| 156187603 | CV2318905 | single nucleotide variant | NM_000862.3(HSD3B1):c.26C>G (p.Thr9Arg) | not specified [RCV004175803] | uncertain significance | 1 | 119507502 | 119507502 | Human | | name |
| 598205611 | CV3968167 | single nucleotide variant | NM_000862.3(HSD3B1):c.20T>C (p.Leu7Pro) | not specified [RCV005337635] | uncertain significance | 1 | 119507496 | 119507496 | Human | | name |
| 14396225 | CV611973 | single nucleotide variant | NM_000862.3(HSD3B1):c.1100= (p.Thr367=) | Androgen deprivation therapy response [RCV000760965] | drug response | 1 | 119514623 | 119514623 | Human | | name |
| 156179192 | CV2287987 | single nucleotide variant | NM_000862.3(HSD3B1):c.98G>C (p.Arg33Thr) | not specified [RCV004147757] | uncertain significance | 1 | 119507574 | 119507574 | Human | | name |
| 329392661 | CV2471467 | single nucleotide variant | NM_000862.3(HSD3B1):c.38G>T (p.Gly13Val) | not specified [RCV004280465] | uncertain significance | 1 | 119507514 | 119507514 | Human | | name |
| 405803583 | CV3274215 | single nucleotide variant | NM_000862.3(HSD3B1):c.61C>T (p.Arg21Cys) | not specified [RCV004404522] | uncertain significance | 1 | 119507537 | 119507537 | Human | | name |
| 405803584 | CV3274216 | single nucleotide variant | NM_000862.3(HSD3B1):c.62G>A (p.Arg21His) | not specified [RCV004404523] | uncertain significance | 1 | 119507538 | 119507538 | Human | | name |
| 598255759 | CV3968169 | single nucleotide variant | NM_000862.3(HSD3B1):c.71T>C (p.Val24Ala) | not specified [RCV005346627] | uncertain significance | 1 | 119507547 | 119507547 | Human | | name |
| 150506382 | CV1213766 | single nucleotide variant | NM_000862.3(HSD3B1):c.235A>G (p.Ile79Val) | not provided [RCV001596023] | benign | 1 | 119511592 | 119511592 | Human | | name |
| 155972939 | CV2334384 | single nucleotide variant | NM_000862.3(HSD3B1):c.247G>A (p.Ala83Thr) | not specified [RCV004188360] | uncertain significance | 1 | 119511604 | 119511604 | Human | | name |
| 156200449 | CV2338191 | single nucleotide variant | NM_000862.3(HSD3B1):c.111G>C (p.Lys37Asn) | not specified [RCV004186261] | uncertain significance | 1 | 119507587 | 119507587 | Human | | name |
| 155922727 | CV2347370 | single nucleotide variant | NM_000862.3(HSD3B1):c.232G>T (p.Val78Phe) | not specified [RCV004207210] | uncertain significance | 1 | 119511589 | 119511589 | Human | | name |
| 401739253 | CV2676466 | single nucleotide variant | NM_000862.3(HSD3B1):c.210G>C (p.Lys70Asn) | not specified [RCV004286480] | uncertain significance | 1 | 119511567 | 119511567 | Human | | name |
| 401877606 | CV2761220 | single nucleotide variant | NM_000862.3(HSD3B1):c.226G>A (p.Val76Ile) | not specified [RCV004341098] | likely benign | 1 | 119511583 | 119511583 | Human | | name |
| 405803579 | CV3274213 | single nucleotide variant | NM_000862.3(HSD3B1):c.279C>G (p.His93Gln) | not specified [RCV004404520] | uncertain significance | 1 | 119511636 | 119511636 | Human | | name |
| 596947051 | CV3547113 | single nucleotide variant | NM_000862.3(HSD3B1):c.212G>T (p.Arg71Ile) | not provided [RCV004810920] | likely benign | 1 | 119511569 | 119511569 | Human | | name |
| 597774119 | CV3689701 | single nucleotide variant | NM_000862.3(HSD3B1):c.181G>C (p.Gly61Arg) | not specified [RCV004929033] | uncertain significance | 1 | 119511538 | 119511538 | Human | | name |
| 9589491 | CV166203 | single nucleotide variant | NM_000862.3(HSD3B1):c.712A>T (p.Arg238Trp) | not provided [RCV000144493] | not provided | 1 | 119514235 | 119514235 | Human | | name |
| 155923147 | CV2217563 | single nucleotide variant | NM_000862.3(HSD3B1):c.835C>T (p.Arg279Cys) | not specified [RCV004090095] | likely benign | 1 | 119514358 | 119514358 | Human | | name |
