| 8581238 | CV115675 | single nucleotide variant | NM_001256732.1(SSBP2):c.712-3131A>T | Lung cancer [RCV000096198] | uncertain significance | 5 | 81451956 | 81451956 | Human | | name |
| 8581240 | CV115677 | single nucleotide variant | NM_001256732.1(SSBP2):c.63-24111C>A | Lung cancer [RCV000096200] | uncertain significance | 5 | 81674450 | 81674450 | Human | | name |
| 8581241 | CV115678 | single nucleotide variant | NM_001256732.1(SSBP2):c.63-46374G>A | Lung cancer [RCV000096201] | uncertain significance | 5 | 81696713 | 81696713 | Human | | name |
| 8581242 | CV115679 | single nucleotide variant | NM_001256732.1(SSBP2):c.63-48753A>G | Lung cancer [RCV000096202] | uncertain significance | 5 | 81699092 | 81699092 | Human | | name |
| 8626049 | CV81193 | single nucleotide variant | NM_012446.3(SSBP2):c.709C>T (p.Pro237Ser) | Malignant melanoma [RCV000061271] | not provided | 5 | 81448804 | 81448804 | Human | | name |
| 8631725 | CV86931 | single nucleotide variant | NM_012446.3(SSBP2):c.731C>T (p.Pro244Leu) | Malignant melanoma [RCV000067022] | not provided | 5 | 81446915 | 81446915 | Human | | name |
| 156079554 | CV2226552 | single nucleotide variant | NM_001256732.3(SSBP2):c.34G>A (p.Val12Ile) | not specified [RCV004101810] | uncertain significance | 5 | 81751009 | 81751009 | Human | | name |
| 156140180 | CV2247008 | single nucleotide variant | NM_001256732.3(SSBP2):c.91C>T (p.Leu31Phe) | not specified [RCV004114573] | uncertain significance | 5 | 81650311 | 81650311 | Human | | name |
| 12741229 | CV359714 | duplication | NM_001256732.3(SSBP2):c.152dup (p.Asn51fs) | not specified [RCV000414474] | uncertain significance | 5 | 81636601 | 81636602 | Human | | name |
| 156226633 | CV2352763 | single nucleotide variant | NM_001256732.3(SSBP2):c.112T>G (p.Ser38Ala) | not specified [RCV004198780] | uncertain significance | 5 | 81650290 | 81650290 | Human | | name |
| 597681256 | CV3611733 | single nucleotide variant | NM_001256732.3(SSBP2):c.239A>G (p.Glu80Gly) | not specified [RCV004857514] | uncertain significance | 5 | 81615516 | 81615516 | Human | | name |
| 9686981 | CV171405 | single nucleotide variant | NM_001256732.3(SSBP2):c.743A>T (p.Tyr248Phe) | Prostate cancer [RCV000149200] | uncertain significance | 5 | 81448794 | 81448794 | Human | 2 | name |
| 156175739 | CV2331119 | single nucleotide variant | NM_001256732.3(SSBP2):c.745G>A (p.Val249Ile) | not specified [RCV004181732] | uncertain significance | 5 | 81448792 | 81448792 | Human | | name |
| 156216458 | CV2348008 | single nucleotide variant | NM_001256732.3(SSBP2):c.962A>G (p.Asp321Gly) | not specified [RCV004197691] | uncertain significance | 5 | 81437449 | 81437449 | Human | | name |
| 401762565 | CV2696167 | single nucleotide variant | NM_001256732.3(SSBP2):c.565C>T (p.Pro189Ser) | not specified [RCV004310221] | uncertain significance | 5 | 81473705 | 81473705 | Human | | name |
| 401734544 | CV2709532 | single nucleotide variant | NM_001256732.3(SSBP2):c.991A>G (p.Asn331Asp) | not specified [RCV004318769] | uncertain significance | 5 | 81428674 | 81428674 | Human | | name |
| 401890542 | CV2778855 | single nucleotide variant | NM_001256732.3(SSBP2):c.830A>G (p.Tyr277Cys) | not specified [RCV004346745] | uncertain significance | 5 | 81442696 | 81442696 | Human | | name |
| 405703474 | CV3326949 | single nucleotide variant | NM_001256732.3(SSBP2):c.674G>A (p.Gly225Asp) | not specified [RCV004460731] | uncertain significance | 5 | 81461092 | 81461092 | Human | | name |
| 407516892 | CV3474909 | single nucleotide variant | NM_001256732.3(SSBP2):c.389G>A (p.Arg130Gln) | not specified [RCV004675453] | uncertain significance | 5 | 81489293 | 81489293 | Human | | name |
| 597681248 | CV3611732 | single nucleotide variant | NM_001256732.3(SSBP2):c.523A>G (p.Met175Val) | not specified [RCV004857513] | uncertain significance | 5 | 81473747 | 81473747 | Human | | name |
| 598174086 | CV3922855 | single nucleotide variant | NM_001256732.3(SSBP2):c.808A>G (p.Thr270Ala) | not specified [RCV005285296] | uncertain significance | 5 | 81442718 | 81442718 | Human | | name |
| 598174094 | CV3922856 | single nucleotide variant | NM_001256732.3(SSBP2):c.837A>C (p.Leu279Phe) | not specified [RCV005285297] | uncertain significance | 5 | 81442689 | 81442689 | Human | | name |
| 41405582 | CV981505 | single nucleotide variant | NM_001256732.3(SSBP2):c.971G>C (p.Ser324Thr) | not provided [RCV001813073] | uncertain significance | 5 | 81437440 | 81437440 | Human | | name |