Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5495 |
| ensemblid | ENSG00000138032.21 |
| hgncid | 9276 |
| symbol | PPM1B |
| name | protein phosphatase, Mg2+/Mn2+ dependent 1B |
| refseq_nuc | NM_002706.6 |
| refseq_prot | NP_002697.1 |
| ensembl_nuc | ENST00000282412.9 |
| ensembl_prot | ENSP00000282412.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 44168875 |
| end | 44231472 |
| strand | + |
| ver | v1.2 |
| region | chr2:44168875-44231472 |
| region5000 | chr2:44163875-44236472 |
| regionname0 | PPM1B_chr2_44168875_44231472 |
| regionname5000 | PPM1B_chr2_44163875_44236472 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 479 | 352 | 89 | 64 | 154 | 12 | 31 | 120 | PPM1B_chr2_44163875_44236472 | PPM1B | MGAFL others(474): Show |
chr2 | 44163875 | 44236472 |
| a0002 | 0/0 | 479 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | MGAFL others(474): Show |
chr2 | 44163875 | 44236472 |
| a0003 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | MGAFL others(474): Show |
chr2 | 44163875 | 44236472 |
| a0004 | 0/0 | 479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | MGAFL others(474): Show |
chr2 | 44163875 | 44236472 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1437 | 352 | 89 | 64 | 154 | 12 | 31 | PPM1B_chr2_44163875_44236472 | PPM1B | ATGGG others(1432): Show |
chr2 | 44163875 | 44236472 | ||
| a0002c0002 | 0/0 | 1437 | 4 | 4 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | ATGGG others(1432): Show |
chr2 | 44163875 | 44236472 | ||
| a0003c0003 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | ATGGG others(1432): Show |
chr2 | 44163875 | 44236472 | ||
| a0004c0004 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | ATGGG others(1432): Show |
chr2 | 44163875 | 44236472 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2617 | 257 | 68 | 43 | 107 | 11 | 27 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0002 | 1/0 | 2608 | 75 | 13 | 15 | 43 | 1 | 2 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2603): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0003 | 0/0 | 2626 | 5 | 5 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2621): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0004 | 0/0 | 2617 | 4 | 0 | 4 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0005 | 0/0 | 2617 | 4 | 0 | 0 | 4 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0006 | 0/0 | 2617 | 2 | 2 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0007 | 0/0 | 2617 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0008 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2621): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0009 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0001c0001t0010 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2603): Show |
chr2 | 44163875 | 44236472 |
| a0002c0002t0001 | 0/0 | 2617 | 4 | 4 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0003c0003t0001 | 0/0 | 2617 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| a0004c0004t0001 | 0/0 | 2617 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | GCAAA others(2612): Show |
chr2 | 44163875 | 44236472 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0333 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0003c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| a0004c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | FIN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00544 | hp1 | a0001 | c0001 | t0005 | g0276 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0217 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0300 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0297 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CDX | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02683 | hp1 | a0001 | c0001 | t0010 | g0050 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0346 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ESN | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | GWD | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0296 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0066 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | STU | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18997 | hp2 | a0001 | c0001 | t0005 | g0262 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | LWK | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ASW | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ASW | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0337 | EUR | TSI | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | GIH | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG02559 | hp2 | a0003 | c0003 | t0001 | g0014 | AFR | ACB | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | USA | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0333 | REF | REF | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0085 | REF | REF | PPM1B_chr2_44163875_44236472 | PPM1B | chr2 | 44163875 | 44236472 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44201251 | G | A | 1 | a0002 | 4 | HG02622.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.52G>A | p.Ala18Thr | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 466/2608 | 52/1440 | 18/479 | chr2 | 44201251 | |||
| chr2:44201266 | C | T | 1 | a0004 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.67C>T | p.Arg23Cys | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 481/2608 | 67/1440 | 23/479 | chr2 | 44201266 | |||
| chr2:44218530 | G | A | 1 | a0003 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1127G>A | p.Ser376Asn | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/6 | 1541/2608 | 1127/1440 | 376/479 | chr2 | 44218530 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44168923 | G | T | 1 | a0001c0001t0007 | 2 | HG01069.hp2 HG01071.hp2 |
5_prime_UTR_variant | MODIFIER | c.-366G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32277 | chr2 | 44168923 | ||||||
| chr2:44169029 | G | A | 1 | a0001c0001t0008 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-260G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32171 | chr2 | 44169029 | ||||||
| chr2:44169088 | A | AGGCGGCA others(2): Show |
2 | a0001c0001t0003 a0001c0001t0008 |
6 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-194_-193insGCGGCG others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32104 | INFO_REALIGN_3_PRIME | chr2 | 44169088 | |||||
| chr2:44169096 | T | G | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(7): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(277): Show |
5_prime_UTR_variant | MODIFIER | c.-193T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32104 | chr2 | 44169096 | ||||||
| chr2:44169140 | C | CCGGAGGC others(2): Show |
11 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(8): Show |
281 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(278): Show |
5_prime_UTR_variant | MODIFIER | c.-145_-137dupAGGCGG others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 32047 | INFO_REALIGN_3_PRIME | chr2 | 44169140 | |||||
| chr2:44169269 | C | T | 1 | a0001c0001t0006 | 2 | HG02647.hp2 HG03579.hp2 |
5_prime_UTR_variant | MODIFIER | c.-20C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/6 | 31931 | chr2 | 44169269 | ||||||
| chr2:44201196 | A | G | 1 | a0001c0001t0008 | 1 | NA20300.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | chr2 | 44201196 | |||||||
| chr2:44201199 | C | T | 1 | a0001c0001t0010 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/6 | 1 | chr2 | 44201199 | ||||||
| chr2:44230781 | T | C | 1 | a0001c0001t0004 | 4 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*63T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 6/6 | 63 | chr2 | 44230781 | ||||||
| chr2:44230999 | A | G | 1 | a0001c0001t0005 | 4 | HG00544.hp1 HG02155.hp1 NA18943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*281A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 6/6 | 281 | chr2 | 44230999 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:44169316 | C | T | 1 | a0001c0001t0001g0347 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-15+42C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169316 | |||||||
| chr2:44169337 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+63G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169337 | |||||||
| chr2:44169363 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-15+89T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169363 | |||||||
| chr2:44169385 | C | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+111C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169385 | |||||||
| chr2:44169480 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+206C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169480 | |||||||
| chr2:44169628 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-15+354C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169628 | |||||||
| chr2:44169646 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0015 others(5): Show |
8 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+372G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169646 | |||||||
| chr2:44169674 | T | A | 1 | a0001c0001t0002g0020 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-15+400T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169674 | |||||||
| chr2:44169716 | C | G | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-15+442C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169716 | |||||||
| chr2:44169770 | C | G | 1 | a0001c0001t0001g0338 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+496C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169770 | |||||||
| chr2:44169905 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(165): Show |
172 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.-15+631A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44169905 | |||||||
| chr2:44169941 | TTAAGAG | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+670_-15+675del others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44169941 | ||||||
| chr2:44170108 | T | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+834T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170108 | |||||||
| chr2:44170166 | T | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-15+892T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170166 | |||||||
| chr2:44170220 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15+946A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170220 | |||||||
| chr2:44170423 | A | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1149A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170423 | |||||||
| chr2:44170433 | T | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG00438.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-15+1159T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170433 | |||||||
| chr2:44170476 | A | G | 5 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(2): Show |
5 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+1202A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170476 | |||||||
| chr2:44170672 | ATTG | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0002c0002t0001g0025 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+1402_-15+1404d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44170672 | ||||||
| chr2:44170731 | A | C | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+1457A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170731 | |||||||
| chr2:44170768 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
7 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+1494T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170768 | |||||||
| chr2:44170871 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15+1597T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170871 | |||||||
| chr2:44170887 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
83 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.-15+1613A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170887 | |||||||
| chr2:44170938 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+1664C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170938 | |||||||
| chr2:44170973 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+1699G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170973 | |||||||
| chr2:44170983 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15+1709C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170983 | |||||||
| chr2:44170988 | CATTT | C | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1715_-15+1718d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44170988 | |||||||
| chr2:44171018 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-15+1744A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171018 | |||||||
| chr2:44171116 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+1842T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171116 | |||||||
| chr2:44171238 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-15+1964A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171238 | |||||||
| chr2:44171250 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+1976C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171250 | |||||||
| chr2:44171292 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+2018A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171292 | |||||||
| chr2:44171310 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+2036A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171310 | |||||||
| chr2:44171347 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2073T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171347 | |||||||
| chr2:44171502 | G | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+2228G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171502 | |||||||
| chr2:44171528 | C | G | 1 | a0001c0001t0001g0338 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-15+2254C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171528 | |||||||
| chr2:44171585 | T | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0103 others(53): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+2311T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171585 | |||||||
| chr2:44171777 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2503C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171777 | |||||||
| chr2:44171829 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0028 others(20): Show |
23 | HG00741.hp2 HG01243.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15+2578dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | ||||||
| chr2:44171829 | CA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-15+2578delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | ||||||
| chr2:44171829 | CAAAAAAA others(1): Show |
C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.-15+2571_-15+2578d others(10): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44171829 | ||||||
| chr2:44171852 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2578A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171852 | |||||||
| chr2:44171954 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2680T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171954 | |||||||
| chr2:44171996 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+2722T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171996 | |||||||
| chr2:44171997 | G | A | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+2723G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44171997 | |||||||
| chr2:44172082 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+2808A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172082 | |||||||
| chr2:44172196 | C | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0040 |
2 | HG00099.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-15+2922C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172196 | |||||||
| chr2:44172199 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-15+2925G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172199 | |||||||
| chr2:44172242 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+2968G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172242 | |||||||
| chr2:44172336 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-15+3062C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172336 | |||||||
| chr2:44172359 | C | T | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3085C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172359 | |||||||
| chr2:44172361 | T | A | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-15+3087T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172361 | |||||||
| chr2:44172497 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-15+3223C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172497 | |||||||
| chr2:44172551 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-15+3277C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172551 | |||||||
| chr2:44172762 | C | G | 16 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
16 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+3488C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172762 | |||||||
| chr2:44172783 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-15+3509C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172783 | |||||||
| chr2:44172980 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+3706C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44172980 | |||||||
| chr2:44173031 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-15+3757G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173031 | |||||||
| chr2:44173041 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-15+3767G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173041 | |||||||
| chr2:44173074 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+3800G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173074 | |||||||
| chr2:44173220 | G | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
15 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+3946G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173220 | |||||||
| chr2:44173384 | CT | C | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+4117delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44173384 | ||||||
| chr2:44173430 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4156G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173430 | |||||||
| chr2:44173508 | C | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+4234C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173508 | |||||||
| chr2:44173534 | G | C | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+4260G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173534 | |||||||
| chr2:44173610 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4336A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173610 | |||||||
| chr2:44173634 | T | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+4360T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173634 | |||||||
| chr2:44173659 | A | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(182): Show |
189 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.-15+4385A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173659 | |||||||
| chr2:44173791 | A | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
21 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+4517A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173791 | |||||||
| chr2:44173916 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(268): Show |
279 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.-15+4642T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173916 | |||||||
| chr2:44173943 | G | A | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG03654.hp2 NA18964.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+4669G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44173943 | |||||||
| chr2:44174213 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-15+4939C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174213 | |||||||
| chr2:44174213 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-15+4939C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174213 | |||||||
| chr2:44174289 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+5015A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174289 | |||||||
| chr2:44174423 | T | C | 336 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(333): Show |
347 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.-15+5149T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174423 | |||||||
| chr2:44174456 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15+5182T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174456 | |||||||
| chr2:44174642 | T | G | 1 | a0001c0001t0002g0043 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15+5368T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174642 | |||||||
| chr2:44174704 | C | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(264): Show |
275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.-15+5430C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174704 | |||||||
| chr2:44174963 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-15+5689A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174963 | |||||||
| chr2:44174975 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-15+5701C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44174975 | |||||||
| chr2:44175119 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0002c0002t0001g0025 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5845C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175119 | |||||||
| chr2:44175322 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-15+6048A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175322 | |||||||
| chr2:44175328 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(265): Show |
276 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.-15+6054T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175328 | |||||||
| chr2:44175591 | T | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(4): Show |
