Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8091 |
| ensemblid | ENSG00000149948.14 |
| hgncid | 5009 |
| symbol | HMGA2 |
| name | high mobility group AT-hook 2 |
| refseq_nuc | NM_003483.6 |
| refseq_prot | NP_003474.1 |
| ensembl_nuc | ENST00000403681.7 |
| ensembl_prot | ENSP00000384026.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 65824483 |
| end | 65966291 |
| strand | + |
| ver | v1.2 |
| region | chr12:65824483-65966291 |
| region5000 | chr12:65819483-65971291 |
| regionname0 | HMGA2_chr12_65824483_65966291 |
| regionname5000 | HMGA2_chr12_65819483_65971291 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 109 | 235 | 64 | 36 | 95 | 8 | 30 | 70 | HMGA2_chr12_65819483_65971291 | HMGA2 | MSARG others(104): Show |
chr12 | 65819483 | 65971291 |
| a0002 | 0/0 | 109 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | MSARG others(104): Show |
chr12 | 65819483 | 65971291 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 327 | 235 | 64 | 36 | 95 | 8 | 30 | HMGA2_chr12_65819483_65971291 | HMGA2 | ATGAG others(322): Show |
chr12 | 65819483 | 65971291 | ||
| a0002c0002 | 0/0 | 327 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | ATGAG others(322): Show |
chr12 | 65819483 | 65971291 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4115 | 29 | 2 | 2 | 23 | 1 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0002 | 0/0 | 4116 | 19 | 1 | 3 | 14 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0003 | 1/0 | 4117 | 15 | 4 | 1 | 3 | 4 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0004 | 0/0 | 4115 | 14 | 0 | 1 | 9 | 0 | 4 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0005 | 0/0 | 4116 | 12 | 4 | 1 | 6 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0006 | 0/0 | 4115 | 10 | 1 | 5 | 0 | 1 | 3 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0007 | 0/0 | 4118 | 9 | 1 | 5 | 1 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0008 | 0/0 | 4117 | 9 | 1 | 0 | 5 | 0 | 3 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0009 | 0/0 | 4115 | 7 | 1 | 0 | 4 | 0 | 2 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0010 | 0/0 | 4119 | 7 | 4 | 2 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4114): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0011 | 0/0 | 4116 | 6 | 1 | 1 | 1 | 0 | 3 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0012 | 0/0 | 4116 | 6 | 1 | 0 | 4 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0013 | 0/0 | 4117 | 6 | 2 | 0 | 4 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0014 | 0/0 | 4117 | 5 | 0 | 3 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0015 | 0/0 | 4117 | 4 | 3 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0016 | 0/0 | 4117 | 4 | 2 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0017 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0018 | 0/0 | 4120 | 3 | 0 | 2 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4115): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0019 | 0/0 | 4116 | 2 | 0 | 2 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0020 | 0/0 | 4115 | 2 | 0 | 2 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0021 | 0/0 | 4118 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0022 | 0/0 | 4118 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0023 | 0/0 | 4117 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0024 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0025 | 0/0 | 4118 | 2 | 2 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0026 | 0/0 | 4119 | 2 | 0 | 0 | 2 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4114): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0027 | 0/0 | 4118 | 2 | 1 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0028 | 0/0 | 4100 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4095): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0029 | 0/1 | 4115 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0030 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0031 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0032 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0033 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0034 | 0/0 | 4119 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4114): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0035 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0036 | 0/0 | 4115 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0037 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0038 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0039 | 0/0 | 4117 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0040 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0041 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0042 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0043 | 0/0 | 4115 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0044 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0045 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0046 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0047 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0048 | 0/0 | 4117 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0049 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0050 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4117): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0051 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0052 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0053 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0054 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0055 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0056 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0057 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0058 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0059 | 0/0 | 4118 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4113): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0060 | 0/0 | 4120 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4115): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0061 | 0/0 | 4120 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4115): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0062 | 0/0 | 4121 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0063 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4112): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0064 | 0/0 | 4122 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4117): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0065 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0066 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0067 | 0/0 | 4121 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0068 | 0/0 | 4121 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0069 | 0/0 | 4122 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4117): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0070 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4120): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0071 | 0/0 | 4121 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4116): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0072 | 0/0 | 4123 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4118): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0073 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4120): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0074 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4120): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0075 | 0/0 | 4115 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4110): Show |
chr12 | 65819483 | 65971291 |
| a0001c0001t0076 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4120): Show |
chr12 | 65819483 | 65971291 |
| a0002c0002t0002 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | AGAAA others(4111): Show |
chr12 | 65819483 | 65971291 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0124 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0009g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0011g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0013g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0014g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0014g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0014g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0014g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0014g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0016g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0016g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0016g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0018g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0018g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0019g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0019g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0020g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0020g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0021g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0021g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0022g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0024g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0024g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0025g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0026g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0026g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0027g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0027g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0028g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0029g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0030g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0031g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0032g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0033g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0034g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0035g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0036g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0037g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0038g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0039g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0040g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0041g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0042g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0043g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0044g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0045g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0046g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0047g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0048g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0049g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0050g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0051g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0052g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0053g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0054g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0055g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0056g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0057g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0058g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0059g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0060g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0061g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0062g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0063g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0064g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0065g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0066g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0067g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0068g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0069g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0070g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0071g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0072g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0073g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0074g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0075g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0001c0001t0076g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | GBR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00140 | hp2 | a0001 | c0001 | t0042 | g0121 | EUR | GBR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0234 | EUR | FIN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0118 | EUR | FIN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00423 | hp1 | a0001 | c0001 | t0015 | g0136 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00423 | hp2 | a0001 | c0001 | t0059 | g0206 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00558 | hp1 | a0001 | c0001 | t0047 | g0011 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0064 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00621 | hp1 | a0001 | c0001 | t0031 | g0195 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00673 | hp2 | a0001 | c0001 | t0028 | g0144 | EAS | CHS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00733 | hp1 | a0001 | c0001 | t0014 | g0022 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00733 | hp2 | a0001 | c0001 | t0038 | g0127 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00735 | hp2 | a0001 | c0001 | t0020 | g0162 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0231 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0083 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01069 | hp1 | a0001 | c0001 | t0020 | g0143 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01069 | hp2 | a0001 | c0001 | t0039 | g0084 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01070 | hp1 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0160 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0081 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01074 | hp2 | a0001 | c0001 | t0014 | g0017 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01167 | hp1 | a0001 | c0001 | t0069 | g0166 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0111 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01169 | hp1 | a0001 | c0001 | t0019 | g0161 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0211 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01192 | hp1 | a0001 | c0001 | t0018 | g0207 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01192 | hp2 | a0001 | c0001 | t0011 | g0027 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0175 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0213 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0214 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01261 | hp1 | a0001 | c0001 | t0062 | g0202 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01261 | hp2 | a0001 | c0001 | t0007 | g0141 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01361 | hp2 | a0001 | c0001 | t0061 | g0219 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0165 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01433 | hp2 | a0001 | c0001 | t0019 | g0117 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0208 | EUR | IBS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0235 | EUR | IBS | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01884 | hp1 | a0001 | c0001 | t0066 | g0005 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01884 | hp2 | a0001 | c0001 | t0033 | g0227 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01891 | hp1 | a0001 | c0001 | t0072 | g0006 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02027 | hp2 | a0001 | c0001 | t0075 | g0087 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0054 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0072 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0058 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02135 | hp2 | a0001 | c0001 | t0011 | g0053 | EAS | KHV | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02155 | hp1 | a0001 | c0001 | t0030 | g0134 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02155 | hp2 | a0001 | c0001 | t0071 | g0212 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02165 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02257 | hp1 | a0001 | c0001 | t0056 | g0228 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0217 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02300 | hp2 | a0001 | c0001 | t0036 | g0086 | AMR | PEL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02451 | hp2 | a0001 | c0001 | t0050 | g0218 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0171 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02615 | hp2 | a0001 | c0001 | t0060 | g0007 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02622 | hp1 | a0001 | c0001 | t0015 | g0170 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02622 | hp2 | a0001 | c0001 | t0045 | g0026 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02647 | hp1 | a0001 | c0001 | t0015 | g0044 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02647 | hp2 | a0001 | c0001 | t0067 | g0230 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0167 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02698 | hp1 | a0001 | c0001 | t0065 | g0203 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0034 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0018 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02735 | hp1 | a0001 | c0001 | t0063 | g0232 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02735 | hp2 | a0001 | c0001 | t0018 | g0209 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0041 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02809 | hp1 | a0001 | c0001 | t0011 | g0169 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02809 | hp2 | a0001 | c0001 | t0041 | g0172 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0023 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0004 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02896 | hp1 | a0001 | c0001 | t0035 | g0010 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02896 | hp2 | a0001 | c0001 | t0043 | g0002 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02922 | hp1 | a0001 | c0001 | t0027 | g0186 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02922 | hp2 | a0001 | c0001 | t0055 | g0182 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02965 | hp1 | a0001 | c0001 | t0037 | g0223 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0045 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0183 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03017 | hp1 | a0001 | c0001 | t0008 | g0035 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0147 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03041 | hp1 | a0001 | c0001 | t0046 | g0216 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0224 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03098 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03098 | hp2 | a0001 | c0001 | t0064 | g0008 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03139 | hp1 | a0001 | c0001 | t0051 | g0019 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03209 | hp1 | a0001 | c0001 | t0058 | g0181 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03209 | hp2 | a0001 | c0001 | t0054 | g0012 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0226 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03239 | hp1 | a0001 | c0001 | t0008 | g0056 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03239 | hp2 | a0001 | c0001 | t0068 | g0200 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0168 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03490 | hp2 | a0001 | c0001 | t0034 | g0149 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03540 | hp2 | a0001 | c0001 | t0024 | g0046 | AFR | GWD | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0003 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03579 | hp2 | a0001 | c0001 | t0052 | g0220 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0163 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03669 | hp2 | a0001 | c0001 | t0070 | g0210 | SAS | PJL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0036 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0159 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0040 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0031 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0184 | SAS | BEB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04204 | hp1 | a0001 | c0001 | t0073 | g0189 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0138 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0042 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0100 | SAS | STU | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18522 | hp1 | a0001 | c0001 | t0053 | g0180 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0049 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18906 | hp1 | a0001 | c0001 | t0023 | g0048 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | YRI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18941 | hp1 | a0001 | c0001 | t0009 | g0065 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18942 | hp1 | a0001 | c0001 | t0014 | g0059 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18943 | hp1 | a0001 | c0001 | t0032 | g0128 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18948 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18952 | hp1 | a0001 | c0001 | t0027 | g0191 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18953 | hp2 | a0001 | c0001 | t0013 | g0198 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18957 | hp2 | a0001 | c0001 | t0013 | g0197 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18959 | hp1 | a0001 | c0001 | t0008 | g0061 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18967 | hp2 | a0001 | c0001 | t0026 | g0199 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18970 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18970 | hp2 | a0001 | c0001 | t0016 | g0062 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18972 | hp2 | a0001 | c0001 | t0048 | g0020 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18978 | hp1 | a0001 | c0001 | t0021 | g0067 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0057 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18984 | hp1 | a0001 | c0001 | t0012 | g0015 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18988 | hp2 | a0001 | c0001 | t0016 | g0063 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18991 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19001 | hp2 | a0001 | c0001 | t0044 | g0071 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19003 | hp1 | a0001 | c0001 | t0012 | g0060 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19010 | hp1 | a0001 | c0001 | t0013 | g0222 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19030 | hp1 | a0001 | c0001 | t0049 | g0039 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19030 | hp2 | a0001 | c0001 | t0025 | g0185 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0047 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19056 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19078 | hp1 | a0001 | c0001 | t0022 | g0073 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0158 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19079 | hp2 | a0001 | c0001 | t0014 | g0068 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19080 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19083 | hp1 | a0001 | c0001 | t0026 | g0215 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19088 | hp1 | a0001 | c0001 | t0076 | g0113 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA19088 | hp2 | a0001 | c0001 | t0012 | g0014 | EAS | JPT | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0013 | AFR | ASW | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0080 | EUR | TSI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | TSI | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | GIH | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | GIH | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0188 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG02559 | hp2 | a0001 | c0001 | t0057 | g0225 | AFR | ACB | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03471 | hp1 | a0001 | c0001 | t0021 | g0043 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | MSL | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | USA | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA21309 | hp1 | a0001 | c0001 | t0024 | g0051 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| NA21309 | hp2 | a0001 | c0001 | t0074 | g0196 | AFR | LWK | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0164 | REF | REF | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0124 | REF | REF | HMGA2_chr12_65819483_65971291 | HMGA2 | chr12 | 65819483 | 65971291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:65963279 | C | G | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.317C>G | p.Ala106Gly | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1105/4117 | 317/330 | 106/109 | chr12 | 65963279 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:65824546 | C | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-725C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 725 | chr12 | 65824546 | ||||||
