| 156000312 | CV2296296 | single nucleotide variant | NM_024622.6(FASTKD1):c.13C>A (p.Pro5Thr) | not specified [RCV004154197] | uncertain significance | 2 | 169572017 | 169572017 | Human | | name |
| 405763492 | CV3253170 | single nucleotide variant | NM_024622.6(FASTKD1):c.21C>A (p.Phe7Leu) | not specified [RCV004383886] | uncertain significance | 2 | 169572009 | 169572009 | Human | | name |
| 401775992 | CV2706842 | single nucleotide variant | NM_024622.6(FASTKD1):c.61A>G (p.Ile21Val) | not specified [RCV004321474] | uncertain significance | 2 | 169571969 | 169571969 | Human | | name |
| 405763508 | CV3253173 | single nucleotide variant | NM_024622.6(FASTKD1):c.49C>T (p.Arg17Cys) | not specified [RCV004383889] | uncertain significance | 2 | 169571981 | 169571981 | Human | | name |
| 156179066 | CV2287975 | single nucleotide variant | NM_024622.6(FASTKD1):c.187C>T (p.Leu63Phe) | not specified [RCV004147747] | uncertain significance | 2 | 169571843 | 169571843 | Human | | name |
| 156195695 | CV2367160 | single nucleotide variant | NM_024622.6(FASTKD1):c.247A>C (p.Thr83Pro) | not specified [RCV004215594] | uncertain significance | 2 | 169571783 | 169571783 | Human | | name |
| 156137456 | CV2375759 | single nucleotide variant | NM_024622.6(FASTKD1):c.272A>G (p.Tyr91Cys) | not specified [RCV004224350] | likely benign | 2 | 169571758 | 169571758 | Human | | name |
| 329397450 | CV2456180 | single nucleotide variant | NM_024622.6(FASTKD1):c.202G>A (p.Val68Met) | not specified [RCV004273370] | uncertain significance | 2 | 169571828 | 169571828 | Human | | name |
| 405763480 | CV3253168 | single nucleotide variant | NM_024622.6(FASTKD1):c.182C>G (p.Ala61Gly) | not specified [RCV004383884] | uncertain significance | 2 | 169571848 | 169571848 | Human | | name |
| 405763486 | CV3253169 | single nucleotide variant | NM_024622.6(FASTKD1):c.190T>G (p.Ser64Ala) | not specified [RCV004383885] | uncertain significance | 2 | 169571840 | 169571840 | Human | | name |
| 597695757 | CV3672182 | single nucleotide variant | NM_024622.6(FASTKD1):c.163T>G (p.Phe55Val) | not specified [RCV004915801] | uncertain significance | 2 | 169571867 | 169571867 | Human | | name |
| 598213320 | CV3966156 | single nucleotide variant | NM_024622.6(FASTKD1):c.268G>A (p.Glu90Lys) | not specified [RCV005339241] | uncertain significance | 2 | 169571762 | 169571762 | Human | | name |
| 156287779 | CV2229669 | single nucleotide variant | NM_024622.6(FASTKD1):c.721G>T (p.Val241Phe) | not specified [RCV004103478] | uncertain significance | 2 | 169560637 | 169560637 | Human | | name |
| 156206727 | CV2249979 | single nucleotide variant | NM_024622.6(FASTKD1):c.422C>T (p.Thr141Ile) | not specified [RCV004122946] | uncertain significance | 2 | 169569208 | 169569208 | Human | | name |
| 156063604 | CV2272368 | single nucleotide variant | NM_024622.6(FASTKD1):c.314C>G (p.Ala105Gly) | not specified [RCV004133294] | uncertain significance | 2 | 169571716 | 169571716 | Human | | name |
| 155953770 | CV2274244 | single nucleotide variant | NM_024622.6(FASTKD1):c.554A>C (p.Glu185Ala) | not specified [RCV004136647] | uncertain significance | 2 | 169563243 | 169563243 | Human | | name |
| 155980464 | CV2343509 | single nucleotide variant | NM_024622.6(FASTKD1):c.815T>A (p.Leu272His) | not specified [RCV004197576] | uncertain significance | 2 | 169560543 | 169560543 | Human | | name |
| 329402307 | CV2454125 | single nucleotide variant | NM_024622.6(FASTKD1):c.962A>G (p.Glu321Gly) | not specified [RCV004265622] | uncertain significance | 2 | 169560396 | 169560396 | Human | | name |
