| 401753293 | CV2720702 | single nucleotide variant | NM_020369.3(FSCN3):c.11C>T (p.Thr4Ile) | not specified [RCV004328061] | uncertain significance | 7 | 127593864 | 127593864 | Human | | name |
| 407495626 | CV3443147 | single nucleotide variant | NM_020369.3(FSCN3):c.65G>A (p.Ser22Asn) | not specified [RCV004621639] | uncertain significance | 7 | 127593918 | 127593918 | Human | | name |
| 597769280 | CV3677403 | single nucleotide variant | NM_020369.3(FSCN3):c.64A>T (p.Ser22Cys) | not specified [RCV004928060] | uncertain significance | 7 | 127593917 | 127593917 | Human | | name |
| 156018741 | CV2272370 | single nucleotide variant | NM_020369.3(FSCN3):c.292C>T (p.Arg98Cys) | not specified [RCV004133296] | uncertain significance | 7 | 127595454 | 127595454 | Human | | name |
| 156107551 | CV2303993 | single nucleotide variant | NM_020369.3(FSCN3):c.197T>C (p.Leu66Pro) | not specified [RCV004170048] | uncertain significance | 7 | 127595359 | 127595359 | Human | | name |
| 156096061 | CV2399036 | single nucleotide variant | NM_020369.3(FSCN3):c.187G>A (p.Val63Met) | not specified [RCV004245338] | uncertain significance | 7 | 127595349 | 127595349 | Human | | name |
| 598231943 | CV3966511 | single nucleotide variant | NM_020369.3(FSCN3):c.269G>T (p.Ser90Ile) | not specified [RCV005342501] | uncertain significance | 7 | 127595431 | 127595431 | Human | | name |
| 156370131 | CV2204121 | single nucleotide variant | NM_020369.3(FSCN3):c.611G>A (p.Arg204Gln) | not specified [RCV004076931] | uncertain significance | 7 | 127595773 | 127595773 | Human | | name |
| 156332564 | CV2214460 | single nucleotide variant | NM_020369.3(FSCN3):c.806G>A (p.Arg269Lys) | not specified [RCV004088517] | likely benign | 7 | 127595968 | 127595968 | Human | | name |
| 156297984 | CV2240909 | single nucleotide variant | NM_020369.3(FSCN3):c.658C>T (p.Arg220Trp) | not specified [RCV004102193] | uncertain significance | 7 | 127595820 | 127595820 | Human | | name |
| 155925781 | CV2258620 | single nucleotide variant | NM_020369.3(FSCN3):c.404T>A (p.Met135Lys) | not specified [RCV004116092] | uncertain significance | 7 | 127595566 | 127595566 | Human | | name |
| 156368688 | CV2267057 | single nucleotide variant | NM_020369.3(FSCN3):c.398A>G (p.Tyr133Cys) | not specified [RCV004131690] | uncertain significance | 7 | 127595560 | 127595560 | Human | | name |
| 156168210 | CV2299367 | single nucleotide variant | NM_020369.3(FSCN3):c.554G>A (p.Arg185Gln) | not specified [RCV004152671] | likely benign | 7 | 127595716 | 127595716 | Human | | name |
| 155966297 | CV2304729 | single nucleotide variant | NM_020369.3(FSCN3):c.511G>A (p.Ala171Thr) | not specified [RCV004166884] | uncertain significance | 7 | 127595673 | 127595673 | Human | | name |
| 155996840 | CV2373119 | single nucleotide variant | NM_020369.3(FSCN3):c.301C>T (p.Arg101Trp) | not specified [RCV004217810] | uncertain significance | 7 | 127595463 | 127595463 | Human | | name |
| 156228272 | CV2388432 | single nucleotide variant | NM_020369.3(FSCN3):c.367G>A (p.Val123Met) | not specified [RCV004236924] | uncertain significance | 7 | 127595529 | 127595529 | Human | | name |
| 156048078 | CV2390985 | single nucleotide variant | NM_020369.3(FSCN3):c.460C>T (p.Arg154Cys) | not specified [RCV004234985] | uncertain significance | 7 | 127595622 | 127595622 | Human | | name |
