| 156061049 | CV2236058 | single nucleotide variant | NM_016479.6(SHISA5):c.247G>A (p.Val83Ile) | not specified [RCV004114218] | uncertain significance | 3 | 48479244 | 48479244 | Human | | name |
| 155986163 | CV2345471 | single nucleotide variant | NM_016479.6(SHISA5):c.274G>A (p.Ala92Thr) | not specified [RCV004198240] | uncertain significance | 3 | 48479217 | 48479217 | Human | | name |
| 156149841 | CV2265377 | single nucleotide variant | NM_016479.6(SHISA5):c.460G>A (p.Val154Met) | not specified [RCV004128259] | uncertain significance | 3 | 48469544 | 48469544 | Human | | name |
| 156283315 | CV2288887 | single nucleotide variant | NM_016479.6(SHISA5):c.572A>G (p.Tyr191Cys) | not specified [RCV004148076] | uncertain significance | 3 | 48469432 | 48469432 | Human | | name |
| 156057568 | CV2322860 | single nucleotide variant | NM_016479.6(SHISA5):c.419G>A (p.Arg140His) | not specified [RCV004185319] | uncertain significance | 3 | 48469739 | 48469739 | Human | | name |
| 156325694 | CV2335345 | single nucleotide variant | NM_016479.6(SHISA5):c.472C>T (p.Pro158Ser) | not specified [RCV004186905] | uncertain significance | 3 | 48469532 | 48469532 | Human | | name |
| 156160798 | CV2371305 | single nucleotide variant | NM_016479.6(SHISA5):c.620C>T (p.Pro207Leu) | not specified [RCV004223317] | uncertain significance | 3 | 48469384 | 48469384 | Human | | name |
| 401720170 | CV2705739 | single nucleotide variant | NM_016479.6(SHISA5):c.497C>T (p.Pro166Leu) | not specified [RCV004318579] | uncertain significance | 3 | 48469507 | 48469507 | Human | | name |
| 405731376 | CV3314473 | single nucleotide variant | NM_016479.6(SHISA5):c.403C>A (p.Leu135Ile) | not specified [RCV004451058] | uncertain significance | 3 | 48469755 | 48469755 | Human | | name |
| 405731385 | CV3314474 | single nucleotide variant | NM_016479.6(SHISA5):c.413C>T (p.Thr138Met) | not specified [RCV004451059] | likely benign | 3 | 48469745 | 48469745 | Human | | name |
| 405731391 | CV3314475 | single nucleotide variant | NM_016479.6(SHISA5):c.577A>G (p.Met193Val) | not specified [RCV004451060] | uncertain significance | 3 | 48469427 | 48469427 | Human | | name |
| 405731402 | CV3314476 | single nucleotide variant | NM_016479.6(SHISA5):c.692C>T (p.Ala231Val) | not specified [RCV004451061] | uncertain significance | 3 | 48469138 | 48469138 | Human | | name |
| 597698779 | CV3602600 | single nucleotide variant | NM_016479.6(SHISA5):c.655G>A (p.Ala219Thr) | not specified [RCV004859674] | uncertain significance | 3 | 48469175 | 48469175 | Human | | name |
| 598241776 | CV3914191 | single nucleotide variant | NM_016479.6(SHISA5):c.427C>T (p.Arg143Cys) | not specified [RCV005276407] | uncertain significance | 3 | 48469731 | 48469731 | Human | | name |
| 598241783 | CV3914192 | single nucleotide variant | NM_016479.6(SHISA5):c.631G>A (p.Glu211Lys) | not specified [RCV005276408] | uncertain significance | 3 | 48469373 | 48469373 | Human | | name |