| 401874489 | CV2759234 | single nucleotide variant | NM_024622.6(FASTKD1):c.598A>G (p.Ile200Val) | not specified [RCV004335832] | uncertain significance | 2 | 169560760 | 169560760 | Human | | name |
| 405763520 | CV3253175 | single nucleotide variant | NM_024622.6(FASTKD1):c.605C>T (p.Ser202Phe) | not specified [RCV004383891] | uncertain significance | 2 | 169560753 | 169560753 | Human | | name |
| 405763527 | CV3253176 | single nucleotide variant | NM_024622.6(FASTKD1):c.667A>G (p.Ile223Val) | not specified [RCV004383892] | uncertain significance | 2 | 169560691 | 169560691 | Human | | name |
| 598213302 | CV3966153 | single nucleotide variant | NM_024622.6(FASTKD1):c.601T>C (p.Ser201Pro) | not specified [RCV005339238] | uncertain significance | 2 | 169560757 | 169560757 | Human | | name |
| 598213310 | CV3966154 | single nucleotide variant | NM_024622.6(FASTKD1):c.731G>T (p.Arg244Leu) | not specified [RCV005339239] | uncertain significance | 2 | 169560627 | 169560627 | Human | | name |
| 598213315 | CV3966155 | single nucleotide variant | NM_024622.6(FASTKD1):c.907C>G (p.Pro303Ala) | not specified [RCV005339240] | uncertain significance | 2 | 169560451 | 169560451 | Human | | name |
| 15153705 | CV719405 | duplication | NM_024622.6(FASTKD1):c.2406dup (p.Arg803fs) | not provided [RCV000880064] | benign | 2 | 169530622 | 169530623 | Human | | name |
| 156083682 | CV2244496 | single nucleotide variant | NM_024622.6(FASTKD1):c.1791C>G (p.Cys597Trp) | not specified [RCV004100453] | uncertain significance | 2 | 169544746 | 169544746 | Human | | name |
| 156100008 | CV2294679 | single nucleotide variant | NM_024622.6(FASTKD1):c.2342T>G (p.Phe781Cys) | not specified [RCV004161926] | uncertain significance | 2 | 169530687 | 169530687 | Human | | name |
| 155943463 | CV2298585 | single nucleotide variant | NM_024622.6(FASTKD1):c.1024C>G (p.Leu342Val) | not specified [RCV004162233] | uncertain significance | 2 | 169557245 | 169557245 | Human | | name |
| 156151918 | CV2318849 | single nucleotide variant | NM_024622.6(FASTKD1):c.2494A>G (p.Met832Val) | not specified [RCV004175758] | uncertain significance | 2 | 169529875 | 169529875 | Human | | name |
| 155972500 | CV2335807 | single nucleotide variant | NM_024622.6(FASTKD1):c.1015G>A (p.Glu339Lys) | not specified [RCV004193996] | uncertain significance | 2 | 169557254 | 169557254 | Human | | name |
| 156123254 | CV2350006 | single nucleotide variant | NM_024622.6(FASTKD1):c.1958C>T (p.Ser653Phe) | not specified [RCV004199932] | uncertain significance | 2 | 169538129 | 169538129 | Human | | name |
| 155989871 | CV2352288 | single nucleotide variant | NM_024622.6(FASTKD1):c.2168C>T (p.Thr723Met) | not specified [RCV004200763] | uncertain significance | 2 | 169537247 | 169537247 | Human | | name |
| 156122443 | CV2354330 | single nucleotide variant | NM_024622.6(FASTKD1):c.2249C>T (p.Ala750Val) | not specified [RCV004206747] | uncertain significance | 2 | 169531430 | 169531430 | Human | | name |
| 156172491 | CV2355083 | single nucleotide variant | NM_024622.6(FASTKD1):c.2228C>T (p.Pro743Leu) | not specified [RCV004198477] | uncertain significance | 2 | 169531451 | 169531451 | Human | | name |
| 155937965 | CV2373913 | single nucleotide variant | NM_024622.6(FASTKD1):c.1178A>C (p.Lys393Thr) | not specified [RCV004224844] | uncertain significance | 2 | 169555160 | 169555160 | Human | | name |
| 156039580 | CV2384277 | single nucleotide variant | NM_024622.6(FASTKD1):c.1590T>A (p.Asp530Glu) | not specified [RCV004227664] | likely benign | 2 | 169546329 | 169546329 | Human | | name |
