| | | Single nucleotide variant (intron variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (G203A +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (R326Q +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (I190T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (Q163K +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (P105T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (R42Q +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (R334H +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | C10orf55, PLAU (V412L +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (Q261H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (V319A +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (Y242C +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (non-coding transcript variant +2 more) | C10orf55-related disorder | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (synonymous variant) | PLAU-related disorder | |
| | | Single nucleotide variant (intron variant) | C10orf55-related disorder | |
| | | Copy number gain | not provided | |
| | C10orf55, PLAU (R201S +2 more) | Single nucleotide variant (missense variant) | PLAU-related disorder +1 more | |
| | C10orf55, LOC126860960 +1 more (I163T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | Distal trisomy 10q | |
| | ABRAXAS2, CHCHD1 +673 more | Copy number loss | Distal 10q deletion syndrome | |
| | C10orf55, LOC126860960 +1 more (P174S +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (R241C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (R387C +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (I47L +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | C10orf55, LOC126860960 +1 more (R115W +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (E166G +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (M166L +2 more) | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Duplication | Genitopatellar syndrome | |
| | C10orf55, PLAU (P301L +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (I110T +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, LOC126860960 +1 more (R159H +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | C10orf55, PLAU (M1T +2 more) | Single nucleotide variant (non-coding transcript variant +2 more) | not specified | |
| | C10orf55, LOC126860960 +1 more (S156P +2 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Duplication | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (P140fs +2 more) | Duplication (frameshift variant) | Quebec platelet disorder | |
| | | Copy number loss | not specified | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | C10orf55, LOC130004104 +1 more | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | C10orf55, PLAU (T393M +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | C10orf55, PLAU (R312L +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (synonymous variant) | Quebec platelet disorder | |
| | C10orf55, PLAU (I31N +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | C10orf55, PLAU (R196H +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (intron variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (N159K +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (I187V +2 more) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (synonymous variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (H132Y +2 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | C10orf55, PLAU (R62P +1 more) | Single nucleotide variant (non-coding transcript variant +2 more) | Quebec platelet disorder | |
| | C10orf55, PLAU (D48G +1 more) | Single nucleotide variant (missense variant +1 more) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Poly (ADP-Ribose) polymerase inhibitor response | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Deletion (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (3 prime UTR variant) | Quebec platelet disorder +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Quebec platelet disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Quebec platelet disorder | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Quebec platelet disorder | |
| | C10orf55, PLAU (V391I +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | | Single nucleotide variant (synonymous variant) | Quebec platelet disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | Quebec platelet disorder | |
| | C10orf55, PLAU (Y350H +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | C10orf55, PLAU (R276Q +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (synonymous variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (I236V +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more (K214Q +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |
| | C10orf55, LOC126860960 +1 more | Single nucleotide variant (intron variant) | Quebec platelet disorder +1 more | |
| | C10orf55, LOC126860960 +1 more (R184L +2 more) | Single nucleotide variant (missense variant) | Quebec platelet disorder | |