| 156224164 | CV2219289 | single nucleotide variant | NM_000862.3(HSD3B1):c.829G>T (p.Gly277Cys) | not specified [RCV004095159] | uncertain significance | 1 | 119514352 | 119514352 | Human | | name |
| 155918077 | CV2236732 | single nucleotide variant | NM_000862.3(HSD3B1):c.822A>C (p.Lys274Asn) | not specified [RCV004110686] | uncertain significance | 1 | 119514345 | 119514345 | Human | | name |
| 156121872 | CV2240975 | single nucleotide variant | NM_000862.3(HSD3B1):c.719T>A (p.Leu240Gln) | not specified [RCV004102248] | uncertain significance | 1 | 119514242 | 119514242 | Human | | name |
| 155971130 | CV2262307 | single nucleotide variant | NM_000862.3(HSD3B1):c.742A>G (p.Ser248Gly) | not specified [RCV004128504] | uncertain significance | 1 | 119514265 | 119514265 | Human | | name |
| 155950862 | CV2302099 | single nucleotide variant | NM_000862.3(HSD3B1):c.949C>A (p.Arg317Ser) | not specified [RCV004158855] | uncertain significance | 1 | 119514472 | 119514472 | Human | | name |
| 156252874 | CV2311410 | single nucleotide variant | NM_000862.3(HSD3B1):c.665A>G (p.Asn222Ser) | not specified [RCV004168259] | uncertain significance | 1 | 119514188 | 119514188 | Human | | name |
| 156305484 | CV2314641 | single nucleotide variant | NM_000862.3(HSD3B1):c.529G>A (p.Gly177Ser) | not specified [RCV004169010] | uncertain significance | 1 | 119514052 | 119514052 | Human | | name |
| 156083541 | CV2330696 | single nucleotide variant | NM_000862.3(HSD3B1):c.674A>G (p.Tyr225Cys) | not specified [RCV004185765] | uncertain significance | 1 | 119514197 | 119514197 | Human | | name |
| 156386304 | CV2364713 | single nucleotide variant | NM_000862.3(HSD3B1):c.736G>T (p.Ala246Ser) | not specified [RCV004219594] | uncertain significance | 1 | 119514259 | 119514259 | Human | | name |
| 156002553 | CV2396593 | single nucleotide variant | NM_000862.3(HSD3B1):c.436C>T (p.Pro146Ser) | not specified [RCV004240422] | uncertain significance | 1 | 119513959 | 119513959 | Human | | name |
| 329402626 | CV2451184 | single nucleotide variant | NM_000862.3(HSD3B1):c.784C>T (p.His262Tyr) | not specified [RCV004270106] | uncertain significance | 1 | 119514307 | 119514307 | Human | | name |
| 401731044 | CV2707672 | single nucleotide variant | NM_000862.3(HSD3B1):c.854G>A (p.Ser285Asn) | not specified [RCV004306932] | uncertain significance | 1 | 119514377 | 119514377 | Human | | name |
| 401862955 | CV2755734 | single nucleotide variant | NM_000862.3(HSD3B1):c.503C>T (p.Ala168Val) | not specified [RCV004342114] | uncertain significance | 1 | 119514026 | 119514026 | Human | | name |
| 401857107 | CV2759973 | single nucleotide variant | NM_000862.3(HSD3B1):c.737C>T (p.Ala246Val) | not specified [RCV004345391] | uncertain significance | 1 | 119514260 | 119514260 | Human | | name |
| 401894234 | CV2770418 | single nucleotide variant | NM_000862.3(HSD3B1):c.855C>A (p.Ser285Arg) | not specified [RCV004358063] | uncertain significance | 1 | 119514378 | 119514378 | Human | | name |
| 405803581 | CV3274214 | single nucleotide variant | NM_000862.3(HSD3B1):c.388G>A (p.Gly130Arg) | not specified [RCV004404521] | uncertain significance | 1 | 119513911 | 119513911 | Human | | name |
| 405803586 | CV3274217 | single nucleotide variant | NM_000862.3(HSD3B1):c.749G>A (p.Arg250Gln) | not specified [RCV004404524] | likely benign | 1 | 119514272 | 119514272 | Human | | name |
| 405803590 | CV3274219 | single nucleotide variant | NM_000862.3(HSD3B1):c.935G>A (p.Arg312Gln) | not specified [RCV004404526] | likely benign | 1 | 119514458 | 119514458 | Human | | name |
| 407510867 | CV3444050 | single nucleotide variant | NM_000862.3(HSD3B1):c.304G>A (p.Val102Met) | not specified [RCV004626273] | uncertain significance | 1 | 119511661 | 119511661 | Human | | name |