| chr12:65824618 | C | T | 1 | a0001c0001t0075 | 1 | HG02027.hp2 | 5_prime_UTR_variant | MODIFIER | c.-653C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 653 | chr12 | 65824618 | ||||||
| chr12:65824708 | ATCTCTTC others(8): Show |
A | 1 | a0001c0001t0028 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-557_-543delTCTCTC others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 543 | INFO_REALIGN_3_PRIME | chr12 | 65824708 | |||||
| chr12:65824713 | T | TTC | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(2): Show |
9 | HG00609.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-503_-502dupTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTC | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0036 others(2): Show |
7 | HG00735.hp1 HG01361.hp1 HG02027.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-505_-502dupTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTCTC | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 |
3 | HG00741.hp2 HG01496.hp2 HG01978.hp1 |
5_prime_UTR_variant | MODIFIER | c.-507_-502dupTCTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTCTCT others(1): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(1): Show |
8 | NA18943.hp1 NA18971.hp1 NA18978.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-509_-502dupTCTCTC others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTCTCT others(3): Show |
1 | a0001c0001t0005 | 1 | NA18994.hp2 | 5_prime_UTR_variant | MODIFIER | c.-511_-502dupTCTCTC others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTCTCT others(5): Show |
2 | a0001c0001t0003 a0001c0001t0006 |
2 | HG01258.hp1 HG01516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-513_-502dupTCTCTC others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | T | TTCTCTCT others(7): Show |
1 | a0001c0001t0003 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-515_-502dupTCTCTC others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 501 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTC | T | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
60 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-503_-502delTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTC | T | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(5): Show |
10 | HG00423.hp1 HG01169.hp1 HG01433.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-505_-502delTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTC | T | 10 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(7): Show |
20 | HG00140.hp1 HG00280.hp2 HG00621.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-507_-502delTCTCTC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(1): Show |
T | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(5): Show |
13 | HG00673.hp1 HG00741.hp1 HG01069.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-509_-502delTCTCTC others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(1): Show |
5 | HG01074.hp1 HG02165.hp2 HG03669.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-511_-502delTCTCTC others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(5): Show |
T | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(4): Show |
11 | HG00735.hp2 HG01243.hp2 HG01256.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-513_-502delTCTCTC others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(7): Show |
T | 3 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0038 |
5 | HG00733.hp2 HG02040.hp2 HG02132.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-515_-502delTCTCTC others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(9): Show |
T | 2 | a0001c0001t0001 a0001c0001t0015 |
3 | HG02615.hp1 HG02622.hp1 NA18981.hp2 |
5_prime_UTR_variant | MODIFIER | c.-517_-502delTCTCTC others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(11): Show |
T | 4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(1): Show |
4 | HG02027.hp1 HG02257.hp2 NA18942.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-519_-502delTCTCTC others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824713 | TTCTCTCT others(15): Show |
T | 5 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(2): Show |
5 | HG02896.hp1 HG03098.hp1 HG03139.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-523_-502delTCTCTC others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 502 | INFO_REALIGN_3_PRIME | chr12 | 65824713 | |||||
| chr12:65824721 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0037 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824721 | |||||
| chr12:65824723 | C | CTCTCTCT others(3): Show |
1 | a0001c0001t0033 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824723 | |||||
| chr12:65824725 | C | CTCTCTCT others(1): Show |
2 | a0001c0001t0073 a0001c0001t0074 |
2 | HG04204.hp1 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824725 | |||||
| chr12:65824727 | C | CTCTCTG | 3 | a0001c0001t0070 a0001c0001t0071 a0001c0001t0072 |
3 | HG01891.hp1 HG02155.hp2 HG03669.hp2 |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824727 | |||||
| chr12:65824729 | C | CTCTG | 6 | a0001c0001t0064 a0001c0001t0065 a0001c0001t0066 others(3): Show |
6 | HG01167.hp1 HG01884.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824729 | |||||
| chr12:65824731 | C | CTG | 10 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0018 others(7): Show |
25 | HG00423.hp2 HG01169.hp2 HG01192.hp1 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-539_-538insGT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 538 | INFO_REALIGN_3_PRIME | chr12 | 65824731 | |||||
| chr12:65824733 | C | CTCTG | 2 | a0001c0001t0050 a0001c0001t0051 |
2 | HG02451.hp2 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-535_-534insGTCT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 534 | INFO_REALIGN_3_PRIME | chr12 | 65824733 | |||||
| chr12:65824733 | C | G | 4 | a0001c0001t0017 a0001c0001t0056 a0001c0001t0057 others(1): Show |
6 | HG02257.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-538C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824733 | |||||||
| chr12:65824735 | C | CTG | 1 | a0001c0001t0024 | 2 | HG03540.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-535_-534insGT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 534 | INFO_REALIGN_3_PRIME | chr12 | 65824735 | |||||
| chr12:65824735 | C | G | 5 | a0001c0001t0025 a0001c0001t0052 a0001c0001t0053 others(2): Show |
6 | HG02922.hp2 HG02976.hp2 HG03209.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-536C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824735 | |||||||
| chr12:65824737 | C | G | 5 | a0001c0001t0014 a0001c0001t0022 a0001c0001t0023 others(2): Show |
11 | HG00733.hp1 HG01070.hp1 HG01074.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-534C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824737 | |||||||
| chr12:65824739 | C | G | 10 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(7): Show |
51 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(48): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-532C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824739 | |||||||
| chr12:65824741 | C | G | 1 | a0001c0001t0044 | 1 | NA19001.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-530C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824741 | |||||||
| chr12:65824877 | G | T | 1 | a0001c0001t0043 | 1 | HG02896.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-394G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65824877 | |||||||
| chr12:65824905 | C | T | 1 | a0001c0001t0042 | 1 | HG00140.hp2 | 5_prime_UTR_variant | MODIFIER | c.-366C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 366 | chr12 | 65824905 | ||||||
| chr12:65825019 | C | T | 1 | a0001c0001t0020 | 2 | HG00735.hp2 HG01069.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-252C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | chr12 | 65825019 | |||||||
| chr12:65825124 | G | C | 1 | a0001c0001t0030 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/5 | 147 | chr12 | 65825124 | ||||||
| chr12:65963427 | A | AG | 23 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(20): Show |
58 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*143dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 144 | INFO_REALIGN_3_PRIME | chr12 | 65963427 | |||||
| chr12:65963427 | AG | A | 7 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0017 others(4): Show |
27 | HG01243.hp1 HG02630.hp1 HG02717.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*143delG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 143 | INFO_REALIGN_3_PRIME | chr12 | 65963427 | |||||
| chr12:65963431 | G | T | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0020 others(4): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*139G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 139 | chr12 | 65963431 | ||||||
| chr12:65963786 | T | A | 1 | a0001c0001t0031 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*494T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 494 | chr12 | 65963786 | ||||||
| chr12:65964007 | A | G | 1 | a0001c0001t0041 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 715 | chr12 | 65964007 | ||||||
| chr12:65964008 | C | T | 6 | a0001c0001t0025 a0001c0001t0040 a0001c0001t0046 others(3): Show |
7 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*716C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 716 | chr12 | 65964008 | ||||||
| chr12:65964166 | A | T | 4 | a0001c0001t0018 a0001c0001t0039 a0001c0001t0069 others(1): Show |
6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*874A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 874 | chr12 | 65964166 | ||||||
| chr12:65964299 | A | AG | 6 | a0001c0001t0018 a0001c0001t0034 a0001c0001t0038 others(3): Show |
8 | HG00733.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008insG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964299 | ||||||
| chr12:65964299 | AAG | A | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0020 others(3): Show |
29 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1008_*1009delAG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964299 | ||||||
| chr12:65964300 | A | G | 7 | a0001c0001t0018 a0001c0001t0034 a0001c0001t0038 others(4): Show |
9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1008A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1008 | chr12 | 65964300 | ||||||
| chr12:65964339 | CTT | C | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(16): Show |
82 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1048_*1049delTT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1048 | chr12 | 65964339 | ||||||
| chr12:65964467 | T | G | 1 | a0001c0001t0065 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1175 | chr12 | 65964467 | ||||||
| chr12:65964567 | C | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
135 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1275C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1275 | chr12 | 65964567 | ||||||
| chr12:65964750 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1458A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1458 | chr12 | 65964750 | ||||||
| chr12:65964760 | T | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1468T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1468 | chr12 | 65964760 | ||||||
| chr12:65964762 | C | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1470C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1470 | chr12 | 65964762 | ||||||
| chr12:65964765 | G | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1473G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1473 | chr12 | 65964765 | ||||||
| chr12:65964774 | T | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1482T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1482 | chr12 | 65964774 | ||||||
| chr12:65964791 | C | A | 1 | a0001c0001t0019 | 2 | HG01169.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1499C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1499 | chr12 | 65964791 | ||||||
| chr12:65964800 | G | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1508 | chr12 | 65964800 | ||||||
| chr12:65964801 | A | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1509 | chr12 | 65964801 | ||||||
| chr12:65964871 | A | T | 1 | a0001c0001t0036 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1579A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1579 | chr12 | 65964871 | ||||||
| chr12:65964962 | A | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1670A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1670 | chr12 | 65964962 | ||||||
| chr12:65964963 | C | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1671 | chr12 | 65964963 | ||||||
| chr12:65964964 | C | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1672 | chr12 | 65964964 | ||||||
| chr12:65964966 | C | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1674C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1674 | chr12 | 65964966 | ||||||
| chr12:65964967 | C | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1675 | chr12 | 65964967 | ||||||
| chr12:65964969 | G | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1677 | chr12 | 65964969 | ||||||
| chr12:65964971 | C | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1679 | chr12 | 65964971 | ||||||
| chr12:65964976 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1684A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1684 | chr12 | 65964976 | ||||||
| chr12:65964977 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1685 | chr12 | 65964977 | ||||||
| chr12:65964978 | A | C | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1686 | chr12 | 65964978 | ||||||
| chr12:65964979 | G | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1687G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1687 | chr12 | 65964979 | ||||||
| chr12:65964981 | A | C | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1689A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1689 | chr12 | 65964981 | ||||||
| chr12:65964982 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1690A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1690 | chr12 | 65964982 | ||||||
| chr12:65964991 | T | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1699T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1699 | chr12 | 65964991 | ||||||
| chr12:65965051 | T | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1759 | chr12 | 65965051 | ||||||
| chr12:65965058 | A | C | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1766A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1766 | chr12 | 65965058 | ||||||
| chr12:65965066 | T | G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1774 | chr12 | 65965066 | ||||||
| chr12:65965121 | GTAAATAA others(19): Show |
G | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1830_*1855delTAAA others(22): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1830 | chr12 | 65965121 | ||||||
| chr12:65965148 | C | T | 1 | a0001c0001t0068 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1856 | chr12 | 65965148 | ||||||
| chr12:65965152 | C | CTTCTAGG others(29): Show |
1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1860_*1861insTTCT others(32): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1861 | chr12 | 65965152 | ||||||
| chr12:65965153 | A | C | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1861 | chr12 | 65965153 | ||||||
| chr12:65965180 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1888A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1888 | chr12 | 65965180 | ||||||
| chr12:65965187 | A | G | 1 | a0001c0001t0047 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1895A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1895 | chr12 | 65965187 | ||||||
| chr12:65965228 | T | C | 1 | a0001c0001t0040 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1936T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1936 | chr12 | 65965228 | ||||||
| chr12:65965274 | A | T | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1982 | chr12 | 65965274 | ||||||
| chr12:65965275 | T | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1983T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1983 | chr12 | 65965275 | ||||||
| chr12:65965276 | T | A | 1 | a0001c0001t0076 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1984T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 1984 | chr12 | 65965276 | ||||||
| chr12:65965403 | C | T | 1 | a0001c0001t0032 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2111C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2111 | chr12 | 65965403 | ||||||
| chr12:65965594 | A | G | 1 | a0001c0001t0035 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2302A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2302 | chr12 | 65965594 | ||||||
| chr12:65965964 | C | T | 4 | a0001c0001t0025 a0001c0001t0040 a0001c0001t0055 others(1): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2672C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2672 | chr12 | 65965964 | ||||||
| chr12:65965972 | C | A | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(55): Show |
175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*2680C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2680 | chr12 | 65965972 | ||||||
| chr12:65966128 | T | C | 1 | a0001c0001t0033 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2836T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2836 | chr12 | 65966128 | ||||||
| chr12:65966288 | C | T | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(16): Show |
82 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2996C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 5/5 | 2996 | chr12 | 65966288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:65825466 | G | A | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.111+85G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825466 | |||||||
| chr12:65825466 | G | C | 7 | a0001c0001t0010g0009 a0001c0001t0013g0003 a0001c0001t0013g0004 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.111+85G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825466 | |||||||
| chr12:65825519 | C | G | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | HG00280.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.111+138C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825519 | |||||||
| chr12:65825596 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.111+215C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65825596 | |||||||
| chr12:65826042 | G | T | 2 | a0001c0001t0007g0231 a0001c0001t0063g0232 |
2 | HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.111+661G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826042 | |||||||
| chr12:65826045 | G | A | 1 | a0001c0001t0035g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.111+664G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826045 | |||||||
| chr12:65826052 | G | C | 1 | a0001c0001t0007g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+671G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826052 | |||||||
| chr12:65826143 | T | A | 1 | a0001c0001t0047g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.111+762T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826143 | |||||||
| chr12:65826364 | G | C | 1 | a0001c0001t0007g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.111+983G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826364 | |||||||
| chr12:65826485 | A | C | 1 | a0001c0001t0067g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.111+1104A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826485 | |||||||
| chr12:65826486 | T | C | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.111+1105T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826486 | |||||||