7 | HG00597.hp1 HG02165.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+6317T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175591 | |||||||
| chr2:44175625 | G | C | 1 | a0001c0001t0002g0044 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-15+6351G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175625 | |||||||
| chr2:44175643 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+6369C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175643 | |||||||
| chr2:44175785 | A | AT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
146 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-15+6529dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44175785 | ||||||
| chr2:44175785 | A | ATT | 25 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0138 others(22): Show |
26 | HG00621.hp1 HG01175.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+6528_-15+6529d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44175785 | ||||||
| chr2:44175846 | T | C | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+6572T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175846 | |||||||
| chr2:44175986 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-15+6712A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44175986 | |||||||
| chr2:44176072 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
164 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-15+6798C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176072 | |||||||
| chr2:44176175 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+6901A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176175 | |||||||
| chr2:44176220 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+6946G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176220 | |||||||
| chr2:44176269 | C | G | 1 | a0001c0001t0001g0317 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-15+6995C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176269 | |||||||
| chr2:44176344 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-15+7070G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176344 | |||||||
| chr2:44176504 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+7230G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176504 | |||||||
| chr2:44176550 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-15+7276G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176550 | |||||||
| chr2:44176665 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-15+7391A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176665 | |||||||
| chr2:44176737 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+7463G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176737 | |||||||
| chr2:44176786 | C | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0002c0002t0001g0025 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+7512C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176786 | |||||||
| chr2:44176929 | C | G | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(56): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+7655C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176929 | |||||||
| chr2:44176937 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7663C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176937 | |||||||
| chr2:44176991 | G | C | 1 | a0001c0001t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15+7717G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44176991 | |||||||
| chr2:44177026 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-15+7752C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177026 | |||||||
| chr2:44177075 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7801C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177075 | |||||||
| chr2:44177134 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7860A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177134 | |||||||
| chr2:44177142 | G | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+7868G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177142 | |||||||
| chr2:44177148 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+7874G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177148 | |||||||
| chr2:44177151 | A | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
186 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.-15+7877A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177151 | |||||||
| chr2:44177226 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+7952T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177226 | |||||||
| chr2:44177418 | C | CT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(18): Show |
21 | HG01074.hp2 HG01099.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+8161dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | ||||||
| chr2:44177418 | C | CTT | 159 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(156): Show |
163 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-15+8160_-15+8161d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | ||||||
| chr2:44177418 | C | CTTT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
13 | HG00642.hp2 HG01070.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+8159_-15+8161d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | ||||||
| chr2:44177418 | C | CTTTT | 69 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(66): Show |
72 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15+8158_-15+8161d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177418 | ||||||
| chr2:44177452 | CTT | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+8179_-15+8180d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177452 | |||||||
| chr2:44177470 | G | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+8196G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177470 | |||||||
| chr2:44177471 | T | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15+8197T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177471 | |||||||
| chr2:44177542 | G | C | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+8268G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177542 | |||||||
| chr2:44177544 | G | C | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+8270G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177544 | |||||||
| chr2:44177700 | G | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+8426G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177700 | |||||||
| chr2:44177763 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(261): Show |
272 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-15+8489T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177763 | |||||||
| chr2:44177915 | C | CT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0149 others(20): Show |
25 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+8660dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177915 | ||||||
| chr2:44177915 | CT | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
11 | HG00323.hp1 HG00609.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+8660delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44177915 | ||||||
| chr2:44177926 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8652T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177926 | |||||||
| chr2:44177934 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+8660T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177934 | |||||||
| chr2:44177963 | G | T | 9 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(6): Show |
9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+8689G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44177963 | |||||||
| chr2:44178024 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00609.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-15+8750C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178024 | |||||||
| chr2:44178093 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-15+8819T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178093 | |||||||
| chr2:44178199 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+8925C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178199 | |||||||
| chr2:44178399 | C | T | 1 | a0001c0001t0003g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-15+9125C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178399 | |||||||
| chr2:44178452 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-15+9178G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178452 | |||||||
| chr2:44178452 | G | GTA | 7 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0327 others(4): Show |
7 | HG00323.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+9200_-15+9201d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | ||||||
| chr2:44178452 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+9179_-15+9180i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | ||||||
| chr2:44178452 | GTA | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0169 others(1): Show |
4 | HG02896.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+9200_-15+9201d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178452 | ||||||
| chr2:44178454 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0002g0044 |
2 | HG03195.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-15+9180A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178454 | |||||||
| chr2:44178472 | A | T | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+9198A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178472 | |||||||
| chr2:44178474 | A | ATATT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0103 others(23): Show |
27 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.-15+9201_-15+9202i others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178474 | A | ATT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0312 a0002c0002t0001g0025 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+9210_-15+9211d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178474 | A | ATTT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+9209_-15+9211d others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178474 | A | ATTTT | 29 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(26): Show |
30 | HG00621.hp1 HG01070.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.-15+9208_-15+9211d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178474 | A | T | 6 | a0001c0001t0001g0114 a0001c0001t0002g0089 a0001c0001t0003g0343 others(3): Show |
6 | HG00609.hp1 HG02055.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+9200A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178474 | |||||||
| chr2:44178474 | AT | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(149): Show |
155 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-15+9211delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178474 | ATT | A | 8 | a0001c0001t0001g0095 a0001c0001t0001g0171 a0001c0001t0001g0172 others(5): Show |
8 | HG01074.hp2 HG01099.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+9210_-15+9211d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44178474 | ||||||
| chr2:44178475 | T | TA | 4 | a0001c0001t0001g0009 a0001c0001t0001g0194 a0001c0001t0001g0213 others(1): Show |
5 | HG01175.hp1 HG01433.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+9201_-15+9202i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178475 | |||||||
| chr2:44178476 | T | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0167 a0001c0001t0001g0168 others(12): Show |
15 | HG02074.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+9202T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178476 | |||||||
| chr2:44178477 | T | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0334 |
2 | HG03017.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-15+9203T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178477 | |||||||
| chr2:44178478 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0008g0021 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-15+9204T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178478 | |||||||
| chr2:44178481 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+9207T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178481 | |||||||
| chr2:44178501 | C | G | 3 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0341 |
3 | HG03239.hp1 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+9227C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178501 | |||||||
| chr2:44178514 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+9240C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178514 | |||||||
| chr2:44178524 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0312 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-15+9250A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178524 | |||||||
| chr2:44178600 | C | G | 1 | a0001c0001t0002g0044 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-15+9326C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178600 | |||||||
| chr2:44178676 | G | C | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-15+9402G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178676 | |||||||
| chr2:44178716 | C | T | 173 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(170): Show |
175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.-15+9442C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178716 | |||||||
| chr2:44178728 | C | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+9454C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178728 | |||||||
| chr2:44178792 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(266): Show |
277 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.-15+9518T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178792 | |||||||
| chr2:44178824 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9550A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178824 | |||||||
| chr2:44178854 | A | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(56): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+9580A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178854 | |||||||
| chr2:44178856 | A | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9582A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178856 | |||||||
| chr2:44178922 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+9648A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178922 | |||||||
| chr2:44178964 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+9690A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44178964 | |||||||
| chr2:44179059 | A | C | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+9785A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179059 | |||||||
| chr2:44179073 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0325 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+9799T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179073 | |||||||
| chr2:44179110 | G | A | 2 | a0001c0001t0007g0216 a0001c0001t0007g0217 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+9836G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179110 | |||||||
| chr2:44179175 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-15+9901A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179175 | |||||||
| chr2:44179489 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+10215T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179489 | |||||||
| chr2:44179535 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15+10261G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179535 | |||||||
| chr2:44179537 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-15+10263C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179537 | |||||||
| chr2:44179547 | C | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(253): Show |
264 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-15+10273C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179547 | |||||||
| chr2:44179693 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+10419A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179693 | |||||||
| chr2:44179774 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-15+10500C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179774 | |||||||
| chr2:44179775 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-15+10501G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179775 | |||||||
| chr2:44179867 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+10593G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179867 | |||||||
| chr2:44179898 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+10624A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179898 | |||||||
| chr2:44179901 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+10627C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179901 | |||||||
| chr2:44179902 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+10628A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179902 | |||||||
| chr2:44179907 | G | T | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(61): Show |
66 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+10633G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179907 | |||||||
| chr2:44179997 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+10723G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44179997 | |||||||
| chr2:44180009 | C | CA | 12 | a0001c0001t0001g0206 a0001c0001t0001g0219 a0001c0001t0001g0220 others(9): Show |
12 | HG01106.hp2 HG01952.hp2 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+10754dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180009 | ||||||
| chr2:44180009 | CA | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-15+10754delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180009 | ||||||
| chr2:44180050 | CT | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(241): Show |
252 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.-15+10778delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44180050 | ||||||
| chr2:44180051 | T | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-15+10777T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180051 | |||||||
| chr2:44180059 | T | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+10785T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180059 | |||||||
| chr2:44180225 | A | T | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-15+10951A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180225 | |||||||
| chr2:44180466 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+11192C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180466 | |||||||
| chr2:44180479 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(253): Show |
264 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-15+11205G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180479 | |||||||
| chr2:44180542 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0328 |
4 | HG02647.hp1 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+11268A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180542 | |||||||
| chr2:44180597 | A | G | 2 | a0001c0001t0007g0216 a0001c0001t0007g0217 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-15+11323A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180597 | |||||||
| chr2:44180641 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+11367C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180641 | |||||||
| chr2:44180664 | G | T | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+11390G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180664 | |||||||
| chr2:44180846 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(264): Show |
275 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.-15+11572G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44180846 | |||||||
| chr2:44181026 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-15+11752C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181026 | |||||||
| chr2:44181033 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15+11759C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181033 | |||||||
| chr2:44181103 | C | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.-15+11829C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181103 | |||||||
| chr2:44181143 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(254): Show |
265 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.-15+11869G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181143 | |||||||
| chr2:44181160 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-15+11886A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181160 | |||||||
| chr2:44181370 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+12096A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181370 | |||||||
| chr2:44181445 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+12171A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181445 | |||||||
| chr2:44181448 | G | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
86 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15+12174G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181448 | |||||||
| chr2:44181726 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+12452C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181726 | |||||||
| chr2:44181731 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+12457A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181731 | |||||||
| chr2:44181781 | C | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0183 a0001c0001t0001g0184 others(84): Show |
89 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15+12507C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181781 | |||||||
| chr2:44181937 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-15+12663G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44181937 | |||||||
| chr2:44182115 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01069.hp1 HG01081.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-15+12841G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182115 | |||||||
