| 407530124 | CV3485502 | single nucleotide variant | NM_001271977.2(STK25):c.9C>G (p.His3Gln) | not specified [RCV004681666] | uncertain significance | 2 | 241508027 | 241508027 | Human | | name |
| 329370115 | CV2461618 | single nucleotide variant | NM_001271977.2(STK25):c.23C>T (p.Ala8Val) | not specified [RCV004269794] | uncertain significance | 2 | 241508013 | 241508013 | Human | | name |
| 401892285 | CV2777390 | single nucleotide variant | NM_001271977.2(STK25):c.154G>A (p.Asp52Asn) | not specified [RCV004354393] | uncertain significance | 2 | 241501585 | 241501585 | Human | | name |
| 598207506 | CV3919683 | single nucleotide variant | NM_001271977.2(STK25):c.295G>T (p.Gly99Cys) | not specified [RCV005291295] | uncertain significance | 2 | 241500763 | 241500763 | Human | | name |
| 156230624 | CV2264187 | single nucleotide variant | NM_001271977.2(STK25):c.301G>A (p.Gly101Ser) | not specified [RCV004136335] | uncertain significance | 2 | 241500757 | 241500757 | Human | | name |
| 156003738 | CV2290061 | single nucleotide variant | NM_001271977.2(STK25):c.764C>T (p.Pro255Leu) | not specified [RCV004152744] | uncertain significance | 2 | 241498996 | 241498996 | Human | | name |
| 329395849 | CV2454649 | single nucleotide variant | NM_001271977.2(STK25):c.976C>T (p.Arg326Trp) | not specified [RCV004268108] | uncertain significance | 2 | 241498291 | 241498291 | Human | | name |
| 329367751 | CV2457039 | single nucleotide variant | NM_001271977.2(STK25):c.953T>G (p.Ile318Ser) | not specified [RCV004264830] | uncertain significance | 2 | 241498314 | 241498314 | Human | | name |
| 329401648 | CV2457268 | single nucleotide variant | NM_001271977.2(STK25):c.386A>G (p.Asp129Gly) | not specified [RCV004267121] | uncertain significance | 2 | 241500214 | 241500214 | Human | | name |
| 405740949 | CV3334491 | single nucleotide variant | NM_001271977.2(STK25):c.577G>A (p.Asp193Asn) | not specified [RCV004465704] | uncertain significance | 2 | 241499265 | 241499265 | Human | | name |
| 405740957 | CV3334492 | single nucleotide variant | NM_001271977.2(STK25):c.767G>A (p.Arg256Gln) | not specified [RCV004465705] | uncertain significance | 2 | 241498993 | 241498993 | Human | | name |
| 405740964 | CV3334493 | single nucleotide variant | NM_001271977.2(STK25):c.856C>T (p.Arg286Cys) | not specified [RCV004465706] | uncertain significance | 2 | 241498700 | 241498700 | Human | | name |
| 405740972 | CV3334494 | single nucleotide variant | NM_001271977.2(STK25):c.865C>T (p.Arg289Cys) | not specified [RCV004465707] | uncertain significance | 2 | 241498691 | 241498691 | Human | | name |
| 405740979 | CV3334495 | single nucleotide variant | NM_001271977.2(STK25):c.875C>T (p.Ser292Leu) | not specified [RCV004465708] | uncertain significance | 2 | 241498681 | 241498681 | Human | | name |
| 405740986 | CV3334496 | single nucleotide variant | NM_001271977.2(STK25):c.929C>T (p.Ala310Val) | not specified [RCV004465709] | uncertain significance | 2 | 241498338 | 241498338 | Human | | name |
| 405740993 | CV3334497 | single nucleotide variant | NM_001271977.2(STK25):c.932A>C (p.Glu311Ala) | not specified [RCV004465710] | uncertain significance | 2 | 241498335 | 241498335 | Human | | name |
| 405741002 | CV3334498 | single nucleotide variant | NM_001271977.2(STK25):c.967C>G (p.Pro323Ala) | not specified [RCV004465711] | uncertain significance | 2 | 241498300 | 241498300 | Human | | name |