| chr12:65826568 | T | C | 2 | a0001c0001t0012g0014 a0001c0001t0012g0015 |
2 | NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.111+1187T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826568 | |||||||
| chr12:65826660 | T | C | 1 | a0001c0001t0003g0016 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.111+1279T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826660 | |||||||
| chr12:65826686 | T | C | 3 | a0001c0001t0014g0017 a0001c0001t0022g0018 a0001c0001t0051g0019 |
3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.111+1305T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826686 | |||||||
| chr12:65826727 | C | T | 1 | a0001c0001t0005g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112-1274C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826727 | |||||||
| chr12:65826754 | T | C | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-1247T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65826754 | |||||||
| chr12:65826780 | C | CA | 10 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0006g0078 others(7): Show |
10 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-1205dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | ||||||
| chr12:65826780 | CA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(63): Show |
66 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.112-1205delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | ||||||
| chr12:65826780 | CAA | C | 13 | a0001c0001t0005g0221 a0001c0001t0013g0222 a0001c0001t0017g0013 others(10): Show |
13 | HG01361.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.112-1206_112-1205d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65826780 | ||||||
| chr12:65827029 | C | T | 1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112-972C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827029 | |||||||
| chr12:65827208 | C | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.112-793C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827208 | |||||||
| chr12:65827241 | C | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.112-760C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827241 | |||||||
| chr12:65827247 | T | G | 10 | a0001c0001t0010g0009 a0001c0001t0013g0003 a0001c0001t0013g0004 others(7): Show |
10 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.112-754T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827247 | |||||||
| chr12:65827280 | A | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(60): Show |
63 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-721A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827280 | |||||||
| chr12:65827282 | A | G | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-719A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827282 | |||||||
| chr12:65827484 | T | C | 1 | a0001c0001t0036g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.112-517T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827484 | |||||||
| chr12:65827540 | T | TAC | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.112-460_112-459ins others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr12 | 65827540 | ||||||
| chr12:65827666 | G | C | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.112-335G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827666 | |||||||
| chr12:65827674 | A | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.112-327A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827674 | |||||||
| chr12:65827928 | T | C | 1 | a0001c0001t0053g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.112-73T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827928 | |||||||
| chr12:65827952 | C | A | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.112-49C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 1/4 | chr12 | 65827952 | |||||||
| chr12:65828238 | C | T | 1 | a0001c0001t0007g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.198+151C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828238 | |||||||
| chr12:65828331 | T | A | 1 | a0001c0001t0067g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.198+244T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828331 | |||||||
| chr12:65828370 | T | TG | 4 | a0001c0001t0008g0167 a0001c0001t0010g0009 a0001c0001t0026g0215 others(1): Show |
4 | HG02683.hp1 HG03098.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+284dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828370 | ||||||
| chr12:65828370 | T | TGG | 4 | a0001c0001t0009g0168 a0001c0001t0011g0169 a0001c0001t0046g0216 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+284_198+285ins others(2): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828370 | ||||||
| chr12:65828371 | GC | G | 7 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0033g0227 others(4): Show |
7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+285delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828371 | |||||||
| chr12:65828372 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(115): Show |
118 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.198+285C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828372 | |||||||
| chr12:65828373 | G | GGGGC | 59 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.198+289_198+290ins others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65828373 | ||||||
| chr12:65828786 | T | G | 1 | a0001c0001t0075g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198+699T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828786 | |||||||
| chr12:65828978 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.198+891T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65828978 | |||||||
| chr12:65829238 | C | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+1151C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829238 | |||||||
| chr12:65829368 | G | A | 1 | a0001c0001t0005g0088 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.198+1281G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829368 | |||||||
| chr12:65829404 | T | A | 3 | a0001c0001t0025g0183 a0001c0001t0055g0182 a0001c0001t0058g0181 |
3 | HG02922.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.198+1317T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829404 | |||||||
| chr12:65829525 | T | G | 13 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+1438T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829525 | |||||||
| chr12:65829766 | T | C | 13 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+1679T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829766 | |||||||
| chr12:65829938 | C | T | 1 | a0001c0001t0008g0069 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.198+1851C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829938 | |||||||
| chr12:65829939 | G | A | 1 | a0001c0001t0011g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.198+1852G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65829939 | |||||||
| chr12:65830681 | A | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(17): Show |
20 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.198+2594A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830681 | |||||||
| chr12:65830765 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+2678A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830765 | |||||||
| chr12:65830968 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.198+2881G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65830968 | |||||||
| chr12:65831060 | A | T | 1 | a0001c0001t0007g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.198+2973A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831060 | |||||||
| chr12:65831186 | C | T | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198+3099C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831186 | |||||||
| chr12:65831224 | T | A | 3 | a0001c0001t0003g0016 a0001c0001t0006g0090 a0001c0001t0007g0165 |
3 | HG01433.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.198+3137T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831224 | |||||||
| chr12:65831408 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(119): Show |
122 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.198+3328dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65831408 | ||||||
| chr12:65831455 | TA | T | 5 | a0001c0001t0006g0159 a0001c0001t0006g0160 a0001c0001t0019g0161 others(2): Show |
5 | HG00735.hp2 HG01070.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+3378delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65831455 | ||||||
| chr12:65831458 | A | G | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.198+3371A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831458 | |||||||
| chr12:65831485 | C | A | 3 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0027g0186 |
3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.198+3398C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831485 | |||||||
| chr12:65831553 | A | G | 66 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(63): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.198+3466A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831553 | |||||||
| chr12:65831749 | C | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(35): Show |
38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+3662C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65831749 | |||||||
| chr12:65832305 | C | T | 1 | a0001c0001t0007g0158 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.198+4218C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65832305 | |||||||
| chr12:65832461 | A | G | 8 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG00673.hp1 HG02074.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+4374A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65832461 | |||||||
| chr12:65833314 | G | A | 1 | a0001c0001t0016g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-5205G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833314 | |||||||
| chr12:65833413 | GT | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(130): Show |
133 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.199-5092delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65833413 | ||||||
| chr12:65833460 | G | T | 1 | a0001c0001t0006g0078 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-5059G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833460 | |||||||
| chr12:65833477 | C | T | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-5042C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833477 | |||||||
| chr12:65833531 | C | T | 1 | a0001c0001t0034g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.199-4988C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833531 | |||||||
| chr12:65833544 | C | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-4975C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833544 | |||||||
| chr12:65833609 | C | G | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.199-4910C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833609 | |||||||
| chr12:65833613 | G | A | 13 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-4906G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833613 | |||||||
| chr12:65833699 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0070 |
2 | HG00609.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.199-4820T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833699 | |||||||
| chr12:65833809 | A | C | 2 | a0001c0001t0010g0213 a0001c0001t0010g0214 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.199-4710A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833809 | |||||||
| chr12:65833810 | C | T | 1 | a0001c0001t0014g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.199-4709C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833810 | |||||||
| chr12:65833902 | G | C | 2 | a0001c0001t0015g0170 a0001c0001t0015g0171 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.199-4617G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65833902 | |||||||
| chr12:65834022 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0002g0092 |
2 | NA18951.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.199-4497T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834022 | |||||||
| chr12:65834065 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.199-4454T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834065 | |||||||
| chr12:65834140 | C | T | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-4379C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834140 | |||||||
| chr12:65834148 | C | G | 3 | a0001c0001t0052g0220 a0001c0001t0061g0219 a0001c0001t0067g0230 |
3 | HG01361.hp2 HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.199-4371C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834148 | |||||||
| chr12:65834162 | G | A | 1 | a0001c0001t0014g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199-4357G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834162 | |||||||
| chr12:65834169 | A | G | 1 | a0001c0001t0012g0055 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.199-4350A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834169 | |||||||
| chr12:65834243 | G | A | 3 | a0001c0001t0008g0056 a0001c0001t0014g0021 a0001c0001t0014g0022 |
3 | HG00733.hp1 HG01070.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.199-4276G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834243 | |||||||
| chr12:65834279 | A | C | 67 | a0001c0001t0001g0075 a0001c0001t0001g0148 a0001c0001t0002g0146 others(64): Show |
67 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.199-4240A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834279 | |||||||
| chr12:65834312 | T | A | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-4207T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834312 | |||||||
| chr12:65834531 | CTCCT | C | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-3982_199-3979d others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65834531 | ||||||
| chr12:65834887 | G | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-3632G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65834887 | |||||||
| chr12:65835052 | C | T | 1 | a0001c0001t0002g0145 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.199-3467C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65835052 | |||||||
| chr12:65835628 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0070 |
2 | HG00609.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.199-2891C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65835628 | |||||||
| chr12:65836074 | G | A | 1 | a0001c0001t0004g0025 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-2445G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836074 | |||||||
| chr12:65836142 | G | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.199-2377G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836142 | |||||||
| chr12:65836156 | G | C | 1 | a0001c0001t0004g0025 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-2363G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836156 | |||||||
| chr12:65836175 | T | C | 4 | a0001c0001t0017g0013 a0001c0001t0040g0217 a0001c0001t0046g0216 others(1): Show |
4 | HG02258.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2344T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836175 | |||||||
| chr12:65836187 | G | C | 1 | a0001c0001t0002g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-2332G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836187 | |||||||
| chr12:65836228 | A | G | 5 | a0001c0001t0001g0085 a0001c0001t0008g0066 a0001c0001t0009g0065 others(2): Show |
5 | NA18941.hp1 NA18951.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2291A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836228 | |||||||
| chr12:65836276 | G | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-2243G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836276 | |||||||
| chr12:65836304 | A | C | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.199-2215A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836304 | |||||||
| chr12:65836364 | GA | G | 80 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0002g0176 others(77): Show |
80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.199-2140delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65836364 | ||||||
| chr12:65836375 | A | G | 1 | a0001c0001t0028g0144 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.199-2144A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836375 | |||||||
| chr12:65836376 | A | G | 2 | a0001c0001t0020g0143 a0001c0001t0020g0162 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.199-2143A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836376 | |||||||
| chr12:65836390 | C | T | 1 | a0001c0001t0004g0052 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199-2129C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836390 | |||||||
| chr12:65836686 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.199-1833G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836686 | |||||||
| chr12:65836699 | C | T | 8 | a0001c0001t0010g0009 a0001c0001t0052g0220 a0001c0001t0060g0007 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-1820C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65836699 | |||||||
| chr12:65837196 | T | C | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.199-1323T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837196 | |||||||
| chr12:65837344 | C | A | 2 | a0001c0001t0001g0075 a0001c0001t0009g0074 |
2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.199-1175C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837344 | |||||||
| chr12:65837389 | G | C | 1 | a0001c0001t0005g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.199-1130G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837389 | |||||||
| chr12:65837585 | C | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-934C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837585 | |||||||
| chr12:65837846 | T | C | 84 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(81): Show |
84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.199-673T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65837846 | |||||||
| chr12:65838393 | C | A | 2 | a0001c0001t0008g0057 a0001c0001t0008g0058 |
2 | HG02132.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.199-126C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838393 | |||||||
| chr12:65838393 | CA | C | 85 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0142 others(82): Show |
85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.199-113delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr12 | 65838393 | ||||||
| chr12:65838394 | A | C | 2 | a0001c0001t0008g0057 a0001c0001t0008g0058 |
2 | HG02132.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.199-125A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838394 | |||||||
| chr12:65838398 | A | C | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-121A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838398 | |||||||
| chr12:65838511 | A | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.199-8A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 2/4 | chr12 | 65838511 | |||||||
| chr12:65838575 | T | A | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
splice_region_variant&intron_variant | LOW | c.249+6T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838575 | |||||||
| chr12:65838598 | T | C | 13 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+29T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838598 | |||||||
| chr12:65838603 | T | TG | 38 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(35): Show |
38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.249+34_249+35insG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838603 | |||||||
| chr12:65838648 | G | A | 3 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0075g0087 |
3 | HG02027.hp2 NA18991.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.249+79G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838648 | |||||||
| chr12:65838962 | C | T | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+393C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838962 | |||||||
| chr12:65838985 | TC | T | 3 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0027g0186 |
3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.249+417delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838985 | |||||||
| chr12:65838986 | C | T | 1 | a0001c0001t0011g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.249+417C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838986 | |||||||
| chr12:65838992 | C | T | 4 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0011g0169 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+423C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838992 | |||||||
| chr12:65838998 | C | CT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00621.hp2 HG02300.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+441dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0014g0059 a0001c0001t0041g0172 a0001c0001t0058g0181 |
3 | HG02809.hp2 HG03209.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.249+430_249+441dup others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(6): Show |
72 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(69): Show |
72 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(7): Show |
15 | a0001c0001t0003g0233 a0001c0001t0007g0178 a0001c0001t0008g0057 others(12): Show |
15 | HG00558.hp1 HG00558.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(8): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(27): Show |
30 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+441_249+442ins others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0071g0212 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.249+441_249+442ins others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+441_249+442ins others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65838998 | C | T | 4 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0011g0169 others(1): Show |
4 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+429C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65838998 | |||||||
| chr12:65838998 | CT | C | 7 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0061g0219 others(4): Show |
7 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+441delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65838998 | ||||||
| chr12:65839030 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(123): Show |
126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.249+461G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839030 | |||||||
