Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4193 |
| ensemblid | ENSG00000135679.27 |
| hgncid | 6973 |
| symbol | MDM2 |
| name | MDM2 proto-oncogene |
| refseq_nuc | NM_002392.6 |
| refseq_prot | NP_002383.2 |
| ensembl_nuc | ENST00000258149.11 |
| ensembl_prot | ENSP00000258149.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 68808177 |
| end | 68845544 |
| strand | + |
| ver | v1.2 |
| region | chr12:68808177-68845544 |
| region5000 | chr12:68803177-68850544 |
| regionname0 | MDM2_chr12_68808177_68845544 |
| regionname5000 | MDM2_chr12_68803177_68850544 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 497 | 386 | 87 | 75 | 172 | 16 | 34 | 134 | MDM2_chr12_68803177_68850544 | MDM2 | MVRSR others(492): Show |
chr12 | 68803177 | 68850544 |
| a0002 | 0/0 | 497 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | MVRSR others(492): Show |
chr12 | 68803177 | 68850544 |
| a0003 | 0/0 | 497 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | MVRSR others(492): Show |
chr12 | 68803177 | 68850544 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1491 | 348 | 65 | 66 | 167 | 16 | 32 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 | ||
| a0001c0002 | 0/0 | 1491 | 34 | 19 | 8 | 5 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 | ||
| a0001c0003 | 0/0 | 1491 | 3 | 2 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 | ||
| a0001c0004 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 | ||
| a0002c0005 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 | ||
| a0003c0006 | 0/0 | 1491 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | ATGGT others(1486): Show |
chr12 | 68803177 | 68850544 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7479 | 84 | 6 | 17 | 47 | 4 | 10 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0002 | 0/1 | 7489 | 64 | 6 | 11 | 41 | 2 | 3 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0003 | 0/0 | 7490 | 30 | 1 | 8 | 17 | 1 | 3 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0004 | 0/0 | 7479 | 22 | 0 | 4 | 17 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0005 | 0/0 | 7490 | 17 | 0 | 9 | 4 | 0 | 4 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0007 | 0/0 | 7491 | 11 | 0 | 1 | 8 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0009 | 0/0 | 7486 | 9 | 8 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7481): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0010 | 0/0 | 7486 | 9 | 1 | 0 | 8 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7481): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0011 | 0/0 | 7488 | 8 | 0 | 0 | 6 | 1 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0012 | 0/0 | 7468 | 6 | 5 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7463): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0013 | 0/0 | 7468 | 4 | 4 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7463): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0015 | 0/0 | 7490 | 4 | 0 | 2 | 0 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0016 | 0/0 | 7493 | 4 | 4 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7488): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0017 | 0/0 | 7482 | 4 | 0 | 2 | 1 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7477): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0018 | 1/0 | 7490 | 3 | 0 | 0 | 0 | 2 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0019 | 0/0 | 7489 | 2 | 0 | 2 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0020 | 0/0 | 7492 | 3 | 3 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7487): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0021 | 0/0 | 7482 | 3 | 0 | 0 | 0 | 3 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7477): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0022 | 0/0 | 7469 | 3 | 3 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7464): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0023 | 0/0 | 7480 | 3 | 0 | 1 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7475): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0024 | 0/0 | 7490 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0025 | 0/0 | 7479 | 2 | 0 | 2 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0027 | 0/0 | 7485 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0028 | 0/0 | 7486 | 2 | 1 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7481): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0029 | 0/0 | 7487 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7482): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0030 | 0/0 | 7481 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7476): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0031 | 0/0 | 7489 | 2 | 0 | 1 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0032 | 0/0 | 7489 | 2 | 0 | 2 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0035 | 0/0 | 7484 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7479): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0036 | 0/0 | 7475 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7470): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0037 | 0/0 | 7489 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0038 | 0/0 | 7479 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0040 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0041 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7473): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0042 | 0/0 | 7478 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7473): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0044 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0045 | 0/0 | 7490 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0046 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0047 | 0/0 | 7489 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0048 | 0/0 | 7489 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0049 | 0/0 | 7491 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0051 | 0/0 | 7490 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0052 | 0/0 | 7490 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0053 | 0/0 | 7490 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0054 | 0/0 | 7493 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7488): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0057 | 0/0 | 7494 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7489): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0058 | 0/0 | 7486 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7481): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0059 | 0/0 | 7486 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7481): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0061 | 0/0 | 7491 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0062 | 0/0 | 7484 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7479): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0063 | 0/0 | 7484 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7479): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0065 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0066 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0067 | 0/0 | 7467 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7462): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0068 | 0/0 | 7468 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7463): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0069 | 0/0 | 7473 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7468): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0070 | 0/0 | 7473 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7468): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0071 | 0/0 | 7479 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0072 | 0/0 | 7488 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0073 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0074 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7486): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0075 | 0/0 | 7479 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0076 | 0/0 | 7479 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0001t0077 | 0/0 | 7479 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7474): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0006 | 0/0 | 7487 | 11 | 8 | 3 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7482): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0008 | 0/0 | 7488 | 10 | 4 | 4 | 0 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0014 | 0/0 | 7488 | 4 | 0 | 0 | 4 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0033 | 0/0 | 7487 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7482): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0034 | 0/0 | 7490 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7485): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0039 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0050 | 0/0 | 7488 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0055 | 0/0 | 7489 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0056 | 0/0 | 7488 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7483): Show |
chr12 | 68803177 | 68850544 |
| a0001c0002t0060 | 0/0 | 7487 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7482): Show |
chr12 | 68803177 | 68850544 |
| a0001c0003t0026 | 0/0 | 7485 | 2 | 1 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| a0001c0003t0043 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| a0001c0004t0013 | 0/0 | 7468 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7463): Show |
chr12 | 68803177 | 68850544 |
| a0002c0005t0019 | 0/0 | 7489 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7484): Show |
chr12 | 68803177 | 68850544 |
| a0003c0006t0064 | 0/0 | 7485 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | GGGCG others(7480): Show |
chr12 | 68803177 | 68850544 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 2 | 6 | 1 | 3 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0005 | 0/0 | 7 | 1 | 4 | 0 | 1 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0001 | 0/0 | 11 | 1 | 1 | 9 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0003 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0012g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0012g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0013g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0013g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0015g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0015g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0016g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0016g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0017g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0017g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0017g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0017g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0018g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0018g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0018g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0019g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0019g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0020g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0020g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0021g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0021g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0022g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0022g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0023g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0023g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0024g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0025g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0025g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0027g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0027g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0028g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0029g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0029g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0030g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0031g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0031g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0032g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0032g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0035g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0035g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0036g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0037g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0037g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0038g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0040g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0041g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0042g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0044g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0045g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0046g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0047g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0048g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0049g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0051g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0052g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0053g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0054g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0057g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0058g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0059g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0061g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0062g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0063g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0065g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0066g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0067g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0068g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0069g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0070g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0071g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0072g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0073g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0074g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0075g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0076g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0001t0077g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0014g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0014g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0014g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0033g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0033g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0034g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0034g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0039g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0050g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0055g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0056g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0002t0060g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0003t0026g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0003t0026g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0003t0043g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0001c0004t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0002c0005t0019g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| a0003c0006t0064g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00099 | hp2 | a0001 | c0001 | t0058 | g0209 | EUR | GBR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0203 | EUR | GBR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00140 | hp2 | a0001 | c0001 | t0011 | g0077 | EUR | GBR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00280 | hp2 | a0001 | c0001 | t0038 | g0022 | EUR | FIN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00544 | hp2 | a0001 | c0001 | t0049 | g0199 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00609 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0071 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0134 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00642 | hp2 | a0001 | c0002 | t0008 | g0035 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00733 | hp2 | a0001 | c0001 | t0032 | g0073 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0097 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG00741 | hp2 | a0001 | c0003 | t0026 | g0133 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0166 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01070 | hp1 | a0001 | c0001 | t0032 | g0066 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01070 | hp2 | a0001 | c0002 | t0006 | g0035 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01071 | hp2 | a0001 | c0002 | t0008 | g0012 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01074 | hp1 | a0001 | c0002 | t0006 | g0034 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01081 | hp1 | a0001 | c0002 | t0008 | g0179 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01109 | hp1 | a0001 | c0001 | t0031 | g0008 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01109 | hp2 | a0001 | c0002 | t0060 | g0173 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01167 | hp1 | a0001 | c0002 | t0006 | g0167 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01167 | hp2 | a0001 | c0001 | t0017 | g0224 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01175 | hp1 | a0001 | c0001 | t0023 | g0016 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01175 | hp2 | a0001 | c0001 | t0015 | g0115 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01261 | hp1 | a0002 | c0005 | t0019 | g0003 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01361 | hp2 | a0001 | c0001 | t0028 | g0032 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01433 | hp2 | a0001 | c0001 | t0007 | g0194 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01496 | hp2 | a0001 | c0001 | t0017 | g0002 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01516 | hp1 | a0001 | c0001 | t0021 | g0038 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01517 | hp1 | a0001 | c0001 | t0021 | g0038 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01891 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01975 | hp2 | a0001 | c0001 | t0025 | g0084 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0208 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01981 | hp2 | a0001 | c0001 | t0005 | g0023 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01993 | hp2 | a0001 | c0001 | t0045 | g0011 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0057 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02015 | hp1 | a0001 | c0001 | t0076 | g0253 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02015 | hp2 | a0001 | c0001 | t0011 | g0076 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02055 | hp1 | a0001 | c0001 | t0065 | g0146 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0185 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0079 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02129 | hp1 | a0001 | c0001 | t0059 | g0112 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CDX | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CDX | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0186 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02258 | hp2 | a0001 | c0001 | t0070 | g0151 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02273 | hp2 | a0001 | c0001 | t0019 | g0078 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02293 | hp2 | a0001 | c0001 | t0025 | g0110 