| chr2:44182161 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-15+12887T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182161 | |||||||
| chr2:44182199 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-15+12925T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182199 | |||||||
| chr2:44182353 | G | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+13079G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182353 | |||||||
| chr2:44182466 | G | A | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+13192G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182466 | |||||||
| chr2:44182620 | G | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-15+13346G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44182620 | |||||||
| chr2:44183056 | T | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(58): Show |
63 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-15+13782T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183056 | |||||||
| chr2:44183094 | T | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-15+13820T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183094 | |||||||
| chr2:44183246 | C | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0167 others(13): Show |
16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+13972C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183246 | |||||||
| chr2:44183392 | A | T | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-15+14118A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183392 | |||||||
| chr2:44183401 | A | C | 72 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(69): Show |
74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-15+14127A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183401 | |||||||
| chr2:44183478 | G | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(53): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+14204G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183478 | |||||||
| chr2:44183601 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+14327C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183601 | |||||||
| chr2:44183658 | AG | A | 5 | a0001c0001t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+14385delG | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183658 | |||||||
| chr2:44183715 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0003g0346 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-15+14441C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183715 | |||||||
| chr2:44183824 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-15+14550C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183824 | |||||||
| chr2:44183887 | C | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(56): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15+14613C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183887 | |||||||
| chr2:44183896 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
196 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-15+14622C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183896 | |||||||
| chr2:44183929 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-15+14655G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183929 | |||||||
| chr2:44183945 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-15+14671A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183945 | |||||||
| chr2:44183981 | G | A | 10 | a0001c0001t0001g0187 a0001c0001t0001g0218 a0001c0001t0001g0257 others(7): Show |
10 | HG01346.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+14707G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44183981 | |||||||
| chr2:44184086 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+14812T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184086 | |||||||
| chr2:44184116 | T | C | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+14842T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184116 | |||||||
| chr2:44184160 | A | C | 1 | a0001c0001t0009g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-15+14886A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184160 | |||||||
| chr2:44184258 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0136 |
2 | HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-15+14984A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184258 | |||||||
| chr2:44184616 | A | G | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(71): Show |
76 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-15+15342A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184616 | |||||||
| chr2:44184719 | T | C | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15445T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184719 | |||||||
| chr2:44184726 | G | A | 1 | a0001c0001t0003g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-15+15452G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184726 | |||||||
| chr2:44184915 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15+15641T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184915 | |||||||
| chr2:44184924 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15650A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184924 | |||||||
| chr2:44184935 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-15+15661C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44184935 | |||||||
| chr2:44185161 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-15+15887A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185161 | |||||||
| chr2:44185190 | T | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-15+15916T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185190 | |||||||
| chr2:44185259 | G | T | 1 | a0001c0001t0002g0089 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14-15927G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185259 | |||||||
| chr2:44185453 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-15733C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185453 | |||||||
| chr2:44185542 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
79 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-14-15644A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185542 | |||||||
| chr2:44185660 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15526A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185660 | |||||||
| chr2:44185724 | TG | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-15461delG | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185724 | |||||||
| chr2:44185725 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
101 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.-14-15461G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185725 | |||||||
| chr2:44185829 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0140 |
3 | HG01070.hp1 HG01123.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-14-15357C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185829 | |||||||
| chr2:44185926 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-15260G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185926 | |||||||
| chr2:44185950 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15236T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185950 | |||||||
| chr2:44185994 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG00741.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-14-15192A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44185994 | |||||||
| chr2:44186026 | G | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15160G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186026 | |||||||
| chr2:44186027 | A | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-15159A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186027 | |||||||
| chr2:44186075 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-14-15111G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186075 | |||||||
| chr2:44186336 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-14-14850A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186336 | |||||||
| chr2:44186523 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-14-14663C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186523 | |||||||
| chr2:44186561 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-14-14625G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186561 | |||||||
| chr2:44186563 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-14-14623C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186563 | |||||||
| chr2:44186575 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-14611A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186575 | |||||||
| chr2:44186640 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-14-14546G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186640 | |||||||
| chr2:44186685 | C | G | 19 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(16): Show |
19 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-14-14501C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186685 | |||||||
| chr2:44186781 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-14405T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186781 | |||||||
| chr2:44186919 | C | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-14267C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186919 | |||||||
| chr2:44186940 | C | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
33 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-14246C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186940 | |||||||
| chr2:44186973 | T | G | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-14-14213T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44186973 | |||||||
| chr2:44187006 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-14180A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187006 | |||||||
| chr2:44187061 | A | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(14): Show |
17 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-14125A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187061 | |||||||
| chr2:44187113 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG02486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-14-14073A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187113 | |||||||
| chr2:44187191 | C | G | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-13995C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187191 | |||||||
| chr2:44187215 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0192 others(10): Show |
15 | HG00642.hp1 HG01099.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.-14-13971A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187215 | |||||||
| chr2:44187282 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-14-13904A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187282 | |||||||
| chr2:44187302 | A | T | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-13884A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187302 | |||||||
| chr2:44187318 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14-13868A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187318 | |||||||
| chr2:44187363 | T | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-13823T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187363 | |||||||
| chr2:44187558 | G | T | 1 | a0001c0001t0001g0302 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-13628G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187558 | |||||||
| chr2:44187642 | C | G | 2 | a0001c0001t0001g0339 a0001c0001t0001g0340 |
2 | HG00621.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-14-13544C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187642 | |||||||
| chr2:44187690 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-13496C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187690 | |||||||
| chr2:44187825 | C | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0160 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-13361C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187825 | |||||||
| chr2:44187836 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0259 |
2 | HG00673.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-14-13350G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187836 | |||||||
| chr2:44187897 | C | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-13289C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187897 | |||||||
| chr2:44187911 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-14-13275C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187911 | |||||||
| chr2:44187991 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-13195C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44187991 | |||||||
| chr2:44188011 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-13175A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188011 | |||||||
| chr2:44188018 | A | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-14-13168A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188018 | |||||||
| chr2:44188247 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14-12939C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188247 | |||||||
| chr2:44188288 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-14-12898C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188288 | |||||||
| chr2:44188377 | GTTTC | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02486.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-12793_-14-1279 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188377 | ||||||
| chr2:44188389 | CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-12793_-14-1278 others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188389 | ||||||
| chr2:44188390 | TTTC | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0167 a0001c0001t0001g0168 others(9): Show |
12 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-12793_-14-1279 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188390 | ||||||
| chr2:44188392 | TC | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0160 a0001c0001t0001g0312 others(4): Show |
7 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-12793delC | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188392 | |||||||
| chr2:44188393 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(16): Show |
21 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-14-12793C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188393 | |||||||
| chr2:44188393 | CT | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.-14-12773delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188393 | ||||||
| chr2:44188393 | CTT | C | 10 | a0001c0001t0001g0178 a0001c0001t0001g0188 a0001c0001t0001g0226 others(7): Show |
10 | HG00639.hp1 HG01070.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-12774_-14-1277 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188393 | ||||||
| chr2:44188397 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-14-12789T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188397 | |||||||
| chr2:44188398 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0002g0067 |
2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-14-12788T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188398 | |||||||
| chr2:44188458 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-12728C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188458 | |||||||
| chr2:44188478 | C | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-12708C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188478 | |||||||
| chr2:44188493 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-14-12693T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188493 | |||||||
| chr2:44188545 | C | T | 1 | a0001c0001t0004g0301 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-14-12641C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188545 | |||||||
| chr2:44188573 | C | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-14-12613C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188573 | |||||||
| chr2:44188575 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
90 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-14-12611T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188575 | |||||||
| chr2:44188577 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-12609C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188577 | |||||||
| chr2:44188578 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-12608G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188578 | |||||||
| chr2:44188627 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-12559C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188627 | |||||||
| chr2:44188713 | G | GCTTTCCT others(17): Show |
1 | a0001c0001t0001g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-14-12426_-14-1240 others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188713 | ||||||
| chr2:44188713 | GCTTTCCT others(17): Show |
G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0199 |
2 | HG02523.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-14-12426_-14-1240 others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188713 | ||||||
| chr2:44188739 | TTTCC | T | 11 | a0001c0001t0001g0095 a0001c0001t0001g0193 a0001c0001t0001g0198 others(8): Show |
11 | HG01934.hp1 HG01943.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-12427_-14-1242 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188739 | ||||||
| chr2:44188743 | CTTCCTTC others(13): Show |
C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-12423_-14-1240 others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188743 | ||||||
| chr2:44188763 | TTTCC | T | 5 | a0001c0001t0001g0225 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-12406_-14-1240 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188763 | ||||||
| chr2:44188788 | T | TTCCC | 47 | a0001c0001t0001g0182 a0001c0001t0001g0252 a0001c0001t0001g0253 others(44): Show |
50 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-14-12393_-14-1239 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44188788 | ||||||
| chr2:44188994 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
156 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-14-12192G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44188994 | |||||||
| chr2:44189053 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-14-12133A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189053 | |||||||
| chr2:44189128 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-14-12058T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189128 | |||||||
| chr2:44189129 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-14-12057C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189129 | |||||||
| chr2:44189142 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-14-12044G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189142 | |||||||
| chr2:44189171 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-14-12015C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189171 | |||||||
| chr2:44189276 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
91 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.-14-11910A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189276 | |||||||
| chr2:44189283 | C | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-11903C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189283 | |||||||
| chr2:44189527 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-14-11659G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189527 | |||||||
| chr2:44189529 | TCTC | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-11656_-14-1165 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189529 | |||||||
| chr2:44189663 | C | T | 5 | a0001c0001t0001g0225 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-11523C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189663 | |||||||
| chr2:44189850 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
89 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.-14-11336T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189850 | |||||||
| chr2:44189877 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-11309C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189877 | |||||||
| chr2:44189934 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-14-11252A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44189934 | |||||||
| chr2:44190154 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-11032G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190154 | |||||||
| chr2:44190155 | A | AT | 10 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0133 others(7): Show |
10 | HG00639.hp2 HG01943.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-11011dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | ||||||
| chr2:44190155 | AT | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(202): Show |
212 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-14-11011delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | ||||||
| chr2:44190155 | ATT | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0261 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-11012_-14-1101 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44190155 | ||||||
| chr2:44190161 | T | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-11025T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190161 | |||||||
| chr2:44190264 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-14-10922C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190264 | |||||||
| chr2:44190268 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0312 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-10918C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190268 | |||||||
| chr2:44190294 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-10892A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190294 | |||||||
| chr2:44190304 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-14-10882G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190304 | |||||||
