| 401725433 | CV2721770 | single nucleotide variant | NM_014280.3(DNAJC8):c.25A>T (p.Thr9Ser) | not specified [RCV004324504] | uncertain significance | 1 | 28232974 | 28232974 | Human | | name |
| 405747696 | CV3240867 | single nucleotide variant | NM_014280.3(DNAJC8):c.21C>A (p.Ser7Arg) | not specified [RCV004381470] | uncertain significance | 1 | 28232978 | 28232978 | Human | | name |
| 405747700 | CV3240868 | single nucleotide variant | NM_014280.3(DNAJC8):c.22G>C (p.Gly8Arg) | not specified [RCV004381471] | uncertain significance | 1 | 28232977 | 28232977 | Human | | name |
| 598163985 | CV3953586 | single nucleotide variant | NM_014280.3(DNAJC8):c.14G>C (p.Gly5Ala) | not specified [RCV005329453] | uncertain significance | 1 | 28232985 | 28232985 | Human | | name |
| 401743293 | CV2674625 | single nucleotide variant | NM_014280.3(DNAJC8):c.47C>T (p.Thr16Ile) | not specified [RCV004293925] | uncertain significance | 1 | 28232952 | 28232952 | Human | | name |
| 405747715 | CV3240870 | single nucleotide variant | NM_014280.3(DNAJC8):c.32G>A (p.Gly11Asp) | not specified [RCV004381473] | uncertain significance | 1 | 28232967 | 28232967 | Human | | name |
| 598163990 | CV3953587 | single nucleotide variant | NM_014280.3(DNAJC8):c.29C>T (p.Ser10Leu) | not specified [RCV005329454] | uncertain significance | 1 | 28232970 | 28232970 | Human | | name |
| 598164002 | CV3953589 | single nucleotide variant | NM_014280.3(DNAJC8):c.43A>G (p.Ser15Gly) | not specified [RCV005329456] | uncertain significance | 1 | 28232956 | 28232956 | Human | | name |
| 329401727 | CV2457340 | single nucleotide variant | NM_014280.3(DNAJC8):c.164A>G (p.Asn55Ser) | not specified [RCV004267180] | uncertain significance | 1 | 28228938 | 28228938 | Human | | name |
| 405747710 | CV3240869 | single nucleotide variant | NM_014280.3(DNAJC8):c.278C>T (p.Ala93Val) | not specified [RCV004381472] | uncertain significance | 1 | 28210597 | 28210597 | Human | | name |
| 597644565 | CV3663048 | single nucleotide variant | NM_014280.3(DNAJC8):c.145C>G (p.Pro49Ala) | not specified [RCV004909620] | uncertain significance | 1 | 28228957 | 28228957 | Human | | name |
| 598163967 | CV3953583 | single nucleotide variant | NM_014280.3(DNAJC8):c.199G>A (p.Glu67Lys) | not specified [RCV005329450] | uncertain significance | 1 | 28214978 | 28214978 | Human | | name |
| 598163995 | CV3953588 | single nucleotide variant | NM_014280.3(DNAJC8):c.283A>G (p.Arg95Gly) | not specified [RCV005329455] | uncertain significance | 1 | 28210592 | 28210592 | Human | | name |
| 405747733 | CV3240872 | single nucleotide variant | NM_014280.3(DNAJC8):c.537G>C (p.Glu179Asp) | not specified [RCV004381475] | uncertain significance | 1 | 28205284 | 28205284 | Human | | name |
| 405747740 | CV3240873 | single nucleotide variant | NM_014280.3(DNAJC8):c.689C>G (p.Thr230Arg) | not specified [RCV004381476] | uncertain significance | 1 | 28201321 | 28201321 | Human | | name |
| 597714102 | CV3663047 | single nucleotide variant | NM_014280.3(DNAJC8):c.653G>A (p.Gly218Asp) | not specified [RCV004918094] | uncertain significance | 1 | 28201357 | 28201357 | Human | | name |
| 597714113 | CV3663049 | single nucleotide variant | NM_014280.3(DNAJC8):c.438A>C (p.Lys146Asn) | not specified [RCV004918095] | uncertain significance | 1 | 28208375 | 28208375 | Human | | name |
| 598163973 | CV3953584 | single nucleotide variant | NM_014280.3(DNAJC8):c.481G>A (p.Ala161Thr) | not specified [RCV005329451] | uncertain significance | 1 | 28205340 | 28205340 | Human | | name |