| 597747636 | CV3614844 | single nucleotide variant | NM_001271977.2(STK25):c.413A>G (p.His138Arg) | not specified [RCV004866106] | uncertain significance | 2 | 241500187 | 241500187 | Human | | name |
| 597747643 | CV3614845 | single nucleotide variant | NM_001271977.2(STK25):c.962T>C (p.Phe321Ser) | not specified [RCV004866107] | uncertain significance | 2 | 241498305 | 241498305 | Human | | name |
| 597747648 | CV3614846 | single nucleotide variant | NM_001271977.2(STK25):c.985C>T (p.Pro329Ser) | not specified [RCV004866108] | uncertain significance | 2 | 241498282 | 241498282 | Human | | name |
| 597747653 | CV3614847 | single nucleotide variant | NM_001271977.2(STK25):c.305C>T (p.Ser102Leu) | not specified [RCV004866109] | uncertain significance | 2 | 241500753 | 241500753 | Human | | name |
| 598251489 | CV3919684 | single nucleotide variant | NM_001271977.2(STK25):c.857G>A (p.Arg286His) | not specified [RCV005277898] | uncertain significance | 2 | 241498699 | 241498699 | Human | | name |
| 598207511 | CV3919686 | single nucleotide variant | NM_001271977.2(STK25):c.652C>T (p.Leu218Phe) | not specified [RCV005291296] | uncertain significance | 2 | 241499108 | 241499108 | Human | | name |
| 155917490 | CV2236568 | single nucleotide variant | NM_001271977.2(STK25):c.1021A>G (p.Ser341Gly) | not specified [RCV004110561] | likely benign | 2 | 241498246 | 241498246 | Human | | name |
| 156336931 | CV2270980 | single nucleotide variant | NM_001271977.2(STK25):c.1034C>T (p.Pro345Leu) | not specified [RCV004132007] | uncertain significance | 2 | 241497686 | 241497686 | Human | | name |
| 156248029 | CV2276945 | single nucleotide variant | NM_001271977.2(STK25):c.1093G>A (p.Val365Ile) | not specified [RCV004140279] | uncertain significance | 2 | 241497627 | 241497627 | Human | | name |
| 155997454 | CV2373184 | single nucleotide variant | NM_001271977.2(STK25):c.1276C>T (p.Arg426Cys) | not specified [RCV004217865] | uncertain significance | 2 | 241495667 | 241495667 | Human | | name |
| 156388963 | CV2376261 | single nucleotide variant | NM_001271977.2(STK25):c.1277G>A (p.Arg426His) | not specified [RCV004220480] | uncertain significance | 2 | 241495666 | 241495666 | Human | | name |
| 329361825 | CV2448059 | single nucleotide variant | NM_001271977.2(STK25):c.1087C>T (p.Arg363Trp) | not specified [RCV004263285] | uncertain significance | 2 | 241497633 | 241497633 | Human | | name |
| 329353515 | CV2466813 | single nucleotide variant | NM_001271977.2(STK25):c.1230G>T (p.Glu410Asp) | not specified [RCV004280757] | uncertain significance | 2 | 241496409 | 241496409 | Human | | name |
| 405740942 | CV3334490 | single nucleotide variant | NM_001271977.2(STK25):c.1045G>A (p.Val349Ile) | not specified [RCV004465703] | uncertain significance | 2 | 241497675 | 241497675 | Human | | name |
| 597747625 | CV3614842 | single nucleotide variant | NM_001271977.2(STK25):c.1276C>A (p.Arg426Ser) | not specified [RCV004866104] | uncertain significance | 2 | 241495667 | 241495667 | Human | | name |
| 597747631 | CV3614843 | single nucleotide variant | NM_001271977.2(STK25):c.1009A>G (p.Thr337Ala) | not specified [RCV004866105] | uncertain significance | 2 | 241498258 | 241498258 | Human | | name |
| 598251494 | CV3919685 | single nucleotide variant | NM_001271977.2(STK25):c.1138G>A (p.Val380Met) | not specified [RCV005277899] | uncertain significance | 2 | 241496501 | 241496501 | Human | | name |