| 155990960 | CV2255595 | single nucleotide variant | NM_001018069.2(SERBP1):c.696-8A>G | not specified [RCV004120012] | uncertain significance | 1 | 67424285 | 67424285 | Human | | name |
| 597737647 | CV3598415 | single nucleotide variant | NM_001018069.2(SERBP1):c.696-10A>G | not specified [RCV004864082] | uncertain significance | 1 | 67424287 | 67424287 | Human | | name |
| 407488712 | CV3473592 | single nucleotide variant | NM_001018069.2(SERBP1):c.4C>T (p.Pro2Ser) | not specified [RCV004665918] | uncertain significance | 1 | 67430297 | 67430297 | Human | | name |
| 155978614 | CV2318102 | single nucleotide variant | NM_001018069.2(SERBP1):c.52G>C (p.Asp18His) | not specified [RCV004177519] | uncertain significance | 1 | 67430249 | 67430249 | Human | | name |
| 8625043 | CV80162 | single nucleotide variant | NM_001018067.1(SERBP1):c.447C>T (p.Gly149=) | Malignant melanoma [RCV000060238] | not provided | 1 | 67426152 | 67426152 | Human | | name |
| 156014075 | CV2300507 | single nucleotide variant | NM_001018069.2(SERBP1):c.203A>G (p.Lys68Arg) | not specified [RCV004153691] | uncertain significance | 1 | 67430098 | 67430098 | Human | | name |
| 405746347 | CV3310818 | single nucleotide variant | NM_001018069.2(SERBP1):c.108C>A (p.Asn36Lys) | not specified [RCV004453118] | uncertain significance | 1 | 67430193 | 67430193 | Human | | name |
| 405746365 | CV3310820 | single nucleotide variant | NM_001018069.2(SERBP1):c.185A>C (p.Asn62Thr) | not specified [RCV004453120] | uncertain significance | 1 | 67430116 | 67430116 | Human | | name |
| 405746371 | CV3310821 | single nucleotide variant | NM_001018069.2(SERBP1):c.284C>T (p.Thr95Met) | not specified [RCV004453121] | uncertain significance | 1 | 67430017 | 67430017 | Human | | name |
| 407488718 | CV3473596 | single nucleotide variant | NM_001018069.2(SERBP1):c.247C>A (p.Pro83Thr) | not specified [RCV004665919] | uncertain significance | 1 | 67430054 | 67430054 | Human | | name |
| 598225237 | CV3900352 | single nucleotide variant | NM_001018069.2(SERBP1):c.247C>T (p.Pro83Ser) | not specified [RCV005273319] | uncertain significance | 1 | 67430054 | 67430054 | Human | | name |
| 598225250 | CV3900354 | single nucleotide variant | NM_001018069.2(SERBP1):c.290C>T (p.Pro97Leu) | not specified [RCV005273321] | uncertain significance | 1 | 67430011 | 67430011 | Human | | name |
| 598225268 | CV3900357 | single nucleotide variant | NM_001018069.2(SERBP1):c.274A>C (p.Lys92Gln) | not specified [RCV005273324] | uncertain significance | 1 | 67430027 | 67430027 | Human | | name |
| 156387375 | CV2221489 | single nucleotide variant | NM_001018069.2(SERBP1):c.745C>G (p.His249Asp) | not specified [RCV004096767] | uncertain significance | 1 | 67424228 | 67424228 | Human | | name |
| 156356673 | CV2257485 | single nucleotide variant | NM_001018069.2(SERBP1):c.953C>T (p.Ala318Val) | not specified [RCV004125554] | uncertain significance | 1 | 67415338 | 67415338 | Human | | name |
| 156360141 | CV2268988 | single nucleotide variant | NM_001018069.2(SERBP1):c.789A>C (p.Glu263Asp) | not specified [RCV004128386] | uncertain significance | 1 | 67420171 | 67420171 | Human | | name |
| 156234537 | CV2271183 | single nucleotide variant | NM_001018069.2(SERBP1):c.392G>A (p.Arg131Gln) | not specified [RCV004134546] | uncertain significance | 1 | 67426207 | 67426207 | Human | | name |
| 155998913 | CV2287208 | single nucleotide variant | NM_001018069.2(SERBP1):c.764C>A (p.Thr255Asn) | not specified [RCV004146858] | uncertain significance | 1 | 67424209 | 67424209 | Human | | name |
| 156149358 | CV2321955 | single nucleotide variant | NM_001018069.2(SERBP1):c.679G>A (p.Val227Ile) | not specified [RCV004173411] | uncertain significance | 1 | 67424904 | 67424904 | Human | | name |