| 156143738 | CV2393602 | single nucleotide variant | NM_020369.3(FSCN3):c.604G>A (p.Val202Ile) | not specified [RCV004231416] | uncertain significance | 7 | 127595766 | 127595766 | Human | | name |
| 329392355 | CV2441479 | single nucleotide variant | NM_020369.3(FSCN3):c.494G>A (p.Arg165His) | not specified [RCV004257274] | uncertain significance | 7 | 127595656 | 127595656 | Human | | name |
| 329396910 | CV2463630 | single nucleotide variant | NM_020369.3(FSCN3):c.508G>A (p.Ala170Thr) | not specified [RCV004277425] | uncertain significance | 7 | 127595670 | 127595670 | Human | | name |
| 401728079 | CV2685815 | single nucleotide variant | NM_020369.3(FSCN3):c.869G>A (p.Arg290His) | not specified [RCV004294804] | likely benign | 7 | 127596355 | 127596355 | Human | | name |
| 401769800 | CV2689952 | single nucleotide variant | NM_020369.3(FSCN3):c.529G>A (p.Glu177Lys) | not specified [RCV004297837] | uncertain significance | 7 | 127595691 | 127595691 | Human | | name |
| 401737502 | CV2699833 | single nucleotide variant | NM_020369.3(FSCN3):c.493C>T (p.Arg165Cys) | not specified [RCV004308478] | uncertain significance | 7 | 127595655 | 127595655 | Human | | name |
| 405782338 | CV3261240 | single nucleotide variant | NM_020369.3(FSCN3):c.493C>G (p.Arg165Gly) | not specified [RCV004386989] | uncertain significance | 7 | 127595655 | 127595655 | Human | | name |
| 405782345 | CV3261241 | single nucleotide variant | NM_020369.3(FSCN3):c.523C>G (p.Leu175Val) | not specified [RCV004386990] | uncertain significance | 7 | 127595685 | 127595685 | Human | | name |
| 405782351 | CV3261242 | single nucleotide variant | NM_020369.3(FSCN3):c.610C>T (p.Arg204Trp) | not specified [RCV004386991] | uncertain significance | 7 | 127595772 | 127595772 | Human | | name |
| 405782357 | CV3261243 | single nucleotide variant | NM_020369.3(FSCN3):c.686A>T (p.Asp229Val) | not specified [RCV004386992] | uncertain significance | 7 | 127595848 | 127595848 | Human | | name |
| 405782362 | CV3261244 | single nucleotide variant | NM_020369.3(FSCN3):c.783C>A (p.His261Gln) | not specified [RCV004386993] | uncertain significance | 7 | 127595945 | 127595945 | Human | | name |
| 405782368 | CV3261245 | single nucleotide variant | NM_020369.3(FSCN3):c.821G>A (p.Arg274Gln) | not specified [RCV004386994] | uncertain significance | 7 | 127595983 | 127595983 | Human | | name |
| 405782374 | CV3261246 | single nucleotide variant | NM_020369.3(FSCN3):c.965G>A (p.Arg322His) | not specified [RCV004386995] | uncertain significance | 7 | 127598439 | 127598439 | Human | | name |
| 597741888 | CV3677400 | single nucleotide variant | NM_020369.3(FSCN3):c.302G>A (p.Arg101Gln) | not specified [RCV004921768] | uncertain significance | 7 | 127595464 | 127595464 | Human | | name |
| 597769271 | CV3677401 | single nucleotide variant | NM_020369.3(FSCN3):c.397T>C (p.Tyr133His) | not specified [RCV004928058] | uncertain significance | 7 | 127595559 | 127595559 | Human | | name |
| 598231933 | CV3966509 | single nucleotide variant | NM_020369.3(FSCN3):c.856G>A (p.Ala286Thr) | not specified [RCV005342499] | uncertain significance | 7 | 127596342 | 127596342 | Human | | name |
| 598231937 | CV3966510 | single nucleotide variant | NM_020369.3(FSCN3):c.548A>G (p.His183Arg) | not specified [RCV005342500] | uncertain significance | 7 | 127595710 | 127595710 | Human | | name |
