| 597800568 | CV3610596 | single nucleotide variant | NM_032936.4(TMEM60):c.17C>T (p.Ala6Val) | not specified [RCV004880278] | uncertain significance | 7 | 77794357 | 77794357 | Human | | name |
| 155934293 | CV2225246 | single nucleotide variant | NM_032936.4(TMEM60):c.266C>T (p.Ala89Val) | not specified [RCV004098897] | uncertain significance | 7 | 77794108 | 77794108 | Human | | name |
| 156079249 | CV2226527 | single nucleotide variant | NM_032936.4(TMEM60):c.277G>A (p.Ala93Thr) | not specified [RCV004101790] | uncertain significance | 7 | 77794097 | 77794097 | Human | | name |
| 156312621 | CV2256895 | single nucleotide variant | NM_032936.4(TMEM60):c.241C>T (p.Leu81Phe) | not specified [RCV004121099] | uncertain significance | 7 | 77794133 | 77794133 | Human | | name |
| 329362096 | CV2448289 | single nucleotide variant | NM_032936.4(TMEM60):c.250A>G (p.Met84Val) | not specified [RCV004263488] | uncertain significance | 7 | 77794124 | 77794124 | Human | | name |
| 405771603 | CV3346615 | single nucleotide variant | NM_032936.4(TMEM60):c.135T>G (p.Phe45Leu) | not specified [RCV004470386] | uncertain significance | 7 | 77794239 | 77794239 | Human | | name |
| 407526833 | CV3482785 | single nucleotide variant | NM_032936.4(TMEM60):c.280C>G (p.Leu94Val) | not specified [RCV004679780] | uncertain significance | 7 | 77794094 | 77794094 | Human | | name |
| 598252599 | CV3913972 | single nucleotide variant | NM_032936.4(TMEM60):c.232G>T (p.Ala78Ser) | not specified [RCV005278112] | uncertain significance | 7 | 77794142 | 77794142 | Human | | name |
| 598227220 | CV3913973 | single nucleotide variant | NM_032936.4(TMEM60):c.233C>A (p.Ala78Asp) | not specified [RCV005294552] | uncertain significance | 7 | 77794141 | 77794141 | Human | | name |
| 156018553 | CV2370294 | single nucleotide variant | NM_032936.4(TMEM60):c.299A>G (p.Gln100Arg) | not specified [RCV004213209] | uncertain significance | 7 | 77794075 | 77794075 | Human | | name |
| 401727813 | CV2678477 | single nucleotide variant | NM_032936.4(TMEM60):c.394A>G (p.Arg132Gly) | not specified [RCV004292494] | uncertain significance | 7 | 77793980 | 77793980 | Human | | name |
| 405771608 | CV3346616 | single nucleotide variant | NM_032936.4(TMEM60):c.313A>T (p.Asn105Tyr) | not specified [RCV004470387] | uncertain significance | 7 | 77794061 | 77794061 | Human | | name |