| 15157894 | CV778836 | single nucleotide variant | NM_007274.4(ACOT7):c.1014+8C>T | not provided [RCV000969395] | benign | 1 | 6281094 | 6281094 | Human | | name |
| 156183045 | CV2222352 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7723A>G | not specified [RCV004099224] | uncertain significance | 1 | 6385534 | 6385534 | Human | | name |
| 155931636 | CV2362605 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7699G>A | not specified [RCV004215258] | uncertain significance | 1 | 6385558 | 6385558 | Human | | name |
| 401739023 | CV2708285 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7604C>T | not specified [RCV004311626] | uncertain significance | 1 | 6385653 | 6385653 | Human | | name |
| 401886150 | CV2774857 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7684C>T | not specified [RCV004343941] | uncertain significance | 1 | 6385573 | 6385573 | Human | | name |
| 405238464 | CV3081228 | insertion | NM_007274.4(ACOT7):c.-62_-61insC | not provided [RCV003736357] | benign | 1 | 6393460 | 6393461 | Human | | name |
| 405292286 | CV3192396 | single nucleotide variant | NM_007274.4(ACOT7):c.144-8956C>T | ACOT7-related disorder [RCV003929666] | benign | 1 | 6358822 | 6358822 | Human | | name , trait , alternate_id |
| 405281839 | CV3216115 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7755T>C | ACOT7-related disorder [RCV003956657] | likely benign | 1 | 6385502 | 6385502 | Human | | name , trait , alternate_id |
| 407500642 | CV3417786 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7615C>G | not specified [RCV004607178] | uncertain significance | 1 | 6385642 | 6385642 | Human | | name |
| 597774299 | CV3643403 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7705G>A | not specified [RCV004897981] | likely benign | 1 | 6385552 | 6385552 | Human | | name |
| 597749142 | CV3643419 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7711G>A | not specified [RCV004892294] | uncertain significance | 1 | 6385546 | 6385546 | Human | | name |
| 597749148 | CV3643429 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7615C>T | not specified [RCV004892295] | uncertain significance | 1 | 6385642 | 6385642 | Human | | name |
| 597774315 | CV3643460 | single nucleotide variant | NM_007274.4(ACOT7):c.143+7603G>T | not specified [RCV004897985] | uncertain significance | 1 | 6385654 | 6385654 | Human | | name |
| 405277334 | CV3195410 | single nucleotide variant | NM_007274.4(ACOT7):c.144-10787G>A | ACOT7-related disorder [RCV003904198] | likely benign | 1 | 6360653 | 6360653 | Human | | name , trait , alternate_id |
| 405292993 | CV3207152 | single nucleotide variant | NM_007274.4(ACOT7):c.306C>T (p.Phe102=) | ACOT7-related disorder [RCV003931558] | likely benign | 1 | 6339545 | 6339545 | Human | | name , trait , alternate_id |
| 405285283 | CV3212277 | single nucleotide variant | NM_007274.4(ACOT7):c.384G>A (p.Val128=) | ACOT7-related disorder [RCV003958902] | benign | 1 | 6339467 | 6339467 | Human | | name , trait , alternate_id |
| 15194469 | CV696829 | single nucleotide variant | NM_007274.4(ACOT7):c.798C>T (p.Asp266=) | not provided [RCV000955656] | benign | 1 | 6294895 | 6294895 | Human | | name |
| 156386265 | CV2228161 | single nucleotide variant | NM_007274.4(ACOT7):c.284C>T (p.Ala95Val) | not specified [RCV004096374] | uncertain significance | 1 | 6339567 | 6339567 | Human | | name |
| 401752427 | CV2707005 | single nucleotide variant | NM_007274.4(ACOT7):c.259G>A (p.Gly87Arg) | not specified [RCV004321602] | uncertain significance | 1 | 6349751 | 6349751 | Human | | name |
| 405272433 | CV3221810 | single nucleotide variant | NM_007274.4(ACOT7):c.1023C>T (p.Thr341=) | ACOT7-related disorder [RCV003972177] | benign | 1 | 6264687 | 6264687 | Human | | name , trait , alternate_id |
| 407489711 | CV3417767 | single nucleotide variant | NM_007274.4(ACOT7):c.187G>A (p.Gly63Arg) | not specified [RCV004604115] | uncertain significance | 1 | 6349823 | 6349823 | Human | | name |
