| 155953357 | CV2379001 | single nucleotide variant | NM_024045.2(DDX50):c.20G>C (p.Trp7Ser) | not specified [RCV004233763] | uncertain significance | 10 | 68901404 | 68901404 | Human | | name |
| 329373402 | CV2434218 | single nucleotide variant | NM_024045.2(DDX50):c.55G>A (p.Glu19Lys) | not specified [RCV004250105] | uncertain significance | 10 | 68901439 | 68901439 | Human | | name |
| 401783759 | CV2723921 | single nucleotide variant | NM_024045.2(DDX50):c.47C>T (p.Pro16Leu) | not specified [RCV004327833] | uncertain significance | 10 | 68901431 | 68901431 | Human | | name |
| 405667627 | CV3239934 | single nucleotide variant | NM_024045.2(DDX50):c.73A>G (p.Lys25Glu) | not specified [RCV004367986] | uncertain significance | 10 | 68901457 | 68901457 | Human | | name |
| 407458822 | CV3426647 | single nucleotide variant | NM_024045.2(DDX50):c.68A>C (p.Gln23Pro) | not specified [RCV004611693] | uncertain significance | 10 | 68901452 | 68901452 | Human | | name |
| 407458825 | CV3426648 | single nucleotide variant | NM_024045.2(DDX50):c.71A>T (p.Lys24Met) | not specified [RCV004611694] | uncertain significance | 10 | 68901455 | 68901455 | Human | | name |
| 15164529 | CV724020 | single nucleotide variant | NM_024045.2(DDX50):c.717C>T (p.Ser239=) | not provided [RCV000882214] | benign | 10 | 68913239 | 68913239 | Human | | name |
| 156143603 | CV2208652 | single nucleotide variant | NM_024045.2(DDX50):c.111C>A (p.His37Gln) | not specified [RCV004091166] | uncertain significance | 10 | 68906734 | 68906734 | Human | | name |
| 10767432 | CV221016 | single nucleotide variant | NM_024045.2(DDX50):c.122C>T (p.Ser41Leu) | Prostate cancer [RCV000204703] | uncertain significance | 10 | 68906745 | 68906745 | Human | 2 | name |
| 156074392 | CV2248171 | single nucleotide variant | NM_024045.2(DDX50):c.164A>C (p.Asp55Ala) | not specified [RCV004117567] | uncertain significance | 10 | 68906787 | 68906787 | Human | | name |
| 405705642 | CV3239925 | single nucleotide variant | NM_024045.2(DDX50):c.165C>G (p.Asp55Glu) | not specified [RCV004375872] | uncertain significance | 10 | 68906788 | 68906788 | Human | | name |
| 405705650 | CV3239926 | single nucleotide variant | NM_024045.2(DDX50):c.197T>C (p.Met66Thr) | not specified [RCV004375873] | uncertain significance | 10 | 68906820 | 68906820 | Human | | name |
| 405667610 | CV3239930 | single nucleotide variant | NM_024045.2(DDX50):c.229G>C (p.Gly77Arg) | not specified [RCV004367982] | uncertain significance | 10 | 68906852 | 68906852 | Human | | name |
| 155903002 | CV2301559 | single nucleotide variant | NM_024045.2(DDX50):c.302T>C (p.Ile101Thr) | not specified [RCV004162468] | uncertain significance | 10 | 68906925 | 68906925 | Human | | name |
| 156249472 | CV2314160 | single nucleotide variant | NM_024045.2(DDX50):c.407A>G (p.Glu136Gly) | not specified [RCV004166245] | uncertain significance | 10 | 68910329 | 68910329 | Human | | name |
| 155927547 | CV2349631 | single nucleotide variant | NM_024045.2(DDX50):c.956A>G (p.Asn319Ser) | not specified [RCV004204051] | uncertain significance | 10 | 68914071 | 68914071 | Human | | name |
| 155931549 | CV2370944 | single nucleotide variant | NM_024045.2(DDX50):c.658A>G (p.Thr220Ala) | not specified [RCV004218671] | uncertain significance | 10 | 68913180 | 68913180 | Human | | name |
| 156142555 | CV2386129 | single nucleotide variant | NM_024045.2(DDX50):c.413C>G (p.Ala138Gly) | not specified [RCV004229180] | uncertain significance | 10 | 68910335 | 68910335 | Human | | name |
| 156156345 | CV2393464 | single nucleotide variant | NM_024045.2(DDX50):c.632C>T (p.Ser211Leu) | not specified [RCV004228956] | uncertain significance | 10 | 68911239 | 68911239 | Human | | name |
| 329399412 | CV2470086 | single nucleotide variant | NM_024045.2(DDX50):c.532A>G (p.Ile178Val) | not specified [RCV004287348] | uncertain significance | 10 | 68911139 | 68911139 | Human | | name |
