| 8602506 | CV40333 | deletion | NM_000524.4(HTR1A):c.-480del | Menstrual cycle-dependent periodic fever [RCV000024351]|not provided [RCV003430640]|not specified [RCV002247394] | pathogenic|likely benign|uncertain significance | 5 | 63962199 | 63962199 | Human | 1 | name |
| 12791673 | CV362497 | single nucleotide variant | NM_000524.3(HTR1A):c.-1019G>C | not specified [RCV000603722] | likely benign|drug response | 5 | 63962738 | 63962738 | Human | | name |
| 15168347 | CV721498 | single nucleotide variant | NM_000524.4(HTR1A):c.96C>G (p.Thr32=) | not provided [RCV000883045] | likely benign | 5 | 63961624 | 63961624 | Human | | name |
| 152156684 | CV1668671 | single nucleotide variant | NM_000524.4(HTR1A):c.390C>A (p.Ile130=) | not specified [RCV002222897] | likely benign | 5 | 63961330 | 63961330 | Human | | name |
| 156253778 | CV2193141 | single nucleotide variant | NM_000524.4(HTR1A):c.32A>C (p.Asn11Thr) | not specified [RCV004071141] | uncertain significance | 5 | 63961688 | 63961688 | Human | | name |
| 401917702 | CV2827788 | single nucleotide variant | NM_000524.4(HTR1A):c.858T>C (p.Asp286=) | not provided [RCV003429654] | likely benign | 5 | 63960862 | 63960862 | Human | | name |
| 405283154 | CV3218457 | single nucleotide variant | NM_000524.4(HTR1A):c.975T>C (p.Asn325=) | HTR1A-related disorder [RCV003957255] | likely benign | 5 | 63960745 | 63960745 | Human | | name , trait , alternate_id |
| 15177578 | CV699136 | single nucleotide variant | NM_000524.4(HTR1A):c.82A>G (p.Ile28Val) | not provided [RCV000951076] | benign | 5 | 63961638 | 63961638 | Human | | name |
| 15181405 | CV721497 | single nucleotide variant | NM_000524.4(HTR1A):c.465G>T (p.Ala155=) | not provided [RCV000885761] | likely benign | 5 | 63961255 | 63961255 | Human | | name |
| 15179590 | CV721499 | single nucleotide variant | NM_000524.4(HTR1A):c.47C>T (p.Pro16Leu) | not provided [RCV000885325] | benign | 5 | 63961673 | 63961673 | Human | | name |
| 15149289 | CV749549 | single nucleotide variant | NM_000524.4(HTR1A):c.423C>T (p.Pro141=) | not provided [RCV000923259] | benign | 5 | 63961297 | 63961297 | Human | | name |
| 15131635 | CV782322 | single nucleotide variant | NM_000524.4(HTR1A):c.861C>T (p.Gly287=) | not provided [RCV000981244] | likely benign | 5 | 63960859 | 63960859 | Human | | name |
| 126910079 | CV1037643 | single nucleotide variant | NM_000524.4(HTR1A):c.275T>C (p.Met92Thr) | not provided [RCV001354346]|not specified [RCV005419100] | uncertain significance | 5 | 63961445 | 63961445 | Human | | name |
| 155952006 | CV2238887 | single nucleotide variant | NM_000524.4(HTR1A):c.295C>T (p.Leu99Phe) | not specified [RCV004109796] | uncertain significance | 5 | 63961425 | 63961425 | Human | | name |
| 401917701 | CV2827787 | single nucleotide variant | NM_000524.4(HTR1A):c.1002G>A (p.Lys334=) | not provided [RCV003429653] | likely benign | 5 | 63960718 | 63960718 | Human | | name |
| 405804157 | CV3270579 | single nucleotide variant | NM_000524.4(HTR1A):c.109G>A (p.Val37Met) | not specified [RCV004404828] | uncertain significance | 5 | 63961611 | 63961611 | Human | | name |