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02300 | hp1 | a0001 | c0001 | t0019 | g0026 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02451 | hp1 | a0001 | c0001 | t0066 | g0148 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02451 | hp2 | a0001 | c0002 | t0033 | g0175 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0013 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02572 | hp2 | a0001 | c0001 | t0022 | g0155 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02615 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0172 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0189 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02630 | hp1 | a0001 | c0002 | t0033 | g0174 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02630 | hp2 | a0001 | c0001 | t0035 | g0029 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0028 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02717 | hp1 | a0001 | c0002 | t0008 | g0160 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02717 | hp2 | a0001 | c0001 | t0022 | g0031 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02723 | hp1 | a0001 | c0001 | t0040 | g0040 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02723 | hp2 | a0001 | c0001 | t0030 | g0039 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02735 | hp2 | a0001 | c0001 | t0051 | g0049 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0114 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02809 | hp1 | a0001 | c0001 | t0073 | g0154 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02809 | hp2 | a0001 | c0001 | t0027 | g0028 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02818 | hp1 | a0001 | c0001 | t0024 | g0040 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02818 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02886 | hp1 | a0001 | c0001 | t0062 | g0150 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02886 | hp2 | a0001 | c0001 | t0028 | g0032 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02895 | hp1 | a0001 | c0001 | t0063 | g0147 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02895 | hp2 | a0001 | c0001 | t0029 | g0165 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0013 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02897 | hp1 | a0001 | c0001 | t0027 | g0135 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02897 | hp2 | a0001 | c0001 | t0029 | g0164 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02922 | hp2 | a0001 | c0001 | t0067 | g0159 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0142 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03041 | hp1 | a0001 | c0001 | t0030 | g0039 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | GWD | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03098 | hp1 | a0001 | c0002 | t0034 | g0136 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03098 | hp2 | a0001 | c0002 | t0055 | g0037 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03130 | hp1 | a0001 | c0001 | t0020 | g0187 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03130 | hp2 | a0001 | c0001 | t0024 | g0190 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03139 | hp1 | a0001 | c0002 | t0008 | g0162 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03209 | hp1 | a0001 | c0001 | t0009 | g0137 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03209 | hp2 | a0001 | c0001 | t0057 | g0013 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03225 | hp1 | a0001 | c0002 | t0006 | g0171 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0157 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0140 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0031 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03486 | hp1 | a0001 | c0003 | t0043 | g0131 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03486 | hp2 | a0001 | c0002 | t0008 | g0161 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03490 | hp2 | a0001 | c0002 | t0008 | g0034 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03491 | hp2 | a0001 | c0001 | t0075 | g0015 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03516 | hp1 | a0001 | c0002 | t0039 | g0037 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03516 | hp2 | a0001 | c0002 | t0006 | g0181 | AFR | ESN | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03579 | hp2 | a0001 | c0001 | t0069 | g0145 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0127 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03688 | hp1 | a0001 | c0001 | t0053 | g0103 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03704 | hp1 | a0001 | c0001 | t0015 | g0020 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03831 | hp2 | a0001 | c0002 | t0008 | g0012 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03834 | hp1 | a0001 | c0001 | t0015 | g0020 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03834 | hp2 | a0001 | c0001 | t0017 | g0244 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0126 | SAS | BEB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04199 | hp1 | a0001 | c0001 | t0048 | g0192 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04204 | hp1 | a0001 | c0001 | t0011 | g0075 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG04204 | hp2 | a0001 | c0001 | t0072 | g0226 | SAS | STU | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0156 | AFR | YRI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18612 | hp2 | a0001 | c0001 | t0011 | g0017 | EAS | CHB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18906 | hp2 | a0001 | c0002 | t0056 | g0176 | AFR | YRI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18943 | hp2 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18953 | hp1 | a0001 | c0001 | t0011 | g0006 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18954 | hp1 | a0001 | c0001 | t0071 | g0238 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18963 | hp1 | a0001 | c0001 | t0036 | g0258 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18964 | hp2 | a0001 | c0001 | t0037 | g0063 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18965 | hp1 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0006 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18968 | hp1 | a0001 | c0001 | t0010 | g0100 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18970 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18973 | hp2 | a0001 | c0001 | t0031 | g0200 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18984 | hp1 | a0001 | c0001 | t0044 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18987 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18990 | hp2 | a0001 | c0001 | t0061 | g0214 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18991 | hp2 | a0001 | c0001 | t0052 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18998 | hp1 | a0001 | c0002 | t0050 | g0036 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18999 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA18999 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19001 | hp1 | a0001 | c0001 | t0017 | g0255 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0219 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19003 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19004 | hp2 | a0001 | c0002 | t0014 | g0180 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19006 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19006 | hp2 | a0001 | c0001 | t0077 | g0277 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19011 | hp2 | a0001 | c0001 | t0041 | g0041 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19030 | hp1 | a0001 | c0004 | t0013 | g0153 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19030 | hp2 | a0001 | c0002 | t0006 | g0183 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0170 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0091 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0195 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19062 | hp1 | a0001 | c0001 | t0023 | g0259 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19062 | hp2 | a0001 | c0002 | t0014 | g0178 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19063 | hp1 | a0001 | c0001 | t0047 | g0042 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19067 | hp1 | a0001 | c0002 | t0014 | g0182 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19067 | hp2 | a0001 | c0001 | t0010 | g0107 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19074 | hp1 | a0001 | c0001 | t0042 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19074 | hp2 | a0001 | c0001 | t0036 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19079 | hp2 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19082 | hp1 | a0001 | c0002 | t0014 | g0036 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19082 | hp2 | a0001 | c0001 | t0010 | g0121 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19088 | hp1 | a0001 | c0001 | t0037 | g0108 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0101 | AFR | ASW | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | ASW | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | TSI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20752 | hp2 | a0001 | c0001 | t0046 | g0003 | EUR | TSI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20805 | hp1 | a0001 | c0001 | t0018 | g0046 | EUR | TSI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20805 | hp2 | a0001 | c0001 | t0021 | g0188 | EUR | TSI | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0008 | SAS | GIH | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0217 | SAS | GIH | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01123 | hp1 | a0001 | c0002 | t0008 | g0012 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0064 | AMR | CLM | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0007 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02109 | hp2 | a0001 | c0001 | t0054 | g0184 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02486 | hp2 | a0003 | c0006 | t0064 | g0029 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02559 | hp1 | a0001 | c0001 | t0074 | g0152 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG02559 | hp2 | a0001 | c0002 | t0008 | g0168 | AFR | ACB | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0030 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG03471 | hp2 | a0001 | c0001 | t0035 | g0149 | AFR | MSL | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0169 | AFR | USA | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | USA | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA20300 | hp2 | a0001 | c0001 | t0068 | g0158 | AFR | USA | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA21309 | hp1 | a0001 | c0003 | t0026 | g0132 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| NA21309 | hp2 | a0001 | c0002 | t0034 | g0163 | AFR | LWK | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0118 | REF | REF | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0018 | g0202 | REF | REF | MDM2_chr12_68803177_68850544 | MDM2 | chr12 | 68803177 | 68850544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68839354 | G | T | 1 | a0003 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.999G>T | p.Glu333Asp | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1300/7490 | 999/1494 | 333/497 | chr12 | 68839354 | |||
| chr12:68839597 | A | C | 1 | a0002 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.1242A>C | p.Gln414His | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1543/7490 | 1242/1494 | 414/497 | chr12 | 68839597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68828854 | C | T | 1 | a0001c0003 | 3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.607C>T | p.Leu203Leu | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/11 | 908/7490 | 607/1494 | 203/497 | chr12 | 68828854 | |||
| chr12:68839357 | T | C | 1 | a0001c0004 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1002T>C | p.Asn334Asn | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1303/7490 | 1002/1494 | 334/497 | chr12 | 68839357 | |||
| chr12:68839435 | A | G | 1 | a0001c0002 | 34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
synonymous_variant | LOW | c.1080A>G | p.Glu360Glu | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1381/7490 | 1080/1494 | 360/497 | chr12 | 68839435 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68808189 | A | C | 1 | a0001c0001t0037 | 2 | NA18964.hp2 NA19088.hp1 |
5_prime_UTR_variant | MODIFIER | c.-289A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/11 | 289 | chr12 | 68808189 | ||||||
| chr12:68808235 | T | G | 1 | a0001c0001t0038 | 1 | HG00280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/11 | 243 | chr12 | 68808235 | ||||||
| chr12:68808384 | A | G | 24 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(21): Show |
119 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-94A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/11 | 94 | chr12 | 68808384 | ||||||
| chr12:68839854 | C | T | 1 | a0001c0001t0021 | 3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5 | chr12 | 68839854 | ||||||
| chr12:68839936 | G | A | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*87G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 87 | chr12 | 68839936 | ||||||
| chr12:68839962 | A | G | 1 | a0001c0001t0061 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 113 | chr12 | 68839962 | ||||||
| chr12:68840106 | G | T | 1 | a0001c0001t0077 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*257G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 257 | chr12 | 68840106 | ||||||
| chr12:68840233 | C | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 384 | chr12 | 68840233 | ||||||
| chr12:68840234 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 385 | chr12 | 68840234 | ||||||
| chr12:68840237 | C | T | 1 | a0001c0001t0075 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 388 | chr12 | 68840237 | ||||||
| chr12:68840311 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*462A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 462 | chr12 | 68840311 | ||||||
| chr12:68840312 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 463 | chr12 | 68840312 | ||||||
| chr12:68840316 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 467 | chr12 | 68840316 | ||||||
| chr12:68840318 | G | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 469 | chr12 | 68840318 | ||||||
| chr12:68840319 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*470T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 470 | chr12 | 68840319 | ||||||
| chr12:68840321 | C | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 472 | chr12 | 68840321 | ||||||
| chr12:68840324 | T | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*475T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 475 | chr12 | 68840324 | ||||||
| chr12:68840326 | A | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 477 | chr12 | 68840326 | ||||||
| chr12:68840327 | G | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*478G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 478 | chr12 | 68840327 | ||||||
| chr12:68840350 | T | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 501 | chr12 | 68840350 | ||||||
| chr12:68840365 | C | T | 1 | a0001c0002t0060 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*516C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 516 | chr12 | 68840365 | ||||||
| chr12:68840409 | G | A | 1 | a0001c0002t0039 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 560 | chr12 | 68840409 | ||||||
| chr12:68840416 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 567 | chr12 | 68840416 | ||||||
| chr12:68840437 | T | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 588 | chr12 | 68840437 | ||||||
| chr12:68840438 | C | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 589 | chr12 | 68840438 | ||||||
| chr12:68840439 | C | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 590 | chr12 | 68840439 | ||||||
| chr12:68840445 | A | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*596A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 596 | chr12 | 68840445 | ||||||
| chr12:68840464 | T | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*615T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 615 | chr12 | 68840464 | ||||||
| chr12:68840466 | A | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 617 | chr12 | 68840466 | ||||||
| chr12:68840472 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 623 | chr12 | 68840472 | ||||||
| chr12:68840474 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 625 | chr12 | 68840474 | ||||||
| chr12:68840478 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*629A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 629 | chr12 | 68840478 | ||||||
| chr12:68840479 | A | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 630 | chr12 | 68840479 | ||||||
| chr12:68840486 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*637A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 637 | chr12 | 68840486 | ||||||
| chr12:68840487 | A | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 638 | chr12 | 68840487 | ||||||
| chr12:68840488 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*639A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 639 | chr12 | 68840488 | ||||||
| chr12:68840489 | G | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 640 | chr12 | 68840489 | ||||||
| chr12:68840496 | T | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*647T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 647 | chr12 | 68840496 | ||||||
| chr12:68840504 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 655 | chr12 | 68840504 | ||||||
| chr12:68840505 | T | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*656T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 656 | chr12 | 68840505 | ||||||
| chr12:68840506 | TTTTG | T | 4 | a0001c0001t0010 a0001c0001t0036 a0001c0001t0058 others(1): Show |
13 | HG00099.hp2 HG00609.hp2 HG02129.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*681_*684delGTTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 681 | INFO_REALIGN_3_PRIME | chr12 | 68840506 | |||||
| chr12:68840506 | TTTTGTTT others(1): Show |
T | 8 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(5): Show |
18 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*677_*684delGTTTGT others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 677 | INFO_REALIGN_3_PRIME | chr12 | 68840506 | |||||
| chr12:68840510 | G | T | 1 | a0001c0001t0015 | 2 | HG03704.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*661G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 661 | chr12 | 68840510 | ||||||
| chr12:68840528 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 679 | chr12 | 68840528 | ||||||
| chr12:68840530 | G | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*681G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 681 | chr12 | 68840530 | ||||||
| chr12:68840531 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 682 | chr12 | 68840531 | ||||||
| chr12:68840560 | C | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*711C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 711 | chr12 | 68840560 | ||||||
| chr12:68840561 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 712 | chr12 | 68840561 | ||||||
| chr12:68840591 | C | G | 8 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(5): Show |
18 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 742 | chr12 | 68840591 | ||||||
| chr12:68840827 | T | A | 2 | a0001c0001t0024 a0001c0001t0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*978T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 978 | chr12 | 68840827 | ||||||
| chr12:68840835 | C | CT | 20 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(17): Show |
