| 401891620 | CV2779258 | single nucleotide variant | NM_003287.4(TPD52L1):c.89T>C (p.Met30Thr) | not specified [RCV004350942] | uncertain significance | 6 | 125220147 | 125220147 | Human | | name |
| 407521376 | CV3492357 | single nucleotide variant | NM_003287.4(TPD52L1):c.85A>G (p.Ser29Gly) | not specified [RCV004677287] | uncertain significance | 6 | 125220143 | 125220143 | Human | | name |
| 598200888 | CV3928316 | single nucleotide variant | NM_003287.4(TPD52L1):c.55G>A (p.Glu19Lys) | not specified [RCV005290068] | uncertain significance | 6 | 125220113 | 125220113 | Human | | name |
| 156002595 | CV2257975 | single nucleotide variant | NM_003287.4(TPD52L1):c.198G>C (p.Glu66Asp) | not specified [RCV004129784] | uncertain significance | 6 | 125229180 | 125229180 | Human | | name |
| 401727908 | CV2678574 | single nucleotide variant | NM_003287.4(TPD52L1):c.503C>T (p.Thr168Met) | not specified [RCV004292582] | uncertain significance | 6 | 125262850 | 125262850 | Human | | name |
| 401727169 | CV2684498 | single nucleotide variant | NM_003287.4(TPD52L1):c.347A>G (p.Asn116Ser) | not specified [RCV004291570] | uncertain significance | 6 | 125248344 | 125248344 | Human | | name |
| 401774363 | CV2727817 | single nucleotide variant | NM_003287.4(TPD52L1):c.604C>G (p.Leu202Val) | not specified [RCV004323840] | uncertain significance | 6 | 125262951 | 125262951 | Human | | name |
| 405774456 | CV3343825 | single nucleotide variant | NM_003287.4(TPD52L1):c.499G>A (p.Gly167Ser) | not specified [RCV004470861] | uncertain significance | 6 | 125262846 | 125262846 | Human | | name |
| 405774462 | CV3343826 | single nucleotide variant | NM_003287.4(TPD52L1):c.535C>G (p.Leu179Val) | not specified [RCV004470862] | uncertain significance | 6 | 125262882 | 125262882 | Human | | name |
| 597795271 | CV3611263 | single nucleotide variant | NM_003287.4(TPD52L1):c.526G>A (p.Glu176Lys) | not specified [RCV004878159] | uncertain significance | 6 | 125262873 | 125262873 | Human | | name |
| 598265197 | CV3928315 | single nucleotide variant | NM_003287.4(TPD52L1):c.488C>T (p.Thr163Met) | not specified [RCV005281006] | uncertain significance | 6 | 125262835 | 125262835 | Human | | name |
| 8631803 | CV87009 | single nucleotide variant | NM_001003396.1(TPD52L1):c.428G>A (p.Arg143Gln) | Malignant melanoma [RCV000067100] | not provided | 6 | 125262836 | 125262836 | Human | | name |