| 401737999 | CV2700887 | single nucleotide variant | NM_024045.2(DDX50):c.413C>A (p.Ala138Asp) | not specified [RCV004307154] | uncertain significance | 10 | 68910335 | 68910335 | Human | | name |
| 401761228 | CV2706264 | single nucleotide variant | NM_024045.2(DDX50):c.700A>G (p.Ile234Val) | not specified [RCV004314929] | uncertain significance | 10 | 68913222 | 68913222 | Human | | name |
| 401891905 | CV2775785 | single nucleotide variant | NM_024045.2(DDX50):c.854G>A (p.Arg285Gln) | not specified [RCV004344832] | uncertain significance | 10 | 68913487 | 68913487 | Human | | name |
| 405667615 | CV3239931 | single nucleotide variant | NM_024045.2(DDX50):c.350C>G (p.Ser117Cys) | not specified [RCV004367983] | uncertain significance | 10 | 68906973 | 68906973 | Human | | name |
| 405667619 | CV3239932 | single nucleotide variant | NM_024045.2(DDX50):c.544C>T (p.Arg182Trp) | not specified [RCV004367984] | uncertain significance | 10 | 68911151 | 68911151 | Human | | name |
| 405667624 | CV3239933 | single nucleotide variant | NM_024045.2(DDX50):c.628C>T (p.Arg210Cys) | not specified [RCV004367985] | uncertain significance | 10 | 68911235 | 68911235 | Human | | name |
| 405667632 | CV3239935 | single nucleotide variant | NM_024045.2(DDX50):c.873A>T (p.Glu291Asp) | not specified [RCV004367987] | uncertain significance | 10 | 68913506 | 68913506 | Human | | name |
| 407458828 | CV3426649 | single nucleotide variant | NM_024045.2(DDX50):c.650T>C (p.Leu217Ser) | not specified [RCV004611695] | uncertain significance | 10 | 68913172 | 68913172 | Human | | name |
| 597805735 | CV3658344 | single nucleotide variant | NM_024045.2(DDX50):c.475T>C (p.Tyr159His) | not specified [RCV004908815] | uncertain significance | 10 | 68911082 | 68911082 | Human | | name |
| 597805736 | CV3658345 | single nucleotide variant | NM_024045.2(DDX50):c.445A>C (p.Ile149Leu) | not specified [RCV004908816] | uncertain significance | 10 | 68910367 | 68910367 | Human | | name |
| 597805733 | CV3662226 | single nucleotide variant | NM_024045.2(DDX50):c.395G>A (p.Arg132His) | not specified [RCV004908813] | uncertain significance | 10 | 68910317 | 68910317 | Human | | name |
| 597783155 | CV3662228 | single nucleotide variant | NM_024045.2(DDX50):c.833G>A (p.Arg278Gln) | not specified [RCV004900172] | uncertain significance | 10 | 68913466 | 68913466 | Human | | name |
| 598222719 | CV3956368 | single nucleotide variant | NM_024045.2(DDX50):c.806G>C (p.Arg269Pro) | not specified [RCV005317961] | uncertain significance | 10 | 68913439 | 68913439 | Human | | name |
| 598222750 | CV3956373 | single nucleotide variant | NM_024045.2(DDX50):c.656C>T (p.Pro219Leu) | not specified [RCV005317966] | uncertain significance | 10 | 68913178 | 68913178 | Human | | name |
| 156188999 | CV2205881 | single nucleotide variant | NM_024045.2(DDX50):c.2057G>A (p.Arg686Gln) | not specified [RCV004078318] | uncertain significance | 10 | 68946473 | 68946473 | Human | | name |
| 156330327 | CV2226983 | single nucleotide variant | NM_024045.2(DDX50):c.2188G>A (p.Gly730Arg) | not specified [RCV004097377] | uncertain significance | 10 | 68946604 | 68946604 | Human | | name |
| 155945452 | CV2292104 | single nucleotide variant | NM_024045.2(DDX50):c.1174G>T (p.Ala392Ser) | not specified [RCV004160368] | uncertain significance | 10 | 68919916 | 68919916 | Human | | name |
| 156087970 | CV2295470 | single nucleotide variant | NM_024045.2(DDX50):c.2122G>A (p.Gly708Arg) | not specified [RCV004160585] | uncertain significance | 10 | 68946538 | 68946538 | Human | | name |
| 156194023 | CV2322022 | single nucleotide variant | NM_024045.2(DDX50):c.1993G>A (p.Glu665Lys) | not specified [RCV004173775] | uncertain significance | 10 | 68946409 | 68946409 | Human | | name |
| 156034233 | CV2338628 | single nucleotide variant | NM_024045.2(DDX50):c.2087G>A (p.Arg696Gln) | not specified [RCV004182212] | uncertain significance | 10 | 68946503 | 68946503 | Human | | name |
| 155921511 | CV2350679 | single nucleotide variant | NM_024045.2(DDX50):c.2053G>C (p.Gly685Arg) | not specified [RCV004207028] | uncertain significance | 10 | 68946469 | 68946469 | Human | | name |
