| 407492182 | CV3428710 | single nucleotide variant | NM_005736.4(ACTR1A):c.114T>C (p.Tyr38=) | not specified [RCV004604901] | likely benign | 10 | 102489138 | 102489138 | Human | | name |
| 156042249 | CV2310956 | single nucleotide variant | NM_005736.4(ACTR1A):c.281A>G (p.Tyr94Cys) | not specified [RCV004163990] | uncertain significance | 10 | 102488184 | 102488184 | Human | | name |
| 597775304 | CV3643912 | single nucleotide variant | NM_005736.4(ACTR1A):c.133G>A (p.Val45Ile) | not specified [RCV004898206] | uncertain significance | 10 | 102489119 | 102489119 | Human | | name |
| 597775308 | CV3643915 | single nucleotide variant | NM_005736.4(ACTR1A):c.238G>A (p.Val80Ile) | not specified [RCV004898207] | uncertain significance | 10 | 102488227 | 102488227 | Human | | name |
| 597775393 | CV3643944 | single nucleotide variant | NM_005736.4(ACTR1A):c.209C>T (p.Ser70Leu) | not specified [RCV004898227] | uncertain significance | 10 | 102488256 | 102488256 | Human | | name |
| 8633469 | CV88684 | single nucleotide variant | NM_005736.3(ACTR1A):c.1017C>T (p.Ser339=) | Malignant melanoma [RCV000068777] | not provided | 10 | 102481143 | 102481143 | Human | | name |
| 156369956 | CV2263448 | single nucleotide variant | NM_005736.4(ACTR1A):c.590A>G (p.Tyr197Cys) | not specified [RCV004133694] | uncertain significance | 10 | 102484227 | 102484227 | Human | | name |
| 156207258 | CV2298028 | single nucleotide variant | NM_005736.4(ACTR1A):c.587T>A (p.Leu196His) | not specified [RCV004157925] | uncertain significance | 10 | 102484230 | 102484230 | Human | | name |
| 156106468 | CV2307641 | single nucleotide variant | NM_005736.4(ACTR1A):c.924A>T (p.Lys308Asn) | not specified [RCV004168059] | uncertain significance | 10 | 102482002 | 102482002 | Human | | name |
| 405761551 | CV3300215 | single nucleotide variant | NM_005736.4(ACTR1A):c.803T>C (p.Ile268Thr) | not specified [RCV004433732] | uncertain significance | 10 | 102482123 | 102482123 | Human | | name |
| 407492139 | CV3428700 | single nucleotide variant | NM_005736.4(ACTR1A):c.574C>T (p.Arg192Cys) | not specified [RCV004604891] | uncertain significance | 10 | 102484243 | 102484243 | Human | | name |
| 597775338 | CV3643924 | single nucleotide variant | NM_005736.4(ACTR1A):c.800T>C (p.Leu267Ser) | not specified [RCV004898214] | uncertain significance | 10 | 102482126 | 102482126 | Human | | name |
| 597775371 | CV3643935 | single nucleotide variant | NM_005736.4(ACTR1A):c.380T>G (p.Val127Gly) | not specified [RCV004898222] | uncertain significance | 10 | 102485669 | 102485669 | Human | | name |
| 598202275 | CV3946551 | single nucleotide variant | NM_005736.4(ACTR1A):c.541A>G (p.Met181Val) | not specified [RCV005314419] | uncertain significance | 10 | 102484276 | 102484276 | Human | | name |
| 598202307 | CV3946560 | single nucleotide variant | NM_005736.4(ACTR1A):c.568G>A (p.Val190Ile) | not specified [RCV005314426] | uncertain significance | 10 | 102484249 | 102484249 | Human | | name |
| 598202346 | CV3946571 | single nucleotide variant | NM_005736.4(ACTR1A):c.698C>T (p.Thr233Met) | not specified [RCV005314434] | uncertain significance | 10 | 102483063 | 102483063 | Human | | name |