| 405804159 | CV3270580 | single nucleotide variant | NM_000524.4(HTR1A):c.215A>G (p.Asn72Ser) | not specified [RCV004404829] | uncertain significance | 5 | 63961505 | 63961505 | Human | | name |
| 407465197 | CV3444199 | single nucleotide variant | NM_000524.4(HTR1A):c.184G>T (p.Ala62Ser) | not specified [RCV004635302] | uncertain significance | 5 | 63961536 | 63961536 | Human | | name |
| 597782975 | CV3686121 | single nucleotide variant | NM_000524.4(HTR1A):c.104A>T (p.Tyr35Phe) | not specified [RCV004931298] | uncertain significance | 5 | 63961616 | 63961616 | Human | | name |
| 598256418 | CV3968378 | single nucleotide variant | NM_000524.4(HTR1A):c.225T>G (p.Ile75Met) | not specified [RCV005346788] | uncertain significance | 5 | 63961495 | 63961495 | Human | | name |
| 150528652 | CV1306014 | single nucleotide variant | NM_000524.4(HTR1A):c.659G>T (p.Arg220Leu) | not provided [RCV001755417] | benign|likely benign | 5 | 63961061 | 63961061 | Human | | name |
| 156223299 | CV2209204 | single nucleotide variant | NM_000524.4(HTR1A):c.748C>T (p.Pro250Ser) | not specified [RCV004093401] | uncertain significance | 5 | 63960972 | 63960972 | Human | | name |
| 156118535 | CV2228691 | single nucleotide variant | NM_000524.4(HTR1A):c.674G>A (p.Arg225His) | not specified [RCV004093176] | uncertain significance | 5 | 63961046 | 63961046 | Human | | name |
| 156360406 | CV2269032 | single nucleotide variant | NM_000524.4(HTR1A):c.955G>A (p.Ala319Thr) | not specified [RCV004128428] | uncertain significance | 5 | 63960765 | 63960765 | Human | | name |
| 156090620 | CV2302583 | single nucleotide variant | NM_000524.4(HTR1A):c.416C>T (p.Thr139Met) | not specified [RCV004160750] | uncertain significance | 5 | 63961304 | 63961304 | Human | | name |
| 401778881 | CV2732952 | single nucleotide variant | NM_000524.4(HTR1A):c.902C>T (p.Ser301Phe) | not specified [RCV004331129] | uncertain significance | 5 | 63960818 | 63960818 | Human | | name |
| 401888313 | CV2788304 | single nucleotide variant | NM_000524.4(HTR1A):c.753G>C (p.Lys251Asn) | not specified [RCV004352889] | uncertain significance | 5 | 63960967 | 63960967 | Human | | name |
| 401914917 | CV2827789 | single nucleotide variant | NM_000524.4(HTR1A):c.709G>A (p.Gly237Arg) | Menstrual cycle-dependent periodic fever [RCV005399389]|not provided [RCV003428527] | likely benign|uncertain significance | 5 | 63961011 | 63961011 | Human | 1 | name |
| 405260051 | CV3186534 | duplication | NM_000524.4(HTR1A):c.1015dup (p.Arg339fs) | not provided [RCV003884293] | uncertain significance | 5 | 63960704 | 63960705 | Human | | name |
| 405804161 | CV3270581 | single nucleotide variant | NM_000524.4(HTR1A):c.737C>A (p.Pro246His) | not specified [RCV004404830] | uncertain significance | 5 | 63960983 | 63960983 | Human | | name |
| 405804163 | CV3270582 | single nucleotide variant | NM_000524.4(HTR1A):c.779G>A (p.Ser260Asn) | not specified [RCV004404831] | uncertain significance | 5 | 63960941 | 63960941 | Human | | name |
| 405804164 | CV3270583 | single nucleotide variant | NM_000524.4(HTR1A):c.855C>G (p.Asp285Glu) | not specified [RCV004404832] | likely benign | 5 | 63960865 | 63960865 | Human | | name |