| chr12:65839344 | A | G | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+775A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839344 | |||||||
| chr12:65839445 | T | C | 1 | a0001c0001t0011g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+876T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839445 | |||||||
| chr12:65839474 | A | AT | 7 | a0001c0001t0001g0148 a0001c0001t0002g0146 a0001c0001t0003g0137 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+915dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65839474 | ||||||
| chr12:65839637 | G | T | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+1068G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839637 | |||||||
| chr12:65839752 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+1183A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839752 | |||||||
| chr12:65839995 | G | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+1426G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65839995 | |||||||
| chr12:65840329 | G | T | 1 | a0001c0001t0004g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.249+1760G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840329 | |||||||
| chr12:65840343 | G | C | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+1774G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840343 | |||||||
| chr12:65840480 | A | G | 1 | a0001c0001t0015g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.249+1911A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840480 | |||||||
| chr12:65840746 | A | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2177A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840746 | |||||||
| chr12:65840747 | T | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2178T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840747 | |||||||
| chr12:65840937 | G | A | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+2368G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840937 | |||||||
| chr12:65840977 | C | G | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+2408C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840977 | |||||||
| chr12:65840978 | G | A | 84 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(81): Show |
84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.249+2409G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65840978 | |||||||
| chr12:65841008 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.249+2439C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841008 | |||||||
| chr12:65841663 | C | T | 1 | a0001c0001t0017g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+3094C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841663 | |||||||
| chr12:65841684 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(34): Show |
37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+3115T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841684 | |||||||
| chr12:65841961 | A | G | 2 | a0001c0001t0063g0232 a0001c0001t0073g0189 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.249+3392A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65841961 | |||||||
| chr12:65842220 | G | T | 1 | a0001c0001t0036g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.249+3651G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842220 | |||||||
| chr12:65842328 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+3759T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842328 | |||||||
| chr12:65842533 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.249+3964G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842533 | |||||||
| chr12:65842650 | G | A | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+4081G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842650 | |||||||
| chr12:65842651 | T | G | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+4082T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842651 | |||||||
| chr12:65842663 | G | C | 1 | a0001c0001t0009g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+4094G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842663 | |||||||
| chr12:65842763 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+4194T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842763 | |||||||
| chr12:65842794 | T | A | 1 | a0001c0001t0037g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.249+4225T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842794 | |||||||
| chr12:65842955 | T | C | 84 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(81): Show |
84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.249+4386T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65842955 | |||||||
| chr12:65843009 | T | A | 1 | a0001c0001t0014g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.249+4440T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843009 | |||||||
| chr12:65843369 | G | A | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+4800G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843369 | |||||||
| chr12:65843380 | A | T | 2 | a0001c0001t0063g0232 a0001c0001t0073g0189 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.249+4811A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843380 | |||||||
| chr12:65843630 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(34): Show |
37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+5061T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65843630 | |||||||
| chr12:65843665 | T | TAC | 20 | a0001c0001t0001g0095 a0001c0001t0002g0135 a0001c0001t0005g0088 others(17): Show |
20 | HG01361.hp2 HG02027.hp2 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+5128_249+5129d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | ||||||
| chr12:65843665 | TAC | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0096 others(64): Show |
67 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.249+5128_249+5129d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | ||||||
| chr12:65843665 | TACAC | T | 22 | a0001c0001t0001g0093 a0001c0001t0001g0150 a0001c0001t0008g0056 others(19): Show |
22 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+5126_249+5129d others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | ||||||
| chr12:65843665 | TACACAC | T | 28 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(25): Show |
28 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.249+5124_249+5129d others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843665 | ||||||
| chr12:65843682 | A | ACACACAC others(5): Show |
1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+5123_249+5124i others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65843682 | ||||||
| chr12:65844026 | G | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+5457G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844026 | |||||||
| chr12:65844050 | C | CA | 26 | a0001c0001t0007g0158 a0001c0001t0008g0167 a0001c0001t0009g0168 others(23): Show |
26 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+5500dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | ||||||
| chr12:65844050 | C | CAA | 12 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+5499_249+5500d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | ||||||
| chr12:65844050 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0093 others(98): Show |
101 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.249+5500delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65844050 | ||||||
| chr12:65844069 | A | G | 6 | a0001c0001t0010g0208 a0001c0001t0018g0207 a0001c0001t0018g0209 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+5500A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844069 | |||||||
| chr12:65844407 | T | A | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+5838T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844407 | |||||||
| chr12:65844473 | C | G | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+5904C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844473 | |||||||
| chr12:65844935 | A | C | 1 | a0001c0001t0072g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.249+6366A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65844935 | |||||||
| chr12:65845037 | T | A | 1 | a0001c0001t0006g0078 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.249+6468T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845037 | |||||||
| chr12:65845044 | A | G | 3 | a0001c0001t0010g0187 a0001c0001t0010g0188 a0001c0001t0027g0186 |
3 | HG02559.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.249+6475A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845044 | |||||||
| chr12:65845195 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.249+6626T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845195 | |||||||
| chr12:65845272 | C | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(34): Show |
37 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.249+6703C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845272 | |||||||
| chr12:65845284 | T | A | 2 | a0001c0001t0002g0140 a0001c0001t0036g0086 |
2 | HG02300.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.249+6715T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845284 | |||||||
| chr12:65845331 | A | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0139 others(124): Show |
127 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.249+6762A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845331 | |||||||
| chr12:65845499 | C | A | 1 | a0001c0001t0004g0028 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.249+6930C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845499 | |||||||
| chr12:65845505 | G | A | 86 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0002g0176 others(83): Show |
86 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.249+6936G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845505 | |||||||
| chr12:65845538 | G | A | 1 | a0001c0001t0014g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.249+6969G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845538 | |||||||
| chr12:65845554 | TCAC | T | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+6989_249+6991d others(5): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65845554 | ||||||
| chr12:65845575 | A | AT | 59 | a0001c0001t0001g0139 a0001c0001t0004g0024 a0001c0001t0004g0025 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+7014dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65845575 | ||||||
| chr12:65845583 | T | A | 2 | a0001c0001t0002g0099 a0001c0001t0005g0094 |
2 | NA18942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.249+7014T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845583 | |||||||
| chr12:65845584 | A | T | 1 | a0001c0001t0063g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+7015A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845584 | |||||||
| chr12:65845754 | C | T | 7 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(4): Show |
7 | HG02258.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+7185C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845754 | |||||||
| chr12:65845793 | C | G | 1 | a0001c0001t0017g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+7224C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845793 | |||||||
| chr12:65845861 | G | C | 85 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(82): Show |
85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.249+7292G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845861 | |||||||
| chr12:65845937 | C | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(123): Show |
126 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.249+7368C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845937 | |||||||
| chr12:65845944 | C | G | 3 | a0001c0001t0008g0069 a0001c0001t0009g0076 a0001c0001t0012g0049 |
3 | HG02451.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.249+7375C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845944 | |||||||
| chr12:65845982 | C | T | 8 | a0001c0001t0010g0009 a0001c0001t0052g0220 a0001c0001t0060g0007 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+7413C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65845982 | |||||||
| chr12:65846090 | C | T | 85 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(82): Show |
85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.249+7521C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846090 | |||||||
| chr12:65846094 | A | G | 88 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(85): Show |
88 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.249+7525A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846094 | |||||||
| chr12:65846105 | C | A | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+7536C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846105 | |||||||
| chr12:65846275 | C | T | 1 | a0001c0001t0059g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.249+7706C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846275 | |||||||
| chr12:65846352 | T | C | 1 | a0001c0001t0007g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+7783T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846352 | |||||||
| chr12:65846562 | G | A | 3 | a0001c0001t0015g0044 a0001c0001t0024g0046 a0001c0001t0024g0051 |
3 | HG02647.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.249+7993G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846562 | |||||||
| chr12:65846809 | G | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+8240G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846809 | |||||||
| chr12:65846994 | T | C | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+8425T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65846994 | |||||||
| chr12:65847311 | G | A | 1 | a0001c0001t0060g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.249+8742G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847311 | |||||||
| chr12:65847406 | C | T | 1 | a0001c0001t0017g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+8837C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847406 | |||||||
| chr12:65847592 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(33): Show |
36 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.249+9023C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847592 | |||||||
| chr12:65847997 | A | G | 24 | a0001c0001t0001g0139 a0001c0001t0008g0056 a0001c0001t0008g0057 others(21): Show |
24 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+9428A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65847997 | |||||||
| chr12:65848118 | G | A | 91 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0002g0176 others(88): Show |
91 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+9549G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848118 | |||||||
| chr12:65848315 | T | C | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.249+9746T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848315 | |||||||
| chr12:65848357 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.249+9788G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848357 | |||||||
| chr12:65848547 | A | G | 64 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0004g0024 others(61): Show |
64 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+9978A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848547 | |||||||
| chr12:65848548 | G | A | 14 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(11): Show |
14 | HG01243.hp1 HG01361.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+9979G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848548 | |||||||
| chr12:65848771 | G | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+10202G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848771 | |||||||
| chr12:65848831 | C | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+10262C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848831 | |||||||
| chr12:65848832 | C | G | 1 | a0001c0001t0003g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.249+10263C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848832 | |||||||
| chr12:65848842 | G | C | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+10273G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848842 | |||||||
| chr12:65848858 | G | A | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+10289G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65848858 | |||||||
| chr12:65849130 | G | A | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+10561G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849130 | |||||||
| chr12:65849555 | C | T | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+10986C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849555 | |||||||
| chr12:65849722 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(32): Show |
35 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.249+11153A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849722 | |||||||
| chr12:65849736 | A | AT | 16 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0131 others(13): Show |
16 | HG00423.hp1 HG00733.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+11191dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT | 22 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0061 others(19): Show |
22 | HG00733.hp1 HG01070.hp1 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.249+11185_249+1119 others(11): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(1): Show |
19 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0029 others(16): Show |
19 | HG00609.hp1 HG01192.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+11184_249+1119 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(2): Show |
16 | a0001c0001t0001g0075 a0001c0001t0004g0028 a0001c0001t0004g0037 others(13): Show |
16 | HG00558.hp1 HG01074.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+11183_249+1119 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0004g0041 a0001c0001t0004g0042 a0001c0001t0011g0040 others(1): Show |
4 | HG02738.hp2 HG04115.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+11182_249+1119 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(5): Show |
3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+11180_249+1119 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(12): Show |
3 | a0001c0001t0025g0183 a0001c0001t0055g0182 a0001c0001t0058g0181 |
3 | HG02922.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.249+11173_249+1119 others(23): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0025g0185 a0001c0001t0053g0180 |
2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.249+11172_249+1119 others(24): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+11170_249+1119 others(26): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | AT | A | 12 | a0001c0001t0002g0145 a0001c0001t0005g0205 a0001c0001t0006g0079 others(9): Show |
12 | HG00423.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+11191delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849736 | ATT | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(36): Show |
39 | HG00609.hp2 HG00621.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.249+11190_249+1119 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849736 | ||||||
| chr12:65849781 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+11212C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849781 | |||||||
| chr12:65849808 | TC | T | 14 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(11): Show |
14 | HG01243.hp1 HG01361.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+11242delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65849808 | ||||||
| chr12:65849839 | C | T | 1 | a0001c0001t0025g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.249+11270C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849839 | |||||||
| chr12:65849984 | G | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+11415G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65849984 | |||||||
| chr12:65850221 | G | A | 6 | a0001c0001t0001g0077 a0001c0001t0006g0078 a0001c0001t0006g0079 others(3): Show |
6 | HG01074.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+11652G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850221 | |||||||
| chr12:65850221 | G | T | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+11652G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850221 | |||||||
| chr12:65850434 | T | C | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+11865T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850434 | |||||||
| chr12:65850512 | G | A | 2 | a0001c0001t0052g0220 a0001c0001t0067g0230 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249+11943G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850512 | |||||||
| chr12:65850515 | T | A | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+11946T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850515 | |||||||
| chr12:65850733 | G | C | 1 | a0001c0001t0027g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.249+12164G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65850733 | |||||||
| chr12:65851032 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+12463T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851032 | |||||||
| chr12:65851256 | G | A | 1 | a0001c0001t0008g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+12687G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851256 | |||||||
| chr12:65851383 | C | T | 3 | a0001c0001t0006g0082 a0001c0001t0013g0204 a0001c0001t0027g0191 |
3 | HG01891.hp2 NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.249+12814C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851383 | |||||||
| chr12:65851421 | C | T | 1 | a0001c0001t0005g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.249+12852C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851421 | |||||||
| chr12:65851646 | C | T | 6 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0050g0218 others(3): Show |
6 | HG02451.hp2 HG02922.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+13077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851646 | |||||||
| chr12:65851788 | C | T | 27 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(24): Show |
27 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+13219C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851788 | |||||||
| chr12:65851808 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+13239A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65851808 | |||||||
| chr12:65852003 | G | C | 1 | a0001c0001t0010g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.249+13434G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852003 | |||||||