| 407489128 | CV3417777 | single nucleotide variant | NM_007274.4(ACOT7):c.265C>T (p.Arg89Cys) | not specified [RCV004604124] | uncertain significance | 1 | 6339586 | 6339586 | Human | | name |
| 597774307 | CV3643443 | single nucleotide variant | NM_007274.4(ACOT7):c.239G>A (p.Arg80Gln) | not specified [RCV004897983] | uncertain significance | 1 | 6349771 | 6349771 | Human | | name |
| 156227527 | CV2203218 | single nucleotide variant | NM_007274.4(ACOT7):c.534G>C (p.Glu178Asp) | not specified [RCV004070909] | uncertain significance | 1 | 6327390 | 6327390 | Human | | name |
| 156345648 | CV2291148 | single nucleotide variant | NM_007274.4(ACOT7):c.872A>G (p.Asn291Ser) | not specified [RCV004153455] | uncertain significance | 1 | 6281244 | 6281244 | Human | | name |
| 156351668 | CV2323809 | single nucleotide variant | NM_007274.4(ACOT7):c.595G>A (p.Gly199Arg) | not specified [RCV004176350] | uncertain significance | 1 | 6327329 | 6327329 | Human | | name |
| 329396321 | CV2462508 | single nucleotide variant | NM_007274.4(ACOT7):c.586T>G (p.Trp196Gly) | not specified [RCV004276684] | uncertain significance | 1 | 6327338 | 6327338 | Human | | name |
| 401866701 | CV2782919 | single nucleotide variant | NM_007274.4(ACOT7):c.889G>A (p.Glu297Lys) | not specified [RCV004361718] | uncertain significance | 1 | 6281227 | 6281227 | Human | | name |
| 405738067 | CV3292004 | single nucleotide variant | NM_007274.4(ACOT7):c.517C>G (p.Arg173Gly) | not specified [RCV004430268] | uncertain significance | 1 | 6327407 | 6327407 | Human | | name |
| 405738145 | CV3292017 | single nucleotide variant | NM_007274.4(ACOT7):c.704T>G (p.Val235Gly) | not specified [RCV004430281] | uncertain significance | 1 | 6318500 | 6318500 | Human | | name |
| 405738166 | CV3292020 | single nucleotide variant | NM_007274.4(ACOT7):c.866C>T (p.Thr289Met) | not specified [RCV004430284] | uncertain significance | 1 | 6281250 | 6281250 | Human | | name |
| 407500647 | CV3417796 | single nucleotide variant | NM_007274.4(ACOT7):c.596G>A (p.Gly199Glu) | not specified [RCV004607179] | uncertain significance | 1 | 6327328 | 6327328 | Human | | name |
| 597774311 | CV3643454 | single nucleotide variant | NM_007274.4(ACOT7):c.518G>A (p.Arg173Gln) | not specified [RCV004897984] | uncertain significance | 1 | 6327406 | 6327406 | Human | | name |
| 13485250 | CV442871 | single nucleotide variant | NM_007274.4(ACOT7):c.937T>C (p.Tyr313His) | not provided [RCV000522552] | uncertain significance | 1 | 6281179 | 6281179 | Human | | name |
| 156041428 | CV2261378 | single nucleotide variant | NM_007274.4(ACOT7):c.1088A>G (p.Gln363Arg) | not specified [RCV004130018] | uncertain significance | 1 | 6264622 | 6264622 | Human | | name |
| 155907502 | CV2302227 | single nucleotide variant | NM_007274.4(ACOT7):c.1099G>A (p.Glu367Lys) | not specified [RCV004159220] | uncertain significance | 1 | 6264611 | 6264611 | Human | | name |
| 405737910 | CV3291981 | single nucleotide variant | NM_007274.4(ACOT7):c.1097C>T (p.Ala366Val) | not specified [RCV004430245] | uncertain significance | 1 | 6264613 | 6264613 | Human | | name |
| 597774337 | CV3639965 | single nucleotide variant | NM_007274.4(ACOT7):c.1018G>A (p.Glu340Lys) | not specified [RCV004897991] | uncertain significance | 1 | 6264692 | 6264692 | Human | | name |
| 597774303 | CV3643435 | single nucleotide variant | NM_007274.4(ACOT7):c.1109C>G (p.Pro370Arg) | not specified [RCV004897982] | uncertain significance | 1 | 6264601 | 6264601 | Human | | name |
| 598248505 | CV3949652 | single nucleotide variant | NM_007274.4(ACOT7):c.1096G>A (p.Ala366Thr) | not specified [RCV005298033] | likely benign | 1 | 6264614 | 6264614 | Human | | name |
| 598161724 | CV3949655 | single nucleotide variant | NM_007274.4(ACOT7):c.1057G>A (p.Gly353Arg) | not specified [RCV005307067] | uncertain significance | 1 | 6264653 | 6264653 | Human | | name |
