| 15098196 | CV777306 | single nucleotide variant | NM_015131.3(WDR43):c.364-10T>A | not provided [RCV000958499] | benign | 2 | 28906450 | 28906450 | Human | | name |
| 597791487 | CV3633622 | single nucleotide variant | NM_015131.3(WDR43):c.22A>G (p.Ser8Gly) | not specified [RCV004876677] | uncertain significance | 2 | 28894720 | 28894720 | Human | | name |
| 401726724 | CV2677322 | single nucleotide variant | NM_015131.3(WDR43):c.95C>T (p.Ala32Val) | not specified [RCV004295938] | uncertain significance | 2 | 28894793 | 28894793 | Human | | name |
| 407523946 | CV3489798 | single nucleotide variant | NM_015131.3(WDR43):c.46G>A (p.Gly16Arg) | not specified [RCV004678245] | uncertain significance | 2 | 28894744 | 28894744 | Human | | name |
| 155926288 | CV2284847 | single nucleotide variant | NM_015131.3(WDR43):c.145C>T (p.His49Tyr) | not specified [RCV004143307] | uncertain significance | 2 | 28894843 | 28894843 | Human | | name |
| 405807015 | CV3356211 | single nucleotide variant | NM_015131.3(WDR43):c.107G>A (p.Gly36Asp) | not specified [RCV004480471] | uncertain significance | 2 | 28894805 | 28894805 | Human | | name |
| 405807021 | CV3356214 | single nucleotide variant | NM_015131.3(WDR43):c.136A>T (p.Asn46Tyr) | not specified [RCV004480474] | uncertain significance | 2 | 28894834 | 28894834 | Human | | name |
| 597791493 | CV3633625 | single nucleotide variant | NM_015131.3(WDR43):c.135C>A (p.Asn45Lys) | not specified [RCV004876679] | uncertain significance | 2 | 28894833 | 28894833 | Human | | name |
| 598219775 | CV3933221 | single nucleotide variant | NM_015131.3(WDR43):c.226G>A (p.Glu76Lys) | not specified [RCV005293374] | uncertain significance | 2 | 28901987 | 28901987 | Human | | name |
| 598219795 | CV3933227 | single nucleotide variant | NM_015131.3(WDR43):c.1266C>T (p.Thr422=) | not specified [RCV005293377] | likely benign | 2 | 28927661 | 28927661 | Human | | name |
| 598257623 | CV3933230 | single nucleotide variant | NM_015131.3(WDR43):c.223A>G (p.Lys75Glu) | not specified [RCV005299863] | uncertain significance | 2 | 28894921 | 28894921 | Human | | name |
| 156290576 | CV2226201 | single nucleotide variant | NM_015131.3(WDR43):c.658A>G (p.Arg220Gly) | not specified [RCV004105599] | uncertain significance | 2 | 28914120 | 28914120 | Human | | name |
| 156035313 | CV2246730 | single nucleotide variant | NM_015131.3(WDR43):c.404A>C (p.His135Pro) | not specified [RCV004112272] | uncertain significance | 2 | 28906500 | 28906500 | Human | | name |
| 155976285 | CV2342754 | single nucleotide variant | NM_015131.3(WDR43):c.505A>G (p.Ser169Gly) | not specified [RCV004189798] | uncertain significance | 2 | 28912609 | 28912609 | Human | | name |
| 156168878 | CV2345484 | single nucleotide variant | NM_015131.3(WDR43):c.346T>G (p.Leu116Val) | not specified [RCV004198251] | uncertain significance | 2 | 28902107 | 28902107 | Human | | name |
| 156014091 | CV2368662 | single nucleotide variant | NM_015131.3(WDR43):c.463G>A (p.Val155Ile) | not specified [RCV004214558] | uncertain significance | 2 | 28906559 | 28906559 | Human | | name |
| 401880496 | CV2763061 | single nucleotide variant | NM_015131.3(WDR43):c.474C>G (p.Cys158Trp) | not specified [RCV004336116] | uncertain significance | 2 | 28906570 | 28906570 | Human | | name |
| 405807028 | CV3356218 | single nucleotide variant | NM_015131.3(WDR43):c.506G>A (p.Ser169Asn) | not specified [RCV004480478] | uncertain significance | 2 | 28912610 | 28912610 | Human | | name |