72 | HG00544.hp2 HG00609.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1013dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1014 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | C | CTT | 7 | a0001c0001t0016 a0001c0001t0035 a0001c0001t0054 others(4): Show |
11 | HG02055.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1013dupTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1014 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | C | CTTT | 5 | a0001c0001t0057 a0001c0001t0065 a0001c0001t0066 others(2): Show |
6 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1011_*1013dupTTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1014 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CT | C | 10 | a0001c0001t0011 a0001c0001t0022 a0001c0001t0029 others(7): Show |
23 | HG00140.hp2 HG00733.hp2 HG01070.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1013delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1013 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CTT | C | 8 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0013 others(5): Show |
29 | HG00639.hp2 HG01069.hp1 HG01175.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1012_*1013delTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1012 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CTTT | C | 10 | a0001c0001t0001 a0001c0001t0027 a0001c0001t0036 others(7): Show |
96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1011_*1013delTTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1011 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0004 a0001c0001t0025 a0001c0001t0038 |
25 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1004_*1013delTTTT others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1004 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0042 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1003_*1013delTTTT others(7): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1003 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68840835 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0041 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1002_*1013delTTTT others(8): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1002 | INFO_REALIGN_3_PRIME | chr12 | 68840835 | |||||
| chr12:68841112 | C | T | 4 | a0001c0001t0015 a0001c0001t0019 a0001c0001t0053 others(1): Show |
8 | HG00738.hp1 HG01175.hp2 HG01261.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1263C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1263 | chr12 | 68841112 | ||||||
| chr12:68841207 | T | TA | 4 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0054 others(1): Show |
9 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1369dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1370 | INFO_REALIGN_3_PRIME | chr12 | 68841207 | |||||
| chr12:68841207 | TA | T | 21 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(18): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1369delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1369 | INFO_REALIGN_3_PRIME | chr12 | 68841207 | |||||
| chr12:68841283 | G | A | 2 | a0001c0003t0026 a0001c0003t0043 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1434G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1434 | chr12 | 68841283 | ||||||
| chr12:68841319 | A | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1470 | chr12 | 68841319 | ||||||
| chr12:68841320 | C | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1471C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1471 | chr12 | 68841320 | ||||||
| chr12:68841321 | T | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1472 | chr12 | 68841321 | ||||||
| chr12:68841322 | C | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1473 | chr12 | 68841322 | ||||||
| chr12:68841338 | C | A | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1489C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1489 | chr12 | 68841338 | ||||||
| chr12:68841383 | T | G | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1534T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1534 | chr12 | 68841383 | ||||||
| chr12:68841407 | A | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1558A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1558 | chr12 | 68841407 | ||||||
| chr12:68841430 | T | G | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1581T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1581 | chr12 | 68841430 | ||||||
| chr12:68841468 | A | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1619A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1619 | chr12 | 68841468 | ||||||
| chr12:68841469 | T | C | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1620 | chr12 | 68841469 | ||||||
| chr12:68841470 | C | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1621C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1621 | chr12 | 68841470 | ||||||
| chr12:68841626 | G | A | 14 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(11): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1777G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1777 | chr12 | 68841626 | ||||||
| chr12:68841626 | G | C | 1 | a0001c0001t0046 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1777G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1777 | chr12 | 68841626 | ||||||
| chr12:68841695 | G | A | 1 | a0001c0001t0030 | 2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1846G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1846 | chr12 | 68841695 | ||||||
| chr12:68841711 | C | T | 1 | a0001c0001t0025 | 2 | HG01975.hp2 HG02293.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1862C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1862 | chr12 | 68841711 | ||||||
| chr12:68841761 | T | A | 1 | a0001c0001t0053 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1912T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 1912 | chr12 | 68841761 | ||||||
| chr12:68841889 | G | A | 1 | a0001c0001t0073 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2040G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2040 | chr12 | 68841889 | ||||||
| chr12:68841966 | C | T | 2 | a0001c0001t0028 a0001c0001t0029 |
4 | HG01361.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2117C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2117 | chr12 | 68841966 | ||||||
| chr12:68842480 | A | C | 1 | a0001c0001t0059 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2631A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2631 | chr12 | 68842480 | ||||||
| chr12:68842490 | C | T | 1 | a0001c0001t0048 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2641C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2641 | chr12 | 68842490 | ||||||
| chr12:68842534 | A | ACAT | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2687_*2688insTCA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2688 | INFO_REALIGN_3_PRIME | chr12 | 68842534 | |||||
| chr12:68842614 | CAT | C | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2767_*2768delTA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2767 | INFO_REALIGN_3_PRIME | chr12 | 68842614 | |||||
| chr12:68842641 | T | C | 1 | a0001c0001t0062 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2792T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2792 | chr12 | 68842641 | ||||||
| chr12:68842794 | C | A | 1 | a0001c0001t0049 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2945C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 2945 | chr12 | 68842794 | ||||||
| chr12:68843106 | T | A | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3257T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3257 | chr12 | 68843106 | ||||||
| chr12:68843117 | A | G | 1 | a0001c0001t0052 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3268A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3268 | chr12 | 68843117 | ||||||
| chr12:68843210 | TA | T | 3 | a0001c0002t0033 a0001c0002t0056 a0001c0002t0060 |
4 | HG01109.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3363delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3363 | INFO_REALIGN_3_PRIME | chr12 | 68843210 | |||||
| chr12:68843256 | C | T | 1 | a0001c0001t0051 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3407C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3407 | chr12 | 68843256 | ||||||
| chr12:68843295 | TGAGA | T | 6 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(3): Show |
16 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3464_*3467delAGAG | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3464 | INFO_REALIGN_3_PRIME | chr12 | 68843295 | |||||
| chr12:68843317 | T | A | 2 | a0001c0002t0014 a0001c0002t0050 |
5 | NA18998.hp1 NA19004.hp2 NA19062.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3468T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3468 | chr12 | 68843317 | ||||||
| chr12:68843504 | ACTT | A | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3659_*3661delCTT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3659 | INFO_REALIGN_3_PRIME | chr12 | 68843504 | |||||
| chr12:68843605 | T | C | 1 | a0001c0001t0044 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3756T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3756 | chr12 | 68843605 | ||||||
| chr12:68843608 | A | G | 68 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(65): Show |
334 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
3_prime_UTR_variant | MODIFIER | c.*3759A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3759 | chr12 | 68843608 | ||||||
| chr12:68843609 | G | A | 1 | a0001c0001t0030 | 2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3760G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3760 | chr12 | 68843609 | ||||||
| chr12:68843621 | A | G | 2 | a0001c0001t0009 a0001c0001t0027 |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3772A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3772 | chr12 | 68843621 | ||||||
| chr12:68843698 | ACT | A | 25 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(22): Show |
151 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*3866_*3867delCT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3866 | INFO_REALIGN_3_PRIME | chr12 | 68843698 | |||||
| chr12:68843698 | ACTCTCT | A | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3862_*3867delCTCT others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 3862 | INFO_REALIGN_3_PRIME | chr12 | 68843698 | |||||
| chr12:68843898 | C | G | 6 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0024 others(3): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4049C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4049 | chr12 | 68843898 | ||||||
| chr12:68843955 | T | C | 8 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(5): Show |
18 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4106T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4106 | chr12 | 68843955 | ||||||
| chr12:68843986 | T | C | 2 | a0001c0001t0073 a0001c0001t0074 |
2 | HG02559.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4137T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4137 | chr12 | 68843986 | ||||||
| chr12:68844009 | G | A | 3 | a0001c0001t0035 a0001c0001t0062 a0003c0006t0064 |
4 | HG02486.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4160G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4160 | chr12 | 68844009 | ||||||
| chr12:68844055 | G | A | 1 | a0001c0002t0050 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4206G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4206 | chr12 | 68844055 | ||||||
| chr12:68844082 | A | G | 1 | a0001c0001t0045 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4233A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4233 | chr12 | 68844082 | ||||||
| chr12:68844146 | A | G | 1 | a0001c0001t0068 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4297A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4297 | chr12 | 68844146 | ||||||
| chr12:68844154 | C | T | 1 | a0001c0001t0066 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4305C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4305 | chr12 | 68844154 | ||||||
| chr12:68844272 | C | T | 1 | a0001c0001t0054 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4423C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4423 | chr12 | 68844272 | ||||||
| chr12:68844295 | C | T | 2 | a0001c0001t0073 a0001c0001t0074 |
2 | HG02559.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4446C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4446 | chr12 | 68844295 | ||||||
| chr12:68844628 | G | T | 78 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(75): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*4779G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4779 | chr12 | 68844628 | ||||||
| chr12:68844657 | CA | C | 10 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0014 others(7): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4815delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4815 | INFO_REALIGN_3_PRIME | chr12 | 68844657 | |||||
| chr12:68844683 | C | T | 1 | a0001c0001t0070 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4834C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4834 | chr12 | 68844683 | ||||||
| chr12:68844727 | A | G | 10 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0014 others(7): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4878A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 4878 | chr12 | 68844727 | ||||||
| chr12:68845055 | G | A | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5206G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5206 | chr12 | 68845055 | ||||||
| chr12:68845059 | C | T | 1 | a0001c0001t0071 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5210C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5210 | chr12 | 68845059 | ||||||
| chr12:68845112 | A | T | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5263A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5263 | chr12 | 68845112 | ||||||
| chr12:68845183 | T | C | 14 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(11): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5334T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5334 | chr12 | 68845183 | ||||||
| chr12:68845203 | TATAAAA | T | 10 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0021 others(7): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5356_*5361delTAAA others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5356 | INFO_REALIGN_3_PRIME | chr12 | 68845203 | |||||
| chr12:68845206 | AAAAAG | A | 5 | a0001c0001t0012 a0001c0001t0013 a0001c0001t0022 others(2): Show |
15 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5362_*5366delGAAA others(1): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5362 | INFO_REALIGN_3_PRIME | chr12 | 68845206 | |||||
| chr12:68845276 | C | T | 1 | a0001c0003t0043 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5427C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5427 | chr12 | 68845276 | ||||||
| chr12:68845403 | G | C | 1 | a0001c0001t0030 | 2 | HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5554G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5554 | chr12 | 68845403 | ||||||
| chr12:68845443 | G | A | 3 | a0001c0001t0009 a0001c0001t0027 a0001c0001t0029 |
13 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5594G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 11/11 | 5594 | chr12 | 68845443 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:68808546 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(71): Show |
98 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.14+55C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808546 | |||||||
| chr12:68808598 | G | A | 1 | a0001c0001t0018g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.14+107G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808598 | |||||||
| chr12:68808717 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.14+226C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808717 | |||||||
| chr12:68808776 | G | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | HG01978.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.14+285G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808776 | |||||||
| chr12:68808800 | T | G | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(110): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.14+309T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808800 | |||||||
| chr12:68808835 | T | A | 15 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(12): Show |
15 | HG00639.hp2 HG00741.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.14+344T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808835 | |||||||
| chr12:68808913 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.15-295C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808913 | |||||||
| chr12:68808917 | T | G | 1 | a0001c0001t0003g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.15-291T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68808917 | |||||||
| chr12:68809132 | G | A | 1 | a0001c0001t0051g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.15-76G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 1/10 | chr12 | 68809132 | |||||||
| chr12:68809532 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(71): Show |
98 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+240G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68809532 | |||||||
| chr12:68809617 | C | CA | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
101 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+331dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68809617 | ||||||
| chr12:68809624 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(267): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.99+332G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68809624 | |||||||
| chr12:68809731 | G | A | 5 | a0001c0001t0002g0017 a0001c0001t0002g0050 a0001c0001t0005g0051 others(2): Show |
5 | HG03579.hp2 NA18612.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+439G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68809731 | |||||||
| chr12:68809744 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(86): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.99+452T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68809744 | |||||||
| chr12:68809774 | T | G | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+482T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68809774 | |||||||
| chr12:68810250 | C | T | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.99+958C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810250 | |||||||
| chr12:68810309 | T | TA | 6 | a0001c0001t0001g0221 a0001c0001t0003g0191 a0001c0002t0008g0160 others(3): Show |
6 | HG02717.hp1 HG03139.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1031dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68810309 | ||||||
| chr12:68810309 | TA | T | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(110): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.99+1031delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68810309 | ||||||
| chr12:68810412 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.99+1120C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810412 | |||||||
| chr12:68810424 | C | CTCCTGCC others(37): Show |
1 | a0001c0001t0001g0222 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.99+1170_99+1171ins others(44): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68810424 | ||||||
| chr12:68810441 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.99+1149T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810441 | |||||||
| chr12:68810468 | A | T | 10 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(7): Show |