| 401742422 | CV2673779 | single nucleotide variant | NM_024045.2(DDX50):c.1558A>G (p.Met520Val) | not specified [RCV004293166] | uncertain significance | 10 | 68936042 | 68936042 | Human | | name |
| 401780427 | CV2674020 | single nucleotide variant | NM_024045.2(DDX50):c.2002T>G (p.Tyr668Asp) | not specified [RCV004293385] | uncertain significance | 10 | 68946418 | 68946418 | Human | | name |
| 401734613 | CV2688575 | single nucleotide variant | NM_024045.2(DDX50):c.1528A>G (p.Thr510Ala) | not specified [RCV004301533] | uncertain significance | 10 | 68936012 | 68936012 | Human | | name |
| 401732897 | CV2691143 | single nucleotide variant | NM_024045.2(DDX50):c.1415A>G (p.Tyr472Cys) | not specified [RCV004301137] | uncertain significance | 10 | 68934812 | 68934812 | Human | | name |
| 401771160 | CV2726384 | single nucleotide variant | NM_024045.2(DDX50):c.1883G>C (p.Gly628Ala) | not specified [RCV004328599] | uncertain significance | 10 | 68941187 | 68941187 | Human | | name |
| 401761372 | CV2726737 | single nucleotide variant | NM_024045.2(DDX50):c.1200G>T (p.Lys400Asn) | not specified [RCV004323064] | uncertain significance | 10 | 68919942 | 68919942 | Human | | name |
| 401891960 | CV2775848 | single nucleotide variant | NM_024045.2(DDX50):c.1883G>A (p.Gly628Glu) | not specified [RCV004344884] | uncertain significance | 10 | 68941187 | 68941187 | Human | | name |
| 405667596 | CV3239927 | single nucleotide variant | NM_024045.2(DDX50):c.2087G>T (p.Arg696Leu) | not specified [RCV004367979] | uncertain significance | 10 | 68946503 | 68946503 | Human | | name |
| 405667601 | CV3239928 | single nucleotide variant | NM_024045.2(DDX50):c.2095G>A (p.Gly699Ser) | not specified [RCV004367980] | uncertain significance | 10 | 68946511 | 68946511 | Human | | name |
| 405667605 | CV3239929 | single nucleotide variant | NM_024045.2(DDX50):c.2108G>A (p.Arg703Lys) | not specified [RCV004367981] | uncertain significance | 10 | 68946524 | 68946524 | Human | | name |
| 407458813 | CV3426644 | single nucleotide variant | NM_024045.2(DDX50):c.1844A>C (p.Asn615Thr) | not specified [RCV004611690] | uncertain significance | 10 | 68941148 | 68941148 | Human | | name |
| 407458816 | CV3426645 | single nucleotide variant | NM_024045.2(DDX50):c.2171G>C (p.Arg724Thr) | not specified [RCV004611691] | uncertain significance | 10 | 68946587 | 68946587 | Human | | name |
| 597805732 | CV3662225 | single nucleotide variant | NM_024045.2(DDX50):c.1928G>A (p.Arg643Lys) | not specified [RCV004908812] | uncertain significance | 10 | 68943250 | 68943250 | Human | | name |
| 597805734 | CV3662227 | single nucleotide variant | NM_024045.2(DDX50):c.1423C>T (p.Arg475Cys) | not specified [RCV004908814] | uncertain significance | 10 | 68934820 | 68934820 | Human | | name |
| 598222707 | CV3956366 | single nucleotide variant | NM_024045.2(DDX50):c.1217C>G (p.Ala406Gly) | not specified [RCV005317959] | uncertain significance | 10 | 68919959 | 68919959 | Human | | name |
| 598222712 | CV3956367 | single nucleotide variant | NM_024045.2(DDX50):c.2147A>G (p.Asp716Gly) | not specified [RCV005317960] | uncertain significance | 10 | 68946563 | 68946563 | Human | | name |
| 598222732 | CV3956370 | single nucleotide variant | NM_024045.2(DDX50):c.1989A>C (p.Glu663Asp) | not specified [RCV005317963] | uncertain significance | 10 | 68946405 | 68946405 | Human | | name |
| 598222738 | CV3956371 | single nucleotide variant | NM_024045.2(DDX50):c.1594A>G (p.Arg532Gly) | not specified [RCV005317964] | uncertain significance | 10 | 68936078 | 68936078 | Human | | name |
| 598222744 | CV3956372 | single nucleotide variant | NM_024045.2(DDX50):c.1439G>A (p.Gly480Asp) | not specified [RCV005317965] | uncertain significance | 10 | 68934836 | 68934836 | Human | | name |
| 15196924 | CV724021 | single nucleotide variant | NM_024045.2(DDX50):c.1975G>A (p.Ala659Thr) | not provided [RCV000889907] | benign | 10 | 68946391 | 68946391 | Human | | name |