| 407464820 | CV3444051 | single nucleotide variant | NM_000862.3(HSD3B1):c.532G>A (p.Gly178Ser) | not specified [RCV004635176] | uncertain significance | 1 | 119514055 | 119514055 | Human | | name |
| 407464829 | CV3444053 | single nucleotide variant | NM_000862.3(HSD3B1):c.377T>C (p.Ile126Thr) | not specified [RCV004635178] | uncertain significance | 1 | 119513900 | 119513900 | Human | | name |
| 407464833 | CV3444054 | single nucleotide variant | NM_000862.3(HSD3B1):c.791G>A (p.Ser264Asn) | not specified [RCV004635179] | uncertain significance | 1 | 119514314 | 119514314 | Human | | name |
| 407464836 | CV3444055 | single nucleotide variant | NM_000862.3(HSD3B1):c.382G>A (p.Val128Ile) | not specified [RCV004635180] | uncertain significance | 1 | 119513905 | 119513905 | Human | | name |
| 597774107 | CV3689698 | single nucleotide variant | NM_000862.3(HSD3B1):c.496G>A (p.Val166Ile) | not specified [RCV004929030] | uncertain significance | 1 | 119514019 | 119514019 | Human | | name |
| 597774111 | CV3689699 | single nucleotide variant | NM_000862.3(HSD3B1):c.949C>T (p.Arg317Cys) | not specified [RCV004929031] | uncertain significance | 1 | 119514472 | 119514472 | Human | | name |
| 597774115 | CV3689700 | single nucleotide variant | NM_000862.3(HSD3B1):c.334T>A (p.Cys112Ser) | not specified [RCV004929032] | uncertain significance | 1 | 119513857 | 119513857 | Human | | name |
| 597774123 | CV3689702 | single nucleotide variant | NM_000862.3(HSD3B1):c.359T>C (p.Phe120Ser) | not specified [RCV004929034] | uncertain significance | 1 | 119513882 | 119513882 | Human | | name |
| 597774130 | CV3689703 | single nucleotide variant | NM_000862.3(HSD3B1):c.731A>G (p.Lys244Arg) | not specified [RCV004929035] | uncertain significance | 1 | 119514254 | 119514254 | Human | | name |
| 598255749 | CV3968165 | single nucleotide variant | NM_000862.3(HSD3B1):c.911T>C (p.Leu304Pro) | not specified [RCV005346625] | uncertain significance | 1 | 119514434 | 119514434 | Human | | name |
| 598255754 | CV3968166 | single nucleotide variant | NM_000862.3(HSD3B1):c.779C>T (p.Thr260Met) | not specified [RCV005346626] | uncertain significance | 1 | 119514302 | 119514302 | Human | | name |
| 598205618 | CV3968168 | single nucleotide variant | NM_000862.3(HSD3B1):c.563T>C (p.Met188Thr) | not specified [RCV005337636] | likely benign | 1 | 119514086 | 119514086 | Human | | name |
| 598205624 | CV3968170 | single nucleotide variant | NM_000862.3(HSD3B1):c.878G>T (p.Trp293Leu) | not specified [RCV005337637] | uncertain significance | 1 | 119514401 | 119514401 | Human | | name |
| 150475201 | CV1263469 | single nucleotide variant | NM_000862.3(HSD3B1):c.1100C>A (p.Thr367Asn) | Androgen deprivation therapy response [RCV004699172]|not provided [RCV001684992] | benign|drug response | 1 | 119514623 | 119514623 | Human | | name |
| 156230572 | CV2227525 | single nucleotide variant | NM_000862.3(HSD3B1):c.1040A>G (p.Glu347Gly) | not specified [RCV004092175] | uncertain significance | 1 | 119514563 | 119514563 | Human | | name |
| 405803573 | CV3274210 | single nucleotide variant | NM_000862.3(HSD3B1):c.1043A>G (p.Glu348Gly) | not specified [RCV004404517] | uncertain significance | 1 | 119514566 | 119514566 | Human | | name |
| 405803575 | CV3274211 | single nucleotide variant | NM_000862.3(HSD3B1):c.1113G>T (p.Lys371Asn) | not specified [RCV004404518] | uncertain significance | 1 | 119514636 | 119514636 | Human | | name |
| 407464823 | CV3444052 | single nucleotide variant | NM_000862.3(HSD3B1):c.1087C>T (p.Arg363Trp) | not specified [RCV004635177] | uncertain significance | 1 | 119514610 | 119514610 | Human | | name |