| chr12:65852017 | C | A | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+13448C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852017 | |||||||
| chr12:65852120 | G | A | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+13551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852120 | |||||||
| chr12:65852122 | GCAAATAA others(6): Show |
G | 10 | a0001c0001t0006g0159 a0001c0001t0006g0160 a0001c0001t0019g0161 others(7): Show |
10 | HG00735.hp2 HG01070.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+13574_249+1358 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65852122 | ||||||
| chr12:65852234 | C | T | 2 | a0001c0001t0015g0170 a0001c0001t0015g0171 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.249+13665C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852234 | |||||||
| chr12:65852401 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(139): Show |
142 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.249+13832A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852401 | |||||||
| chr12:65852464 | C | T | 15 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(12): Show |
15 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.249+13895C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852464 | |||||||
| chr12:65852535 | T | C | 1 | a0001c0001t0038g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.249+13966T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852535 | |||||||
| chr12:65852629 | T | C | 1 | a0001c0001t0007g0158 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+14060T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852629 | |||||||
| chr12:65852674 | T | C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0001g0151 others(6): Show |
9 | HG00673.hp1 HG02074.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+14105T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65852674 | |||||||
| chr12:65853017 | A | G | 22 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(19): Show |
22 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+14448A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853017 | |||||||
| chr12:65853088 | G | A | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+14519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853088 | |||||||
| chr12:65853108 | G | A | 22 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(19): Show |
22 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.249+14539G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853108 | |||||||
| chr12:65853120 | G | A | 3 | a0001c0001t0003g0016 a0001c0001t0006g0090 a0001c0001t0007g0165 |
3 | HG01433.hp1 NA20752.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249+14551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853120 | |||||||
| chr12:65853230 | C | G | 80 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(77): Show |
80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.249+14661C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853230 | |||||||
| chr12:65853271 | C | T | 91 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(88): Show |
91 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+14702C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853271 | |||||||
| chr12:65853464 | T | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+14895T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853464 | |||||||
| chr12:65853477 | G | A | 2 | a0001c0001t0013g0003 a0001c0001t0013g0004 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.249+14908G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853477 | |||||||
| chr12:65853660 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.249+15091G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853660 | |||||||
| chr12:65853711 | G | T | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+15142G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853711 | |||||||
| chr12:65853819 | A | G | 17 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(14): Show |
17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+15250A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65853819 | |||||||
| chr12:65854308 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.249+15739C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854308 | |||||||
| chr12:65854438 | T | C | 21 | a0001c0001t0001g0139 a0001c0001t0008g0056 a0001c0001t0008g0057 others(18): Show |
21 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+15869T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854438 | |||||||
| chr12:65854543 | C | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+15974C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854543 | |||||||
| chr12:65854819 | A | T | 1 | a0001c0001t0001g0095 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.249+16250A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854819 | |||||||
| chr12:65854874 | C | A | 1 | a0001c0001t0017g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+16305C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65854874 | |||||||
| chr12:65855400 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+16831A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855400 | |||||||
| chr12:65855448 | T | TCA | 4 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16880_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855448 | ||||||
| chr12:65855450 | T | A | 4 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16881T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855450 | |||||||
| chr12:65855450 | T | TCA | 7 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0033g0227 others(4): Show |
7 | HG01884.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+16882_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855450 | ||||||
| chr12:65855452 | T | A | 14 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(11): Show |
14 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+16883T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855452 | |||||||
| chr12:65855452 | T | TCA | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+16884_249+1688 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855452 | ||||||
| chr12:65855454 | T | A | 17 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(14): Show |
17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+16885T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855454 | |||||||
| chr12:65855456 | T | A | 17 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(14): Show |
17 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.249+16887T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855456 | |||||||
| chr12:65855458 | T | A | 18 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(15): Show |
18 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.249+16889T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855458 | |||||||
| chr12:65855458 | T | TCA | 12 | a0001c0001t0001g0123 a0001c0001t0002g0099 a0001c0001t0003g0122 others(9): Show |
12 | HG00673.hp2 HG02630.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+16920_249+1692 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCACA | 93 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(90): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.249+16918_249+1692 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCACACA | 38 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0103 others(35): Show |
38 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.249+16916_249+1692 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCACACAC others(1): Show |
8 | a0001c0001t0001g0075 a0001c0001t0004g0029 a0001c0001t0005g0229 others(5): Show |
8 | HG02074.hp1 HG02165.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+16914_249+1692 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCTCA | 3 | a0001c0001t0003g0125 a0001c0001t0005g0094 a0001c0001t0061g0219 |
3 | HG01361.hp2 NA18994.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.249+16890_249+1689 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCTCACA | 9 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(6): Show |
9 | HG02257.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+16890_249+1689 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCTCACAC others(1): Show |
8 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(5): Show |
8 | HG00733.hp1 HG01070.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+16890_249+1689 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | T | TCTCTCAC others(5): Show |
1 | a0001c0001t0041g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+16890_249+1689 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855458 | TCA | T | 4 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+16920_249+1692 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855458 | ||||||
| chr12:65855460 | A | T | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+16891A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855460 | |||||||
| chr12:65855462 | A | T | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+16893A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855462 | |||||||
| chr12:65855565 | G | A | 1 | a0001c0001t0007g0158 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+16996G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855565 | |||||||
| chr12:65855687 | T | C | 1 | a0001c0001t0035g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.249+17118T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855687 | |||||||
| chr12:65855699 | A | AGAT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0095 others(100): Show |
103 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.249+17167_249+1716 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | ||||||
| chr12:65855699 | A | AGATGAT | 61 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0091 others(58): Show |
61 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.249+17164_249+1716 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | ||||||
| chr12:65855699 | A | AGATGATG others(2): Show |
13 | a0001c0001t0003g0177 a0001c0001t0003g0233 a0001c0001t0006g0079 others(10): Show |
13 | HG00140.hp2 HG01070.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+17161_249+1716 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855699 | ||||||
| chr12:65855716 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+17147A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855716 | |||||||
| chr12:65855801 | T | C | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+17232T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855801 | |||||||
| chr12:65855825 | G | T | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0025 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+17256G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855825 | |||||||
| chr12:65855888 | C | CT | 20 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(17): Show |
20 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.249+17332dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65855888 | ||||||
| chr12:65855942 | G | A | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+17373G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855942 | |||||||
| chr12:65855992 | A | G | 2 | a0001c0001t0014g0059 a0001c0001t0022g0073 |
2 | NA18942.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.249+17423A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65855992 | |||||||
| chr12:65856157 | A | T | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+17588A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856157 | |||||||
| chr12:65856181 | G | A | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+17612G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856181 | |||||||
| chr12:65856288 | G | C | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+17719G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856288 | |||||||
| chr12:65856312 | A | G | 4 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(1): Show |
4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+17743A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856312 | |||||||
| chr12:65856684 | G | A | 1 | a0001c0001t0049g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249+18115G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856684 | |||||||
| chr12:65856793 | C | T | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.249+18224C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65856793 | |||||||
| chr12:65857160 | T | G | 91 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+18591T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857160 | |||||||
| chr12:65857375 | T | C | 4 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(1): Show |
4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+18806T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857375 | |||||||
| chr12:65857755 | A | T | 1 | a0001c0001t0063g0232 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.249+19186A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65857755 | |||||||
| chr12:65858347 | A | G | 1 | a0001c0001t0038g0127 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.249+19778A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858347 | |||||||
| chr12:65858514 | A | G | 113 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.249+19945A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858514 | |||||||
| chr12:65858847 | A | G | 1 | a0001c0001t0005g0221 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.249+20278A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65858847 | |||||||
| chr12:65859081 | G | A | 21 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.249+20512G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859081 | |||||||
| chr12:65859173 | C | T | 1 | a0001c0001t0011g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+20604C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859173 | |||||||
| chr12:65859374 | A | T | 1 | a0001c0001t0003g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+20805A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859374 | |||||||
| chr12:65859713 | G | A | 23 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(20): Show |
23 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.249+21144G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859713 | |||||||
| chr12:65859807 | T | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(4): Show |
7 | HG00609.hp2 HG00621.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+21238T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65859807 | |||||||
| chr12:65859918 | T | TA | 21 | a0001c0001t0001g0139 a0001c0001t0008g0056 a0001c0001t0008g0057 others(18): Show |
21 | HG00558.hp2 HG00621.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+21365dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65859918 | ||||||
| chr12:65860239 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0074g0196 |
2 | HG00140.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.249+21670G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860239 | |||||||
| chr12:65860448 | A | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+21879A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860448 | |||||||
| chr12:65860599 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.249+22030C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860599 | |||||||
| chr12:65860745 | T | G | 1 | a0001c0001t0067g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.249+22176T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65860745 | |||||||
| chr12:65861021 | T | C | 1 | a0001c0001t0015g0044 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249+22452T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861021 | |||||||
| chr12:65861089 | C | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22520C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861089 | |||||||
| chr12:65861150 | G | A | 78 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(75): Show |
78 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.249+22581G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861150 | |||||||
| chr12:65861199 | C | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22630C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861199 | |||||||
| chr12:65861223 | G | A | 78 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(75): Show |
78 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.249+22654G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861223 | |||||||
| chr12:65861225 | G | C | 94 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.249+22656G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861225 | |||||||
| chr12:65861364 | T | TCAAAA | 2 | a0001c0001t0003g0016 a0001c0001t0008g0035 |
2 | HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.249+22821_249+2282 others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861364 | ||||||
| chr12:65861370 | C | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+22801C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861370 | |||||||
| chr12:65861469 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.249+22900G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861469 | |||||||
| chr12:65861623 | T | TA | 79 | a0001c0001t0001g0139 a0001c0001t0002g0176 a0001c0001t0002g0179 others(76): Show |
79 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.249+23072dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861623 | ||||||
| chr12:65861623 | T | TAA | 8 | a0001c0001t0001g0075 a0001c0001t0007g0178 a0001c0001t0011g0027 others(5): Show |
8 | HG01192.hp2 HG02074.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+23071_249+2307 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861623 | ||||||
| chr12:65861680 | T | C | 2 | a0001c0001t0005g0229 a0001c0001t0061g0219 |
2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+23111T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861680 | |||||||
| chr12:65861733 | T | TATTTATT others(5): Show |
1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23165_249+2316 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861733 | ||||||
| chr12:65861735 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23166G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861735 | |||||||
| chr12:65861736 | A | T | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23167A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861736 | |||||||
| chr12:65861740 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23171T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861740 | |||||||
| chr12:65861741 | A | T | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23172A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861741 | |||||||
| chr12:65861748 | T | A | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23179T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861748 | |||||||
| chr12:65861752 | T | TATCTAGT others(3): Show |
1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23183_249+2318 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861752 | |||||||
| chr12:65861772 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23203T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861772 | |||||||
| chr12:65861780 | T | G | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23211T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861780 | |||||||
| chr12:65861782 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.249+23213T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861782 | |||||||
| chr12:65861790 | C | T | 11 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(8): Show |
11 | HG01361.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23221C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861790 | |||||||
| chr12:65861794 | T | A | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23225T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861794 | |||||||
| chr12:65861806 | A | C | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23237A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861806 | |||||||
| chr12:65861810 | T | A | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23241T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861810 | |||||||
| chr12:65861811 | T | G | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23242T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861811 | |||||||
| chr12:65861827 | G | A | 1 | a0001c0001t0003g0233 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.249+23258G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861827 | |||||||
| chr12:65861828 | T | G | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23259T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861828 | |||||||
| chr12:65861833 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23264G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861833 | |||||||
| chr12:65861835 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23266G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861835 | |||||||
| chr12:65861846 | C | CT | 5 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+23292dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65861846 | ||||||
| chr12:65861846 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23277C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861846 | |||||||
| chr12:65861849 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.249+23280T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861849 | |||||||
| chr12:65861855 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.249+23286T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861855 | |||||||
| chr12:65861856 | T | C | 2 | a0001c0001t0005g0229 a0001c0001t0061g0219 |
2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+23287T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861856 | |||||||
| chr12:65861874 | C | T | 1 | a0001c0001t0041g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+23305C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65861874 | |||||||
| chr12:65862017 | G | A | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+23448G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862017 | |||||||
| chr12:65862097 | G | T | 1 | a0001c0001t0066g0005 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.249+23528G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862097 | |||||||
| chr12:65862127 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.249+23558G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862127 | |||||||
