| 401923118 | CV2796630 | single nucleotide variant | NM_019087.3(ARL15):c.253+3A>T | ARL15-related disorder [RCV003404249] | uncertain significance | 5 | 54154577 | 54154577 | Human | | name , trait , alternate_id |
| 405287926 | CV3218035 | single nucleotide variant | NM_019087.3(ARL15):c.15A>G (p.Arg5=) | ARL15-related disorder [RCV003982159] | benign | 5 | 54310465 | 54310465 | Human | 4 | name , trait , alternate_id |
| 401771269 | CV2722773 | single nucleotide variant | NM_019087.3(ARL15):c.89G>A (p.Arg30Gln) | not specified [RCV004325201] | uncertain significance | 5 | 54171888 | 54171888 | Human | | name |
| 405662854 | CV3290115 | single nucleotide variant | NM_019087.3(ARL15):c.95A>T (p.Glu32Val) | not specified [RCV004417888] | uncertain significance | 5 | 54171882 | 54171882 | Human | | name |
| 401758878 | CV2705216 | single nucleotide variant | NM_019087.3(ARL15):c.124G>A (p.Gly42Ser) | not specified [RCV004311920] | uncertain significance | 5 | 54171853 | 54171853 | Human | | name |
| 329390581 | CV2437096 | single nucleotide variant | NM_019087.3(ARL15):c.484G>C (p.Glu162Gln) | not specified [RCV004262903] | uncertain significance | 5 | 53886692 | 53886692 | Human | | name |
| 405662841 | CV3290112 | single nucleotide variant | NM_019087.3(ARL15):c.347T>C (p.Leu116Ser) | not specified [RCV004417885] | uncertain significance | 5 | 54113317 | 54113317 | Human | | name |
| 405662844 | CV3290113 | single nucleotide variant | NM_019087.3(ARL15):c.425A>G (p.Asn142Ser) | not specified [RCV004417886] | uncertain significance | 5 | 54113239 | 54113239 | Human | | name |
| 405662849 | CV3290114 | single nucleotide variant | NM_019087.3(ARL15):c.499G>A (p.Gly167Arg) | not specified [RCV004417887] | uncertain significance | 5 | 53886677 | 53886677 | Human | | name |
| 598183261 | CV3901732 | single nucleotide variant | NM_019087.3(ARL15):c.349G>A (p.Glu117Lys) | not specified [RCV005265574] | uncertain significance | 5 | 54113315 | 54113315 | Human | | name |