12 | HG02559.hp1 HG02572.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+1176A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810468 | |||||||
| chr12:68810471 | A | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(105): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.99+1179A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810471 | |||||||
| chr12:68810521 | G | A | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.99+1229G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810521 | |||||||
| chr12:68810551 | C | G | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99+1259C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810551 | |||||||
| chr12:68810561 | A | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0128 a0001c0001t0002g0129 others(1): Show |
5 | HG02135.hp2 NA18971.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+1269A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810561 | |||||||
| chr12:68810562 | C | T | 1 | a0001c0001t0016g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.99+1270C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810562 | |||||||
| chr12:68810685 | T | C | 1 | a0001c0001t0074g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+1393T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810685 | |||||||
| chr12:68810797 | A | G | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+1505A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810797 | |||||||
| chr12:68810850 | C | A | 1 | a0001c0001t0048g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.99+1558C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68810850 | |||||||
| chr12:68811091 | C | T | 1 | a0001c0001t0005g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+1799C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811091 | |||||||
| chr12:68811132 | T | A | 1 | a0001c0001t0004g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.99+1840T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811132 | |||||||
| chr12:68811266 | C | G | 3 | a0001c0001t0021g0038 a0001c0001t0021g0188 a0001c0001t0030g0039 |
5 | HG01516.hp1 HG01517.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1974C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811266 | |||||||
| chr12:68811348 | A | C | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99+2056A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811348 | |||||||
| chr12:68811409 | T | C | 1 | a0001c0001t0009g0134 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+2117T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811409 | |||||||
| chr12:68811507 | A | G | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-2047A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811507 | |||||||
| chr12:68811541 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(105): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.100-2013T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811541 | |||||||
| chr12:68811601 | A | AT | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(137): Show |
175 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.100-1932dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68811601 | ||||||
| chr12:68811601 | A | ATT | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG01099.hp1 HG01993.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-1933_100-1932d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68811601 | ||||||
| chr12:68811601 | AT | A | 6 | a0001c0001t0002g0055 a0001c0001t0003g0193 a0001c0001t0004g0056 others(3): Show |
6 | HG02004.hp1 HG02897.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-1932delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68811601 | ||||||
| chr12:68811880 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(154): Show |
194 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.100-1674A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811880 | |||||||
| chr12:68811895 | T | C | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-1659T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811895 | |||||||
| chr12:68811943 | A | G | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-1611A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811943 | |||||||
| chr12:68811967 | C | T | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-1587C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811967 | |||||||
| chr12:68811971 | C | T | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-1583C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68811971 | |||||||
| chr12:68812011 | G | T | 1 | a0001c0001t0007g0217 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100-1543G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812011 | |||||||
| chr12:68812139 | T | C | 1 | a0001c0001t0051g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100-1415T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812139 | |||||||
| chr12:68812173 | G | A | 4 | a0001c0002t0033g0174 a0001c0002t0033g0175 a0001c0002t0056g0176 others(1): Show |
4 | HG01109.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1381G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812173 | |||||||
| chr12:68812197 | TA | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(115): Show |
150 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.100-1344delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68812197 | ||||||
| chr12:68812197 | TAAA | T | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-1346_100-1344d others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68812197 | ||||||
| chr12:68812229 | A | C | 1 | a0001c0002t0056g0176 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100-1325A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812229 | |||||||
| chr12:68812242 | A | G | 3 | a0001c0001t0004g0024 a0001c0001t0004g0058 a0001c0001t0011g0024 |
3 | NA18965.hp1 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.100-1312A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812242 | |||||||
| chr12:68812393 | G | A | 3 | a0001c0002t0008g0160 a0001c0002t0008g0161 a0001c0002t0008g0162 |
3 | HG02717.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1161G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812393 | |||||||
| chr12:68812661 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.100-893G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812661 | |||||||
| chr12:68812699 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(86): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.100-855A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812699 | |||||||
| chr12:68812730 | A | T | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-824A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812730 | |||||||
| chr12:68812733 | G | A | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-821G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812733 | |||||||
| chr12:68812738 | C | T | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-816C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812738 | |||||||
| chr12:68812907 | A | G | 1 | a0001c0002t0033g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-647A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68812907 | |||||||
| chr12:68813030 | GACTA | G | 12 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(9): Show |
12 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-518_100-515del others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr12 | 68813030 | ||||||
| chr12:68813111 | G | A | 1 | a0001c0001t0020g0177 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100-443G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813111 | |||||||
| chr12:68813262 | G | A | 1 | a0001c0001t0005g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.100-292G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813262 | |||||||
| chr12:68813365 | C | G | 19 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(16): Show |
21 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-189C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813365 | |||||||
| chr12:68813382 | G | A | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(267): Show |
335 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.100-172G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813382 | |||||||
| chr12:68813414 | A | G | 4 | a0001c0001t0028g0032 a0001c0001t0029g0164 a0001c0001t0029g0165 others(1): Show |
5 | HG01361.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-140A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813414 | |||||||
| chr12:68813544 | C | A | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.100-10C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 2/10 | chr12 | 68813544 | |||||||
| chr12:68814075 | C | T | 1 | a0001c0001t0021g0038 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.174+447C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814075 | |||||||
| chr12:68814084 | G | C | 2 | a0001c0001t0028g0032 a0001c0002t0056g0176 |
3 | HG01361.hp2 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.174+456G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814084 | |||||||
| chr12:68814122 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(154): Show |
194 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.174+494A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814122 | |||||||
| chr12:68814127 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.174+499A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814127 | |||||||
| chr12:68814238 | G | A | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+610G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814238 | |||||||
| chr12:68814743 | A | G | 4 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+1115A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814743 | |||||||
| chr12:68814798 | A | C | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(268): Show |
337 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.174+1170A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68814798 | |||||||
| chr12:68815107 | A | G | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.174+1479A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815107 | |||||||
| chr12:68815119 | T | C | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.174+1491T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815119 | |||||||
| chr12:68815148 | T | C | 1 | a0001c0001t0004g0060 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.174+1520T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815148 | |||||||
| chr12:68815231 | A | G | 2 | a0001c0001t0012g0007 a0001c0001t0012g0166 |
6 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-1581A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815231 | |||||||
| chr12:68815315 | A | G | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00738.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.175-1497A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815315 | |||||||
| chr12:68815355 | G | T | 1 | a0001c0001t0005g0023 | 2 | HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.175-1457G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815355 | |||||||
| chr12:68815380 | A | G | 1 | a0001c0001t0004g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.175-1432A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815380 | |||||||
| chr12:68815392 | G | A | 1 | a0001c0001t0007g0194 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.175-1420G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815392 | |||||||
| chr12:68815433 | C | CT | 40 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(37): Show |
45 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.175-1355dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68815433 | ||||||
| chr12:68815433 | C | CTT | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
93 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.175-1356_175-1355d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68815433 | ||||||
| chr12:68815433 | C | CTTT | 9 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(6): Show |
9 | HG00738.hp2 HG01261.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-1357_175-1355d others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68815433 | ||||||
| chr12:68815433 | C | CTTTT | 11 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(8): Show |
17 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-1358_175-1355d others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68815433 | ||||||
| chr12:68815433 | CT | C | 11 | a0001c0001t0002g0062 a0001c0001t0002g0065 a0001c0001t0002g0119 others(8): Show |
11 | HG01081.hp1 HG01123.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.175-1355delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68815433 | ||||||
| chr12:68815436 | T | C | 3 | a0001c0001t0002g0061 a0001c0001t0030g0039 a0001c0002t0008g0160 |
4 | HG02717.hp1 HG02723.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1376T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815436 | |||||||
| chr12:68815470 | C | T | 1 | a0001c0001t0074g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175-1342C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815470 | |||||||
| chr12:68815490 | G | A | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.175-1322G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815490 | |||||||
| chr12:68815509 | A | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0045 others(43): Show |
59 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.175-1303A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815509 | |||||||
| chr12:68815745 | A | G | 1 | a0001c0001t0002g0109 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.175-1067A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815745 | |||||||
| chr12:68815792 | A | G | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.175-1020A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68815792 | |||||||
| chr12:68816126 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.175-686T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816126 | |||||||
| chr12:68816151 | A | T | 1 | a0001c0001t0037g0108 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.175-661A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816151 | |||||||
| chr12:68816261 | T | A | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.175-551T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816261 | |||||||
| chr12:68816362 | C | CT | 24 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0265 others(21): Show |
24 | HG00099.hp2 HG01175.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.175-422dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0070g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175-431_175-422dup others(10): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0069g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.175-432_175-422dup others(11): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | CT | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(118): Show |
155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-422delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | CTT | C | 66 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0002g0001 others(63): Show |
85 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.175-423_175-422del others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | CTTT | C | 5 | a0001c0001t0002g0067 a0001c0001t0012g0007 a0001c0001t0012g0166 others(2): Show |
9 | HG01069.hp1 HG01070.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.175-424_175-422del others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | CTTTT | C | 6 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(3): Show |
8 | HG02572.hp2 HG02717.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.175-425_175-422del others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816362 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0063g0147 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.175-432_175-422del others(11): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816362 | ||||||
| chr12:68816400 | T | C | 1 | a0001c0004t0013g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175-412T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816400 | |||||||
| chr12:68816421 | G | A | 1 | a0001c0001t0004g0068 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.175-391G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816421 | |||||||
| chr12:68816425 | T | A | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-387T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816425 | |||||||
| chr12:68816430 | TGGCGCAA others(4): Show |
T | 12 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(9): Show |
18 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.175-378_175-368del others(11): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr12 | 68816430 | ||||||
| chr12:68816573 | G | A | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.175-239G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816573 | |||||||
| chr12:68816585 | C | T | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.175-227C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816585 | |||||||
| chr12:68816681 | G | C | 2 | a0001c0003t0026g0132 a0001c0003t0043g0131 |
2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175-131G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816681 | |||||||
| chr12:68816725 | CT | C | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-86delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 3/10 | chr12 | 68816725 | |||||||
| chr12:68817208 | A | T | 1 | a0001c0001t0028g0032 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.308+263A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817208 | |||||||
| chr12:68817264 | T | C | 2 | a0001c0001t0012g0007 a0001c0001t0012g0166 |
6 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.308+319T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817264 | |||||||
| chr12:68817429 | A | T | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.308+484A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817429 | |||||||
| chr12:68817485 | C | T | 1 | a0001c0001t0005g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.308+540C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817485 | |||||||
| chr12:68817559 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(73): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.308+614G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817559 | |||||||
| chr12:68817641 | C | T | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.308+696C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817641 | |||||||
| chr12:68817676 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(105): Show |
138 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.308+731C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817676 | |||||||
| chr12:68817844 | C | T | 1 | a0001c0001t0010g0107 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.308+899C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817844 | |||||||
| chr12:68817845 | T | C | 1 | a0001c0001t0010g0107 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.308+900T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817845 | |||||||
| chr12:68817880 | C | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(73): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.308+935C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817880 | |||||||
| chr12:68817947 | G | C | 1 | a0001c0001t0004g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.308+1002G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817947 | |||||||