| chr12:65862276 | T | TAC | 94 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0085 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.249+23737_249+2373 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862276 | T | TACAC | 57 | a0001c0001t0001g0139 a0001c0001t0003g0112 a0001c0001t0004g0024 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.249+23735_249+2373 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862276 | T | TACACAC | 11 | a0001c0001t0004g0042 a0001c0001t0008g0057 a0001c0001t0008g0058 others(8): Show |
11 | HG01891.hp1 HG02040.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23733_249+2373 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862276 | T | TACACACA others(3): Show |
7 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0013 others(4): Show |
7 | HG01884.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+23729_249+2373 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862276 | T | TACACACA others(7): Show |
1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.249+23725_249+2373 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862276 | TAC | T | 2 | a0001c0001t0002g0156 a0001c0001t0007g0158 |
2 | NA18991.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.249+23737_249+2373 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862276 | ||||||
| chr12:65862296 | C | CACAT | 11 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(8): Show |
11 | HG01361.hp2 HG02257.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+23730_249+2373 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65862296 | ||||||
| chr12:65862374 | A | C | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+23805A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862374 | |||||||
| chr12:65862457 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.249+23888A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862457 | |||||||
| chr12:65862615 | G | C | 100 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0002g0176 others(97): Show |
100 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.249+24046G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862615 | |||||||
| chr12:65862708 | T | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+24139T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862708 | |||||||
| chr12:65862764 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0002g0092 a0001c0001t0013g0197 others(1): Show |
4 | NA18951.hp2 NA18953.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+24195G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862764 | |||||||
| chr12:65862921 | A | G | 4 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(1): Show |
4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+24352A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65862921 | |||||||
| chr12:65863105 | C | T | 1 | a0001c0001t0032g0128 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.249+24536C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65863105 | |||||||
| chr12:65863167 | A | C | 64 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0004g0024 others(61): Show |
64 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.249+24598A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65863167 | |||||||
| chr12:65863447 | GTCCTGGT | G | 5 | a0001c0001t0005g0229 a0001c0001t0015g0170 a0001c0001t0015g0171 others(2): Show |
5 | HG01361.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+24882_249+2488 others(11): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65863447 | ||||||
| chr12:65863575 | GA | G | 27 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0109 others(24): Show |
27 | HG00733.hp2 HG01167.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.249+25015delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65863575 | ||||||
| chr12:65864456 | C | G | 99 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(96): Show |
99 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.249+25887C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864456 | |||||||
| chr12:65864515 | G | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+25946G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864515 | |||||||
| chr12:65864715 | T | C | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+26146T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864715 | |||||||
| chr12:65864925 | A | G | 2 | a0001c0001t0009g0054 a0001c0001t0011g0053 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.249+26356A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864925 | |||||||
| chr12:65864997 | C | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+26428C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65864997 | |||||||
| chr12:65865042 | C | T | 66 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0177 others(63): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.249+26473C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865042 | |||||||
| chr12:65865119 | C | T | 2 | a0001c0001t0005g0229 a0001c0001t0061g0219 |
2 | HG01361.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.249+26550C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865119 | |||||||
| chr12:65865150 | T | C | 2 | a0001c0001t0002g0135 a0001c0001t0030g0134 |
2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.249+26581T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865150 | |||||||
| chr12:65865192 | G | T | 199 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0085 others(196): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.249+26623G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865192 | |||||||
| chr12:65865276 | G | A | 4 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(1): Show |
4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+26707G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865276 | |||||||
| chr12:65865336 | G | C | 199 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0085 others(196): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.249+26767G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865336 | |||||||
| chr12:65865633 | C | CT | 9 | a0001c0001t0002g0146 a0001c0001t0005g0205 a0001c0001t0006g0138 others(6): Show |
9 | HG00621.hp1 HG02083.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+27083dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65865633 | ||||||
| chr12:65865690 | A | G | 1 | a0001c0001t0005g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.249+27121A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865690 | |||||||
| chr12:65865884 | T | C | 200 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0085 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.249+27315T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865884 | |||||||
| chr12:65865885 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0135 others(3): Show |
6 | HG02027.hp2 HG02135.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+27316G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865885 | |||||||
| chr12:65865933 | C | T | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+27364C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865933 | |||||||
| chr12:65865949 | T | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+27380T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865949 | |||||||
| chr12:65865949 | TC | T | 4 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(1): Show |
4 | HG02683.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+27381delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65865949 | |||||||
| chr12:65866294 | A | T | 20 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.249+27725A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866294 | |||||||
| chr12:65866430 | A | G | 1 | a0001c0001t0034g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.249+27861A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866430 | |||||||
| chr12:65866516 | T | G | 1 | a0001c0001t0003g0112 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.249+27947T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866516 | |||||||
| chr12:65866778 | TA | T | 7 | a0001c0001t0005g0229 a0001c0001t0014g0017 a0001c0001t0022g0018 others(4): Show |
7 | HG01074.hp2 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+28220delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65866778 | ||||||
| chr12:65866885 | G | T | 1 | a0001c0001t0004g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+28316G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866885 | |||||||
| chr12:65866936 | G | A | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+28367G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866936 | |||||||
| chr12:65866953 | C | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+28384C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65866953 | |||||||
| chr12:65867003 | A | T | 3 | a0001c0001t0016g0023 a0001c0001t0016g0045 a0001c0001t0021g0043 |
3 | HG02818.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.249+28434A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867003 | |||||||
| chr12:65867034 | A | G | 1 | a0001c0001t0007g0158 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+28465A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867034 | |||||||
| chr12:65867144 | A | G | 95 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.249+28575A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867144 | |||||||
| chr12:65867145 | C | G | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+28576C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867145 | |||||||
| chr12:65867211 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+28642C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867211 | |||||||
| chr12:65867226 | T | A | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+28657T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867226 | |||||||
| chr12:65867993 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0006g0078 a0001c0001t0006g0079 others(3): Show |
6 | HG01074.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+29424C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65867993 | |||||||
| chr12:65868197 | A | G | 96 | a0001c0001t0001g0075 a0001c0001t0001g0139 a0001c0001t0002g0176 others(93): Show |
96 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.249+29628A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868197 | |||||||
| chr12:65868287 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.249+29718G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868287 | |||||||
| chr12:65868618 | G | A | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+30049G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868618 | |||||||
| chr12:65868911 | G | A | 2 | a0001c0001t0017g0013 a0001c0001t0054g0012 |
2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.249+30342G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868911 | |||||||
| chr12:65868961 | G | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+30392G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868961 | |||||||
| chr12:65868978 | G | A | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+30409G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65868978 | |||||||
| chr12:65869170 | G | C | 5 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(2): Show |
5 | HG02257.hp1 HG02683.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+30601G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869170 | |||||||
| chr12:65869208 | A | T | 199 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0085 others(196): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.249+30639A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869208 | |||||||
| chr12:65869253 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.249+30684T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869253 | |||||||
| chr12:65869328 | T | C | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+30759T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869328 | |||||||
| chr12:65869420 | C | T | 1 | a0001c0001t0014g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.249+30851C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869420 | |||||||
| chr12:65869542 | T | C | 1 | a0001c0001t0005g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.249+30973T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869542 | |||||||
| chr12:65869795 | A | G | 1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+31226A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65869795 | |||||||
| chr12:65870120 | G | A | 1 | a0001c0001t0009g0065 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.249+31551G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870120 | |||||||
| chr12:65870211 | C | T | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+31642C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870211 | |||||||
| chr12:65870222 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+31653G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870222 | |||||||
| chr12:65870276 | C | G | 6 | a0001c0001t0002g0176 a0001c0001t0003g0177 a0001c0001t0003g0233 others(3): Show |
6 | HG02257.hp2 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+31707C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870276 | |||||||
| chr12:65870426 | T | C | 20 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.249+31857T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870426 | |||||||
| chr12:65870530 | A | G | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+31961A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870530 | |||||||
| chr12:65870616 | G | C | 1 | a0001c0001t0015g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.249+32047G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870616 | |||||||
| chr12:65870742 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+32173A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870742 | |||||||
| chr12:65870976 | A | G | 2 | a0001c0001t0052g0220 a0001c0001t0067g0230 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.249+32407A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65870976 | |||||||
| chr12:65871165 | T | C | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+32596T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871165 | |||||||
| chr12:65871230 | G | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+32661G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871230 | |||||||
| chr12:65871262 | C | T | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+32693C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871262 | |||||||
| chr12:65871300 | C | T | 1 | a0001c0001t0021g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.249+32731C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871300 | |||||||
| chr12:65871338 | C | T | 6 | a0001c0001t0006g0159 a0001c0001t0006g0160 a0001c0001t0019g0161 others(3): Show |
6 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+32769C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871338 | |||||||
| chr12:65871534 | G | T | 2 | a0001c0001t0012g0060 a0001c0001t0048g0020 |
2 | NA18972.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.249+32965G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871534 | |||||||
| chr12:65871637 | T | C | 63 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.249+33068T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871637 | |||||||
| chr12:65871901 | G | A | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+33332G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65871901 | |||||||
| chr12:65872274 | T | C | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.249+33705T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872274 | |||||||
| chr12:65872353 | G | A | 2 | a0001c0001t0009g0054 a0001c0001t0011g0053 |
2 | HG02040.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.249+33784G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872353 | |||||||
| chr12:65872394 | G | A | 1 | a0001c0001t0019g0117 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.249+33825G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872394 | |||||||
| chr12:65872504 | G | A | 7 | a0001c0001t0017g0013 a0001c0001t0025g0183 a0001c0001t0025g0185 others(4): Show |
7 | HG02922.hp2 HG02976.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+33935G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872504 | |||||||
| chr12:65872613 | A | G | 58 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(55): Show |
58 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.249+34044A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872613 | |||||||
| chr12:65872740 | T | G | 3 | a0001c0001t0001g0089 a0001c0001t0003g0112 a0001c0001t0003g0234 |
3 | HG00280.hp1 NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.249+34171T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872740 | |||||||
| chr12:65872787 | A | G | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+34218A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872787 | |||||||
| chr12:65872837 | G | A | 1 | a0001c0001t0058g0181 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.249+34268G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872837 | |||||||
| chr12:65872941 | C | T | 9 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+34372C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65872941 | |||||||
| chr12:65873198 | C | T | 3 | a0001c0001t0014g0017 a0001c0001t0022g0018 a0001c0001t0051g0019 |
3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+34629C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873198 | |||||||
| chr12:65873356 | G | A | 11 | a0001c0001t0005g0229 a0001c0001t0008g0069 a0001c0001t0009g0076 others(8): Show |
11 | HG01891.hp1 HG02451.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+34787G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873356 | |||||||
| chr12:65873596 | G | A | 1 | a0001c0001t0004g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.249+35027G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873596 | |||||||
| chr12:65873692 | A | G | 1 | a0001c0001t0037g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.249+35123A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873692 | |||||||
| chr12:65873923 | GTAGGTAA others(5): Show |
G | 1 | a0001c0001t0076g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.249+35359_249+3537 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65873923 | ||||||
| chr12:65873939 | G | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+35370G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65873939 | |||||||
| chr12:65874159 | C | T | 1 | a0001c0001t0074g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.249+35590C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874159 | |||||||
| chr12:65874189 | C | T | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+35620C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874189 | |||||||
| chr12:65874325 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.249+35756C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874325 | |||||||
| chr12:65874451 | G | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+35882G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874451 | |||||||
| chr12:65874968 | C | G | 1 | a0001c0001t0007g0111 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.249+36399C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65874968 | |||||||
| chr12:65875002 | C | G | 57 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(54): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.249+36433C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875002 | |||||||
| chr12:65875011 | C | T | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+36442C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875011 | |||||||
| chr12:65875110 | T | TA | 70 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(67): Show |
70 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.249+36542dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875110 | ||||||
| chr12:65875112 | T | A | 70 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(67): Show |
70 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.249+36543T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875112 | |||||||
| chr12:65875187 | A | G | 1 | a0001c0001t0065g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249+36618A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875187 | |||||||
| chr12:65875188 | T | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+36619T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875188 | |||||||
| chr12:65875589 | A | AT | 9 | a0001c0001t0001g0194 a0001c0001t0007g0178 a0001c0001t0010g0214 others(6): Show |
9 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+37061dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(3): Show |
9 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0002g0140 others(6): Show |
9 | HG00280.hp1 HG01074.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37052_249+3706 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(4): Show |
21 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0131 others(18): Show |
21 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+37051_249+3706 others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(5): Show |
14 | a0001c0001t0001g0089 a0001c0001t0001g0106 a0001c0001t0001g0109 others(11): Show |
14 | HG01256.hp2 HG01496.hp2 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+37050_249+3706 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0002g0135 others(7): Show |
10 | HG00733.hp2 HG01167.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+37049_249+3706 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(7): Show |
5 | a0001c0001t0002g0105 a0001c0001t0002g0116 a0001c0001t0002g0120 others(2): Show |
5 | HG01261.hp2 HG01361.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+37048_249+3706 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0007g0163 a0001c0001t0075g0087 |
2 | HG02027.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.249+37047_249+3706 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0001g0123 a0001c0001t0001g0139 a0001c0001t0003g0137 others(1): Show |
4 | HG00621.hp2 HG00673.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+37046_249+3706 others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0003g0110 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.249+37045_249+3706 others(21): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0002g0146 a0001c0001t0007g0158 |