| 405807030 | CV3356219 | single nucleotide variant | NM_015131.3(WDR43):c.543G>T (p.Lys181Asn) | not specified [RCV004480479] | uncertain significance | 2 | 28912647 | 28912647 | Human | | name |
| 405807032 | CV3356220 | single nucleotide variant | NM_015131.3(WDR43):c.750G>C (p.Gln250His) | not specified [RCV004480480] | uncertain significance | 2 | 28917896 | 28917896 | Human | | name |
| 597791478 | CV3633619 | single nucleotide variant | NM_015131.3(WDR43):c.815A>G (p.Tyr272Cys) | not specified [RCV004876674] | uncertain significance | 2 | 28917961 | 28917961 | Human | | name |
| 597791490 | CV3633623 | single nucleotide variant | NM_015131.3(WDR43):c.514A>G (p.Ser172Gly) | not specified [RCV004876678] | uncertain significance | 2 | 28912618 | 28912618 | Human | | name |
| 597791498 | CV3633628 | single nucleotide variant | NM_015131.3(WDR43):c.614C>T (p.Thr205Ile) | not specified [RCV004876681] | uncertain significance | 2 | 28914076 | 28914076 | Human | | name |
| 598219789 | CV3933224 | single nucleotide variant | NM_015131.3(WDR43):c.980A>G (p.Lys327Arg) | not specified [RCV005293376] | uncertain significance | 2 | 28925047 | 28925047 | Human | | name |
| 598257609 | CV3933226 | single nucleotide variant | NM_015131.3(WDR43):c.563G>A (p.Arg188Gln) | not specified [RCV005299860] | uncertain significance | 2 | 28912667 | 28912667 | Human | | name |
| 598257614 | CV3933228 | single nucleotide variant | NM_015131.3(WDR43):c.786G>A (p.Met262Ile) | not specified [RCV005299861] | uncertain significance | 2 | 28917932 | 28917932 | Human | | name |
| 598257618 | CV3933229 | single nucleotide variant | NM_015131.3(WDR43):c.724C>T (p.His242Tyr) | not specified [RCV005299862] | uncertain significance | 2 | 28914186 | 28914186 | Human | | name |
| 155919800 | CV2209717 | single nucleotide variant | NM_015131.3(WDR43):c.1321C>T (p.Arg441Cys) | not specified [RCV004083042] | uncertain significance | 2 | 28929594 | 28929594 | Human | | name |
| 155981351 | CV2233070 | single nucleotide variant | NM_015131.3(WDR43):c.1826A>G (p.Asp609Gly) | not specified [RCV004103700] | uncertain significance | 2 | 28946471 | 28946471 | Human | | name |
| 155983530 | CV2240745 | single nucleotide variant | NM_015131.3(WDR43):c.1553A>G (p.Asn518Ser) | not specified [RCV004119357] | uncertain significance | 2 | 28936950 | 28936950 | Human | | name |
| 156041111 | CV2310864 | single nucleotide variant | NM_015131.3(WDR43):c.1336G>C (p.Asp446His) | not specified [RCV004163907] | uncertain significance | 2 | 28929609 | 28929609 | Human | | name |
| 156181006 | CV2327785 | single nucleotide variant | NM_015131.3(WDR43):c.1084G>T (p.Val362Leu) | not specified [RCV004179130] | uncertain significance | 2 | 28925151 | 28925151 | Human | | name |
| 156175816 | CV2331124 | single nucleotide variant | NM_015131.3(WDR43):c.1681A>G (p.Thr561Ala) | not specified [RCV004181736] | uncertain significance | 2 | 28941521 | 28941521 | Human | | name |
| 156271032 | CV2333813 | single nucleotide variant | NM_015131.3(WDR43):c.1771C>G (p.Pro591Ala) | not specified [RCV004181313] | uncertain significance | 2 | 28942348 | 28942348 | Human | | name |
| 156079816 | CV2341286 | single nucleotide variant | NM_015131.3(WDR43):c.1076T>C (p.Ile359Thr) | not specified [RCV004186696] | uncertain significance | 2 | 28925143 | 28925143 | Human | | name |
| 329368231 | CV2442664 | single nucleotide variant | NM_015131.3(WDR43):c.1231C>T (p.His411Tyr) | not specified [RCV004265016] | uncertain significance | 2 | 28927626 | 28927626 | Human | | name |