| chr12:68817952 | C | A | 1 | a0001c0001t0010g0107 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.308+1007C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817952 | |||||||
| chr12:68817976 | T | C | 8 | a0001c0001t0016g0013 a0001c0001t0016g0185 a0001c0001t0016g0189 others(5): Show |
9 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.308+1031T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68817976 | |||||||
| chr12:68818054 | A | C | 8 | a0001c0001t0003g0011 a0001c0001t0003g0196 a0001c0001t0003g0205 others(5): Show |
10 | HG01255.hp2 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.308+1109A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818054 | |||||||
| chr12:68818230 | A | G | 114 | a0001c0001t0001g0274 a0001c0001t0002g0001 a0001c0001t0002g0003 others(111): Show |
142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.308+1285A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818230 | |||||||
| chr12:68818272 | T | A | 1 | a0001c0001t0004g0058 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.308+1327T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818272 | |||||||
| chr12:68818273 | A | T | 1 | a0001c0001t0004g0058 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.308+1328A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818273 | |||||||
| chr12:68818275 | T | A | 1 | a0001c0001t0004g0058 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.308+1330T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818275 | |||||||
| chr12:68818356 | T | C | 7 | a0001c0001t0004g0024 a0001c0001t0004g0054 a0001c0001t0004g0058 others(4): Show |
7 | HG00558.hp2 HG00621.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.308+1411T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818356 | |||||||
| chr12:68818437 | T | C | 3 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0022g0155 |
4 | HG02572.hp2 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+1492T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818437 | |||||||
| chr12:68818550 | ATAT | A | 3 | a0001c0001t0016g0013 a0001c0001t0054g0184 a0001c0001t0057g0013 |
4 | HG02109.hp2 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.308+1609_308+1611d others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr12 | 68818550 | ||||||
| chr12:68818864 | G | A | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.309-1461G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818864 | |||||||
| chr12:68818999 | T | A | 1 | a0001c0001t0004g0058 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.309-1326T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68818999 | |||||||
| chr12:68819012 | G | A | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.309-1313G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819012 | |||||||
| chr12:68819051 | T | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.309-1274T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819051 | |||||||
| chr12:68819060 | G | C | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.309-1265G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819060 | |||||||
| chr12:68819174 | C | G | 4 | a0001c0001t0003g0008 a0001c0001t0003g0144 a0001c0001t0007g0008 others(1): Show |
6 | HG01106.hp2 HG01109.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.309-1151C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819174 | |||||||
| chr12:68819358 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.309-967T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819358 | |||||||
| chr12:68819544 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.309-781T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819544 | |||||||
| chr12:68819585 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.309-740G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819585 | |||||||
| chr12:68819596 | A | T | 1 | a0001c0001t0004g0058 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.309-729A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819596 | |||||||
| chr12:68819875 | G | C | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.309-450G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819875 | |||||||
| chr12:68819883 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.309-442G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 4/10 | chr12 | 68819883 | |||||||
| chr12:68820779 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.358+405T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68820779 | |||||||
| chr12:68820868 | T | A | 1 | a0001c0001t0073g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.358+494T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68820868 | |||||||
| chr12:68820911 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(142): Show |
181 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.358+537G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68820911 | |||||||
| chr12:68820956 | C | T | 1 | a0001c0001t0003g0204 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.358+582C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68820956 | |||||||
| chr12:68821044 | C | CT | 23 | a0001c0001t0001g0015 a0001c0001t0001g0231 a0001c0001t0001g0246 others(20): Show |
31 | HG01069.hp1 HG01891.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.358+691dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68821044 | ||||||
| chr12:68821044 | CT | C | 45 | a0001c0001t0001g0247 a0001c0001t0002g0018 a0001c0001t0002g0022 others(42): Show |
46 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.358+691delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68821044 | ||||||
| chr12:68821044 | CTT | C | 116 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(113): Show |
147 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.358+690_358+691del others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68821044 | ||||||
| chr12:68821046 | T | C | 1 | a0001c0001t0004g0072 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.358+672T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821046 | |||||||
| chr12:68821114 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(264): Show |
331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.358+740T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821114 | |||||||
| chr12:68821114 | T | G | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.358+740T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821114 | |||||||
| chr12:68821208 | C | T | 11 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.358+834C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821208 | |||||||
| chr12:68821289 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.358+915G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821289 | |||||||
| chr12:68821348 | A | G | 1 | a0001c0001t0021g0038 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.358+974A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821348 | |||||||
| chr12:68821490 | A | C | 1 | a0001c0001t0021g0038 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.358+1116A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821490 | |||||||
| chr12:68821553 | ACT | A | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.358+1182_358+1183d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68821553 | ||||||
| chr12:68821570 | A | G | 1 | a0001c0001t0013g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.358+1196A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821570 | |||||||
| chr12:68821728 | A | AAAAAC | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.358+1369_358+1373d others(7): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68821728 | ||||||
| chr12:68821745 | A | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(73): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.358+1371A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821745 | |||||||
| chr12:68821858 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.358+1484G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821858 | |||||||
| chr12:68821878 | G | A | 1 | a0001c0002t0008g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.358+1504G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821878 | |||||||
| chr12:68821946 | C | T | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.358+1572C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821946 | |||||||
| chr12:68821960 | A | G | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.358+1586A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821960 | |||||||
| chr12:68821968 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.358+1594C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821968 | |||||||
| chr12:68821997 | G | A | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.358+1623G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68821997 | |||||||
| chr12:68822015 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0043 others(47): Show |
64 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.358+1641T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822015 | |||||||
| chr12:68822365 | A | G | 12 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(9): Show |
18 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.358+1991A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822365 | |||||||
| chr12:68822371 | C | CT | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(221): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.359-1981dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822371 | ||||||
| chr12:68822371 | C | CTT | 17 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0009g0028 others(14): Show |
17 | HG00639.hp2 HG02145.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.359-1982_359-1981d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822371 | ||||||
| chr12:68822371 | C | CTTTT | 5 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0022g0155 others(2): Show |
9 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-1984_359-1981d others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822371 | ||||||
| chr12:68822371 | C | CTTTTT | 16 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(13): Show |
18 | HG02055.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.359-1985_359-1981d others(7): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822371 | ||||||
| chr12:68822449 | A | G | 1 | a0001c0001t0053g0103 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.359-1914A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822449 | |||||||
| chr12:68822522 | C | T | 4 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-1841C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822522 | |||||||
| chr12:68822574 | G | A | 25 | a0001c0001t0002g0087 a0001c0001t0002g0104 a0001c0001t0004g0009 others(22): Show |
28 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.359-1789G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822574 | |||||||
| chr12:68822741 | T | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(70): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.359-1622T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822741 | |||||||
| chr12:68822746 | C | CT | 6 | a0001c0001t0002g0125 a0001c0002t0006g0167 a0001c0002t0006g0171 others(3): Show |
6 | HG01167.hp1 HG02615.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-1605dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822746 | ||||||
| chr12:68822746 | C | CTTTTTT | 17 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0157 others(14): Show |
22 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.359-1610_359-1605d others(8): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822746 | ||||||
| chr12:68822746 | CT | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.359-1605delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68822746 | ||||||
| chr12:68822885 | T | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(307): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(381): Show |
intron_variant | MODIFIER | c.359-1478T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822885 | |||||||
| chr12:68822985 | C | T | 1 | a0001c0001t0019g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.359-1378C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68822985 | |||||||
| chr12:68823018 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(144): Show |
183 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.359-1345A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823018 | |||||||
| chr12:68823145 | T | A | 1 | a0001c0001t0003g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.359-1218T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823145 | |||||||
| chr12:68823253 | A | AG | 114 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(111): Show |
142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.359-1104dupG | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68823253 | ||||||
| chr12:68823256 | G | C | 9 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(6): Show |
14 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-1107G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823256 | |||||||
| chr12:68823300 | C | A | 21 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(18): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.359-1063C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823300 | |||||||
| chr12:68823660 | A | C | 1 | a0001c0004t0013g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.359-703A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823660 | |||||||
| chr12:68823697 | G | A | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.359-666G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823697 | |||||||
| chr12:68823699 | G | C | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.359-664G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823699 | |||||||
| chr12:68823785 | G | A | 2 | a0001c0001t0032g0066 a0001c0001t0032g0073 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.359-578G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823785 | |||||||
| chr12:68823799 | G | A | 2 | a0001c0001t0002g0089 a0001c0001t0005g0088 |
2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.359-564G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823799 | |||||||
| chr12:68823892 | T | G | 6 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0013g0157 others(3): Show |
7 | HG02572.hp2 HG02922.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-471T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68823892 | |||||||
| chr12:68824062 | C | G | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-301C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68824062 | |||||||
| chr12:68824130 | AAC | A | 104 | a0001c0001t0001g0264 a0001c0001t0002g0001 a0001c0001t0002g0003 others(101): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.359-231_359-230del others(2): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr12 | 68824130 | ||||||
| chr12:68824217 | A | T | 1 | a0001c0001t0035g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.359-146A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68824217 | |||||||
| chr12:68824258 | T | G | 173 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0001g0232 others(170): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.359-105T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 5/10 | chr12 | 68824258 | |||||||
| chr12:68824468 | T | C | 1 | a0001c0001t0004g0126 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.426+38T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 6/10 | chr12 | 68824468 | |||||||
| chr12:68824705 | C | G | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+54C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68824705 | |||||||
| chr12:68824920 | G | C | 6 | a0001c0001t0002g0017 a0001c0001t0002g0050 a0001c0001t0002g0106 others(3): Show |
6 | HG01928.hp1 NA18612.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.523+269G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68824920 | |||||||
| chr12:68824950 | T | G | 3 | a0001c0001t0028g0032 a0001c0001t0029g0164 a0001c0001t0029g0165 |
4 | HG01361.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+299T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68824950 | |||||||
| chr12:68824974 | C | T | 2 | a0001c0001t0073g0154 a0001c0001t0074g0152 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.523+323C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68824974 | |||||||
| chr12:68825044 | T | TA | 5 | a0001c0001t0002g0074 a0001c0001t0002g0128 a0001c0001t0028g0032 others(2): Show |
6 | HG01361.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.523+401dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 68825044 | ||||||
| chr12:68825053 | T | A | 4 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0022g0155 others(1): Show |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+402T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825053 | |||||||
| chr12:68825079 | G | A | 2 | a0001c0001t0009g0137 a0001c0002t0060g0173 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.523+428G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825079 | |||||||
| chr12:68825133 | C | T | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.523+482C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825133 | |||||||
| chr12:68825201 | T | G | 10 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(7): Show |
16 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.523+550T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825201 | |||||||
| chr12:68825439 | G | C | 11 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.523+788G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825439 | |||||||
| chr12:68825522 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0262 a0001c0001t0001g0276 |
3 | HG01099.hp1 NA19087.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.523+871G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825522 | |||||||
| chr12:68825655 | AAG | A | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.523+1016_523+1017d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 68825655 | ||||||
| chr12:68825668 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.523+1017A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825668 | |||||||
| chr12:68825680 | A | G | 1 | a0001c0001t0022g0031 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.523+1029A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825680 | |||||||
| chr12:68825712 | G | A | 111 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(108): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.523+1061G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825712 | |||||||
| chr12:68825761 | G | A | 1 | a0001c0001t0011g0077 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.523+1110G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825761 | |||||||
| chr12:68825828 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG00408.hp2 NA18992.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.523+1177G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68825828 | |||||||
| chr12:68826002 | G | A | 3 | a0001c0001t0028g0032 a0001c0001t0029g0164 a0001c0001t0029g0165 |
4 | HG01361.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+1351G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826002 | |||||||
| chr12:68826205 | G | A | 1 | a0001c0001t0037g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.523+1554G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826205 | |||||||
| chr12:68826419 | C | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.523+1768C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826419 | |||||||
| chr12:68826446 | C | T | 1 | a0001c0001t0011g0076 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.523+1795C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826446 | |||||||