2 | HG02738.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.249+37044_249+3706 others(22): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | AT | A | 8 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+37061delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTT | A | 6 | a0001c0001t0006g0160 a0001c0001t0007g0165 a0001c0001t0017g0013 others(3): Show |
6 | HG00735.hp2 HG01070.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+37057_249+3706 others(9): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0005g0229 a0001c0001t0010g0009 a0001c0001t0015g0136 others(4): Show |
7 | HG00423.hp1 HG01891.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.249+37054_249+3706 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0008g0069 a0001c0001t0009g0076 a0001c0001t0012g0049 others(3): Show |
6 | HG02451.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+37053_249+3706 others(13): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(3): Show |
A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0151 others(11): Show |
14 | HG02074.hp2 HG02165.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+37052_249+3706 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0152 a0001c0001t0007g0231 |
2 | HG00673.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.249+37051_249+3706 others(15): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0150 a0001c0001t0003g0122 |
2 | HG02083.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+37050_249+3706 others(16): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(6): Show |
A | 15 | a0001c0001t0001g0075 a0001c0001t0004g0029 a0001c0001t0004g0030 others(12): Show |
15 | HG01496.hp1 HG02074.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.249+37049_249+3706 others(17): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(7): Show |
A | 41 | a0001c0001t0004g0024 a0001c0001t0004g0028 a0001c0001t0004g0042 others(38): Show |
41 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.249+37048_249+3706 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0003g0129 a0001c0001t0014g0017 a0001c0001t0074g0196 |
3 | HG01074.hp2 HG03942.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.249+37047_249+3706 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+37046_249+3706 others(20): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(12): Show |
A | 1 | a0001c0001t0027g0191 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.249+37043_249+3706 others(23): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(14): Show |
A | 4 | a0001c0001t0001g0107 a0001c0001t0002g0108 a0001c0001t0003g0118 others(1): Show |
4 | HG00280.hp2 HG01516.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+37041_249+3706 others(25): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875589 | ATTTTTTT others(17): Show |
A | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+37038_249+3706 others(28): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65875589 | ||||||
| chr12:65875965 | G | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.249+37396G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65875965 | |||||||
| chr12:65876125 | T | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37556T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876125 | |||||||
| chr12:65876226 | CA | C | 59 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.249+37667delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65876226 | ||||||
| chr12:65876329 | G | C | 1 | a0001c0001t0033g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.249+37760G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876329 | |||||||
| chr12:65876393 | T | A | 1 | a0001c0001t0002g0140 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.249+37824T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876393 | |||||||
| chr12:65876498 | T | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+37929T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876498 | |||||||
| chr12:65876610 | A | G | 1 | a0001c0001t0005g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+38041A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876610 | |||||||
| chr12:65876695 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249+38126T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876695 | |||||||
| chr12:65876904 | G | A | 2 | a0001c0001t0001g0115 a0002c0002t0002g0098 |
2 | HG02027.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.249+38335G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65876904 | |||||||
| chr12:65877208 | G | A | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.249+38639G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877208 | |||||||
| chr12:65877265 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.249+38696G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877265 | |||||||
| chr12:65877439 | G | C | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+38870G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877439 | |||||||
| chr12:65877649 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.249+39080C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877649 | |||||||
| chr12:65877814 | C | CA | 18 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(15): Show |
18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+39255dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65877814 | ||||||
| chr12:65877860 | A | C | 5 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0033g0227 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+39291A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877860 | |||||||
| chr12:65877896 | G | A | 1 | a0001c0001t0008g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.249+39327G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877896 | |||||||
| chr12:65877901 | C | T | 1 | a0001c0001t0006g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.249+39332C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65877901 | |||||||
| chr12:65878422 | G | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(26): Show |
29 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.249+39853G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878422 | |||||||
| chr12:65878579 | G | T | 5 | a0001c0001t0001g0075 a0001c0001t0009g0054 a0001c0001t0009g0074 others(2): Show |
5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+40010G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878579 | |||||||
| chr12:65878952 | A | G | 18 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(15): Show |
18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+40383A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878952 | |||||||
| chr12:65878990 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.249+40421T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65878990 | |||||||
| chr12:65879000 | T | C | 1 | a0001c0001t0007g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.249+40431T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879000 | |||||||
| chr12:65879291 | T | TA | 80 | a0001c0001t0001g0075 a0001c0001t0003g0122 a0001c0001t0004g0024 others(77): Show |
80 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.249+40723dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65879291 | ||||||
| chr12:65879292 | A | AAT | 31 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(28): Show |
31 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.249+40723_249+4072 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879292 | |||||||
| chr12:65879292 | AT | A | 11 | a0001c0001t0001g0115 a0001c0001t0002g0105 a0001c0001t0007g0163 others(8): Show |
11 | HG01361.hp1 HG02683.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.249+40739delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65879292 | ||||||
| chr12:65879294 | T | A | 8 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 others(5): Show |
8 | HG02683.hp1 HG02809.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.249+40725T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879294 | |||||||
| chr12:65879483 | T | G | 2 | a0001c0001t0046g0216 a0001c0001t0054g0012 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.249+40914T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879483 | |||||||
| chr12:65879719 | G | A | 2 | a0001c0001t0013g0204 a0001c0001t0027g0191 |
2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.249+41150G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879719 | |||||||
| chr12:65879833 | T | A | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+41264T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879833 | |||||||
| chr12:65879871 | A | G | 3 | a0001c0001t0009g0054 a0001c0001t0011g0053 a0001c0001t0012g0055 |
3 | HG02040.hp1 HG02135.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.249+41302A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65879871 | |||||||
| chr12:65880789 | A | G | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.249+42220A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880789 | |||||||
| chr12:65880815 | A | T | 3 | a0001c0001t0014g0017 a0001c0001t0022g0018 a0001c0001t0051g0019 |
3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+42246A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880815 | |||||||
| chr12:65880931 | C | T | 4 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+42362C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65880931 | |||||||
| chr12:65881052 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+42483T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881052 | |||||||
| chr12:65881271 | T | A | 1 | a0001c0001t0005g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+42702T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881271 | |||||||
| chr12:65881293 | TC | T | 2 | a0001c0001t0026g0199 a0001c0001t0026g0215 |
2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.249+42725delC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881293 | |||||||
| chr12:65881455 | T | TA | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+42894dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65881455 | ||||||
| chr12:65881979 | C | A | 1 | a0001c0001t0004g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.249+43410C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65881979 | |||||||
| chr12:65882303 | G | C | 1 | a0001c0001t0007g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.249+43734G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882303 | |||||||
| chr12:65882419 | C | T | 18 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(15): Show |
18 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.249+43850C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882419 | |||||||
| chr12:65882662 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+44093G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882662 | |||||||
| chr12:65882902 | G | A | 1 | a0001c0001t0004g0041 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.249+44333G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882902 | |||||||
| chr12:65882973 | G | A | 1 | a0001c0001t0017g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+44404G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65882973 | |||||||
| chr12:65883194 | C | T | 2 | a0001c0001t0016g0062 a0001c0001t0016g0063 |
2 | NA18970.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.249+44625C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883194 | |||||||
| chr12:65883233 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.249+44664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883233 | |||||||
| chr12:65883283 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+44714G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883283 | |||||||
| chr12:65883420 | A | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+44851A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883420 | |||||||
| chr12:65883529 | C | T | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+44960C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883529 | |||||||
| chr12:65883869 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.249+45300C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883869 | |||||||
| chr12:65883918 | A | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(110): Show |
113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.249+45349A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65883918 | |||||||
| chr12:65884011 | G | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+45442G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884011 | |||||||
| chr12:65884083 | C | A | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+45514C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884083 | |||||||
| chr12:65884132 | C | G | 1 | a0001c0001t0045g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.249+45563C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884132 | |||||||
| chr12:65884218 | T | C | 5 | a0001c0001t0001g0075 a0001c0001t0009g0054 a0001c0001t0009g0074 others(2): Show |
5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+45649T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884218 | |||||||
| chr12:65884952 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.249+46383C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65884952 | |||||||
| chr12:65885141 | A | G | 1 | a0001c0001t0062g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.249+46572A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885141 | |||||||
| chr12:65885193 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.249+46624G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885193 | |||||||
| chr12:65885313 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0002g0108 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.249+46744G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885313 | |||||||
| chr12:65885319 | T | A | 44 | a0001c0001t0001g0075 a0001c0001t0003g0122 a0001c0001t0004g0024 others(41): Show |
44 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.249+46750T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885319 | |||||||
| chr12:65885382 | A | C | 1 | a0001c0001t0011g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.249+46813A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885382 | |||||||
| chr12:65885489 | C | A | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+46920C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885489 | |||||||
| chr12:65885520 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.249+46951A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885520 | |||||||
| chr12:65885816 | T | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+47247T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885816 | |||||||
| chr12:65885838 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+47269G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885838 | |||||||
| chr12:65885931 | T | G | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+47362T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65885931 | |||||||
| chr12:65886042 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(21): Show |
24 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.249+47473C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886042 | |||||||
| chr12:65886095 | A | G | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+47526A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886095 | |||||||
| chr12:65886363 | C | CT | 7 | a0001c0001t0010g0208 a0001c0001t0018g0207 a0001c0001t0018g0209 others(4): Show |
7 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.249+47808dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65886363 | ||||||
| chr12:65886364 | T | TC | 41 | a0001c0001t0001g0075 a0001c0001t0003g0122 a0001c0001t0004g0024 others(38): Show |
41 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.249+47795_249+4779 others(5): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886364 | |||||||
| chr12:65886365 | T | C | 3 | a0001c0001t0004g0037 a0001c0001t0046g0216 a0001c0001t0054g0012 |
3 | HG03041.hp1 HG03209.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.249+47796T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886365 | |||||||
| chr12:65886463 | G | A | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.249+47894G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886463 | |||||||
| chr12:65886471 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+47902T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886471 | |||||||
| chr12:65886705 | C | A | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+48136C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886705 | |||||||
| chr12:65886734 | C | T | 1 | a0001c0001t0070g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.249+48165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886734 | |||||||
| chr12:65886804 | C | G | 1 | a0001c0001t0008g0069 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.249+48235C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886804 | |||||||
| chr12:65886965 | C | T | 1 | a0001c0001t0036g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.249+48396C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886965 | |||||||
| chr12:65886967 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.249+48398G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65886967 | |||||||
| chr12:65887143 | A | G | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+48574A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887143 | |||||||
| chr12:65887173 | A | G | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+48604A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887173 | |||||||
| chr12:65887394 | C | A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+48825C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887394 | |||||||
| chr12:65887568 | C | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.249+48999C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887568 | |||||||
| chr12:65887815 | C | T | 1 | a0001c0001t0014g0017 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.249+49246C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887815 | |||||||
| chr12:65887828 | T | C | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+49259T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887828 | |||||||
| chr12:65887877 | TA | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(110): Show |
113 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.249+49322delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65887877 | ||||||
| chr12:65887878 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249+49309A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65887878 | |||||||
| chr12:65888100 | C | T | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+49531C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888100 | |||||||
| chr12:65888228 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+49659G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888228 | |||||||
| chr12:65888479 | A | G | 1 | a0001c0001t0012g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.249+49910A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888479 | |||||||
| chr12:65888512 | A | G | 1 | a0001c0001t0009g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.249+49943A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888512 | |||||||
| chr12:65888551 | GCT | G | 2 | a0001c0001t0003g0235 a0001c0001t0005g0147 |
2 | HG01516.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.249+49985_249+4998 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888551 | ||||||
| chr12:65888554 | C | CT | 61 | a0001c0001t0001g0096 a0001c0001t0001g0107 a0001c0001t0001g0109 others(58): Show |
61 | HG00558.hp1 HG00609.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.249+50012dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | ||||||
| chr12:65888554 | C | CTT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0154 others(47): Show |
50 | HG00423.hp2 HG00621.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.249+50011_249+5001 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | ||||||
| chr12:65888554 | C | CTTT | 21 | a0001c0001t0001g0194 a0001c0001t0004g0041 a0001c0001t0005g0088 others(18): Show |
21 | HG00609.hp2 HG01074.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.249+50010_249+5001 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | ||||||
| chr12:65888554 | CT | C | 52 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.249+50012delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | ||||||
| chr12:65888554 | CTT | C | 15 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0001g0103 others(12): Show |
15 | HG01258.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+50011_249+5001 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888554 | ||||||
| chr12:65888595 | ACT | A | 38 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(35): Show |
38 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(35): Show |
intron_variant | MODIFIER | c.249+50029_249+5003 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65888595 | ||||||
| chr12:65888664 | T | C | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+50095T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888664 | |||||||
| chr12:65888688 | T | C | 1 | a0001c0001t0064g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.249+50119T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888688 | |||||||
| chr12:65888721 | G | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG01258.hp1 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+50152G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888721 | |||||||
| chr12:65888725 | G | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(24): Show |
27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+50156G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888725 | |||||||
| chr12:65888731 | C | T | 1 | a0001c0001t0065g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.249+50162C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888731 | |||||||
| chr12:65888772 | C | T | 1 | a0001c0001t0016g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.249+50203C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888772 | |||||||
| chr12:65888814 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+50245C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888814 | |||||||
| chr12:65888852 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(100): Show |
103 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.249+50283G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888852 | |||||||