| 405804166 | CV3270584 | single nucleotide variant | NM_000524.4(HTR1A):c.889C>G (p.Arg297Gly) | not specified [RCV004404833] | uncertain significance | 5 | 63960831 | 63960831 | Human | | name |
| 407510925 | CV3444197 | single nucleotide variant | NM_000524.4(HTR1A):c.928G>A (p.Glu310Lys) | not specified [RCV004626294] | uncertain significance | 5 | 63960792 | 63960792 | Human | | name |
| 407465632 | CV3444200 | single nucleotide variant | NM_000524.4(HTR1A):c.730G>A (p.Ala244Thr) | not specified [RCV004635303] | likely benign | 5 | 63960990 | 63960990 | Human | | name |
| 597782979 | CV3686122 | single nucleotide variant | NM_000524.4(HTR1A):c.340G>A (p.Ala114Thr) | not specified [RCV004931299] | uncertain significance | 5 | 63961380 | 63961380 | Human | | name |
| 598122103 | CV3884191 | single nucleotide variant | NM_000524.4(HTR1A):c.667C>T (p.Arg223Cys) | not specified [RCV005236881] | uncertain significance | 5 | 63961053 | 63961053 | Human | | name |
| 598256408 | CV3968374 | single nucleotide variant | NM_000524.4(HTR1A):c.898A>G (p.Asn300Asp) | not specified [RCV005346785] | uncertain significance | 5 | 63960822 | 63960822 | Human | | name |
| 598256412 | CV3968375 | single nucleotide variant | NM_000524.4(HTR1A):c.311T>C (p.Leu104Pro) | not specified [RCV005346786] | uncertain significance | 5 | 63961409 | 63961409 | Human | | name |
| 598256416 | CV3968376 | single nucleotide variant | NM_000524.4(HTR1A):c.673C>A (p.Arg225Ser) | not specified [RCV005346787] | uncertain significance | 5 | 63961047 | 63961047 | Human | | name |
| 598205911 | CV3968377 | single nucleotide variant | NM_000524.4(HTR1A):c.439A>G (p.Lys147Glu) | not specified [RCV005337685] | uncertain significance | 5 | 63961281 | 63961281 | Human | | name |
| 15110207 | CV709965 | single nucleotide variant | NM_000524.4(HTR1A):c.818G>A (p.Gly273Asp) | not provided [RCV000960854] | benign | 5 | 63960902 | 63960902 | Human | | name |
| 15122079 | CV709966 | single nucleotide variant | NM_000524.4(HTR1A):c.464C>G (p.Ala155Gly) | HTR1A-related disorder [RCV003943124]|not provided [RCV000963012] | likely benign | 5 | 63961256 | 63961256 | Human | 1 | name , trait , alternate_id |
| 15140639 | CV735150 | single nucleotide variant | NM_000524.4(HTR1A):c.545C>T (p.Ser182Leu) | not provided [RCV000899353] | benign|likely benign | 5 | 63961175 | 63961175 | Human | | name |
| 153349713 | CV1693869 | single nucleotide variant | NM_000524.4(HTR1A):c.1000A>C (p.Lys334Gln) | not provided [RCV002276130] | likely benign | 5 | 63960720 | 63960720 | Human | | name |
| 407510928 | CV3444198 | single nucleotide variant | NM_000524.4(HTR1A):c.1022G>A (p.Arg341Lys) | not specified [RCV004626295] | uncertain significance | 5 | 63960698 | 63960698 | Human | | name |
| 598256404 | CV3968373 | single nucleotide variant | NM_000524.4(HTR1A):c.1247A>T (p.Lys416Met) | not specified [RCV005346784] | uncertain significance | 5 | 63960473 | 63960473 | Human | | name |
| 243062488 | CV2404934 | deletion | NM_000524.4(HTR1A):c.980_1039del (p.Arg327_Thr346del) | Menstrual cycle-dependent periodic fever [RCV003225791] | uncertain significance | 5 | 63960681 | 63960740 | Human | 1 | name |