| chr12:68826517 | C | T | 1 | a0001c0001t0004g0056 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.523+1866C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826517 | |||||||
| chr12:68826601 | G | A | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.523+1950G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826601 | |||||||
| chr12:68826643 | C | CAT | 3 | a0001c0001t0010g0100 a0001c0001t0069g0145 a0001c0001t0070g0151 |
3 | HG02258.hp2 HG03579.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.523+1992_523+1993i others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826643 | |||||||
| chr12:68826644 | C | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(264): Show |
332 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.523+1993C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826644 | |||||||
| chr12:68826646 | CT | C | 8 | a0001c0001t0002g0099 a0001c0001t0002g0104 a0001c0001t0004g0060 others(5): Show |
8 | HG00423.hp2 HG02027.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.523+1997delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 68826646 | ||||||
| chr12:68826647 | T | A | 3 | a0001c0001t0010g0100 a0001c0001t0069g0145 a0001c0001t0070g0151 |
3 | HG02258.hp2 HG03579.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.523+1996T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826647 | |||||||
| chr12:68826647 | T | TC | 4 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0235 others(1): Show |
4 | HG00408.hp2 NA18992.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+1996_523+1997i others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826647 | |||||||
| chr12:68826647 | T | TCAA | 18 | a0001c0001t0010g0019 a0001c0001t0010g0090 a0001c0001t0010g0091 others(15): Show |
25 | HG00609.hp2 HG01069.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.523+1996_523+1997i others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826647 | |||||||
| chr12:68826647 | T | TCAAA | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.523+1996_523+1997i others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826647 | |||||||
| chr12:68826648 | T | A | 32 | a0001c0001t0001g0228 a0001c0001t0001g0232 a0001c0001t0001g0235 others(29): Show |
39 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.523+1997T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826648 | |||||||
| chr12:68826648 | T | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(225): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.523+1997T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826648 | |||||||
| chr12:68826649 | A | C | 8 | a0001c0001t0002g0099 a0001c0001t0002g0104 a0001c0001t0004g0060 others(5): Show |
8 | HG00423.hp2 HG02027.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.523+1998A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826649 | |||||||
| chr12:68826653 | A | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0271 |
2 | HG00639.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.523+2002A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826653 | |||||||
| chr12:68826727 | A | G | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.524-2044A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826727 | |||||||
| chr12:68826856 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(70): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.524-1915C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826856 | |||||||
| chr12:68826884 | G | A | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.524-1887G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826884 | |||||||
| chr12:68826975 | G | A | 1 | a0001c0001t0015g0020 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.524-1796G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68826975 | |||||||
| chr12:68827126 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.524-1645C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827126 | |||||||
| chr12:68827205 | A | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.524-1566A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827205 | |||||||
| chr12:68827298 | G | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0249 a0001c0001t0001g0256 others(1): Show |
4 | HG00544.hp1 NA18964.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1473G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827298 | |||||||
| chr12:68827300 | AAG | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(72): Show |
99 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.524-1468_524-1467d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 68827300 | ||||||
| chr12:68827304 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.524-1467G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827304 | |||||||
| chr12:68827438 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.524-1333T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827438 | |||||||
| chr12:68827850 | G | A | 4 | a0001c0001t0013g0030 a0001c0001t0013g0156 a0001c0001t0022g0155 others(1): Show |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-921G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827850 | |||||||
| chr12:68827950 | G | A | 1 | a0001c0001t0005g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.524-821G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68827950 | |||||||
| chr12:68828045 | C | G | 24 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0050 others(21): Show |
27 | HG00423.hp1 HG00609.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.524-726C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828045 | |||||||
| chr12:68828074 | T | C | 2 | a0001c0001t0073g0154 a0001c0001t0074g0152 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.524-697T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828074 | |||||||
| chr12:68828230 | C | T | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.524-541C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828230 | |||||||
| chr12:68828300 | A | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.524-471A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828300 | |||||||
| chr12:68828560 | C | T | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.524-211C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828560 | |||||||
| chr12:68828577 | C | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(140): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.524-194C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828577 | |||||||
| chr12:68828598 | A | C | 4 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-173A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828598 | |||||||
| chr12:68828599 | A | G | 27 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(24): Show |
30 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.524-172A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828599 | |||||||
| chr12:68828620 | TCTG | T | 11 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.524-147_524-145del others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr12 | 68828620 | ||||||
| chr12:68828636 | G | T | 1 | a0001c0001t0073g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.524-135G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828636 | |||||||
| chr12:68828681 | A | G | 1 | a0001c0001t0020g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.524-90A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828681 | |||||||
| chr12:68828684 | C | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(87): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.524-87C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 7/10 | chr12 | 68828684 | |||||||
| chr12:68829029 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0098 |
3 | HG00735.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.684+98C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68829029 | |||||||
| chr12:68829247 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.684+316A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68829247 | |||||||
| chr12:68829254 | AGTT | A | 31 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(28): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.684+327_684+329del others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68829254 | ||||||
| chr12:68829512 | A | G | 1 | a0001c0001t0077g0277 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.684+581A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68829512 | |||||||
| chr12:68829765 | C | CA | 29 | a0001c0001t0002g0092 a0001c0001t0002g0129 a0001c0001t0003g0004 others(26): Show |
39 | HG00544.hp2 HG01069.hp1 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.684+852dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68829765 | ||||||
| chr12:68829765 | CA | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(86): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.684+852delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68829765 | ||||||
| chr12:68829885 | C | T | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.684+954C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68829885 | |||||||
| chr12:68829986 | G | C | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(266): Show |
334 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.684+1055G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68829986 | |||||||
| chr12:68830046 | C | T | 1 | a0001c0002t0006g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.684+1115C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830046 | |||||||
| chr12:68830060 | A | ATT | 20 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(17): Show |
27 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.684+1139_684+1140d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68830060 | ||||||
| chr12:68830139 | A | G | 1 | a0001c0001t0003g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.684+1208A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830139 | |||||||
| chr12:68830162 | A | G | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.684+1231A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830162 | |||||||
| chr12:68830179 | G | A | 1 | a0001c0001t0068g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.684+1248G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830179 | |||||||
| chr12:68830262 | A | G | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.684+1331A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830262 | |||||||
| chr12:68830283 | C | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.684+1352C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830283 | |||||||
| chr12:68830549 | G | GGA | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+1621_684+1622d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68830549 | ||||||
| chr12:68830617 | C | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(140): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.684+1686C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68830617 | |||||||
| chr12:68831112 | T | G | 31 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(28): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.684+2181T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831112 | |||||||
| chr12:68831338 | G | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.684+2407G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831338 | |||||||
| chr12:68831654 | G | C | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.684+2723G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831654 | |||||||
| chr12:68831775 | TA | T | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+2850delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68831775 | ||||||
| chr12:68831786 | A | G | 2 | a0001c0001t0009g0137 a0001c0001t0009g0141 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.684+2855A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831786 | |||||||
| chr12:68831793 | C | T | 2 | a0001c0001t0009g0137 a0001c0001t0009g0141 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.684+2862C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831793 | |||||||
| chr12:68831828 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(268): Show |
336 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.684+2897A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831828 | |||||||
| chr12:68831854 | G | C | 1 | a0001c0001t0005g0113 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.684+2923G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831854 | |||||||
| chr12:68831895 | A | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(106): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.684+2964A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831895 | |||||||
| chr12:68831908 | A | G | 11 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+2977A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68831908 | |||||||
| chr12:68832365 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.684+3434A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832365 | |||||||
| chr12:68832372 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.684+3441G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832372 | |||||||
| chr12:68832374 | T | TCCCTTTT others(6): Show |
1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.684+3443_684+3444i others(15): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832374 | |||||||
| chr12:68832377 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.684+3446G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832377 | |||||||
| chr12:68832385 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3444T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832385 | |||||||
| chr12:68832388 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3441T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832388 | |||||||
| chr12:68832391 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3438A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832391 | |||||||
| chr12:68832392 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3437T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832392 | |||||||
| chr12:68832393 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3436A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832393 | |||||||
| chr12:68832394 | A | T | 11 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(8): Show |
11 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.685-3435A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832394 | |||||||
| chr12:68832396 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3433T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832396 | |||||||
| chr12:68832397 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3432T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832397 | |||||||
| chr12:68832398 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3431G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832398 | |||||||
| chr12:68832400 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3429T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832400 | |||||||
| chr12:68832401 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3428T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832401 | |||||||
| chr12:68832402 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3427A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832402 | |||||||
| chr12:68832408 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3421C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832408 | |||||||
| chr12:68832421 | G | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3408G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832421 | |||||||
| chr12:68832429 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3400T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832429 | |||||||
| chr12:68832441 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3388A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832441 | |||||||
| chr12:68832443 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3386T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832443 | |||||||
| chr12:68832444 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3385T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832444 | |||||||
| chr12:68832452 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3377T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832452 | |||||||
| chr12:68832466 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3363G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832466 | |||||||
| chr12:68832467 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3362A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832467 | |||||||
| chr12:68832468 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3361T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832468 | |||||||
| chr12:68832472 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3357A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832472 | |||||||
| chr12:68832473 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3356G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832473 | |||||||
| chr12:68832476 | C | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3353C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832476 | |||||||
| chr12:68832477 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3352T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832477 | |||||||
| chr12:68832480 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3349G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832480 | |||||||
| chr12:68832491 | C | T | 2 | a0001c0001t0073g0154 a0001c0001t0074g0152 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.685-3338C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832491 | |||||||
| chr12:68832494 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3335T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832494 | |||||||
| chr12:68832497 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3332G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832497 | |||||||
| chr12:68832500 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3329G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832500 | |||||||
| chr12:68832503 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3326T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832503 | |||||||
| chr12:68832511 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3318T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832511 | |||||||
| chr12:68832513 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3316T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832513 | |||||||
| chr12:68832516 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3313A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832516 | |||||||
| chr12:68832521 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3308T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832521 | |||||||
| chr12:68832524 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3305A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832524 | |||||||
| chr12:68832525 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3304A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832525 | |||||||
| chr12:68832527 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3302T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832527 | |||||||
| chr12:68832536 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3293A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832536 | |||||||
| chr12:68832538 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3291T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832538 | |||||||
| chr12:68832544 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3285A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832544 | |||||||
