| 150454710 | CV1277053 | single nucleotide variant | NM_175061.4(JAZF1):c.115+30671A>G | not provided [RCV001708844] | benign | 7 | 28149792 | 28149792 | Human | | name |
| 617153047 | CV4021021 | single nucleotide variant | NM_175061.4(JAZF1):c.702G>A (p.Ser234=) | not provided [RCV005428774] | likely benign | 7 | 27832830 | 27832830 | Human | | name |
| 156277317 | CV2255889 | single nucleotide variant | NM_175061.4(JAZF1):c.117T>A (p.Asp39Glu) | not specified [RCV004122042] | uncertain significance | 7 | 27991980 | 27991980 | Human | | name |
| 156090371 | CV2299957 | single nucleotide variant | NM_175061.4(JAZF1):c.128G>A (p.Arg43Gln) | not specified [RCV004151175] | uncertain significance | 7 | 27991969 | 27991969 | Human | | name |
| 156224070 | CV2395076 | single nucleotide variant | NM_175061.4(JAZF1):c.251T>C (p.Leu84Pro) | not specified [RCV004236760] | uncertain significance | 7 | 27895354 | 27895354 | Human | | name |
| 598211998 | CV3969356 | single nucleotide variant | NM_175061.4(JAZF1):c.208C>T (p.Arg70Cys) | not specified [RCV005358768] | uncertain significance | 7 | 27895397 | 27895397 | Human | | name |
| 598172494 | CV3969357 | single nucleotide variant | NM_175061.4(JAZF1):c.194T>C (p.Met65Thr) | not specified [RCV005370784] | uncertain significance | 7 | 27895411 | 27895411 | Human | | name |
| 329353281 | CV2469089 | single nucleotide variant | NM_175061.4(JAZF1):c.695C>T (p.Pro232Leu) | not specified [RCV004274326] | uncertain significance | 7 | 27832837 | 27832837 | Human | | name |
| 401744411 | CV2696995 | single nucleotide variant | NM_175061.4(JAZF1):c.312C>A (p.Ser104Arg) | not specified [RCV004292987] | uncertain significance | 7 | 27895293 | 27895293 | Human | | name |
| 401861131 | CV2769530 | single nucleotide variant | NM_175061.4(JAZF1):c.488T>C (p.Met163Thr) | not specified [RCV004351187] | uncertain significance | 7 | 27840765 | 27840765 | Human | | name |
| 405795255 | CV3275384 | single nucleotide variant | NM_175061.4(JAZF1):c.433G>A (p.Asp145Asn) | not specified [RCV004401158] | uncertain significance | 7 | 27840820 | 27840820 | Human | | name |
| 597777333 | CV3691251 | single nucleotide variant | NM_175061.4(JAZF1):c.320G>A (p.Ser107Asn) | not specified [RCV004929846] | uncertain significance | 7 | 27895285 | 27895285 | Human | | name |
| 597777337 | CV3691252 | single nucleotide variant | NM_175061.4(JAZF1):c.608G>A (p.Arg203His) | not specified [RCV004929847] | uncertain significance | 7 | 27832924 | 27832924 | Human | | name |
| 597777341 | CV3691253 | single nucleotide variant | NM_175061.4(JAZF1):c.691C>A (p.Pro231Thr) | not specified [RCV004929848] | uncertain significance | 7 | 27832841 | 27832841 | Human | | name |
| 598258684 | CV3969355 | single nucleotide variant | NM_175061.4(JAZF1):c.503G>A (p.Gly168Glu) | not specified [RCV005347257] | uncertain significance | 7 | 27840750 | 27840750 | Human | | name |