| 401760877 | CV2695193 | single nucleotide variant | NM_018639.5(WSB2):c.64G>C (p.Asp22His) | not specified [RCV004303335] | uncertain significance | 12 | 118052428 | 118052428 | Human | | name |
| 401932471 | CV2816917 | single nucleotide variant | NM_018639.5(WSB2):c.747C>T (p.Pro249=) | not provided [RCV003392067] | likely benign | 12 | 118036424 | 118036424 | Human | | name |
| 401932473 | CV2816918 | single nucleotide variant | NM_018639.5(WSB2):c.648T>C (p.Ala216=) | not provided [RCV003392068] | likely benign | 12 | 118038300 | 118038300 | Human | | name |
| 15160507 | CV702157 | single nucleotide variant | NM_001278557.1(WSB2):c.12C>T (p.Asp4=) | not provided [RCV000947499] | benign | 12 | 118062151 | 118062151 | Human | | name |
| 15135227 | CV713368 | single nucleotide variant | NM_018639.5(WSB2):c.738C>T (p.Asp246=) | not provided [RCV000965253] | benign | 12 | 118036433 | 118036433 | Human | | name |
| 156088382 | CV2241395 | single nucleotide variant | NM_018639.5(WSB2):c.236G>A (p.Gly79Glu) | not specified [RCV004102525] | uncertain significance | 12 | 118043324 | 118043324 | Human | | name |
| 156216178 | CV2386046 | single nucleotide variant | NM_018639.5(WSB2):c.238C>T (p.Arg80Trp) | not specified [RCV004229108] | uncertain significance | 12 | 118043322 | 118043322 | Human | | name |
| 405812302 | CV3353019 | single nucleotide variant | NM_018639.5(WSB2):c.262C>G (p.Leu88Val) | not specified [RCV004483219] | uncertain significance | 12 | 118043298 | 118043298 | Human | | name |
| 405812304 | CV3353020 | single nucleotide variant | NM_018639.5(WSB2):c.287G>C (p.Gly96Ala) | not specified [RCV004483220] | uncertain significance | 12 | 118043273 | 118043273 | Human | | name |
| 617148416 | CV3550516 | single nucleotide variant | NM_018639.5(WSB2):c.128G>A (p.Trp43Ter) | not provided [RCV005429197] | uncertain significance | 12 | 118052364 | 118052364 | Human | | name |
| 617148415 | CV3550517 | deletion | NM_018639.5(WSB2):c.399del (p.Gln134fs) | not provided [RCV005429198] | uncertain significance | 12 | 118043161 | 118043161 | Human | | name |
| 597800055 | CV3633847 | single nucleotide variant | NM_018639.5(WSB2):c.167C>T (p.Pro56Leu) | not specified [RCV004880040] | uncertain significance | 12 | 118052325 | 118052325 | Human | | name |
| 156146021 | CV2218867 | single nucleotide variant | NM_018639.5(WSB2):c.659C>T (p.Ser220Leu) | not specified [RCV004085105] | uncertain significance | 12 | 118038289 | 118038289 | Human | | name |
| 156383535 | CV2220092 | single nucleotide variant | NM_018639.5(WSB2):c.331T>C (p.Trp111Arg) | not specified [RCV004093965] | uncertain significance | 12 | 118043229 | 118043229 | Human | | name |
| 156193024 | CV2344166 | single nucleotide variant | NM_018639.5(WSB2):c.338G>A (p.Arg113His) | not specified [RCV004195763] | uncertain significance | 12 | 118043222 | 118043222 | Human | | name |
| 156114342 | CV2349201 | single nucleotide variant | NM_018639.5(WSB2):c.317C>A (p.Pro106His) | not specified [RCV004199158] | uncertain significance | 12 | 118043243 | 118043243 | Human | | name |
| 329376999 | CV2456804 | single nucleotide variant | NM_018639.5(WSB2):c.538A>G (p.Ile180Val) | not specified [RCV004270775] | uncertain significance | 12 | 118042862 | 118042862 | Human | | name |
| 401774395 | CV2727828 | single nucleotide variant | NM_018639.5(WSB2):c.871G>A (p.Val291Ile) | not specified [RCV004323850] | uncertain significance | 12 | 118035287 | 118035287 | Human | | name |
| 401870577 | CV2758948 | single nucleotide variant | NM_018639.5(WSB2):c.865A>G (p.Ser289Gly) | not specified [RCV004342264] | uncertain significance | 12 | 118035293 | 118035293 | Human | | name |
| 401932474 | CV2816919 | single nucleotide variant | NM_018639.5(WSB2):c.358G>A (p.Asp120Asn) | not provided [RCV003392069] | likely benign | 12 | 118043202 | 118043202 | Human | | name |
| 405812308 | CV3353022 | single nucleotide variant | NM_018639.5(WSB2):c.853G>A (p.Ala285Thr) | not specified [RCV004483222] | uncertain significance | 12 | 118035305 | 118035305 | Human | | name |
| 407455536 | CV3488044 | single nucleotide variant | NM_018639.5(WSB2):c.785A>G (p.Asn262Ser) | not specified [RCV004685608] | uncertain significance | 12 | 118036386 | 118036386 | Human | | name |
| 597741095 | CV3633845 | single nucleotide variant | NM_018639.5(WSB2):c.997A>T (p.Met333Leu) | not specified [RCV004890686] | uncertain significance | 12 | 118035041 | 118035041 | Human | | name |
| 597741100 | CV3633846 | single nucleotide variant | NM_018639.5(WSB2):c.689C>T (p.Thr230Met) | not specified [RCV004890687] | uncertain significance | 12 | 118036482 | 118036482 | Human | | name |
| 597800057 | CV3633848 | single nucleotide variant | NM_018639.5(WSB2):c.887T>C (p.Leu296Pro) | not specified [RCV004880041] | uncertain significance | 12 | 118035271 | 118035271 | Human | | name |
| 15199732 | CV702156 | single nucleotide variant | NM_018639.5(WSB2):c.484A>G (p.Thr162Ala) | not provided [RCV000957122] | benign | 12 | 118042916 | 118042916 | Human | | name |
| 401772530 | CV2687723 | single nucleotide variant | NM_018639.5(WSB2):c.1082C>G (p.Thr361Arg) | not specified [RCV004302712] | uncertain significance | 12 | 118034329 | 118034329 | Human | | name |
| 405812300 | CV3353018 | single nucleotide variant | NM_018639.5(WSB2):c.1205G>A (p.Arg402Lys) | not specified [RCV004483218] | uncertain significance | 12 | 118034206 | 118034206 | Human | | name |
| 597800053 | CV3633844 | single nucleotide variant | NM_018639.5(WSB2):c.1185G>A (p.Met395Ile) | not specified [RCV004880039] | uncertain significance | 12 | 118034226 | 118034226 | Human | | name |
| 597800059 | CV3633849 | single nucleotide variant | NM_018639.5(WSB2):c.1066C>T (p.His356Tyr) | not specified [RCV004880042] | uncertain significance | 12 | 118034345 | 118034345 | Human | | name |
| 617148414 | CV3550518 | deletion | NM_018639.5(WSB2):c.1187_1188del (p.Lys396fs) | not provided [RCV005429199] | uncertain significance | 12 | 118034223 | 118034224 | Human | | name |