| 155958539 | CV2395203 | single nucleotide variant | NM_001018069.2(SERBP1):c.775G>A (p.Glu259Lys) | not specified [RCV004236871] | uncertain significance | 1 | 67420185 | 67420185 | Human | | name |
| 329374895 | CV2431085 | single nucleotide variant | NM_001018069.2(SERBP1):c.731C>A (p.Pro244His) | not specified [RCV004250449] | uncertain significance | 1 | 67424242 | 67424242 | Human | | name |
| 329353293 | CV2469109 | single nucleotide variant | NM_001018069.2(SERBP1):c.841A>C (p.Ile281Leu) | not specified [RCV004274341] | uncertain significance | 1 | 67420119 | 67420119 | Human | | name |
| 401758680 | CV2700693 | single nucleotide variant | NM_001018069.2(SERBP1):c.542G>T (p.Arg181Leu) | not specified [RCV004313406] | uncertain significance | 1 | 67425146 | 67425146 | Human | | name |
| 401857150 | CV2759986 | single nucleotide variant | NM_001018069.2(SERBP1):c.467C>T (p.Pro156Leu) | not specified [RCV004345404] | uncertain significance | 1 | 67425221 | 67425221 | Human | | name |
| 405746379 | CV3310822 | single nucleotide variant | NM_001018069.2(SERBP1):c.569A>G (p.Lys190Arg) | not specified [RCV004453122] | uncertain significance | 1 | 67425119 | 67425119 | Human | | name |
| 405746386 | CV3310823 | single nucleotide variant | NM_001018069.2(SERBP1):c.710C>T (p.Ser237Leu) | not specified [RCV004453123] | uncertain significance | 1 | 67424263 | 67424263 | Human | | name |
| 407492421 | CV3473593 | single nucleotide variant | NM_001018069.2(SERBP1):c.793G>A (p.Val265Ile) | not specified [RCV004667120] | uncertain significance | 1 | 67420167 | 67420167 | Human | | name |
| 597737637 | CV3598413 | single nucleotide variant | NM_001018069.2(SERBP1):c.383C>T (p.Pro128Leu) | not specified [RCV004864080] | uncertain significance | 1 | 67426216 | 67426216 | Human | | name |
| 597737642 | CV3598414 | single nucleotide variant | NM_001018069.2(SERBP1):c.511G>A (p.Gly171Ser) | not specified [RCV004864081] | uncertain significance | 1 | 67425177 | 67425177 | Human | | name |
| 598225244 | CV3900353 | single nucleotide variant | NM_001018069.2(SERBP1):c.354G>C (p.Gln118His) | not specified [RCV005273320] | uncertain significance | 1 | 67426245 | 67426245 | Human | | name |
| 598225257 | CV3900355 | single nucleotide variant | NM_001018069.2(SERBP1):c.723G>C (p.Glu241Asp) | not specified [RCV005273322] | uncertain significance | 1 | 67424250 | 67424250 | Human | | name |
| 598225263 | CV3900356 | single nucleotide variant | NM_001018069.2(SERBP1):c.326T>C (p.Val109Ala) | not specified [RCV005273323] | uncertain significance | 1 | 67426273 | 67426273 | Human | | name |
| 598225273 | CV3900358 | single nucleotide variant | NM_001018069.2(SERBP1):c.394C>A (p.Pro132Thr) | not specified [RCV005273325] | uncertain significance | 1 | 67426205 | 67426205 | Human | | name |
| 155903297 | CV2274854 | single nucleotide variant | NM_001018069.2(SERBP1):c.1028A>G (p.Asn343Ser) | not specified [RCV004133052] | uncertain significance | 1 | 67415263 | 67415263 | Human | | name |
| 405746357 | CV3310819 | single nucleotide variant | NM_001018069.2(SERBP1):c.1121A>G (p.Asp374Gly) | not specified [RCV004453119] | uncertain significance | 1 | 67415170 | 67415170 | Human | | name |
| 407492424 | CV3473594 | single nucleotide variant | NM_001018069.2(SERBP1):c.1045C>T (p.Arg349Cys) | not specified [RCV004667121] | uncertain significance | 1 | 67415246 | 67415246 | Human | | name |
| 597737627 | CV3598410 | single nucleotide variant | NM_001018069.2(SERBP1):c.1120G>A (p.Asp374Asn) | not specified [RCV004864078] | uncertain significance | 1 | 67415171 | 67415171 | Human | | name |
| 597737632 | CV3598411 | single nucleotide variant | NM_001018069.2(SERBP1):c.1109G>T (p.Gly370Val) | not specified [RCV004864079] | uncertain significance | 1 | 67415182 | 67415182 | Human | | name |