384 | HTR2A | c.1299G= (p.Lys433=) c.810G= (p.Lys270=) c.1047G= (p.Lys349=) | |
13 | g.46834954C>G | CA388150477 | HTR2A | c.1299G>C (p.Lys433Asn) c.810G>C (p.Lys270Asn) c.1047G>C (p.Lys349Asn) | |
13 | g.46834954C>T | CA483739171 | HTR2A | c.1299G>A (p.Lys433=) c.810G>A (p.Lys270=) c.1047G>A (p.Lys349=) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834955T>A | CA388150479 | HTR2A | c.1298A>T (p.Lys433Met) c.809A>T (p.Lys270Met) c.1046A>T (p.Lys349Met) | |
13 | g.46834955T>C | CA388150481 | HTR2A | c.1298A>G (p.Lys433Arg) c.809A>G (p.Lys270Arg) c.1046A>G (p.Lys349Arg) | |
13 | g.46834955T>G | CA388150483 | HTR2A | c.1298A>C (p.Lys433Thr) c.809A>C (p.Lys270Thr) c.1046A>C (p.Lys349Thr) | |
13 | g.46834956T>A | CA388150484 | HTR2A | c.1297A>T (p.Lys433Ter) c.808A>T (p.Lys270Ter) c.1045A>T (p.Lys349Ter) | |
13 | g.46834956T>C | CA388150485 | HTR2A | c.1297A>G (p.Lys433Glu) c.808A>G (p.Lys270Glu) c.1045A>G (p.Lys349Glu) | |
13 | g.46834956T>G | CA388150486 | HTR2A | c.1297A>C (p.Lys433Gln) c.808A>C (p.Lys270Gln) c.1045A>C (p.Lys349Gln) | |
13 | g.46834957T>A | CA483739175 | HTR2A | c.1296A>T (p.Ser432=) c.807A>T (p.Ser269=) c.1044A>T (p.Ser348=) | |
13 | g.46834957T>C | CA483739176 | HTR2A | c.1296A>G (p.Ser432=) c.807A>G (p.Ser269=) c.1044A>G (p.Ser348=) | |
13 | g.46834957T>G | CA483739177 | HTR2A | c.1296A>C (p.Ser432=) c.807A>C (p.Ser269=) c.1044A>C (p.Ser348=) | |
13 | g.46834958G>A | CA388150488 | HTR2A | c.1295C>T (p.Ser432Leu) c.806C>T (p.Ser269Leu) c.1043C>T (p.Ser348Leu) | dbSNP |
13 | g.46834958G>C | CA388150490 | HTR2A | c.1295C>G (p.Ser432Ter) c.806C>G (p.Ser269Ter) c.1043C>G (p.Ser348Ter) | |
13 | g.46834958G= | CA2089283385 | HTR2A | c.1295C= (p.Ser432=) c.806C= (p.Ser269=) c.1043C= (p.Ser348=) | |
13 | g.46834958G>T | CA388150491 | HTR2A | c.1295C>A (p.Ser432Ter) c.806C>A (p.Ser269Ter) c.1043C>A (p.Ser348Ter) | gnomAD v4 |
13 | g.46834959A= | CA2089283386 | HTR2A | c.1294T= (p.Ser432=) c.805T= (p.Ser269=) c.1042T= (p.Ser348=) | |
13 | g.46834959A>C | CA388150495 | HTR2A | c.1294T>G (p.Ser432Ala) c.805T>G (p.Ser269Ala) c.1042T>G (p.Ser348Ala) | |
13 | g.46834959A>G | CA388150494 | HTR2A | c.1294T>C (p.Ser432Pro) c.805T>C (p.Ser269Pro) c.1042T>C (p.Ser348Pro) | dbSNP gnomAD v4 |
13 | g.46834959A>T | CA388150493 | HTR2A | c.1294T>A (p.Ser432Thr) c.805T>A (p.Ser269Thr) c.1042T>A (p.Ser348Thr) | |
13 | g.46834960A>C | CA388150497 | HTR2A | c.1293T>G (p.Asn431Lys) c.804T>G (p.Asn268Lys) c.1041T>G (p.Asn347Lys) | |
13 | g.46834960A>G | CA483739181 | HTR2A | c.1293T>C (p.Asn431=) c.804T>C (p.Asn268=) c.1041T>C (p.Asn347=) | |
13 | g.46834960A>T | CA388150499 | HTR2A | c.1293T>A (p.Asn431Lys) c.804T>A (p.Asn268Lys) c.1041T>A (p.Asn347Lys) | |
13 | g.46834961T>A | CA388150501 | HTR2A | c.1292A>T (p.Asn431Ile) c.803A>T (p.Asn268Ile) c.1040A>T (p.Asn347Ile) | |
13 | g.46834961T>C | CA388150503 | HTR2A | c.1292A>G (p.Asn431Ser) c.803A>G (p.Asn268Ser) c.1040A>G (p.Asn347Ser) | COSMIC |
13 | g.46834961T>G | CA388150505 | HTR2A | c.1292A>C (p.Asn431Thr) c.803A>C (p.Asn268Thr) c.1040A>C (p.Asn347Thr) | |