| chr12:68832545 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3284C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832545 | |||||||
| chr12:68832561 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3268G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832561 | |||||||
| chr12:68832598 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3231A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832598 | |||||||
| chr12:68832605 | G | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3224G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832605 | |||||||
| chr12:68832615 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3214A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832615 | |||||||
| chr12:68832616 | A | G | 31 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(28): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.685-3213A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832616 | |||||||
| chr12:68832618 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3211C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832618 | |||||||
| chr12:68832620 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3209T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832620 | |||||||
| chr12:68832646 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3183G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832646 | |||||||
| chr12:68832648 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3181G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832648 | |||||||
| chr12:68832649 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3180A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832649 | |||||||
| chr12:68832650 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3179C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832650 | |||||||
| chr12:68832670 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3159A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832670 | |||||||
| chr12:68832671 | C | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3158C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832671 | |||||||
| chr12:68832673 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3156T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832673 | |||||||
| chr12:68832674 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3155G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832674 | |||||||
| chr12:68832686 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3143T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832686 | |||||||
| chr12:68832689 | C | CT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
113 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.685-3129dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68832689 | ||||||
| chr12:68832698 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3131T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832698 | |||||||
| chr12:68832699 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3130T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832699 | |||||||
| chr12:68832711 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3118A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832711 | |||||||
| chr12:68832712 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3117T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832712 | |||||||
| chr12:68832713 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3116C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832713 | |||||||
| chr12:68832715 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3114T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832715 | |||||||
| chr12:68832716 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3113G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832716 | |||||||
| chr12:68832717 | G | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3112G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832717 | |||||||
| chr12:68832718 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3111C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832718 | |||||||
| chr12:68832727 | C | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3102C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832727 | |||||||
| chr12:68832738 | C | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3091C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832738 | |||||||
| chr12:68832739 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3090A>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832739 | |||||||
| chr12:68832742 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3087C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832742 | |||||||
| chr12:68832751 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3078T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832751 | |||||||
| chr12:68832754 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3075T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832754 | |||||||
| chr12:68832762 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3067T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832762 | |||||||
| chr12:68832770 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-3059T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832770 | |||||||
| chr12:68832901 | C | T | 1 | a0001c0001t0003g0210 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.685-2928C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832901 | |||||||
| chr12:68832922 | C | G | 1 | a0001c0001t0074g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.685-2907C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68832922 | |||||||
| chr12:68833084 | C | T | 1 | a0001c0001t0028g0032 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.685-2745C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833084 | |||||||
| chr12:68833126 | C | CA | 11 | a0001c0001t0002g0021 a0001c0001t0003g0207 a0001c0001t0005g0010 others(8): Show |
15 | HG01192.hp2 HG01928.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-2679dupA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CA | C | 8 | a0001c0001t0001g0227 a0001c0001t0001g0257 a0001c0001t0002g0096 others(5): Show |
8 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.685-2679delA | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAA | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0225 a0001c0001t0001g0233 others(9): Show |
13 | HG01081.hp1 HG01167.hp2 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.685-2680_685-2679d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAA | C | 10 | a0001c0002t0006g0034 a0001c0002t0006g0035 a0001c0002t0008g0012 others(7): Show |
12 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.685-2682_685-2679d others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAA | C | 10 | a0001c0002t0006g0033 a0001c0002t0006g0167 a0001c0002t0006g0169 others(7): Show |
11 | HG01167.hp1 HG02257.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.685-2683_685-2679d others(7): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAAAA | C | 6 | a0001c0002t0006g0170 a0001c0002t0008g0161 a0001c0002t0008g0162 others(3): Show |
6 | HG02559.hp2 HG02630.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.685-2685_685-2679d others(9): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0138 others(5): Show |
8 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-2686_685-2679d others(10): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0009g0140 a0001c0001t0009g0142 a0001c0001t0035g0029 others(6): Show |
9 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.685-2687_685-2679d others(11): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0013g0157 a0001c0001t0062g0150 a0001c0001t0068g0158 |
3 | HG02886.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685-2688_685-2679d others(12): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833126 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0009g0137 a0001c0001t0009g0141 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.685-2690_685-2679d others(14): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833126 | ||||||
| chr12:68833141 | AAAAAAAA others(3): Show |
A | 9 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(6): Show |
15 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-2686_685-2677d others(12): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833141 | ||||||
| chr12:68833143 | A | T | 3 | a0001c0002t0006g0183 a0001c0002t0008g0179 a0001c0002t0014g0036 |
3 | HG01081.hp1 NA19030.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.685-2686A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833143 | |||||||
| chr12:68833145 | A | T | 19 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(16): Show |
22 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.685-2684A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833145 | |||||||
| chr12:68833147 | A | AATATATA others(7): Show |
1 | a0001c0001t0016g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.685-2681_685-2680i others(16): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833147 | ||||||
| chr12:68833147 | A | AATATATA others(19): Show |
1 | a0001c0001t0054g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.685-2681_685-2680i others(28): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833147 | ||||||
| chr12:68833147 | A | AT | 14 | a0001c0001t0002g0006 a0001c0001t0002g0047 a0001c0001t0002g0048 others(11): Show |
15 | HG00621.hp2 HG01978.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-2682_685-2681i others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833147 | |||||||
| chr12:68833147 | A | T | 30 | a0001c0001t0001g0002 a0001c0001t0009g0028 a0001c0001t0009g0134 others(27): Show |
33 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.685-2682A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833147 | |||||||
| chr12:68833148 | AAAT | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0247 a0001c0001t0001g0250 others(2): Show |
6 | HG00280.hp1 HG01361.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-2679_685-2677d others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833148 | ||||||
| chr12:68833149 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0024g0190 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.685-2679_685-2678i others(15): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AAAAATAT others(8): Show |
1 | a0001c0001t0020g0186 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.685-2679_685-2678i others(17): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AAAATATA others(5): Show |
2 | a0001c0001t0020g0177 a0001c0001t0020g0187 |
2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.685-2679_685-2678i others(14): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AAAATATA others(7): Show |
1 | a0001c0001t0016g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.685-2679_685-2678i others(16): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AAATATAT others(6): Show |
1 | a0001c0001t0016g0185 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.685-2679_685-2678i others(15): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AAT | 13 | a0001c0001t0004g0009 a0001c0001t0004g0054 a0001c0001t0004g0068 others(10): Show |
15 | HG01361.hp1 HG01516.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.685-2663_685-2662d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AATATATA others(7): Show |
1 | a0001c0001t0057g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685-2675_685-2662d others(16): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AATATATA others(15): Show |
1 | a0001c0001t0024g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685-2662_685-2661i others(24): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AATATATA others(19): Show |
1 | a0001c0001t0016g0013 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.685-2662_685-2661i others(28): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833149 | A | AT | 70 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(67): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.685-2680_685-2679i others(3): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833149 | |||||||
| chr12:68833149 | A | ATAT | 3 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0004g0064 |
3 | HG00735.hp2 HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.685-2680_685-2679i others(5): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833149 | |||||||
| chr12:68833149 | A | ATATATAT others(10): Show |
1 | a0001c0001t0040g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.685-2680_685-2679i others(19): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833149 | |||||||
| chr12:68833149 | A | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0002g0006 others(62): Show |
70 | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.685-2680A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833149 | |||||||
| chr12:68833149 | AAT | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(43): Show |
64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.685-2663_685-2662d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833149 | ||||||
| chr12:68833150 | AT | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0221 others(6): Show |
9 | HG01975.hp1 HG02056.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-2678delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833150 | |||||||
| chr12:68833153 | T | A | 4 | a0001c0001t0001g0229 a0001c0001t0001g0234 a0001c0001t0001g0262 others(1): Show |
4 | HG01975.hp1 HG02148.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2676T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833153 | |||||||
| chr12:68833187 | AAATATAT | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0193 a0001c0001t0003g0197 others(11): Show |
19 | HG02040.hp1 HG02074.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-2631_685-2625d others(9): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833187 | ||||||
| chr12:68833235 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-2594T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833235 | |||||||
| chr12:68833236 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-2593A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833236 | |||||||
| chr12:68833237 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-2592T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833237 | |||||||
| chr12:68833247 | TTATATAT others(33): Show |
T | 3 | a0001c0001t0003g0042 a0001c0001t0003g0191 a0001c0001t0047g0042 |
3 | NA18947.hp2 NA18978.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.685-2564_685-2525d others(42): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833247 | ||||||
| chr12:68833265 | T | TTATATAT others(17): Show |
1 | a0001c0001t0002g0062 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.685-2541_685-2518d others(26): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833265 | ||||||
| chr12:68833266 | T | TATATATT others(39): Show |
1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.685-2557_685-2512d others(48): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833266 | ||||||
| chr12:68833280 | A | AATATAAA others(153): Show |
1 | a0001c0001t0028g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.685-2533_685-2532i others(162): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(193): Show |
1 | a0001c0001t0028g0032 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.685-2533_685-2532i others(202): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(97): Show |
1 | a0001c0001t0009g0141 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.685-2512_685-2511i others(106): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(33): Show |
1 | a0001c0001t0002g0111 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.685-2512_685-2511i others(42): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(79): Show |
12 | a0001c0002t0006g0033 a0001c0002t0006g0167 a0001c0002t0006g0169 others(9): Show |
13 | HG01167.hp1 HG02257.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.685-2512_685-2511i others(88): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(149): Show |
1 | a0001c0001t0021g0188 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.685-2512_685-2511i others(158): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(65): Show |
2 | a0001c0001t0029g0164 a0001c0001t0029g0165 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.685-2512_685-2511i others(74): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(73): Show |
2 | a0001c0001t0009g0140 a0001c0001t0009g0142 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.685-2512_685-2511i others(82): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(181): Show |
1 | a0001c0002t0008g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.685-2512_685-2511i others(190): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(149): Show |
1 | a0001c0001t0021g0038 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.685-2518_685-2517i others(158): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(97): Show |
7 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0138 others(4): Show |
7 | HG00639.hp2 HG02145.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-2518_685-2517i others(106): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(97): Show |
1 | a0001c0001t0009g0137 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.685-2518_685-2517i others(106): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATAAA others(119): Show |
3 | a0001c0002t0033g0174 a0001c0002t0056g0176 a0001c0002t0060g0173 |
3 | HG01109.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.685-2525_685-2524i others(128): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(141): Show |
1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-2544_685-2543i others(150): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(79): Show |
12 | a0001c0002t0006g0034 a0001c0002t0006g0035 a0001c0002t0006g0170 others(9): Show |
14 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(88): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(77): Show |
2 | a0001c0002t0008g0034 a0001c0002t0014g0178 |
2 | HG03490.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.685-2544_685-2543i others(86): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(107): Show |
1 | a0001c0001t0001g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.685-2544_685-2543i others(116): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(45): Show |
3 | a0001c0001t0001g0243 a0001c0001t0001g0268 a0001c0001t0071g0238 |
3 | HG02165.hp1 NA18949.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.685-2544_685-2543i others(54): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(67): Show |
1 | a0001c0001t0001g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.685-2544_685-2543i others(76): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(85): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0222 a0001c0001t0001g0227 |
4 | HG00558.hp1 NA19065.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(94): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(107): Show |
1 | a0001c0001t0023g0002 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.685-2544_685-2543i others(116): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(125): Show |
9 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0251 others(6): Show |
10 | HG00639.hp1 HG01261.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(134): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(183): Show |
1 | a0001c0001t0077g0277 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.685-2544_685-2543i others(192): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(201): Show |
1 | a0001c0001t0001g0266 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.685-2544_685-2543i others(210): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(143): Show |