| chr2:44190417 | C | A | 1 | a0001c0001t0002g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-10769C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190417 | |||||||
| chr2:44190438 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-14-10748C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190438 | |||||||
| chr2:44190514 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-14-10672G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190514 | |||||||
| chr2:44190606 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0023 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-14-10580T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190606 | |||||||
| chr2:44190667 | C | G | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-14-10519C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190667 | |||||||
| chr2:44190786 | T | G | 1 | a0001c0001t0005g0262 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10400T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190786 | |||||||
| chr2:44190787 | G | A | 1 | a0001c0001t0005g0262 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10399G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190787 | |||||||
| chr2:44190823 | T | G | 1 | a0001c0001t0005g0262 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-14-10363T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190823 | |||||||
| chr2:44190826 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-10360G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190826 | |||||||
| chr2:44190895 | C | G | 1 | a0001c0001t0002g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-10291C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190895 | |||||||
| chr2:44190953 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0153 a0001c0001t0001g0154 others(7): Show |
12 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-10233A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190953 | |||||||
| chr2:44190993 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-14-10193A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44190993 | |||||||
| chr2:44191112 | C | A | 1 | a0001c0001t0002g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-14-10074C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191112 | |||||||
| chr2:44191139 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-10047C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191139 | |||||||
| chr2:44191157 | C | T | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0167 others(13): Show |
16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-10029C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191157 | |||||||
| chr2:44191191 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-14-9995G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191191 | |||||||
| chr2:44191245 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-9941G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191245 | |||||||
| chr2:44191318 | A | G | 4 | a0001c0001t0004g0221 a0001c0001t0004g0297 a0001c0001t0004g0300 others(1): Show |
4 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-9868A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191318 | |||||||
| chr2:44191669 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-14-9517G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191669 | |||||||
| chr2:44191721 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-9465A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191721 | |||||||
| chr2:44191768 | T | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0260 a0001c0001t0001g0263 others(1): Show |
4 | NA18986.hp1 NA18988.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-9418T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191768 | |||||||
| chr2:44191791 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-14-9395G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191791 | |||||||
| chr2:44191841 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-9345G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44191841 | |||||||
| chr2:44192017 | C | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-9169C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192017 | |||||||
| chr2:44192049 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-9137C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192049 | |||||||
| chr2:44192077 | C | G | 1 | a0001c0001t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-9109C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192077 | |||||||
| chr2:44192165 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-14-9021T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192165 | |||||||
| chr2:44192185 | G | GGTATT | 3 | a0001c0001t0001g0179 a0001c0001t0003g0343 a0001c0001t0003g0345 |
3 | HG01361.hp1 HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-14-9001_-14-9000i others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192185 | |||||||
| chr2:44192185 | G | GGTATTGT others(3): Show |
3 | a0001c0001t0002g0046 a0001c0001t0003g0344 a0001c0001t0003g0346 |
3 | HG02074.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-14-9001_-14-9000i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192185 | |||||||
| chr2:44192186 | T | G | 6 | a0001c0001t0001g0179 a0001c0001t0002g0046 a0001c0001t0003g0343 others(3): Show |
6 | HG01361.hp1 HG02055.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-9000T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192186 | |||||||
| chr2:44192190 | G | GGTATT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(110): Show |
115 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.-14-8954_-14-8950d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | G | GGTATTGT others(3): Show |
81 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
88 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-14-8959_-14-8950d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | G | GGTATTGT others(8): Show |
23 | a0001c0001t0001g0040 a0001c0001t0001g0153 a0001c0001t0001g0187 others(20): Show |
23 | HG00673.hp2 HG01346.hp1 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-14-8964_-14-8950d others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | G | GGTATTGT others(13): Show |
3 | a0001c0001t0001g0037 a0001c0001t0002g0060 a0001c0001t0010g0050 |
3 | HG00099.hp2 HG02683.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-14-8969_-14-8950d others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | G | GGTATTGT others(18): Show |
2 | a0001c0001t0001g0248 a0001c0001t0002g0049 |
2 | NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-14-8974_-14-8950d others(27): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | G | GTTATGGT others(3): Show |
2 | a0001c0001t0001g0169 a0001c0001t0002g0074 |
2 | HG03486.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-14-8996_-14-8995i others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | |||||||
| chr2:44192190 | G | GTTATGGT others(8): Show |
2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-14-8996_-14-8995i others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | |||||||
| chr2:44192190 | G | T | 6 | a0001c0001t0001g0179 a0001c0001t0002g0046 a0001c0001t0003g0343 others(3): Show |
6 | HG01361.hp1 HG02055.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8996G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192190 | |||||||
| chr2:44192190 | GGTATT | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0095 others(50): Show |
55 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-8954_-14-8950d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | GGTATTGT others(3): Show |
G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-8959_-14-8950d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192190 | GGTATTGT others(8): Show |
G | 1 | a0001c0001t0001g0200 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-14-8964_-14-8950d others(17): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192190 | ||||||
| chr2:44192195 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8991T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192195 | |||||||
| chr2:44192200 | T | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8986T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192200 | |||||||
| chr2:44192234 | T | TTGTATTG others(7): Show |
1 | a0001c0001t0002g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-14-8950_-14-8949i others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44192234 | ||||||
| chr2:44192277 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8909G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192277 | |||||||
| chr2:44192342 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-8844C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192342 | |||||||
| chr2:44192364 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8822A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192364 | |||||||
| chr2:44192375 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0001g0287 a0001c0001t0004g0221 others(3): Show |
6 | HG01081.hp1 HG01106.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-8811C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192375 | |||||||
| chr2:44192429 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-8757T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192429 | |||||||
| chr2:44192630 | C | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(15): Show |
19 | HG00621.hp1 NA18945.hp2 NA18950.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-8556C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192630 | |||||||
| chr2:44192722 | G | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8464G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192722 | |||||||
| chr2:44192852 | A | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-8334A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192852 | |||||||
| chr2:44192852 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-14-8334A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192852 | |||||||
| chr2:44192923 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-14-8263A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192923 | |||||||
| chr2:44192928 | A | T | 1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-14-8258A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192928 | |||||||
| chr2:44192960 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-8226C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44192960 | |||||||
| chr2:44193023 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-8163G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193023 | |||||||
| chr2:44193135 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0179 a0001c0001t0001g0181 |
4 | HG00733.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-8051A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193135 | |||||||
| chr2:44193155 | A | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-8031A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193155 | |||||||
| chr2:44193272 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-7914T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193272 | |||||||
| chr2:44193351 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-7835A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193351 | |||||||
| chr2:44193384 | CCTCTGAA others(42): Show |
C | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-7796_-14-7748d others(51): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193384 | ||||||
| chr2:44193575 | C | CT | 13 | a0001c0001t0001g0095 a0001c0001t0001g0184 a0001c0001t0001g0248 others(10): Show |
13 | HG00621.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7591dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | ||||||
| chr2:44193575 | CT | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
47 | HG01069.hp1 HG01074.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-14-7591delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | ||||||
| chr2:44193575 | CTT | C | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(49): Show |
54 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14-7592_-14-7591d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44193575 | ||||||
| chr2:44193636 | G | C | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-7550G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193636 | |||||||
| chr2:44193639 | C | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
88 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-14-7547C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193639 | |||||||
| chr2:44193740 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0160 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-7446G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193740 | |||||||
| chr2:44193885 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-7301A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193885 | |||||||
| chr2:44193933 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-7253C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193933 | |||||||
| chr2:44193939 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 |
3 | HG01243.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-7247A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44193939 | |||||||
| chr2:44194028 | A | G | 2 | a0001c0001t0007g0216 a0001c0001t0007g0217 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-7158A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194028 | |||||||
| chr2:44194129 | T | C | 1 | a0001c0001t0003g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14-7057T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194129 | |||||||
| chr2:44194324 | T | C | 7 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | NA18949.hp1 NA18969.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-6862T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194324 | |||||||
| chr2:44194351 | C | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0095 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-6835C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194351 | |||||||
| chr2:44194403 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0160 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6783T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194403 | |||||||
| chr2:44194489 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-6697C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194489 | |||||||
| chr2:44194596 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
85 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14-6590G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194596 | |||||||
| chr2:44194756 | A | G | 1 | a0001c0001t0002g0073 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-6430A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194756 | |||||||
| chr2:44194807 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-6379G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194807 | |||||||
| chr2:44194853 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-6333A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194853 | |||||||
| chr2:44194882 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
96 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.-14-6304G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194882 | |||||||
| chr2:44194898 | C | CT | 99 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
103 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.-14-6270dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44194898 | ||||||
| chr2:44194959 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-14-6227C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194959 | |||||||
| chr2:44194963 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0318 |
2 | HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-14-6223A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194963 | |||||||
| chr2:44194972 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(261): Show |
272 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.-14-6214G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44194972 | |||||||
| chr2:44195027 | G | T | 1 | a0001c0001t0003g0343 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-14-6159G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195027 | |||||||
| chr2:44195036 | C | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-6150C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195036 | |||||||
| chr2:44195100 | C | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0160 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6086C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195100 | |||||||
| chr2:44195112 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02145.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-14-6074C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195112 | |||||||
| chr2:44195140 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-14-6046G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195140 | |||||||
| chr2:44195205 | C | CT | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
94 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-14-5968dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44195205 | ||||||
| chr2:44195232 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-14-5954C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195232 | |||||||
| chr2:44195323 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-14-5863C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195323 | |||||||
| chr2:44195364 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-5822A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195364 | |||||||
| chr2:44195455 | C | G | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(59): Show |
64 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-14-5731C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195455 | |||||||
| chr2:44195470 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-14-5716C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195470 | |||||||
| chr2:44195620 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-5566T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195620 | |||||||
| chr2:44195721 | C | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(74): Show |
81 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.-14-5465C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195721 | |||||||
| chr2:44195788 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0018 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-5398C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195788 | |||||||
| chr2:44195852 | A | T | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-5334A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195852 | |||||||
| chr2:44195946 | A | T | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-14-5240A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44195946 | |||||||
| chr2:44196094 | T | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-5092T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196094 | |||||||
| chr2:44196175 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14-5011C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196175 | |||||||
| chr2:44196401 | G | A | 4 | a0002c0002t0001g0025 a0002c0002t0001g0026 a0002c0002t0001g0027 others(1): Show |
4 | HG02622.hp2 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-4785G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196401 | |||||||
| chr2:44196419 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0174 |
2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-14-4767C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196419 | |||||||
| chr2:44196464 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14-4722T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196464 | |||||||
| chr2:44196675 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-4511C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196675 | |||||||
| chr2:44196832 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-4354G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196832 | |||||||
| chr2:44196837 | A | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-4349A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44196837 | |||||||
| chr2:44197039 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-14-4147A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197039 | |||||||
| chr2:44197051 | T | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(14): Show |
17 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-14-4135T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197051 | |||||||
| chr2:44197123 | C | CT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-4054dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44197123 | ||||||
| chr2:44197169 | G | A | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-4017G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197169 | |||||||
| chr2:44197204 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-14-3982T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197204 | |||||||
| chr2:44197361 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14-3825C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197361 | |||||||
| chr2:44197378 | C | G | 1 | a0001c0001t0001g0347 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-14-3808C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197378 | |||||||
| chr2:44197798 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-14-3388T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197798 | |||||||
| chr2:44197837 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-14-3349G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197837 | |||||||
| chr2:44197923 | G | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-3263G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197923 | |||||||
| chr2:44197955 | C | G | 1 | a0001c0001t0001g0331 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-3231C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197955 | |||||||
