| 405736506 | CV3323252 | single nucleotide variant | NM_014471.3(SPINK4):c.25G>A (p.Ala9Thr) | not specified [RCV004465024] | likely benign | 9 | 33240233 | 33240233 | Human | | name |
| 401770791 | CV2707415 | single nucleotide variant | NM_014471.3(SPINK4):c.80G>A (p.Gly27Glu) | not specified [RCV004312802] | uncertain significance | 9 | 33245130 | 33245130 | Human | | name |
| 156295214 | CV2233712 | single nucleotide variant | NM_014471.3(SPINK4):c.134C>A (p.Thr45Asn) | not specified [RCV004100159] | uncertain significance | 9 | 33246647 | 33246647 | Human | | name |
| 156056381 | CV2308903 | single nucleotide variant | NM_014471.3(SPINK4):c.229G>C (p.Asp77His) | not specified [RCV004169195] | uncertain significance | 9 | 33248439 | 33248439 | Human | | name |
| 156142282 | CV2386034 | single nucleotide variant | NM_014471.3(SPINK4):c.133A>G (p.Thr45Ala) | not specified [RCV004229099] | uncertain significance | 9 | 33246646 | 33246646 | Human | | name |
| 156039862 | CV2390380 | single nucleotide variant | NM_014471.3(SPINK4):c.185C>T (p.Thr62Met) | not specified [RCV004240736] | uncertain significance | 9 | 33246698 | 33246698 | Human | | name |
| 329402844 | CV2451446 | single nucleotide variant | NM_014471.3(SPINK4):c.157G>C (p.Val53Leu) | not specified [RCV004272119] | uncertain significance | 9 | 33246670 | 33246670 | Human | | name |
| 401780477 | CV2674043 | single nucleotide variant | NM_014471.3(SPINK4):c.212G>A (p.Arg71Gln) | not specified [RCV004295455] | uncertain significance | 9 | 33246725 | 33246725 | Human | | name |
| 401878121 | CV2767412 | single nucleotide variant | NM_014471.3(SPINK4):c.107T>G (p.Ile36Ser) | not specified [RCV004349568] | uncertain significance | 9 | 33246620 | 33246620 | Human | | name |
| 405736467 | CV3323247 | single nucleotide variant | NM_014471.3(SPINK4):c.161G>A (p.Cys54Tyr) | not specified [RCV004465019] | uncertain significance | 9 | 33246674 | 33246674 | Human | | name |
| 405736474 | CV3323248 | single nucleotide variant | NM_014471.3(SPINK4):c.163G>C (p.Gly55Arg) | not specified [RCV004465020] | uncertain significance | 9 | 33246676 | 33246676 | Human | | name |
| 405736484 | CV3323249 | single nucleotide variant | NM_014471.3(SPINK4):c.181T>C (p.Tyr61His) | not specified [RCV004465021] | uncertain significance | 9 | 33246694 | 33246694 | Human | | name |
| 405736488 | CV3323250 | single nucleotide variant | NM_014471.3(SPINK4):c.199C>T (p.Leu67Phe) | not specified [RCV004465022] | uncertain significance | 9 | 33246712 | 33246712 | Human | | name |
| 597768623 | CV3607592 | single nucleotide variant | NM_014471.3(SPINK4):c.248A>G (p.Asp83Gly) | not specified [RCV004871074] | uncertain significance | 9 | 33248458 | 33248458 | Human | | name |
| 597768628 | CV3607593 | single nucleotide variant | NM_014471.3(SPINK4):c.193T>C (p.Cys65Arg) | not specified [RCV004871075] | uncertain significance | 9 | 33246706 | 33246706 | Human | | name |