| 329392834 | CV2468983 | single nucleotide variant | NM_015131.3(WDR43):c.1271A>G (p.Gln424Arg) | not specified [RCV004274246] | uncertain significance | 2 | 28927666 | 28927666 | Human | | name |
| 401726349 | CV2674110 | single nucleotide variant | NM_015131.3(WDR43):c.1390G>A (p.Val464Ile) | not specified [RCV004295516] | uncertain significance | 2 | 28929663 | 28929663 | Human | | name |
| 401753918 | CV2716932 | single nucleotide variant | NM_015131.3(WDR43):c.1993G>A (p.Asp665Asn) | not specified [RCV004330022] | uncertain significance | 2 | 28946738 | 28946738 | Human | | name |
| 405807013 | CV3356210 | single nucleotide variant | NM_015131.3(WDR43):c.1012G>T (p.Ala338Ser) | not specified [RCV004480470] | uncertain significance | 2 | 28925079 | 28925079 | Human | | name |
| 405807017 | CV3356212 | single nucleotide variant | NM_015131.3(WDR43):c.1235A>C (p.His412Pro) | not specified [RCV004480472] | uncertain significance | 2 | 28927630 | 28927630 | Human | | name |
| 405807019 | CV3356213 | single nucleotide variant | NM_015131.3(WDR43):c.1322G>A (p.Arg441His) | not specified [RCV004480473] | uncertain significance | 2 | 28929595 | 28929595 | Human | | name |
| 405807022 | CV3356215 | single nucleotide variant | NM_015131.3(WDR43):c.1468A>G (p.Ile490Val) | not specified [RCV004480475] | uncertain significance | 2 | 28935551 | 28935551 | Human | | name |
| 405807024 | CV3356216 | single nucleotide variant | NM_015131.3(WDR43):c.1637C>A (p.Pro546His) | not specified [RCV004480476] | uncertain significance | 2 | 28941477 | 28941477 | Human | | name |
| 405807026 | CV3356217 | single nucleotide variant | NM_015131.3(WDR43):c.1813G>A (p.Glu605Lys) | not specified [RCV004480477] | uncertain significance | 2 | 28946458 | 28946458 | Human | | name |
| 597791481 | CV3633620 | single nucleotide variant | NM_015131.3(WDR43):c.1967C>T (p.Thr656Ile) | not specified [RCV004876675] | likely benign | 2 | 28946712 | 28946712 | Human | | name |
| 597791484 | CV3633621 | single nucleotide variant | NM_015131.3(WDR43):c.1504A>G (p.Ile502Val) | not specified [RCV004876676] | likely benign | 2 | 28935587 | 28935587 | Human | | name |
| 597739459 | CV3633624 | single nucleotide variant | NM_015131.3(WDR43):c.1118T>C (p.Leu373Ser) | not specified [RCV004890271] | uncertain significance | 2 | 28926499 | 28926499 | Human | | name |
| 597791496 | CV3633626 | single nucleotide variant | NM_015131.3(WDR43):c.1045C>A (p.Leu349Ile) | not specified [RCV004876680] | uncertain significance | 2 | 28925112 | 28925112 | Human | | name |
| 597739455 | CV3633629 | single nucleotide variant | NM_015131.3(WDR43):c.1973G>C (p.Ser658Thr) | not specified [RCV004890272] | uncertain significance | 2 | 28946718 | 28946718 | Human | | name |
| 597791501 | CV3633630 | single nucleotide variant | NM_015131.3(WDR43):c.1678A>C (p.Lys560Gln) | not specified [RCV004876682] | uncertain significance | 2 | 28941518 | 28941518 | Human | | name |
| 598219770 | CV3933219 | single nucleotide variant | NM_015131.3(WDR43):c.1351A>C (p.Lys451Gln) | not specified [RCV005293373] | uncertain significance | 2 | 28929624 | 28929624 | Human | | name |
| 598257595 | CV3933220 | single nucleotide variant | NM_015131.3(WDR43):c.1387C>G (p.Pro463Ala) | not specified [RCV005299857] | uncertain significance | 2 | 28929660 | 28929660 | Human | | name |
| 598257605 | CV3933225 | single nucleotide variant | NM_015131.3(WDR43):c.1376C>T (p.Thr459Met) | not specified [RCV005299859] | uncertain significance | 2 | 28929649 | 28929649 | Human | | name |