| 597767631 | CV3648854 | single nucleotide variant | NM_001127893.3(CEACAM19):c.85G>A (p.Gly29Ser) | not specified [RCV004896394] | uncertain significance | 19 | 44672625 | 44672625 | Human | | name |
| 156294657 | CV2302975 | single nucleotide variant | NM_001127893.3(CEACAM19):c.138C>G (p.Asn46Lys) | not specified [RCV004156775] | uncertain significance | 19 | 44672678 | 44672678 | Human | | name |
| 156263997 | CV2384533 | single nucleotide variant | NM_001127893.3(CEACAM19):c.176C>T (p.Thr59Ile) | not specified [RCV004232331] | uncertain significance | 19 | 44672716 | 44672716 | Human | | name |
| 329369443 | CV2424822 | single nucleotide variant | NM_001127893.3(CEACAM19):c.217G>A (p.Gly73Arg) | not specified [RCV004248710] | uncertain significance | 19 | 44672757 | 44672757 | Human | | name |
| 401719386 | CV2706281 | single nucleotide variant | NM_001127893.3(CEACAM19):c.126G>T (p.Gln42His) | not specified [RCV004314942] | uncertain significance | 19 | 44672666 | 44672666 | Human | | name |
| 405743775 | CV3303684 | single nucleotide variant | NM_001127893.3(CEACAM19):c.205G>A (p.Glu69Lys) | not specified [RCV004431134] | uncertain significance | 19 | 44672745 | 44672745 | Human | | name |
| 405743779 | CV3303685 | single nucleotide variant | NM_001127893.3(CEACAM19):c.212C>T (p.Thr71Met) | not specified [RCV004431135] | likely benign | 19 | 44672752 | 44672752 | Human | | name |
| 597767621 | CV3648852 | single nucleotide variant | NM_001127893.3(CEACAM19):c.123G>C (p.Glu41Asp) | not specified [RCV004896392] | uncertain significance | 19 | 44672663 | 44672663 | Human | | name |
| 156288879 | CV2229822 | single nucleotide variant | NM_001127893.3(CEACAM19):c.334G>A (p.Ala112Thr) | not specified [RCV004105393] | uncertain significance | 19 | 44672874 | 44672874 | Human | | name |
| 156045376 | CV2234426 | single nucleotide variant | NM_001127893.3(CEACAM19):c.703G>T (p.Ala235Ser) | not specified [RCV004100639] | uncertain significance | 19 | 44680331 | 44680331 | Human | | name |
| 155975440 | CV2342665 | single nucleotide variant | NM_001127893.3(CEACAM19):c.329G>A (p.Arg110His) | not specified [RCV004196747] | uncertain significance | 19 | 44672869 | 44672869 | Human | | name |
| 156108248 | CV2390217 | single nucleotide variant | NM_001127893.3(CEACAM19):c.805C>G (p.Pro269Ala) | not specified [RCV004240598] | uncertain significance | 19 | 44682579 | 44682579 | Human | | name |
| 401876760 | CV2754473 | single nucleotide variant | NM_001127893.3(CEACAM19):c.662T>G (p.Met221Arg) | not specified [RCV004336683] | uncertain significance | 19 | 44680290 | 44680290 | Human | | name |
| 401855237 | CV2757198 | single nucleotide variant | NM_001127893.3(CEACAM19):c.527G>A (p.Cys176Tyr) | not specified [RCV004338802] | uncertain significance | 19 | 44676373 | 44676373 | Human | | name |
| 405743786 | CV3303686 | single nucleotide variant | NM_001127893.3(CEACAM19):c.448A>T (p.Thr150Ser) | not specified [RCV004431136] | uncertain significance | 19 | 44676294 | 44676294 | Human | | name |
| 405743790 | CV3303687 | single nucleotide variant | NM_001127893.3(CEACAM19):c.710A>T (p.Asp237Val) | not specified [RCV004431137] | uncertain significance | 19 | 44681230 | 44681230 | Human | | name |
| 407460837 | CV3418733 | single nucleotide variant | NM_001127893.3(CEACAM19):c.734C>G (p.Pro245Arg) | not specified [RCV004612434] | uncertain significance | 19 | 44681254 | 44681254 | Human | | name |
| 407460841 | CV3418734 | single nucleotide variant | NM_001127893.3(CEACAM19):c.571C>T (p.His191Tyr) | not specified [RCV004612435] | uncertain significance | 19 | 44676417 | 44676417 | Human | | name |
| 597767611 | CV3648850 | single nucleotide variant | NM_001127893.3(CEACAM19):c.490A>T (p.Ile164Phe) | not specified [RCV004896390] | uncertain significance | 19 | 44676336 | 44676336 | Human | | name |
| 597767616 | CV3648851 | single nucleotide variant | NM_001127893.3(CEACAM19):c.395T>C (p.Met132Thr) | not specified [RCV004896391] | uncertain significance | 19 | 44672935 | 44672935 | Human | | name |
| 597767626 | CV3648853 | single nucleotide variant | NM_001127893.3(CEACAM19):c.452A>C (p.His151Pro) | not specified [RCV004896393] | uncertain significance | 19 | 44676298 | 44676298 | Human | | name |
| 598193870 | CV3940482 | single nucleotide variant | NM_001127893.3(CEACAM19):c.854T>C (p.Leu285Pro) | not specified [RCV005313066] | uncertain significance | 19 | 44683444 | 44683444 | Human | | name |