| | LOC130057927, LOC130057928 +1764 more | Copy number gain | See cases | |
| | LOC116268473, LOC116268474 +1244 more | Copy number gain | See cases | |
| | LOC130057943, LOC130057944 +664 more | Copy number gain | See cases | |
| | LOC130057907, LOC130057908 +630 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | MIR11181, MIR1179 +517 more | Copy number gain | See cases | |
| | LOC130057997, LOC130057998 +500 more | Copy number gain | See cases | |
| | LOC130057929, LOC130057930 +311 more | Copy number gain | See cases | |
| | ADAMTS17, ALDH1A3 +422 more | Copy number gain | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial cancer of breast | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial cancer of breast | |
| | | Single nucleotide variant (3 prime UTR variant) | Familial cancer of breast | |
| | PRC1, PRC1-AS1 (S587L +1 more) | Single nucleotide variant (synonymous variant +1 more) | not specified | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PRC1, PRC1-AS1 (A517S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (G553S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (N504K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (G540D +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R497C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (P479L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (L477R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R517Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (V474M +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (Y470C +1 more) | Single nucleotide variant (missense variant) | Familial cancer of breast | |
| | PRC1, PRC1-AS1 (R462W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (N458S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Breast carcinoma | |
| | PRC1, PRC1-AS1 (R445L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R434G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R469Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Insertion | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | PRC1, PRC1-AS1 (E444G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R399G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (M381I +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (L371S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (Y304C +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R340W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Breast carcinoma | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | PRC1, PRC1-AS1 (Q271R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (V299A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R257Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (K292T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (Q247R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (D207N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R240H +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (G197R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (M186T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R182W +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (I215T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (E205K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (V106A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | PRC1, PRC1-AS1 (R70Q +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Familial cancer of breast | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | LOC126862223, PRC1 +1 more (T78I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC126862223, PRC1 +1 more | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | Familial cancer of breast | |
| | | Copy number loss | not specified | |
| | | Copy number gain | See cases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Duplication | D-2-hydroxyglutaric aciduria 2 | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Duplication | Bloom syndrome | |
| | | Copy number loss | See cases | |
| | | Duplication | Bloom syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | ADAMTS17, ALDH1A3 +54 more | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Duplication | 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 | |
| | ADAMTS17, ALDH1A3 +51 more | Copy number loss | See cases | |