| 155907865 | CV2387139 | single nucleotide variant | NM_024622.6(FASTKD1):c.2096C>T (p.Thr699Ile) | not specified [RCV004238248] | uncertain significance | 2 | 169537319 | 169537319 | Human | | name |
| 329370910 | CV2431807 | single nucleotide variant | NM_024622.6(FASTKD1):c.2089G>A (p.Asp697Asn) | not specified [RCV004254954] | likely benign | 2 | 169537326 | 169537326 | Human | | name |
| 329361027 | CV2436603 | single nucleotide variant | NM_024622.6(FASTKD1):c.1262G>A (p.Arg421His) | not specified [RCV004257983] | uncertain significance | 2 | 169546657 | 169546657 | Human | | name |
| 329392978 | CV2449418 | single nucleotide variant | NM_024622.6(FASTKD1):c.1730T>C (p.Ile577Thr) | not specified [RCV004266578] | uncertain significance | 2 | 169544807 | 169544807 | Human | | name |
| 401743257 | CV2674616 | single nucleotide variant | NM_024622.6(FASTKD1):c.2240A>G (p.His747Arg) | not specified [RCV004293920] | uncertain significance | 2 | 169531439 | 169531439 | Human | | name |
| 401772189 | CV2708190 | single nucleotide variant | NM_024622.6(FASTKD1):c.1502G>A (p.Arg501Gln) | not specified [RCV004311550] | uncertain significance | 2 | 169546417 | 169546417 | Human | | name |
| 401765655 | CV2717795 | single nucleotide variant | NM_024622.6(FASTKD1):c.2051G>A (p.Arg684His) | not specified [RCV004321779] | uncertain significance | 2 | 169538036 | 169538036 | Human | | name |
| 401883619 | CV2754511 | single nucleotide variant | NM_024622.6(FASTKD1):c.2533T>C (p.Ser845Pro) | not specified [RCV004336718] | uncertain significance | 2 | 169529836 | 169529836 | Human | | name |
| 401878468 | CV2770561 | single nucleotide variant | NM_024622.6(FASTKD1):c.1160T>C (p.Phe387Ser) | not specified [RCV004349628] | uncertain significance | 2 | 169555178 | 169555178 | Human | | name |
| 405763433 | CV3253160 | single nucleotide variant | NM_024622.6(FASTKD1):c.1037G>A (p.Gly346Glu) | not specified [RCV004383876] | uncertain significance | 2 | 169557232 | 169557232 | Human | | name |
| 405763439 | CV3253161 | single nucleotide variant | NM_024622.6(FASTKD1):c.1053G>A (p.Met351Ile) | not specified [RCV004383877] | uncertain significance | 2 | 169557216 | 169557216 | Human | | name |
| 405763445 | CV3253162 | single nucleotide variant | NM_024622.6(FASTKD1):c.1144A>C (p.Thr382Pro) | not specified [RCV004383878] | uncertain significance | 2 | 169555194 | 169555194 | Human | | name |
| 405763452 | CV3253163 | single nucleotide variant | NM_024622.6(FASTKD1):c.1249T>C (p.Ser417Pro) | not specified [RCV004383879] | uncertain significance | 2 | 169546670 | 169546670 | Human | | name |
| 405763456 | CV3253164 | single nucleotide variant | NM_024622.6(FASTKD1):c.1270T>C (p.Ser424Pro) | not specified [RCV004383880] | uncertain significance | 2 | 169546649 | 169546649 | Human | | name |
| 405763462 | CV3253165 | single nucleotide variant | NM_024622.6(FASTKD1):c.1313G>A (p.Arg438Gln) | not specified [RCV004383881] | uncertain significance | 2 | 169546606 | 169546606 | Human | | name |
| 405763469 | CV3253166 | single nucleotide variant | NM_024622.6(FASTKD1):c.1477C>T (p.His493Tyr) | not specified [RCV004383882] | uncertain significance | 2 | 169546442 | 169546442 | Human | | name |
| 405763474 | CV3253167 | single nucleotide variant | NM_024622.6(FASTKD1):c.1564G>A (p.Ala522Thr) | not specified [RCV004383883] | uncertain significance | 2 | 169546355 | 169546355 | Human | | name |
