| 155978708 | CV2318141 | single nucleotide variant | NM_015994.4(ATP6V1D):c.89G>A (p.Arg30Gln) | not specified [RCV004177552] | uncertain significance | 14 | 67352993 | 67352993 | Human | | name |
| 405667313 | CV3297701 | single nucleotide variant | NM_015994.4(ATP6V1D):c.65G>A (p.Arg22His) | not specified [RCV004418779] | uncertain significance | 14 | 67353017 | 67353017 | Human | | name |
| 405667318 | CV3297702 | single nucleotide variant | NM_015994.4(ATP6V1D):c.89G>T (p.Arg30Leu) | not specified [RCV004418780] | uncertain significance | 14 | 67352993 | 67352993 | Human | | name |
| 401877469 | CV2790181 | single nucleotide variant | NM_015994.4(ATP6V1D):c.169T>A (p.Leu57Met) | not specified [RCV004364105] | uncertain significance | 14 | 67350681 | 67350681 | Human | | name |
| 598199542 | CV3920707 | single nucleotide variant | NM_015994.4(ATP6V1D):c.178G>A (p.Glu60Lys) | not specified [RCV005289864] | uncertain significance | 14 | 67350672 | 67350672 | Human | | name |
| 155919508 | CV2360282 | single nucleotide variant | NM_015994.4(ATP6V1D):c.599A>T (p.Tyr200Phe) | not specified [RCV004208623] | uncertain significance | 14 | 67340443 | 67340443 | Human | | name |
| 401762771 | CV2720068 | single nucleotide variant | NM_015994.4(ATP6V1D):c.425T>C (p.Val142Ala) | not specified [RCV004323640] | uncertain significance | 14 | 67345799 | 67345799 | Human | | name |
| 405667289 | CV3297696 | single nucleotide variant | NM_015994.4(ATP6V1D):c.446C>T (p.Ala149Val) | not specified [RCV004418774] | uncertain significance | 14 | 67345778 | 67345778 | Human | | name |
| 405667292 | CV3297697 | single nucleotide variant | NM_015994.4(ATP6V1D):c.484A>G (p.Ile162Val) | not specified [RCV004418775] | uncertain significance | 14 | 67343411 | 67343411 | Human | | name |
| 405667297 | CV3297698 | single nucleotide variant | NM_015994.4(ATP6V1D):c.490A>G (p.Ile164Val) | not specified [RCV004418776] | uncertain significance | 14 | 67343405 | 67343405 | Human | | name |
| 405667303 | CV3297699 | single nucleotide variant | NM_015994.4(ATP6V1D):c.587G>A (p.Arg196Gln) | not specified [RCV004418777] | uncertain significance | 14 | 67340455 | 67340455 | Human | | name |
| 405667309 | CV3297700 | single nucleotide variant | NM_015994.4(ATP6V1D):c.613A>C (p.Ile205Leu) | not specified [RCV004418778] | uncertain significance | 14 | 67338752 | 67338752 | Human | | name |