| 598231959 | CV3966514 | single nucleotide variant | NM_020369.3(FSCN3):c.746A>G (p.Asn249Ser) | not specified [RCV005342504] | likely benign | 7 | 127595908 | 127595908 | Human | | name |
| 151662632 | CV1330568 | single nucleotide variant | NM_020369.3(FSCN3):c.1154A>G (p.Asn385Ser) | Hypospadias [RCV001824105] | uncertain significance | 7 | 127599414 | 127599414 | Human | 2 | name |
| 156313426 | CV2196502 | single nucleotide variant | NM_020369.3(FSCN3):c.1000G>A (p.Glu334Lys) | not specified [RCV004073794] | uncertain significance | 7 | 127598474 | 127598474 | Human | | name |
| 156242596 | CV2210715 | single nucleotide variant | NM_020369.3(FSCN3):c.1388A>G (p.Asn463Ser) | not specified [RCV004083854] | uncertain significance | 7 | 127600290 | 127600290 | Human | | name |
| 156381449 | CV2215523 | single nucleotide variant | NM_020369.3(FSCN3):c.1240C>T (p.Pro414Ser) | not specified [RCV004089305] | uncertain significance | 7 | 127599500 | 127599500 | Human | | name |
| 156303588 | CV2331931 | single nucleotide variant | NM_020369.3(FSCN3):c.1268G>A (p.Arg423Gln) | not specified [RCV004599564] | uncertain significance | 7 | 127599528 | 127599528 | Human | | name |
| 401893715 | CV2765421 | single nucleotide variant | NM_020369.3(FSCN3):c.1060A>G (p.Arg354Gly) | not specified [RCV004341742] | uncertain significance | 7 | 127598534 | 127598534 | Human | | name |
| 405782298 | CV3261234 | single nucleotide variant | NM_020369.3(FSCN3):c.1023G>A (p.Met341Ile) | not specified [RCV004386983] | uncertain significance | 7 | 127598497 | 127598497 | Human | | name |
| 405782305 | CV3261235 | single nucleotide variant | NM_020369.3(FSCN3):c.1064G>T (p.Gly355Val) | not specified [RCV004386984] | uncertain significance | 7 | 127598538 | 127598538 | Human | | name |
| 405782310 | CV3261236 | single nucleotide variant | NM_020369.3(FSCN3):c.1067G>A (p.Arg356His) | not specified [RCV004386985] | uncertain significance | 7 | 127598541 | 127598541 | Human | | name |
| 405782319 | CV3261237 | single nucleotide variant | NM_020369.3(FSCN3):c.1137T>G (p.Phe379Leu) | not specified [RCV004386986] | uncertain significance | 7 | 127599397 | 127599397 | Human | | name |
| 405782326 | CV3261238 | single nucleotide variant | NM_020369.3(FSCN3):c.1159T>A (p.Ser387Thr) | not specified [RCV004386987] | uncertain significance | 7 | 127599419 | 127599419 | Human | | name |
| 405782335 | CV3261239 | single nucleotide variant | NM_020369.3(FSCN3):c.1336C>T (p.Arg446Cys) | not specified [RCV004386988] | uncertain significance | 7 | 127600238 | 127600238 | Human | | name |
| 407495622 | CV3443146 | single nucleotide variant | NM_020369.3(FSCN3):c.1283A>T (p.His428Leu) | not specified [RCV004621638] | uncertain significance | 7 | 127599543 | 127599543 | Human | | name |
| 597769267 | CV3677399 | single nucleotide variant | NM_020369.3(FSCN3):c.1075G>A (p.Gly359Ser) | not specified [RCV004928057] | uncertain significance | 7 | 127598549 | 127598549 | Human | | name |
| 597769275 | CV3677402 | single nucleotide variant | NM_020369.3(FSCN3):c.1397C>T (p.Thr466Ile) | not specified [RCV004928059] | uncertain significance | 7 | 127600299 | 127600299 | Human | | name |
| 598231949 | CV3966512 | single nucleotide variant | NM_020369.3(FSCN3):c.1156C>T (p.Arg386Cys) | not specified [RCV005342502] | uncertain significance | 7 | 127599416 | 127599416 | Human | | name |