| 405763499 | CV3253171 | single nucleotide variant | NM_024622.6(FASTKD1):c.2325A>C (p.Glu775Asp) | not specified [RCV004383887] | uncertain significance | 2 | 169531354 | 169531354 | Human | | name |
| 405763504 | CV3253172 | single nucleotide variant | NM_024622.6(FASTKD1):c.2441A>G (p.Gln814Arg) | not specified [RCV004383888] | uncertain significance | 2 | 169530588 | 169530588 | Human | | name |
| 407492716 | CV3432160 | single nucleotide variant | NM_024622.6(FASTKD1):c.1425A>T (p.Lys475Asn) | not specified [RCV004620858] | uncertain significance | 2 | 169546494 | 169546494 | Human | | name |
| 407492720 | CV3432161 | single nucleotide variant | NM_024622.6(FASTKD1):c.1094T>G (p.Val365Gly) | not specified [RCV004620859] | uncertain significance | 2 | 169555244 | 169555244 | Human | | name |
| 597695730 | CV3672179 | single nucleotide variant | NM_024622.6(FASTKD1):c.1841T>C (p.Val614Ala) | not specified [RCV004915798] | uncertain significance | 2 | 169540155 | 169540155 | Human | | name |
| 597695740 | CV3672180 | single nucleotide variant | NM_024622.6(FASTKD1):c.1501C>T (p.Arg501Trp) | not specified [RCV004915799] | likely benign | 2 | 169546418 | 169546418 | Human | | name |
| 597695750 | CV3672181 | single nucleotide variant | NM_024622.6(FASTKD1):c.2105A>G (p.Gln702Arg) | not specified [RCV004915800] | uncertain significance | 2 | 169537310 | 169537310 | Human | | name |
| 597695765 | CV3672183 | single nucleotide variant | NM_024622.6(FASTKD1):c.1862C>A (p.Ala621Asp) | not specified [RCV004915802] | uncertain significance | 2 | 169540134 | 169540134 | Human | | name |
| 597695771 | CV3672184 | single nucleotide variant | NM_024622.6(FASTKD1):c.1622C>G (p.Ser541Cys) | not specified [RCV004915803] | uncertain significance | 2 | 169546297 | 169546297 | Human | | name |
| 597695779 | CV3672185 | single nucleotide variant | NM_024622.6(FASTKD1):c.1354A>G (p.Ser452Gly) | not specified [RCV004915804] | uncertain significance | 2 | 169546565 | 169546565 | Human | | name |
| 597695789 | CV3672186 | single nucleotide variant | NM_024622.6(FASTKD1):c.1868T>C (p.Leu623Pro) | not specified [RCV004915805] | uncertain significance | 2 | 169540128 | 169540128 | Human | | name |
| 597695797 | CV3672187 | single nucleotide variant | NM_024622.6(FASTKD1):c.1613A>G (p.Glu538Gly) | not specified [RCV004915806] | likely benign | 2 | 169546306 | 169546306 | Human | | name |
| 598213283 | CV3966149 | single nucleotide variant | NM_024622.6(FASTKD1):c.1732C>T (p.Arg578Cys) | not specified [RCV005339235] | uncertain significance | 2 | 169544805 | 169544805 | Human | | name |
| 598213288 | CV3966150 | single nucleotide variant | NM_024622.6(FASTKD1):c.2359C>A (p.Leu787Ile) | not specified [RCV005339236] | uncertain significance | 2 | 169530670 | 169530670 | Human | | name |
| 598213294 | CV3966151 | single nucleotide variant | NM_024622.6(FASTKD1):c.2491C>T (p.Arg831Trp) | not specified [RCV005339237] | uncertain significance | 2 | 169529878 | 169529878 | Human | | name |
| 598271519 | CV3966152 | single nucleotide variant | NM_024622.6(FASTKD1):c.1479C>G (p.His493Gln) | not specified [RCV005327762] | uncertain significance | 2 | 169546440 | 169546440 | Human | | name |
| 13706973 | CV539434 | single nucleotide variant | NM_024622.6(FASTKD1):c.2230T>A (p.Tyr744Asn) | Glaucoma 1, open angle, B [RCV000663362] | pathogenic | 2 | 169531449 | 169531449 | Human | 1 | name |
| 15187758 | CV697157 | single nucleotide variant | NM_024622.6(FASTKD1):c.2303C>G (p.Ser768Ter) | not provided [RCV000953682] | benign | 2 | 169531376 | 169531376 | Human | | name |