| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CLEC12A, CLEC1B (G189A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (K127E +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (R118T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (Y114F +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (R107K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (R46L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (L43F +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (Q42E +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (T70A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (E32G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number gain | not specified | |
| | | Duplication | not provided | |
| | CLEC12A, CLEC1B (G63C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CLEC12A, CLEC1B (R36G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (N159I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | Pallister-Killian syndrome | |
| | CLEC12A, CLEC1B (M222K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | CLEC12A, CLEC1B (R79H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (Y61H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (Q63K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (C48S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (N87S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (W137S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | CLEC12A, CLEC1B (N101K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Complex | Breast ductal adenocarcinoma | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126861648, LOC126861649 +4836 more | Copy number gain | See cases | |
| | LOC130007425, LOC130007426 +1257 more | Copy number gain | See cases | |
| | LOC130007339, LOC130007340 +698 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC124625919, LOC124625920 +1009 more | Copy number gain | See cases | |
| | LOC130007649, LOC130007650 +1258 more | Copy number gain | See cases | |