13 | g.46834962T>A | CA388150508 | HTR2A | c.1291A>T (p.Asn431Tyr) c.802A>T (p.Asn268Tyr) c.1039A>T (p.Asn347Tyr) | |
13 | g.46834962T>C | CA388150510 | HTR2A | c.1291A>G (p.Asn431Asp) c.802A>G (p.Asn268Asp) c.1039A>G (p.Asn347Asp) | |
13 | g.46834962T>G | CA388150511 | HTR2A | c.1291A>C (p.Asn431His) c.802A>C (p.Asn268His) c.1039A>C (p.Asn347His) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834962T= | CA2089283387 | HTR2A | c.1291A= (p.Asn431=) c.802A= (p.Asn268=) c.1039A= (p.Asn347=) | |
13 | g.46834963C>A | CA388150513 | HTR2A | c.1290G>T (p.Lys430Asn) c.801G>T (p.Lys267Asn) c.1038G>T (p.Lys346Asn) | |
13 | g.46834963C= | CA2089283389 | HTR2A | c.1290G= (p.Lys430=) c.801G= (p.Lys267=) c.1038G= (p.Lys346=) | |
13 | g.46834963C>G | CA388150515 | HTR2A | c.1290G>C (p.Lys430Asn) c.801G>C (p.Lys267Asn) c.1038G>C (p.Lys346Asn) | dbSNP gnomAD v4 |
13 | g.46834963C>T | CA483739183 | HTR2A | c.1290G>A (p.Lys430=) c.801G>A (p.Lys267=) c.1038G>A (p.Lys346=) | |
13 | g.46834963_46834964delinsCT | CA2089283388 | HTR2A | c.1289_1290delinsAG (p.Lys430=) c.800_801delinsAG (p.Lys267=) c.1037_1038delinsAG (p.Lys346=) | |
13 | g.46834964T>A | CA388150517 | HTR2A | c.1289A>T (p.Lys430Met) c.800A>T (p.Lys267Met) c.1037A>T (p.Lys346Met) | |
13 | g.46834964T>C | CA388150519 | HTR2A | c.1289A>G (p.Lys430Arg) c.800A>G (p.Lys267Arg) c.1037A>G (p.Lys346Arg) | |
13 | g.46834964T>G | CA388150520 | HTR2A | c.1289A>C (p.Lys430Thr) c.800A>C (p.Lys267Thr) c.1037A>C (p.Lys346Thr) | |
13 | g.46834970dup | CA2622958752 | HTR2A | c.1289dup (p.Asn431GlufsTer11) c.800dup (p.Asn268GlufsTer11) c.1037dup (p.Asn347GlufsTer11) | gnomAD v4 |
13 | g.46834970del | CA609929162 | HTR2A | c.1289del (p.Lys430ArgfsTer19) c.800del (p.Lys267ArgfsTer19) c.1037del (p.Lys346ArgfsTer19) | dbSNP gnomAD v2 gnomAD v4 |
13 | g.46834965T>A | CA388150524 | HTR2A | c.1288A>T (p.Lys430Ter) c.799A>T (p.Lys267Ter) c.1036A>T (p.Lys346Ter) | |
13 | g.46834965T>C | CA388150526 | HTR2A | c.1288A>G (p.Lys430Glu) c.799A>G (p.Lys267Glu) c.1036A>G (p.Lys346Glu) | |
13 | g.46834965T>G | CA388150522 | HTR2A | c.1288A>C (p.Lys430Gln) c.799A>C (p.Lys267Gln) c.1036A>C (p.Lys346Gln) | |
13 | g.46834966T>A | CA388150531 | HTR2A | c.1287A>T (p.Lys429Asn) c.798A>T (p.Lys266Asn) c.1035A>T (p.Lys345Asn) | |
13 | g.46834966T>C | CA6977510 | HTR2A | c.1287A>G (p.Lys429=) c.798A>G (p.Lys266=) c.1035A>G (p.Lys345=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.46834966T>G | CA388150529 | HTR2A | c.1287A>C (p.Lys429Asn) c.798A>C (p.Lys266Asn) c.1035A>C (p.Lys345Asn) | |
13 | g.46834966T= | CA2089283390 | HTR2A | c.1287A= (p.Lys429=) c.798A= (p.Lys266=) c.1035A= (p.Lys345=) | |
13 | g.46834967T>A | CA388150533 | HTR2A | c.1286A>T (p.Lys429Ile) c.797A>T (p.Lys266Ile) c.1034A>T (p.Lys345Ile) | |
13 | g.46834967T>C | CA388150535 | HTR2A | c.1286A>G (p.Lys429Arg) c.797A>G (p.Lys266Arg) c.1034A>G (p.Lys345Arg) | |
13 | g.46834967T>G | CA388150537 | HTR2A | c.1286A>C (p.Lys429Thr) c.797A>C (p.Lys266Thr) c.1034A>C (p.Lys345Thr) | |