38 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(35): Show |
54 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(152): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(161): Show |
5 | a0001c0001t0001g0221 a0001c0001t0001g0249 a0001c0001t0001g0261 others(2): Show |
5 | HG00544.hp1 NA18953.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(170): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(179): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0016 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.685-2544_685-2543i others(188): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(197): Show |
1 | a0001c0001t0001g0232 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.685-2544_685-2543i others(206): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(103): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0250 others(2): Show |
5 | HG01175.hp1 HG01515.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(112): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(161): Show |
1 | a0001c0001t0001g0252 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.685-2544_685-2543i others(170): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(63): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG02056.hp2 NA18966.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2544_685-2543i others(72): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833280 | A | AATATATA others(177): Show |
1 | a0001c0001t0001g0280 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.685-2544_685-2543i others(186): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833280 | ||||||
| chr12:68833286 | A | AATATATA others(119): Show |
1 | a0001c0002t0033g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.685-2525_685-2524i others(128): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833286 | ||||||
| chr12:68833286 | AAT | A | 10 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(7): Show |
16 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-2534_685-2533d others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833286 | ||||||
| chr12:68833286 | AATAT | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0096 a0001c0001t0002g0119 others(1): Show |
4 | HG02145.hp2 HG02976.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2536_685-2533d others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833286 | ||||||
| chr12:68833288 | T | A | 1 | a0001c0001t0048g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.685-2541T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833288 | |||||||
| chr12:68833288 | TATATATA others(39): Show |
T | 3 | a0001c0001t0004g0056 a0001c0001t0004g0080 a0001c0001t0004g0117 |
3 | NA18982.hp1 NA18986.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.685-2528_685-2483d others(48): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833288 | ||||||
| chr12:68833289 | A | G | 11 | a0001c0001t0016g0013 a0001c0001t0016g0185 a0001c0001t0016g0189 others(8): Show |
12 | HG02055.hp2 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-2540A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833289 | |||||||
| chr12:68833290 | T | A | 10 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(7): Show |
16 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-2539T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833290 | |||||||
| chr12:68833296 | T | A | 10 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(7): Show |
16 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-2533T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833296 | |||||||
| chr12:68833296 | TTTATATA others(15): Show |
T | 1 | a0001c0001t0003g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.685-2511_685-2490d others(24): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833296 | ||||||
| chr12:68833308 | TAAAA | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(80): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.685-2519_685-2516d others(6): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833308 | ||||||
| chr12:68833312 | A | AATATATT others(11): Show |
1 | a0001c0001t0001g0005 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.685-2512_685-2511i others(20): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833312 | ||||||
| chr12:68833312 | A | AATATATT others(103): Show |
1 | a0001c0003t0043g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.685-2512_685-2511i others(112): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833312 | ||||||
| chr12:68833312 | A | AATATATT others(143): Show |
2 | a0001c0003t0026g0132 a0001c0003t0026g0133 |
2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.685-2512_685-2511i others(152): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833312 | ||||||
| chr12:68833318 | A | ATTATATA others(11): Show |
2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.685-2498_685-2497i others(20): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833318 | ||||||
| chr12:68833318 | A | ATTATATA others(33): Show |
2 | a0001c0001t0035g0029 a0003c0006t0064g0029 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.685-2498_685-2497i others(42): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833318 | ||||||
| chr12:68833318 | A | ATTATATA others(55): Show |
5 | a0001c0001t0035g0149 a0001c0001t0062g0150 a0001c0001t0063g0147 others(2): Show |
5 | HG02055.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-2498_685-2497i others(64): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68833318 | ||||||
| chr12:68833318 | A | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(294): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.685-2511A>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833318 | |||||||
| chr12:68833416 | T | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-2413T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833416 | |||||||
| chr12:68833452 | T | G | 1 | a0001c0001t0002g0128 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.685-2377T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833452 | |||||||
| chr12:68833454 | G | T | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(272): Show |
343 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.685-2375G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833454 | |||||||
| chr12:68833493 | G | A | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.685-2336G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833493 | |||||||
| chr12:68833556 | G | A | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.685-2273G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833556 | |||||||
| chr12:68833657 | A | G | 1 | a0001c0001t0073g0154 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.685-2172A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833657 | |||||||
| chr12:68833785 | C | T | 1 | a0001c0001t0028g0032 | 2 | HG01361.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.685-2044C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833785 | |||||||
| chr12:68833924 | C | T | 2 | a0001c0001t0073g0154 a0001c0001t0074g0152 |
2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.685-1905C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68833924 | |||||||
| chr12:68834062 | TTGTTTC | T | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.685-1761_685-1756d others(8): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr12 | 68834062 | ||||||
| chr12:68834169 | G | A | 1 | a0001c0002t0008g0161 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.685-1660G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834169 | |||||||
| chr12:68834263 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(89): Show |
117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.685-1566G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834263 | |||||||
| chr12:68834302 | T | G | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.685-1527T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834302 | |||||||
| chr12:68834368 | G | A | 10 | a0001c0001t0004g0024 a0001c0001t0004g0058 a0001c0001t0011g0024 others(7): Show |
10 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.685-1461G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834368 | |||||||
| chr12:68834381 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.685-1448G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834381 | |||||||
| chr12:68834398 | T | C | 6 | a0001c0002t0006g0034 a0001c0002t0006g0035 a0001c0002t0008g0012 others(3): Show |
8 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.685-1431T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834398 | |||||||
| chr12:68834414 | C | T | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.685-1415C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834414 | |||||||
| chr12:68834450 | A | G | 3 | a0001c0003t0026g0132 a0001c0003t0026g0133 a0001c0003t0043g0131 |
3 | HG00741.hp2 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.685-1379A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834450 | |||||||
| chr12:68834457 | C | G | 1 | a0001c0001t0002g0055 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.685-1372C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834457 | |||||||
| chr12:68834601 | G | A | 7 | a0001c0001t0002g0087 a0001c0001t0004g0009 a0001c0001t0004g0052 others(4): Show |
10 | HG00408.hp1 HG01099.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.685-1228G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834601 | |||||||
| chr12:68834708 | G | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(73): Show |
100 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.685-1121G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834708 | |||||||
| chr12:68834837 | A | G | 2 | a0001c0001t0009g0137 a0001c0001t0009g0141 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.685-992A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834837 | |||||||
| chr12:68834930 | T | C | 1 | a0001c0001t0002g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.685-899T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68834930 | |||||||
| chr12:68835011 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.685-818A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835011 | |||||||
| chr12:68835072 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.685-757A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835072 | |||||||
| chr12:68835101 | C | T | 1 | a0001c0001t0003g0211 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.685-728C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835101 | |||||||
| chr12:68835112 | C | T | 1 | a0001c0001t0058g0209 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.685-717C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835112 | |||||||
| chr12:68835201 | C | T | 1 | a0001c0001t0067g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-628C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835201 | |||||||
| chr12:68835251 | A | G | 1 | a0001c0001t0019g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.685-578A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835251 | |||||||
| chr12:68835307 | G | T | 1 | a0001c0001t0001g0272 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.685-522G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835307 | |||||||
| chr12:68835343 | A | G | 39 | a0001c0001t0016g0013 a0001c0001t0016g0185 a0001c0001t0016g0189 others(36): Show |
43 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.685-486A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835343 | |||||||
| chr12:68835408 | C | T | 1 | a0001c0001t0030g0039 | 2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.685-421C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835408 | |||||||
| chr12:68835448 | T | A | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-381T>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835448 | |||||||
| chr12:68835628 | A | G | 4 | a0001c0001t0009g0134 a0001c0001t0009g0138 a0001c0001t0009g0139 others(1): Show |
4 | HG00639.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-201A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835628 | |||||||
| chr12:68835637 | G | A | 7 | a0001c0001t0035g0029 a0001c0001t0035g0149 a0001c0001t0062g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-192G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835637 | |||||||
| chr12:68835647 | G | T | 1 | a0001c0001t0048g0192 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.685-182G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 8/10 | chr12 | 68835647 | |||||||
| chr12:68836213 | G | T | 1 | a0001c0001t0002g0099 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.840+229G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 9/10 | chr12 | 68836213 | |||||||
| chr12:68836252 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.840+268A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 9/10 | chr12 | 68836252 | |||||||
| chr12:68836263 | C | A | 1 | a0001c0001t0022g0031 | 2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.840+279C>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 9/10 | chr12 | 68836263 | |||||||
| chr12:68836409 | G | T | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(231): Show |
293 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.841-263G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 9/10 | chr12 | 68836409 | |||||||
| chr12:68836517 | T | G | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.841-155T>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 9/10 | chr12 | 68836517 | |||||||
| chr12:68836955 | C | CT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(74): Show |
102 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.918+224dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 68836955 | ||||||
| chr12:68836955 | CT | C | 24 | a0001c0001t0002g0094 a0001c0001t0003g0198 a0001c0001t0012g0007 others(21): Show |
30 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.918+224delT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 68836955 | ||||||
| chr12:68837061 | C | G | 4 | a0001c0001t0016g0189 a0001c0001t0020g0177 a0001c0001t0020g0186 others(1): Show |
4 | HG02257.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+312C>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837061 | |||||||
| chr12:68837088 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.918+339G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837088 | |||||||
| chr12:68837089 | A | G | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.918+340A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837089 | |||||||
| chr12:68837097 | G | T | 113 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(110): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.918+348G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837097 | |||||||
| chr12:68837143 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.918+394G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837143 | |||||||
| chr12:68837274 | T | C | 1 | a0001c0002t0008g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.918+525T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837274 | |||||||
| chr12:68837334 | A | G | 1 | a0001c0001t0018g0203 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.918+585A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837334 | |||||||
| chr12:68837450 | C | T | 2 | a0001c0001t0069g0145 a0001c0001t0070g0151 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.918+701C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837450 | |||||||
| chr12:68837854 | A | AT | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(148): Show |
188 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.918+1111dupT | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 68837854 | ||||||
| chr12:68837934 | T | C | 2 | a0001c0001t0021g0038 a0001c0001t0021g0188 |
3 | HG01516.hp1 HG01517.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.918+1185T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68837934 | |||||||
| chr12:68838010 | T | C | 2 | a0001c0003t0026g0132 a0001c0003t0026g0133 |
2 | HG00741.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.918+1261T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838010 | |||||||
| chr12:68838200 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(70): Show |
97 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.919-1074G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838200 | |||||||
| chr12:68838219 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
2 | HG01978.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.919-1055G>A | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838219 | |||||||
| chr12:68838290 | A | G | 9 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(6): Show |
14 | HG01069.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.919-984A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838290 | |||||||
| chr12:68838354 | T | C | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.919-920T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838354 | |||||||
| chr12:68838460 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.919-814C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838460 | |||||||
| chr12:68838533 | G | T | 1 | a0001c0001t0002g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.919-741G>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838533 | |||||||
| chr12:68838621 | G | C | 2 | a0001c0001t0002g0129 a0001c0001t0002g0130 |
2 | HG02135.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.919-653G>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838621 | |||||||
| chr12:68838726 | C | T | 3 | a0001c0001t0024g0040 a0001c0001t0024g0190 a0001c0001t0040g0040 |
3 | HG02723.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.919-548C>T | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838726 | |||||||
| chr12:68838729 | T | C | 2 | a0001c0001t0029g0164 a0001c0001t0029g0165 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.919-545T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838729 | |||||||
| chr12:68838806 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.919-468A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838806 | |||||||
| chr12:68838896 | G | GTTACATA others(7): Show |
14 | a0001c0001t0009g0028 a0001c0001t0009g0134 a0001c0001t0009g0137 others(11): Show |
15 | HG00639.hp2 HG01361.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.919-374_919-361dup others(14): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 68838896 | ||||||
| chr12:68838932 | A | G | 2 | a0001c0001t0009g0139 a0001c0001t0027g0135 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.919-342A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68838932 | |||||||
| chr12:68839013 | A | G | 31 | a0001c0002t0006g0033 a0001c0002t0006g0034 a0001c0002t0006g0035 others(28): Show |
34 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.919-261A>G | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68839013 | |||||||
| chr12:68839099 | ATAAC | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0014 others(87): Show |
115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.919-168_919-165del others(4): Show |
MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr12 | 68839099 | ||||||
| chr12:68839126 | T | C | 19 | a0001c0001t0012g0007 a0001c0001t0012g0166 a0001c0001t0013g0030 others(16): Show |
25 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.919-148T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68839126 | |||||||
| chr12:68839263 | T | C | 1 | a0001c0001t0004g0052 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.919-11T>C | MDM2 | ENSG00000135679.27 | transcript | ENST00000258149.11 | protein_coding | 10/10 | chr12 | 68839263 |