| chr2:44197964 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-14-3222A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44197964 | |||||||
| chr2:44198004 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3182C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198004 | |||||||
| chr2:44198284 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18960.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-14-2902C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198284 | |||||||
| chr2:44198369 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-2817C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198369 | |||||||
| chr2:44198407 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2779C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198407 | |||||||
| chr2:44198450 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-14-2736C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198450 | |||||||
| chr2:44198777 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-14-2409A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198777 | |||||||
| chr2:44198837 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2349A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198837 | |||||||
| chr2:44198975 | A | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(338): Show |
352 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(349): Show |
intron_variant | MODIFIER | c.-14-2211A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44198975 | |||||||
| chr2:44199071 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-14-2115A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199071 | |||||||
| chr2:44199149 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2037C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199149 | |||||||
| chr2:44199150 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0107 |
2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-14-2036C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199150 | |||||||
| chr2:44199151 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-2035G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199151 | |||||||
| chr2:44199170 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(87): Show |
94 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-14-2016G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199170 | |||||||
| chr2:44199244 | C | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0258 a0001c0001t0001g0313 |
3 | HG01346.hp1 HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-1942C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199244 | |||||||
| chr2:44199257 | C | CA | 9 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0148 others(6): Show |
9 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-1917dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199257 | ||||||
| chr2:44199274 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-14-1912C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199274 | |||||||
| chr2:44199303 | C | CA | 8 | a0001c0001t0001g0032 a0001c0001t0001g0170 a0001c0001t0001g0205 others(5): Show |
8 | HG02559.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-1869dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199303 | ||||||
| chr2:44199311 | A | T | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-14-1875A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199311 | |||||||
| chr2:44199311 | AAAAAAAT others(6): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0112 others(13): Show |
18 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1856d others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199311 | ||||||
| chr2:44199312 | A | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0324 |
2 | NA18999.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-14-1874A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199312 | |||||||
| chr2:44199312 | AAAAAATA others(5): Show |
A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(51): Show |
56 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1857d others(14): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199312 | ||||||
| chr2:44199313 | AAAAATAA others(4): Show |
A | 7 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0109 others(4): Show |
7 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1868_-14-1858d others(13): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199313 | ||||||
| chr2:44199314 | A | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18969.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-14-1872A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199314 | |||||||
| chr2:44199317 | AT | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | NA18949.hp1 NA18969.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1868delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199317 | |||||||
| chr2:44199318 | T | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0170 others(6): Show |
9 | HG01934.hp1 HG01943.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-1868T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199318 | |||||||
| chr2:44199324 | T | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(30): Show |
34 | HG00323.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1862T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199324 | |||||||
| chr2:44199324 | T | TA | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-1848dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr2 | 44199324 | ||||||
| chr2:44199325 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-1861A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199325 | |||||||
| chr2:44199327 | A | AT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0002g0090 others(4): Show |
7 | HG01074.hp2 HG01099.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-1859_-14-1858i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199327 | |||||||
| chr2:44199327 | A | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-14-1859A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199327 | |||||||
| chr2:44199330 | A | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0001g0186 others(4): Show |
7 | HG00438.hp1 NA18953.hp2 NA18989.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-1856A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199330 | |||||||
| chr2:44199331 | A | AT | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1855_-14-1854i others(3): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199331 | |||||||
| chr2:44199335 | A | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-14-1851A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199335 | |||||||
| chr2:44199350 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-1836A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199350 | |||||||
| chr2:44199430 | A | G | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(338): Show |
352 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(349): Show |
intron_variant | MODIFIER | c.-14-1756A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199430 | |||||||
| chr2:44199712 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-1474A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199712 | |||||||
| chr2:44199855 | T | C | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1331T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199855 | |||||||
| chr2:44199899 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
95 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-14-1287C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199899 | |||||||
| chr2:44199943 | A | G | 15 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(12): Show |
15 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-14-1243A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199943 | |||||||
| chr2:44199994 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-14-1192C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44199994 | |||||||
| chr2:44200053 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-14-1133C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200053 | |||||||
| chr2:44200148 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-14-1038T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200148 | |||||||
| chr2:44200265 | T | A | 1 | a0001c0001t0002g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-14-921T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200265 | |||||||
| chr2:44200405 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0008g0021 |
2 | HG00323.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-14-781A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200405 | |||||||
| chr2:44200540 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-14-646A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200540 | |||||||
| chr2:44200628 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-558T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200628 | |||||||
| chr2:44200800 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-386C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200800 | |||||||
| chr2:44200808 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-14-378A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200808 | |||||||
| chr2:44200880 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-14-306A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200880 | |||||||
| chr2:44200930 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14-256T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200930 | |||||||
| chr2:44200956 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-14-230C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44200956 | |||||||
| chr2:44201065 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-14-121C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201065 | |||||||
| chr2:44201096 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-14-90T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201096 | |||||||
| chr2:44201103 | G | A | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0167 others(13): Show |
16 | HG01074.hp2 HG01099.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-83G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201103 | |||||||
| chr2:44201144 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-14-42C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 1/5 | chr2 | 44201144 | |||||||
| chr2:44202135 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+90T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44202135 | |||||||
| chr2:44202222 | C | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | HG02040.hp1 HG02083.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.846+177C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44202222 | |||||||
| chr2:44202604 | C | CTATG | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.846+561_846+562ins others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44202604 | ||||||
| chr2:44203096 | A | T | 1 | a0001c0001t0002g0044 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.846+1051A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203096 | |||||||
| chr2:44203099 | T | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.846+1054T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203099 | |||||||
| chr2:44203120 | A | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.846+1075A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203120 | |||||||
| chr2:44203166 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+1121C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203166 | |||||||
| chr2:44203473 | T | TA | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.846+1436dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44203473 | ||||||
| chr2:44203528 | A | G | 1 | a0001c0001t0001g0007 | 2 | NA18945.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.846+1483A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203528 | |||||||
| chr2:44203630 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
98 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.846+1585A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203630 | |||||||
| chr2:44203676 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.846+1631C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203676 | |||||||
| chr2:44203710 | G | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(57): Show |
62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.846+1665G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203710 | |||||||
| chr2:44203850 | C | A | 1 | a0001c0001t0002g0056 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.846+1805C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44203850 | |||||||
| chr2:44204011 | C | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+1966C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204011 | |||||||
| chr2:44204092 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.846+2047C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204092 | |||||||
| chr2:44204316 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+2271T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204316 | |||||||
| chr2:44204316 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.846+2271T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204316 | |||||||
| chr2:44204517 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.846+2472A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204517 | |||||||
| chr2:44204535 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.846+2490G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204535 | |||||||
| chr2:44204573 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.846+2528C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204573 | |||||||
| chr2:44204580 | A | G | 72 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(69): Show |
75 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.846+2535A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204580 | |||||||
| chr2:44204661 | A | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2616A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204661 | |||||||
| chr2:44204732 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+2687G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204732 | |||||||
| chr2:44204783 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.846+2738C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204783 | |||||||
| chr2:44204816 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
165 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.846+2771G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204816 | |||||||
| chr2:44204856 | C | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+2811C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44204856 | |||||||
| chr2:44204858 | C | CA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0039 others(35): Show |
39 | HG00609.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.846+2839dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | C | CAA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0192 others(9): Show |
14 | HG00642.hp1 HG01099.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.846+2838_846+2839d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | CA | C | 13 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0137 others(10): Show |
13 | HG00544.hp1 HG01109.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.846+2839delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | CAA | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0312 a0001c0001t0003g0343 others(7): Show |
10 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.846+2838_846+2839d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | CAAAAAAA | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.846+2833_846+2839d others(9): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+2830_846+2839d others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44204858 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.846+2827_846+2839d others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44204858 | ||||||
| chr2:44205142 | G | C | 5 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(2): Show |
5 | HG01074.hp2 HG01099.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+3097G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205142 | |||||||
| chr2:44205332 | AGTGGGT | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
153 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.846+3309_846+3314d others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205332 | ||||||
| chr2:44205336 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.846+3291G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205336 | |||||||
| chr2:44205337 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(92): Show |
99 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.846+3292G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205337 | |||||||
| chr2:44205348 | G | GGTGTGTG others(15): Show |
1 | a0001c0001t0001g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.846+3308_846+3309i others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205348 | ||||||
| chr2:44205350 | TGTGG | T | 13 | a0001c0001t0001g0176 a0001c0001t0001g0202 a0001c0001t0001g0205 others(10): Show |
13 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.846+3309_846+3312d others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205350 | ||||||
| chr2:44205354 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0001g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.846+3319_846+3320i others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(13): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0028 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(15): Show |
2 | a0001c0001t0001g0095 a0001c0001t0003g0031 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(24): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(17): Show |
3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0008g0021 |
3 | HG02809.hp1 NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(26): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(19): Show |
18 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0122 others(15): Show |
18 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(28): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(21): Show |
56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(53): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(30): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(23): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0119 others(7): Show |
12 | HG01106.hp1 HG02015.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(32): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(25): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0135 |
2 | HG02922.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.846+3319_846+3320i others(34): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(27): Show |
4 | a0001c0001t0001g0132 a0001c0001t0001g0157 a0001c0001t0001g0165 others(1): Show |
4 | HG02280.hp2 HG02486.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3319_846+3320i others(36): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(24): Show |
1 | a0001c0001t0001g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.846+3319_846+3320i others(33): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | GGTGTGTG others(24): Show |
1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.846+3319_846+3320i others(33): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205354 | ||||||
| chr2:44205354 | G | T | 4 | a0001c0001t0001g0148 a0001c0001t0001g0283 a0001c0001t0001g0295 others(1): Show |
4 | HG01934.hp2 HG02015.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3309G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205354 | |||||||
| chr2:44205356 | T | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0219 a0001c0001t0001g0241 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+3311T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205356 | |||||||
| chr2:44205374 | T | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0003c0003t0001g0014 |
3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.846+3329T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205374 | |||||||
| chr2:44205380 | T | TAA | 4 | a0001c0001t0001g0151 a0001c0001t0003g0031 a0001c0001t0006g0150 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+3336_846+3337d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44205380 | ||||||
| chr2:44205523 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.846+3478C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205523 | |||||||
| chr2:44205630 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG01070.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.847-3580A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205630 | |||||||
| chr2:44205713 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.847-3497A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205713 | |||||||
| chr2:44205769 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.847-3441A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205769 | |||||||
| chr2:44205860 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.847-3350C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205860 | |||||||
| chr2:44205986 | A | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(59): Show |
64 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.847-3224A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44205986 | |||||||
| chr2:44206044 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-3166A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206044 | |||||||
| chr2:44206259 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847-2951A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206259 | |||||||
| chr2:44206564 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.847-2646C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206564 | |||||||
