| 405683381 | CV3286018 | single nucleotide variant | NM_031944.3(MIXL1):c.20G>A (p.Arg7His) | not specified [RCV004422148] | uncertain significance | 1 | 226223701 | 226223701 | Human | | name |
| 598187165 | CV3993411 | single nucleotide variant | NM_031944.3(MIXL1):c.17C>T (p.Ser6Phe) | not specified [RCV005373523] | uncertain significance | 1 | 226223698 | 226223698 | Human | | name |
| 155978783 | CV2215092 | single nucleotide variant | NM_031944.3(MIXL1):c.76G>T (p.Gly26Cys) | not specified [RCV004084859] | uncertain significance | 1 | 226223757 | 226223757 | Human | | name |
| 156402294 | CV2363727 | single nucleotide variant | NM_031944.3(MIXL1):c.62G>C (p.Arg21Pro) | not specified [RCV004218717] | uncertain significance | 1 | 226223743 | 226223743 | Human | | name |
| 405683391 | CV3286021 | single nucleotide variant | NM_031944.3(MIXL1):c.92C>A (p.Pro31Gln) | not specified [RCV004422151] | uncertain significance | 1 | 226223773 | 226223773 | Human | | name |
| 597647847 | CV3560622 | single nucleotide variant | NM_031944.3(MIXL1):c.72C>A (p.His24Gln) | not specified [RCV004833265] | uncertain significance | 1 | 226223753 | 226223753 | Human | | name |
| 156029617 | CV2238330 | single nucleotide variant | NM_031944.3(MIXL1):c.151A>C (p.Thr51Pro) | not specified [RCV004113404] | likely benign | 1 | 226223832 | 226223832 | Human | | name |
| 156290850 | CV2305998 | single nucleotide variant | NM_031944.3(MIXL1):c.289C>A (p.Gln97Lys) | not specified [RCV004160987] | uncertain significance | 1 | 226223970 | 226223970 | Human | | name |
| 156362764 | CV2330356 | single nucleotide variant | NM_031944.3(MIXL1):c.190C>T (p.Pro64Ser) | not specified [RCV004180932] | uncertain significance | 1 | 226223871 | 226223871 | Human | | name |
| 155996759 | CV2393227 | single nucleotide variant | NM_031944.3(MIXL1):c.149C>T (p.Ala50Val) | not specified [RCV004226698] | uncertain significance | 1 | 226223830 | 226223830 | Human | | name |
| 156146022 | CV2397385 | single nucleotide variant | NM_031944.3(MIXL1):c.280A>G (p.Ser94Gly) | not specified [RCV004238906] | uncertain significance | 1 | 226223961 | 226223961 | Human | | name |
| 329391093 | CV2452027 | single nucleotide variant | NM_031944.3(MIXL1):c.206G>A (p.Ser69Asn) | not specified [RCV004278759] | uncertain significance | 1 | 226223887 | 226223887 | Human | | name |
| 405683371 | CV3286016 | single nucleotide variant | NM_031944.3(MIXL1):c.170G>C (p.Gly57Ala) | not specified [RCV004422146] | uncertain significance | 1 | 226223851 | 226223851 | Human | | name |
| 407518611 | CV3457205 | single nucleotide variant | NM_031944.3(MIXL1):c.227C>G (p.Pro76Arg) | not specified [RCV004628932] | uncertain significance | 1 | 226223908 | 226223908 | Human | | name |
| 597647829 | CV3560618 | single nucleotide variant | NM_031944.3(MIXL1):c.227C>A (p.Pro76His) | not specified [RCV004833262] | uncertain significance | 1 | 226223908 | 226223908 | Human | | name |
| 597647835 | CV3560619 | single nucleotide variant | NM_031944.3(MIXL1):c.125C>A (p.Ala42Glu) | not specified [RCV004833263] | uncertain significance | 1 | 226223806 | 226223806 | Human | | name |
| 597647840 | CV3560621 | single nucleotide variant | NM_031944.3(MIXL1):c.289C>G (p.Gln97Glu) | not specified [RCV004833264] | uncertain significance | 1 | 226223970 | 226223970 | Human | | name |
| 598255105 | CV3993405 | single nucleotide variant | NM_031944.3(MIXL1):c.238G>A (p.Ala80Thr) | not specified [RCV005367303] | uncertain significance | 1 | 226223919 | 226223919 | Human | | name |
| 598255121 | CV3993408 | single nucleotide variant | NM_031944.3(MIXL1):c.242C>T (p.Ala81Val) | not specified [RCV005367305] | uncertain significance | 1 | 226223923 | 226223923 | Human | | name |
| 598187158 | CV3993409 | single nucleotide variant | NM_031944.3(MIXL1):c.194C>A (p.Pro65Gln) | not specified [RCV005373522] | uncertain significance | 1 | 226223875 | 226223875 | Human | | name |
| 155965033 | CV2330523 | single nucleotide variant | NM_031944.3(MIXL1):c.304G>C (p.Glu102Gln) | not specified [RCV004181087] | uncertain significance | 1 | 226223985 | 226223985 | Human | | name |
| 156219498 | CV2393603 | single nucleotide variant | NM_031944.3(MIXL1):c.611T>C (p.Phe204Ser) | not specified [RCV004231417] | uncertain significance | 1 | 226225724 | 226225724 | Human | | name |
| 156003475 | CV2396738 | single nucleotide variant | NM_031944.3(MIXL1):c.632C>T (p.Ser211Phe) | not specified [RCV004233887] | uncertain significance | 1 | 226225745 | 226225745 | Human | | name |
| 329372450 | CV2424096 | single nucleotide variant | NM_031944.3(MIXL1):c.620G>T (p.Cys207Phe) | not specified [RCV004248000] | uncertain significance | 1 | 226225733 | 226225733 | Human | | name |
| 329385448 | CV2432152 | single nucleotide variant | NM_031944.3(MIXL1):c.628C>G (p.Leu210Val) | not specified [RCV004249298] | uncertain significance | 1 | 226225741 | 226225741 | Human | | name |
| 401761528 | CV2702376 | single nucleotide variant | NM_031944.3(MIXL1):c.694T>G (p.Phe232Val) | not specified [RCV004316902] | uncertain significance | 1 | 226225807 | 226225807 | Human | | name |
| 401894953 | CV2785313 | single nucleotide variant | NM_031944.3(MIXL1):c.556G>A (p.Glu186Lys) | not specified [RCV004357070] | uncertain significance | 1 | 226225669 | 226225669 | Human | | name |
| 405683384 | CV3286019 | single nucleotide variant | NM_031944.3(MIXL1):c.487G>T (p.Ala163Ser) | not specified [RCV004422149] | uncertain significance | 1 | 226225600 | 226225600 | Human | | name |
| 407486146 | CV3457204 | single nucleotide variant | NM_031944.3(MIXL1):c.600A>C (p.Gln200His) | not specified [RCV004640837] | uncertain significance | 1 | 226225713 | 226225713 | Human | | name |
| 597647857 | CV3560623 | single nucleotide variant | NM_031944.3(MIXL1):c.404A>G (p.Gln135Arg) | not specified [RCV004833266] | uncertain significance | 1 | 226225517 | 226225517 | Human | | name |
| 598255127 | CV3993410 | single nucleotide variant | NM_031944.3(MIXL1):c.454T>G (p.Leu152Val) | not specified [RCV005367306] | uncertain significance | 1 | 226225567 | 226225567 | Human | | name |
