| 405816023 | CV3280954 | single nucleotide variant | NM_177477.4(LYNX1):c.5C>T (p.Thr2Met) | not specified [RCV004411008] | uncertain significance | 8 | 142775953 | 142775953 | Human | | name |
| 407481110 | CV3449349 | single nucleotide variant | NM_177477.4(LYNX1):c.8C>T (p.Pro3Leu) | not specified [RCV004640331] | uncertain significance | 8 | 142775950 | 142775950 | Human | | name |
| 329365179 | CV2440108 | single nucleotide variant | NM_177477.4(LYNX1):c.73G>A (p.Val25Met) | not specified [RCV004260572] | uncertain significance | 8 | 142775674 | 142775674 | Human | | name |
| 401772576 | CV2719684 | single nucleotide variant | NM_177477.4(LYNX1):c.70C>T (p.His24Tyr) | not specified [RCV004329128] | uncertain significance | 8 | 142775677 | 142775677 | Human | | name |
| 155922188 | CV2240645 | single nucleotide variant | NM_177477.4(LYNX1):c.119C>T (p.Pro40Leu) | not specified [RCV004599477] | uncertain significance | 8 | 142775628 | 142775628 | Human | | name |
| 156251173 | CV2394282 | single nucleotide variant | NM_177477.4(LYNX1):c.146C>T (p.Thr49Met) | not specified [RCV004238512] | uncertain significance | 8 | 142775601 | 142775601 | Human | | name |
| 329361849 | CV2448090 | single nucleotide variant | NM_177477.4(LYNX1):c.110T>G (p.Met37Arg) | not specified [RCV004263313] | uncertain significance | 8 | 142775637 | 142775637 | Human | | name |
| 405816021 | CV3280952 | single nucleotide variant | NM_177477.4(LYNX1):c.113G>A (p.Arg38His) | not specified [RCV004411006] | uncertain significance | 8 | 142775634 | 142775634 | Human | | name |
| 405816022 | CV3280953 | single nucleotide variant | NM_177477.4(LYNX1):c.116G>C (p.Cys39Ser) | not specified [RCV004411007] | uncertain significance | 8 | 142775631 | 142775631 | Human | | name |
| 407481103 | CV3449348 | single nucleotide variant | NM_177477.4(LYNX1):c.149G>A (p.Arg50His) | not specified [RCV004640330] | uncertain significance | 8 | 142775598 | 142775598 | Human | | name |
| 597644938 | CV3696898 | single nucleotide variant | NM_177477.4(LYNX1):c.124A>G (p.Met42Val) | not specified [RCV004942301] | uncertain significance | 8 | 142775623 | 142775623 | Human | | name |
| 15158453 | CV758773 | single nucleotide variant | NM_023946.5(LYNX1-SLURP2):c.360C>T (p.Ile120=) | not provided [RCV000925073] | benign | 8 | 142764641 | 142764641 | Human | | name |