| chr2:44206572 | G | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-2638G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206572 | |||||||
| chr2:44206638 | TTAAAAGA others(11): Show |
T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-2565_847-2548d others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44206638 | ||||||
| chr2:44206656 | C | G | 66 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(63): Show |
69 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.847-2554C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206656 | |||||||
| chr2:44206688 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.847-2522A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206688 | |||||||
| chr2:44206726 | T | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2484T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206726 | |||||||
| chr2:44206728 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2482T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206728 | |||||||
| chr2:44206730 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2480T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206730 | |||||||
| chr2:44206731 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2479T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206731 | |||||||
| chr2:44206732 | G | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2478G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206732 | |||||||
| chr2:44206733 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2477T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206733 | |||||||
| chr2:44206735 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2475G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206735 | |||||||
| chr2:44206736 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2474T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206736 | |||||||
| chr2:44206737 | T | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0246 |
2 | HG01169.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.847-2473T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206737 | |||||||
| chr2:44206776 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.847-2434A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206776 | |||||||
| chr2:44206855 | A | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-2355A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206855 | |||||||
| chr2:44206867 | C | G | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.847-2343C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44206867 | |||||||
| chr2:44207078 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.847-2132A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207078 | |||||||
| chr2:44207145 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.847-2065C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207145 | |||||||
| chr2:44207166 | AC | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-2043delC | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207166 | |||||||
| chr2:44207190 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.847-2020G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207190 | |||||||
| chr2:44207329 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-1881G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207329 | |||||||
| chr2:44207493 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.847-1717G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207493 | |||||||
| chr2:44207579 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.847-1631G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207579 | |||||||
| chr2:44207635 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0218 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.847-1575G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207635 | |||||||
| chr2:44207639 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.847-1571C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207639 | |||||||
| chr2:44207669 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.847-1541A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207669 | |||||||
| chr2:44207888 | C | CT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(23): Show |
26 | HG01169.hp1 HG01258.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.847-1303dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44207888 | ||||||
| chr2:44207888 | CT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
151 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.847-1303delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr2 | 44207888 | ||||||
| chr2:44207973 | C | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(4): Show |
10 | HG00733.hp1 NA18953.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.847-1237C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44207973 | |||||||
| chr2:44208041 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-1169A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208041 | |||||||
| chr2:44208121 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-1089C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208121 | |||||||
| chr2:44208150 | A | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-1060A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208150 | |||||||
| chr2:44208186 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
119 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.847-1024T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208186 | |||||||
| chr2:44208384 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.847-826C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208384 | |||||||
| chr2:44208386 | C | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.847-824C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208386 | |||||||
| chr2:44208544 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(161): Show |
168 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.847-666C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208544 | |||||||
| chr2:44208572 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-638G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208572 | |||||||
| chr2:44208583 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.847-627G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208583 | |||||||
| chr2:44208669 | C | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0139 |
4 | HG00642.hp2 HG01981.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.847-541C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208669 | |||||||
| chr2:44208868 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.847-342A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208868 | |||||||
| chr2:44208874 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.847-336G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44208874 | |||||||
| chr2:44209180 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.847-30T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44209180 | |||||||
| chr2:44209188 | C | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.847-22C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 2/5 | chr2 | 44209188 | |||||||
| chr2:44209431 | C | CAA | 11 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0095 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.964+116_964+117dup others(2): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209431 | ||||||
| chr2:44209456 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.964+129A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209456 | |||||||
| chr2:44209518 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.964+191A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209518 | |||||||
| chr2:44209604 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.964+277C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209604 | |||||||
| chr2:44209629 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.964+302T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209629 | |||||||
| chr2:44209632 | C | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+305C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209632 | |||||||
| chr2:44209777 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0018 others(27): Show |
32 | HG00438.hp1 HG00642.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.964+468dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209777 | ||||||
| chr2:44209777 | CA | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
101 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.964+468delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209777 | ||||||
| chr2:44209833 | GA | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(4): Show |
7 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+512delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44209833 | ||||||
| chr2:44209874 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.964+547C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44209874 | |||||||
| chr2:44210078 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
112 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.964+751G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210078 | |||||||
| chr2:44210101 | G | C | 1 | a0001c0001t0003g0343 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964+774G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210101 | |||||||
| chr2:44210127 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+800C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210127 | |||||||
| chr2:44210161 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.964+834T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210161 | |||||||
| chr2:44210170 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0003c0003t0001g0014 |
3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.964+843C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210170 | |||||||
| chr2:44210172 | A | G | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+845A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210172 | |||||||
| chr2:44210215 | A | AT | 11 | a0001c0001t0001g0184 a0001c0001t0001g0260 a0001c0001t0001g0263 others(8): Show |
11 | HG01358.hp1 HG01975.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.964+907dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44210215 | ||||||
| chr2:44210215 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
116 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.964+907delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44210215 | ||||||
| chr2:44210339 | C | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+1012C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210339 | |||||||
| chr2:44210458 | A | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+1131A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210458 | |||||||
| chr2:44210802 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.964+1475C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210802 | |||||||
| chr2:44210858 | C | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.964+1531C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210858 | |||||||
| chr2:44210931 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+1604T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210931 | |||||||
| chr2:44210968 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964+1641T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210968 | |||||||
| chr2:44210973 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.964+1646T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44210973 | |||||||
| chr2:44211002 | G | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(5): Show |
8 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+1675G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211002 | |||||||
| chr2:44211029 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0218 |
3 | HG02486.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.964+1702C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211029 | |||||||
| chr2:44211034 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.964+1707G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211034 | |||||||
| chr2:44211107 | G | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
160 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.964+1780G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211107 | |||||||
| chr2:44211114 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.964+1787T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211114 | |||||||
| chr2:44211169 | A | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+1842A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211169 | |||||||
| chr2:44211464 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+2137T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211464 | |||||||
| chr2:44211485 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.964+2158T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211485 | |||||||
| chr2:44211589 | AAT | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
166 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.964+2265_964+2266d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211589 | ||||||
| chr2:44211742 | CT | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(213): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.964+2439delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211742 | ||||||
| chr2:44211742 | CTT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
107 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.964+2438_964+2439d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44211742 | ||||||
| chr2:44211792 | C | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.964+2465C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211792 | |||||||
| chr2:44211827 | G | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+2500G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211827 | |||||||
| chr2:44211836 | G | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.964+2509G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211836 | |||||||
| chr2:44211993 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.964+2666G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44211993 | |||||||
| chr2:44212084 | G | A | 59 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(56): Show |
61 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.964+2757G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212084 | |||||||
| chr2:44212205 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.964+2878C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212205 | |||||||
| chr2:44212333 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.964+3006C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212333 | |||||||
| chr2:44212361 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.964+3034C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212361 | |||||||
| chr2:44212516 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.964+3189C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212516 | |||||||
| chr2:44212586 | G | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.964+3259G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212586 | |||||||
| chr2:44212628 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.964+3301A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212628 | |||||||
| chr2:44212721 | G | A | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(336): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(347): Show |
intron_variant | MODIFIER | c.964+3394G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212721 | |||||||
| chr2:44212749 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0154 others(6): Show |
11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.964+3422G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212749 | |||||||
| chr2:44212773 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
75 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.964+3446G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212773 | |||||||
| chr2:44212781 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.964+3454C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212781 | |||||||
| chr2:44212872 | G | T | 1 | a0002c0002t0001g0027 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.964+3545G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212872 | |||||||
| chr2:44212894 | T | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(150): Show |
157 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.964+3567T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212894 | |||||||
| chr2:44212896 | C | T | 9 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(6): Show |
9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.964+3569C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212896 | |||||||
| chr2:44212978 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
93 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.964+3651A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212978 | |||||||
| chr2:44212991 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.964+3664C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44212991 | |||||||
| chr2:44213013 | C | CA | 25 | a0001c0001t0001g0040 a0001c0001t0001g0101 a0001c0001t0001g0124 others(22): Show |
25 | HG00597.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.964+3706dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213013 | ||||||
| chr2:44213013 | CA | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(19): Show |
22 | HG01884.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.964+3706delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213013 | ||||||
| chr2:44213104 | C | CT | 15 | a0001c0001t0001g0039 a0001c0001t0001g0160 a0001c0001t0001g0161 others(12): Show |
15 | HG00323.hp1 HG00438.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.964+3794dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213104 | ||||||
| chr2:44213104 | CT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
82 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.964+3794delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213104 | ||||||
| chr2:44213382 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.964+4055C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213382 | |||||||
| chr2:44213398 | A | T | 1 | a0001c0001t0003g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.964+4071A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213398 | |||||||
| chr2:44213405 | C | T | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(334): Show |
348 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.964+4078C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213405 | |||||||
| chr2:44213480 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.964+4153T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213480 | |||||||
| chr2:44213499 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.964+4172A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213499 | |||||||
| chr2:44213714 | T | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.965-4253T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213714 | |||||||
| chr2:44213889 | ATAGTT | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-4075_965-4071d others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44213889 | ||||||
| chr2:44213921 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.965-4046A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213921 | |||||||
| chr2:44213954 | G | A | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-4013G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44213954 | |||||||
| chr2:44214013 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.965-3954T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214013 | |||||||
| chr2:44214039 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-3928C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214039 | |||||||
| chr2:44214140 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0260 a0001c0001t0001g0263 others(2): Show |
5 | NA18944.hp1 NA18986.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-3827C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214140 | |||||||
| chr2:44214149 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.965-3818G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214149 | |||||||
| chr2:44214169 | G | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-3798G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214169 | |||||||
| chr2:44214270 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3697G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214270 | |||||||
| chr2:44214320 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3647C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214320 | |||||||
| chr2:44214378 | T | G | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-3589T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214378 | |||||||
| chr2:44214410 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.965-3557A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214410 | |||||||
| chr2:44214525 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0008g0021 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.965-3442A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214525 | |||||||
| chr2:44214558 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0170 |
3 | HG02145.hp2 HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.965-3409G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214558 | |||||||
| chr2:44214643 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.965-3324G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214643 | |||||||
| chr2:44214704 | C | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-3263C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214704 | |||||||
| chr2:44214722 | G | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-3245G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214722 | |||||||