13 | g.46834968T>A | CA388150539 | HTR2A | c.1285A>T (p.Lys429Ter) c.796A>T (p.Lys266Ter) c.1033A>T (p.Lys345Ter) | |
13 | g.46834968T>C | CA388150541 | HTR2A | c.1285A>G (p.Lys429Glu) c.796A>G (p.Lys266Glu) c.1033A>G (p.Lys345Glu) | |
13 | g.46834968T>G | CA388150542 | HTR2A | c.1285A>C (p.Lys429Gln) c.796A>C (p.Lys266Gln) c.1033A>C (p.Lys345Gln) | |
13 | g.46834969T>A | CA388150544 | HTR2A | c.1284A>T (p.Gln428His) c.795A>T (p.Gln265His) c.1032A>T (p.Gln344His) | |
13 | g.46834969T>C | CA483739188 | HTR2A | c.1284A>G (p.Gln428=) c.795A>G (p.Gln265=) c.1032A>G (p.Gln344=) | gnomAD v4 |
13 | g.46834969T>G | CA388150546 | HTR2A | c.1284A>C (p.Gln428His) c.795A>C (p.Gln265His) c.1032A>C (p.Gln344His) | |
13 | g.46834970T>A | CA388150548 | HTR2A | c.1283A>T (p.Gln428Leu) c.794A>T (p.Gln265Leu) c.1031A>T (p.Gln344Leu) | |
13 | g.46834970T>C | CA388150549 | HTR2A | c.1283A>G (p.Gln428Arg) c.794A>G (p.Gln265Arg) c.1031A>G (p.Gln344Arg) | |
13 | g.46834970T>G | CA388150551 | HTR2A | c.1283A>C (p.Gln428Pro) c.794A>C (p.Gln265Pro) c.1031A>C (p.Gln344Pro) | gnomAD v4 |
13 | g.46834971G>A | CA388150557 | HTR2A | c.1282C>T (p.Gln428Ter) c.793C>T (p.Gln265Ter) c.1030C>T (p.Gln344Ter) | |
13 | g.46834971G>C | CA388150553 | HTR2A | c.1282C>G (p.Gln428Glu) c.793C>G (p.Gln265Glu) c.1030C>G (p.Gln344Glu) | |
13 | g.46834971G>T | CA388150555 | HTR2A | c.1282C>A (p.Gln428Lys) c.793C>A (p.Gln265Lys) c.1030C>A (p.Gln344Lys) | |
13 | g.46834972T>A | CA483739192 | HTR2A | c.1281A>T (p.Gly427=) c.792A>T (p.Gly264=) c.1029A>T (p.Gly343=) | dbSNP gnomAD v3 gnomAD v4 |
13 | g.46834972T>C | CA483739193 | HTR2A | c.1281A>G (p.Gly427=) c.792A>G (p.Gly264=) c.1029A>G (p.Gly343=) | |
13 | g.46834972T>G | CA483739194 | HTR2A | c.1281A>C (p.Gly427=) c.792A>C (p.Gly264=) c.1029A>C (p.Gly343=) | |
13 | g.46834972T= | CA2089283391 | HTR2A | c.1281A= (p.Gly427=) c.792A= (p.Gly264=) c.1029A= (p.Gly343=) | |
13 | g.46834973C>A | CA388150558 | HTR2A | c.1280G>T (p.Gly427Val) c.791G>T (p.Gly264Val) c.1028G>T (p.Gly343Val) | |
13 | g.46834973C>G | CA388150559 | HTR2A | c.1280G>C (p.Gly427Ala) c.791G>C (p.Gly264Ala) c.1028G>C (p.Gly343Ala) | |
13 | g.46834973C>T | CA388150560 | HTR2A | c.1280G>A (p.Gly427Glu) c.791G>A (p.Gly264Glu) c.1028G>A (p.Gly343Glu) | |
13 | g.46834974C>A | CA388150562 | HTR2A | c.1279G>T (p.Gly427Ter) c.790G>T (p.Gly264Ter) c.1027G>T (p.Gly343Ter) | |
13 | g.46834974C>G | CA388150564 | HTR2A | c.1279G>C (p.Gly427Arg) c.790G>C (p.Gly264Arg) c.1027G>C (p.Gly343Arg) | |
13 | g.46834974C>T | CA388150566 | HTR2A | c.1279G>A (p.Gly427Arg) c.790G>A (p.Gly264Arg) c.1027G>A (p.Gly343Arg) | gnomAD v4 |
13 | g.46834975C>A | CA388150569 | HTR2A | c.1278G>T (p.Met426Ile) c.789G>T (p.Met263Ile) c.1026G>T (p.Met342Ile) | |
13 | g.46834975C>G | CA388150570 | HTR2A | c.1278G>C (p.Met426Ile) c.789G>C (p.Met263Ile) c.1026G>C (p.Met342Ile) | |
13 | g.46834975C>T | CA388150572 | HTR2A | c.1278G>A (p.Met426Ile) c.789G>A (p.Met263Ile) c.1026G>A (p.Met342Ile) | gnomAD v4 |