| chr2:44214868 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.965-3099T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214868 | |||||||
| chr2:44214961 | G | A | 17 | a0001c0001t0001g0184 a0001c0001t0001g0197 a0001c0001t0001g0202 others(14): Show |
17 | HG00597.hp1 HG01167.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.965-3006G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44214961 | |||||||
| chr2:44215008 | G | A | 9 | a0001c0001t0001g0184 a0001c0001t0001g0260 a0001c0001t0001g0263 others(6): Show |
9 | HG02015.hp2 HG02040.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-2959G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215008 | |||||||
| chr2:44215104 | G | C | 5 | a0001c0001t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-2863G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215104 | |||||||
| chr2:44215187 | T | TA | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2776dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44215187 | ||||||
| chr2:44215373 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.965-2594A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215373 | |||||||
| chr2:44215383 | A | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2584A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215383 | |||||||
| chr2:44215418 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2549A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215418 | |||||||
| chr2:44215420 | T | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2547T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215420 | |||||||
| chr2:44215461 | G | GA | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(11): Show |
14 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.965-2494dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44215461 | ||||||
| chr2:44215617 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-2350T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215617 | |||||||
| chr2:44215828 | G | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-2139G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215828 | |||||||
| chr2:44215929 | C | A | 1 | a0001c0001t0002g0096 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.965-2038C>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215929 | |||||||
| chr2:44215940 | C | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(336): Show |
350 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(347): Show |
intron_variant | MODIFIER | c.965-2027C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44215940 | |||||||
| chr2:44216040 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.965-1927A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216040 | |||||||
| chr2:44216216 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-1751A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216216 | |||||||
| chr2:44216240 | G | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(9): Show |
12 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.965-1727G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216240 | |||||||
| chr2:44216388 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965-1579C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216388 | |||||||
| chr2:44216449 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0240 a0001c0001t0001g0241 others(2): Show |
5 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-1518C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216449 | |||||||
| chr2:44216717 | G | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-1250G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216717 | |||||||
| chr2:44216728 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.965-1239C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216728 | |||||||
| chr2:44216837 | A | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-1130A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216837 | |||||||
| chr2:44216902 | C | CA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.965-1052dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44216902 | ||||||
| chr2:44216902 | C | CAA | 9 | a0001c0001t0001g0012 a0001c0001t0001g0184 a0001c0001t0001g0260 others(6): Show |
9 | HG01358.hp1 HG03704.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-1053_965-1052d others(4): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44216902 | ||||||
| chr2:44216933 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.965-1034G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216933 | |||||||
| chr2:44216967 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.965-1000C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216967 | |||||||
| chr2:44216971 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.965-996C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44216971 | |||||||
| chr2:44217025 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-942G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217025 | |||||||
| chr2:44217058 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0204 |
2 | NA18964.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.965-909G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217058 | |||||||
| chr2:44217068 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.965-899G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217068 | |||||||
| chr2:44217068 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.965-899G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217068 | |||||||
| chr2:44217148 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.965-819C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217148 | |||||||
| chr2:44217264 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.965-703T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217264 | |||||||
| chr2:44217350 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.965-617G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217350 | |||||||
| chr2:44217380 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.965-587C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217380 | |||||||
| chr2:44217399 | C | CA | 28 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0024 others(25): Show |
28 | HG00735.hp2 HG01243.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.965-553dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr2 | 44217399 | ||||||
| chr2:44217414 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.965-553A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217414 | |||||||
| chr2:44217468 | A | G | 9 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(6): Show |
9 | HG00408.hp2 NA18980.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-499A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217468 | |||||||
| chr2:44217568 | C | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.965-399C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217568 | |||||||
| chr2:44217620 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-347G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217620 | |||||||
| chr2:44217686 | T | A | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-281T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217686 | |||||||
| chr2:44217778 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.965-189C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217778 | |||||||
| chr2:44217861 | T | A | 2 | a0001c0001t0001g0157 a0001c0001t0008g0021 |
2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.965-106T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217861 | |||||||
| chr2:44217902 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.965-65T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 3/5 | chr2 | 44217902 | |||||||
| chr2:44218096 | C | G | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1076+18C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 4/5 | chr2 | 44218096 | |||||||
| chr2:44218465 | GT | G | 6 | a0001c0001t0001g0266 a0001c0001t0001g0286 a0001c0001t0001g0334 others(3): Show |
6 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1077-3delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr2 | 44218465 | ||||||
| chr2:44218547 | A | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0153 others(8): Show |
13 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1134+10A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44218547 | |||||||
| chr2:44218711 | A | ACTTC | 5 | a0001c0001t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+174_1134+175i others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44218711 | |||||||
| chr2:44219068 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1134+531A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219068 | |||||||
| chr2:44219084 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1134+547A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219084 | |||||||
| chr2:44219198 | C | CT | 9 | a0001c0001t0001g0173 a0001c0001t0001g0182 a0001c0001t0001g0220 others(6): Show |
9 | HG01106.hp2 HG01517.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1134+674dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44219198 | ||||||
| chr2:44219230 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+693A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219230 | |||||||
| chr2:44219353 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(273): Show |
284 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1134+816T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219353 | |||||||
| chr2:44219396 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1134+859A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219396 | |||||||
| chr2:44219424 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1134+887A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219424 | |||||||
| chr2:44219640 | G | A | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(339): Show |
353 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.1134+1103G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219640 | |||||||
| chr2:44219792 | T | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(271): Show |
282 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1134+1255T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219792 | |||||||
| chr2:44219835 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+1298C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219835 | |||||||
| chr2:44219930 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1134+1393C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44219930 | |||||||
| chr2:44220054 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1134+1517T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220054 | |||||||
| chr2:44220101 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+1564T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220101 | |||||||
| chr2:44220104 | C | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+1567C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220104 | |||||||
| chr2:44220158 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1134+1621A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220158 | |||||||
| chr2:44220190 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0146 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1134+1653A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220190 | |||||||
| chr2:44220237 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1134+1700A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220237 | |||||||
| chr2:44220263 | C | CAT | 55 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
58 | HG00408.hp2 HG00544.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.1134+1744_1134+174 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220263 | C | CATAT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0017 others(72): Show |
78 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.1134+1742_1134+174 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220263 | C | CATATAT | 4 | a0001c0001t0001g0006 a0001c0001t0001g0110 a0001c0001t0001g0139 others(1): Show |
5 | HG00642.hp2 HG01981.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+1740_1134+174 others(10): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220263 | C | CATATATA others(1): Show |
9 | a0001c0001t0001g0024 a0001c0001t0001g0143 a0001c0001t0001g0151 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+1738_1134+174 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220263 | C | CATATATA others(3): Show |
6 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1736_1134+174 others(14): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220263 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1134+1734_1134+174 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44220263 | ||||||
| chr2:44220371 | T | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+1834T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220371 | |||||||
| chr2:44220430 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1134+1893C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220430 | |||||||
| chr2:44220659 | G | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(11): Show |
14 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1134+2122G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220659 | |||||||
| chr2:44220687 | A | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
174 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1134+2150A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220687 | |||||||
| chr2:44220722 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1134+2185A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220722 | |||||||
| chr2:44220786 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1134+2249T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220786 | |||||||
| chr2:44220824 | T | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(167): Show |
174 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1134+2287T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220824 | |||||||
| chr2:44220856 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1134+2319C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44220856 | |||||||
| chr2:44221042 | T | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1134+2505T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221042 | |||||||
| chr2:44221252 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1134+2715T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221252 | |||||||
| chr2:44221362 | C | T | 2 | a0001c0001t0001g0330 a0001c0001t0001g0332 |
2 | HG02523.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1134+2825C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221362 | |||||||
| chr2:44221493 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
261 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.1134+2956G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221493 | |||||||
| chr2:44221515 | G | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1134+2978G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221515 | |||||||
| chr2:44221540 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1134+3003G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221540 | |||||||
| chr2:44221596 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+3059A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221596 | |||||||
| chr2:44221618 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1134+3081A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221618 | |||||||
| chr2:44221625 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1134+3088A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221625 | |||||||
| chr2:44221917 | C | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0229 others(6): Show |
9 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1134+3380C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221917 | |||||||
| chr2:44221942 | C | G | 1 | a0001c0001t0001g0310 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1134+3405C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44221942 | |||||||
| chr2:44222007 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
109 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1134+3470G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222007 | |||||||
| chr2:44222014 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1134+3477C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222014 | |||||||
| chr2:44222048 | C | T | 5 | a0001c0001t0001g0266 a0001c0001t0001g0334 a0001c0001t0001g0335 others(2): Show |
5 | HG03017.hp1 HG03239.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1134+3511C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222048 | |||||||
| chr2:44222121 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | NA18968.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1134+3584G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222121 | |||||||
| chr2:44222201 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0287 |
2 | NA18944.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1134+3664G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222201 | |||||||
| chr2:44222458 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1134+3921A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222458 | |||||||
| chr2:44222525 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+3988C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222525 | |||||||
| chr2:44222551 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
153 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1134+4014C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222551 | |||||||
| chr2:44222573 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1134+4036C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222573 | |||||||
| chr2:44222606 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1134+4069C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222606 | |||||||
| chr2:44222642 | G | C | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+4105G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222642 | |||||||
| chr2:44222882 | G | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+4345G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44222882 | |||||||
| chr2:44223111 | C | T | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1134+4574C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223111 | |||||||
| chr2:44223296 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(258): Show |
269 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.1134+4759T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223296 | |||||||
| chr2:44223385 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.1134+4848G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223385 | |||||||
| chr2:44223456 | T | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0146 |
2 | HG01884.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1134+4919T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223456 | |||||||
| chr2:44223692 | T | G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0024 others(69): Show |
74 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1134+5155T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223692 | |||||||
| chr2:44223752 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+5215C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223752 | |||||||
| chr2:44223814 | T | TA | 30 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0039 others(27): Show |
31 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1134+5307dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223814 | TA | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(50): Show |
55 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.1134+5307delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223814 | TAA | T | 40 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0160 others(37): Show |
40 | HG00544.hp1 HG00597.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1134+5306_1134+530 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223814 | TAAA | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
118 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1134+5305_1134+530 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223814 | TAAAA | T | 8 | a0001c0001t0001g0231 a0001c0001t0001g0246 a0001c0001t0001g0251 others(5): Show |
8 | HG02897.hp2 HG03486.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.1134+5304_1134+530 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223814 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1134+5297_1134+530 others(15): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223814 | ||||||
| chr2:44223815 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0003c0003t0001g0014 |
3 | HG02559.hp2 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1134+5278A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223815 | |||||||
| chr2:44223831 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1134+5296_1134+531 others(22): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44223831 | ||||||
| chr2:44223843 | A | AG | 4 | a0001c0001t0001g0107 a0001c0001t0001g0198 a0001c0001t0001g0263 others(1): Show |
4 | HG01975.hp2 NA18522.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+5306_1134+530 others(5): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223843 | |||||||
| chr2:44223843 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0101 a0001c0001t0001g0105 others(2): Show |
5 | HG00741.hp1 HG02683.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+5306A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223843 | |||||||
| chr2:44223858 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1134+5321A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223858 | |||||||
| chr2:44223881 | A | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(60): Show |
65 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1134+5344A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223881 | |||||||
| chr2:44223896 | G | C | 5 | a0001c0001t0001g0261 a0001c0001t0001g0265 a0001c0001t0001g0270 others(2): Show |
5 | HG00639.hp1 HG01934.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.1134+5359G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223896 | |||||||
| chr2:44223908 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0312 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1134+5371A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223908 | |||||||
| chr2:44223969 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0001t0006g0152 |
3 | HG01884.hp1 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1134+5432T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223969 | |||||||
| chr2:44223975 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1134+5438A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44223975 | |||||||
| chr2:44224067 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1134+5530A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224067 | |||||||
| chr2:44224128 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1134+5591T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224128 | |||||||
| chr2:44224178 | G | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0342 a0001c0001t0002g0034 others(1): Show |
4 | HG00741.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1134+5641G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224178 | |||||||
| chr2:44224231 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1134+5694G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224231 | |||||||
| chr2:44224323 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+5786C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224323 | |||||||
| chr2:44224380 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
110 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1134+5843G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224380 | |||||||
| chr2:44224455 | C | CA | 12 | a0001c0001t0001g0028 a0001c0001t0001g0193 a0001c0001t0001g0269 others(9): Show |
12 | HG02056.hp1 HG02074.hp1 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1134+5938dupA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224455 | ||||||
| chr2:44224455 | CA | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(241): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.1134+5938delA | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224455 | ||||||
| chr2:44224617 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1135-5796A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224617 | |||||||
| chr2:44224694 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1135-5719A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224694 | |||||||
| chr2:44224700 | TAA | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
153 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1135-5709_1135-570 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44224700 | ||||||
| chr2:44224710 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1135-5703G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224710 | |||||||
| chr2:44224729 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1135-5684G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224729 | |||||||
| chr2:44224988 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0213 a0001c0001t0001g0222 others(10): Show |
13 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135-5425C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44224988 | |||||||
| chr2:44225015 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(57): Show |
62 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1135-5398T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225015 | |||||||
| chr2:44225168 | A | T | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-5245A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225168 | |||||||
| chr2:44225205 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
241 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1135-5208T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225205 | |||||||
| chr2:44225215 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1135-5198G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225215 | |||||||
| chr2:44225251 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
152 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1135-5162C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225251 | |||||||
| chr2:44225415 | A | C | 6 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 others(3): Show |
6 | HG01074.hp2 HG01099.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-4998A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225415 | |||||||
| chr2:44225541 | C | G | 1 | a0001c0001t0002g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1135-4872C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225541 | |||||||
| chr2:44225598 | G | C | 2 | a0001c0001t0002g0030 a0001c0001t0002g0053 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1135-4815G>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225598 | |||||||
| chr2:44225679 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-4734C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225679 | |||||||
| chr2:44225722 | T | A | 1 | a0001c0001t0002g0077 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1135-4691T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225722 | |||||||
| chr2:44225777 | C | G | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1135-4636C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225777 | |||||||
| chr2:44225972 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0342 |
2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-4441A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44225972 | |||||||
| chr2:44225976 | C | CT | 6 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0257 others(3): Show |
6 | HG01169.hp1 HG02145.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-4420dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44225976 | ||||||
| chr2:44225976 | CT | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
98 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.1135-4420delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44225976 | ||||||
| chr2:44226062 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-4351G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226062 | |||||||
| chr2:44226124 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1135-4289C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226124 | |||||||
| chr2:44226135 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1135-4278C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226135 | |||||||
| chr2:44226293 | G | A | 5 | a0001c0001t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-4120G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226293 | |||||||
| chr2:44226304 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-4109T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226304 | |||||||
| chr2:44226429 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1135-3984G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226429 | |||||||
| chr2:44226444 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1135-3969C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226444 | |||||||
| chr2:44226517 | T | C | 10 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0095 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135-3896T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226517 | |||||||
| chr2:44226541 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1135-3872C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226541 | |||||||
| chr2:44226683 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG00741.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1135-3730A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226683 | |||||||
| chr2:44226735 | CT | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(50): Show |
57 | HG00323.hp1 HG00642.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.1135-3654delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | ||||||
| chr2:44226735 | CTT | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
195 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.1135-3655_1135-365 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | ||||||
| chr2:44226735 | CTTT | C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0206 a0001c0001t0001g0234 others(5): Show |
8 | HG01069.hp2 HG01981.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135-3656_1135-365 others(7): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226735 | ||||||
| chr2:44226778 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1135-3635G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226778 | |||||||
| chr2:44226899 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1135-3514C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226899 | |||||||
| chr2:44226908 | C | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0218 |
3 | HG02486.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1135-3505C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226908 | |||||||
| chr2:44226932 | T | TTTTA | 116 | a0001c0001t0001g0018 a0001c0001t0001g0125 a0001c0001t0001g0153 others(113): Show |
116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1135-3443_1135-344 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | T | TTTTATTT others(1): Show |
47 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(44): Show |
48 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.1135-3447_1135-344 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | T | TTTTATTT others(5): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0186 a0001c0001t0001g0265 others(3): Show |
6 | HG01934.hp2 HG02074.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3451_1135-344 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | TTTTA | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0028 others(25): Show |
30 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1135-3443_1135-344 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | TTTTATTT others(1): Show |
T | 7 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 others(4): Show |
7 | HG02055.hp2 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-3447_1135-344 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | TTTTATTT others(5): Show |
T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0002c0002t0001g0025 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-3451_1135-344 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226932 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0307 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1135-3455_1135-344 others(20): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226932 | ||||||
| chr2:44226967 | TATTTATG others(5): Show |
T | 1 | a0001c0001t0001g0128 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1135-3443_1135-343 others(16): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226967 | ||||||
| chr2:44226970 | T | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-3443T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226970 | |||||||
| chr2:44226971 | T | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1135-3442T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226971 | |||||||
| chr2:44226971 | TATGA | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0103 others(26): Show |
31 | HG00609.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1135-3421_1135-341 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226971 | ||||||
| chr2:44226971 | TATGAATG others(1): Show |
T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0148 |
3 | HG02735.hp1 HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1135-3425_1135-341 others(12): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44226971 | ||||||
| chr2:44226974 | G | T | 29 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0109 others(26): Show |
29 | HG00438.hp2 HG00621.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1135-3439G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226974 | |||||||
| chr2:44226975 | A | T | 29 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0109 others(26): Show |
29 | HG00438.hp2 HG00621.hp1 HG01943.hp1 others(26): Show |
intron_variant | MODIFIER | c.1135-3438A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226975 | |||||||
| chr2:44226978 | G | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(53): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1135-3435G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226978 | |||||||
| chr2:44226979 | A | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0101 others(53): Show |
58 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1135-3434A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44226979 | |||||||
| chr2:44227301 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1135-3112T>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227301 | |||||||
| chr2:44227454 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1135-2959G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227454 | |||||||
| chr2:44227464 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0032 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1135-2949A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227464 | |||||||
| chr2:44227482 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0263 a0001c0001t0001g0302 |
3 | NA18944.hp1 NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.1135-2931A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227482 | |||||||
| chr2:44227495 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-2918G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227495 | |||||||
| chr2:44227503 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1135-2910C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227503 | |||||||
| chr2:44227518 | C | CT | 17 | a0001c0001t0001g0018 a0001c0001t0001g0136 a0001c0001t0001g0169 others(14): Show |
17 | HG00544.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1135-2879dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227518 | ||||||
| chr2:44227518 | C | CTT | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(61): Show |
66 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.1135-2880_1135-287 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227518 | ||||||
| chr2:44227643 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1135-2770C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227643 | |||||||
| chr2:44227740 | G | A | 74 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(71): Show |
77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1135-2673G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227740 | |||||||
| chr2:44227785 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1135-2628G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227785 | |||||||
| chr2:44227879 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1135-2534G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227879 | |||||||
| chr2:44227912 | T | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0255 |
2 | HG00597.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1135-2501T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44227912 | |||||||
| chr2:44227922 | C | CT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1135-2474dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227922 | ||||||
| chr2:44227922 | CT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
114 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.1135-2474delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44227922 | ||||||
| chr2:44228007 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0167 others(4): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1135-2406C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228007 | |||||||
| chr2:44228073 | C | T | 2 | a0001c0001t0003g0344 a0001c0001t0003g0346 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1135-2340C>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228073 | |||||||
| chr2:44228080 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-2333G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228080 | |||||||
| chr2:44228158 | G | A | 1 | a0001c0001t0008g0021 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-2255G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228158 | |||||||
| chr2:44228187 | C | CT | 279 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(276): Show |
288 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1135-2206dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | ||||||
| chr2:44228187 | C | CTT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0121 others(7): Show |
10 | HG00438.hp2 HG01169.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1135-2207_1135-220 others(6): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | ||||||
| chr2:44228187 | CT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0153 others(7): Show |
12 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1135-2206delT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228187 | ||||||
| chr2:44228227 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-2186G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228227 | |||||||
| chr2:44228249 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1135-2164A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228249 | |||||||
| chr2:44228255 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1135-2158A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228255 | |||||||
| chr2:44228269 | CCTCAACC others(12): Show |
C | 4 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0237 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2134_1135-211 others(23): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228269 | ||||||
| chr2:44228331 | G | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0237 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2082G>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228331 | |||||||
| chr2:44228348 | A | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0237 others(1): Show |
4 | HG00099.hp1 HG00735.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1135-2065A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228348 | |||||||
| chr2:44228513 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-1900A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228513 | |||||||
| chr2:44228572 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1135-1841A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228572 | |||||||
| chr2:44228593 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1135-1820T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228593 | |||||||
| chr2:44228622 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1135-1791A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228622 | |||||||
| chr2:44228724 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0151 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1135-1689A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228724 | |||||||
| chr2:44228811 | TTGAC | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0212 a0001c0001t0001g0312 others(1): Show |
4 | HG02886.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-1598_1135-159 others(8): Show |
PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44228811 | ||||||
| chr2:44228971 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1135-1442T>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44228971 | |||||||
| chr2:44229109 | G | A | 5 | a0001c0001t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(2): Show |
5 | HG01243.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-1304G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229109 | |||||||
| chr2:44229190 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1135-1223A>C | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229190 | |||||||
| chr2:44229272 | A | T | 1 | a0001c0001t0001g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1135-1141A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229272 | |||||||
| chr2:44229304 | A | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(36): Show |
41 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.1135-1109A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229304 | |||||||
| chr2:44229397 | C | G | 1 | a0001c0001t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1135-1016C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229397 | |||||||
| chr2:44229408 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1135-1005A>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229408 | |||||||
| chr2:44229515 | A | T | 1 | a0001c0001t0001g0012 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1135-898A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229515 | |||||||
| chr2:44229610 | A | T | 1 | a0001c0001t0001g0335 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1135-803A>T | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229610 | |||||||
| chr2:44229700 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1135-713T>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229700 | |||||||
| chr2:44229708 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(21): Show |
26 | HG01106.hp1 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1135-705G>A | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44229708 | |||||||
| chr2:44230095 | G | GT | 4 | a0001c0001t0003g0343 a0001c0001t0003g0344 a0001c0001t0003g0345 others(1): Show |
4 | HG02055.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135-315dupT | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | 44230095 | ||||||
| chr2:44230192 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0312 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1135-221C>G | PPM1B | ENSG00000138032.21 | transcript | ENST00000282412.9 | protein_coding | 5/5 | chr2 | 44230192 |