| chr12:65888864 | C | T | 37 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(34): Show |
37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.249+50295C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65888864 | |||||||
| chr12:65889031 | G | C | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+50462G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889031 | |||||||
| chr12:65889139 | C | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+50570C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889139 | |||||||
| chr12:65889378 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.249+50809A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889378 | |||||||
| chr12:65889444 | A | G | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+50875A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889444 | |||||||
| chr12:65889453 | T | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(24): Show |
27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+50884T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889453 | |||||||
| chr12:65889455 | C | T | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+50886C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889455 | |||||||
| chr12:65889742 | A | G | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249+51173A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889742 | |||||||
| chr12:65889794 | G | A | 12 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(9): Show |
12 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.249+51225G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889794 | |||||||
| chr12:65889820 | T | C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(24): Show |
27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+51251T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889820 | |||||||
| chr12:65889865 | T | A | 1 | a0001c0001t0007g0158 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.249+51296T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889865 | |||||||
| chr12:65889893 | T | C | 19 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(16): Show |
19 | HG00558.hp2 HG00733.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+51324T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65889893 | |||||||
| chr12:65890019 | T | C | 1 | a0001c0001t0024g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.249+51450T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890019 | |||||||
| chr12:65890556 | C | T | 75 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.249+51987C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890556 | |||||||
| chr12:65890655 | T | C | 1 | a0001c0001t0070g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.249+52086T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890655 | |||||||
| chr12:65890710 | C | T | 1 | a0001c0001t0008g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.249+52141C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890710 | |||||||
| chr12:65890727 | C | CT | 10 | a0001c0001t0009g0034 a0001c0001t0013g0003 a0001c0001t0013g0004 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+52173dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65890727 | ||||||
| chr12:65890727 | CT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(36): Show |
39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.249+52173delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65890727 | ||||||
| chr12:65890765 | C | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.249+52196C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65890765 | |||||||
| chr12:65891051 | A | G | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+52482A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891051 | |||||||
| chr12:65891065 | C | A | 2 | a0001c0001t0002g0140 a0001c0001t0036g0086 |
2 | HG02300.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.249+52496C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891065 | |||||||
| chr12:65891093 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(109): Show |
112 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.249+52524T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891093 | |||||||
| chr12:65891405 | CAAT | C | 2 | a0001c0001t0026g0199 a0001c0001t0026g0215 |
2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.249+52841_249+5284 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65891405 | ||||||
| chr12:65891479 | G | A | 1 | a0001c0001t0002g0135 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.249+52910G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891479 | |||||||
| chr12:65891578 | C | T | 1 | a0001c0001t0004g0024 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.249+53009C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891578 | |||||||
| chr12:65891605 | G | A | 1 | a0001c0001t0067g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.249+53036G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891605 | |||||||
| chr12:65891788 | G | T | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.249+53219G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65891788 | |||||||
| chr12:65892354 | C | T | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.249+53785C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892354 | |||||||
| chr12:65892742 | G | A | 3 | a0001c0001t0014g0017 a0001c0001t0022g0018 a0001c0001t0051g0019 |
3 | HG01074.hp2 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.249+54173G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892742 | |||||||
| chr12:65892785 | C | T | 1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.249+54216C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892785 | |||||||
| chr12:65892815 | T | A | 1 | a0001c0001t0005g0229 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.249+54246T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892815 | |||||||
| chr12:65892831 | A | G | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54262A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892831 | |||||||
| chr12:65892957 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0002g0092 a0001c0001t0013g0197 |
3 | NA18951.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.249+54388G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65892957 | |||||||
| chr12:65893005 | G | A | 1 | a0001c0001t0007g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.249+54436G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893005 | |||||||
| chr12:65893035 | G | A | 1 | a0001c0001t0052g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.249+54466G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893035 | |||||||
| chr12:65893106 | C | A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54537C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893106 | |||||||
| chr12:65893160 | A | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+54591A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893160 | |||||||
| chr12:65893539 | A | G | 1 | a0001c0001t0019g0161 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.249+54970A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65893539 | |||||||
| chr12:65894000 | G | A | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+55431G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894000 | |||||||
| chr12:65894194 | C | G | 3 | a0001c0001t0015g0170 a0001c0001t0015g0171 a0001c0001t0041g0172 |
3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.249+55625C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894194 | |||||||
| chr12:65894484 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.249+55915T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894484 | |||||||
| chr12:65894748 | A | G | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+56179A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894748 | |||||||
| chr12:65894854 | T | C | 1 | a0001c0001t0033g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.249+56285T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894854 | |||||||
| chr12:65894999 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-56384G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65894999 | |||||||
| chr12:65895344 | A | G | 1 | a0001c0001t0005g0114 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-56039A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895344 | |||||||
| chr12:65895441 | C | T | 9 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-55942C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895441 | |||||||
| chr12:65895844 | T | G | 2 | a0001c0001t0045g0026 a0001c0001t0057g0225 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.250-55539T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895844 | |||||||
| chr12:65895953 | A | C | 40 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(37): Show |
40 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.250-55430A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65895953 | |||||||
| chr12:65896072 | G | A | 1 | a0001c0001t0007g0111 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.250-55311G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896072 | |||||||
| chr12:65896597 | C | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-54786C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896597 | |||||||
| chr12:65896768 | C | T | 3 | a0001c0001t0007g0141 a0001c0001t0010g0213 a0001c0001t0010g0214 |
3 | HG01256.hp1 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.250-54615C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896768 | |||||||
| chr12:65896786 | T | G | 1 | a0001c0001t0007g0231 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.250-54597T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65896786 | |||||||
| chr12:65897147 | T | C | 3 | a0001c0001t0016g0023 a0001c0001t0016g0045 a0001c0001t0021g0043 |
3 | HG02818.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.250-54236T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897147 | |||||||
| chr12:65897452 | T | C | 39 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(36): Show |
39 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.250-53931T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897452 | |||||||
| chr12:65897462 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0002g0092 a0001c0001t0013g0197 |
3 | NA18951.hp2 NA18957.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.250-53921G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897462 | |||||||
| chr12:65897594 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(24): Show |
27 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.250-53789C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897594 | |||||||
| chr12:65897620 | G | A | 1 | a0001c0001t0055g0182 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.250-53763G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897620 | |||||||
| chr12:65897652 | A | C | 20 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(17): Show |
20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-53731A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897652 | |||||||
| chr12:65897681 | C | T | 1 | a0001c0001t0008g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-53702C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897681 | |||||||
| chr12:65897685 | C | T | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897685 | |||||||
| chr12:65897831 | G | T | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53552G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897831 | |||||||
| chr12:65897941 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(95): Show |
98 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.250-53442A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65897941 | |||||||
| chr12:65897964 | C | CA | 42 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(39): Show |
42 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.250-53403dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65897964 | ||||||
| chr12:65897964 | CA | C | 22 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(19): Show |
22 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.250-53403delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65897964 | ||||||
| chr12:65898005 | G | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0152 a0001c0001t0002g0092 others(4): Show |
7 | HG00673.hp1 HG02155.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-53378G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898005 | |||||||
| chr12:65898202 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(6): Show |
9 | HG00609.hp2 HG00621.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-53181A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898202 | |||||||
| chr12:65898208 | T | A | 1 | a0001c0001t0037g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-53175T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898208 | |||||||
| chr12:65898451 | G | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-52932G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898451 | |||||||
| chr12:65898644 | G | A | 6 | a0001c0001t0001g0148 a0001c0001t0002g0146 a0001c0001t0003g0118 others(3): Show |
6 | HG00140.hp1 HG00280.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-52739G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898644 | |||||||
| chr12:65898656 | T | G | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-52727T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898656 | |||||||
| chr12:65898771 | G | A | 4 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-52612G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898771 | |||||||
| chr12:65898841 | G | C | 1 | a0001c0001t0008g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-52542G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898841 | |||||||
| chr12:65898904 | C | T | 1 | a0001c0001t0059g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.250-52479C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898904 | |||||||
| chr12:65898913 | G | A | 1 | a0001c0001t0072g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.250-52470G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898913 | |||||||
| chr12:65898936 | C | T | 1 | a0001c0001t0042g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-52447C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898936 | |||||||
| chr12:65898991 | C | T | 7 | a0001c0001t0006g0082 a0001c0001t0006g0090 a0001c0001t0006g0159 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-52392C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65898991 | |||||||
| chr12:65899043 | C | CA | 31 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0001g0104 others(28): Show |
31 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.250-52311dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | ||||||
| chr12:65899043 | C | CAA | 11 | a0001c0001t0001g0085 a0001c0001t0001g0103 a0001c0001t0001g0106 others(8): Show |
11 | HG00741.hp2 HG01258.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-52312_250-5231 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | ||||||
| chr12:65899043 | CA | C | 23 | a0001c0001t0001g0075 a0001c0001t0001g0096 a0001c0001t0001g0123 others(20): Show |
23 | HG00280.hp2 HG00733.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.250-52311delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | ||||||
| chr12:65899043 | CAA | C | 59 | a0001c0001t0004g0024 a0001c0001t0004g0028 a0001c0001t0004g0029 others(56): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.250-52312_250-5231 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | ||||||
| chr12:65899043 | CAAA | C | 7 | a0001c0001t0003g0122 a0001c0001t0007g0231 a0001c0001t0014g0017 others(4): Show |
7 | HG00741.hp1 HG01070.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-52313_250-5231 others(7): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65899043 | ||||||
| chr12:65899097 | G | A | 1 | a0001c0001t0062g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.250-52286G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899097 | |||||||
| chr12:65899291 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(5): Show |
8 | HG00609.hp2 HG00621.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-52092T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899291 | |||||||
| chr12:65899918 | A | G | 1 | a0001c0001t0018g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-51465A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899918 | |||||||
| chr12:65899993 | T | G | 4 | a0001c0001t0008g0057 a0001c0001t0008g0058 a0001c0001t0008g0061 others(1): Show |
4 | HG00558.hp2 HG02132.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-51390T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65899993 | |||||||
| chr12:65900015 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-51368C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900015 | |||||||
| chr12:65900096 | T | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-51287T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900096 | |||||||
| chr12:65900814 | G | A | 4 | a0001c0001t0002g0126 a0001c0001t0002g0140 a0001c0001t0036g0086 others(1): Show |
4 | HG00735.hp1 HG02300.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-50569G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900814 | |||||||
| chr12:65900854 | G | T | 5 | a0001c0001t0001g0075 a0001c0001t0009g0054 a0001c0001t0009g0074 others(2): Show |
5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-50529G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65900854 | |||||||
| chr12:65901010 | G | A | 1 | a0001c0001t0023g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-50373G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901010 | |||||||
| chr12:65901072 | G | C | 1 | a0001c0001t0011g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250-50311G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901072 | |||||||
| chr12:65901232 | A | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-50151A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901232 | |||||||
| chr12:65901316 | C | T | 1 | a0001c0001t0004g0033 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.250-50067C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901316 | |||||||
| chr12:65901323 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-50060A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901323 | |||||||
| chr12:65901493 | C | T | 7 | a0001c0001t0009g0072 a0001c0001t0012g0060 a0001c0001t0014g0059 others(4): Show |
7 | HG02083.hp2 NA18942.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.250-49890C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901493 | |||||||
| chr12:65901790 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-49593T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901790 | |||||||
| chr12:65901906 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-49477A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901906 | |||||||
| chr12:65901992 | A | G | 1 | a0001c0001t0023g0047 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.250-49391A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65901992 | |||||||
| chr12:65902010 | C | G | 1 | a0001c0001t0053g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-49373C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902010 | |||||||
| chr12:65902026 | T | G | 1 | a0001c0001t0053g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.250-49357T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902026 | |||||||
| chr12:65902056 | A | G | 1 | a0001c0001t0032g0128 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.250-49327A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902056 | |||||||
| chr12:65902067 | T | G | 4 | a0001c0001t0017g0224 a0001c0001t0017g0226 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-49316T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902067 | |||||||
| chr12:65902166 | GT | G | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-49207delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65902166 | ||||||
| chr12:65902167 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.250-49216T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902167 | |||||||
| chr12:65902218 | A | G | 1 | a0001c0001t0070g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.250-49165A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902218 | |||||||
| chr12:65902295 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.250-49088C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902295 | |||||||
| chr12:65902540 | T | C | 2 | a0001c0001t0003g0112 a0001c0001t0003g0234 |
2 | HG00280.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.250-48843T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902540 | |||||||
| chr12:65902958 | T | A | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-48425T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902958 | |||||||
| chr12:65902973 | G | A | 1 | a0001c0001t0034g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-48410G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65902973 | |||||||
| chr12:65903045 | G | T | 20 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(17): Show |
20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-48338G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903045 | |||||||
| chr12:65903316 | T | C | 1 | a0001c0001t0010g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.250-48067T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903316 | |||||||
| chr12:65903499 | T | C | 39 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(36): Show |
39 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.250-47884T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65903499 | |||||||
| chr12:65903629 | A | AT | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-47745dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65903629 | ||||||
| chr12:65904031 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-47352C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904031 | |||||||
| chr12:65904175 | TCATAGAA others(20): Show |
T | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-47206_250-4718 others(31): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65904175 | ||||||
| chr12:65904251 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(98): Show |
101 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.250-47132C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904251 | |||||||
| chr12:65904254 | G | A | 8 | a0001c0001t0010g0208 a0001c0001t0010g0213 a0001c0001t0010g0214 others(5): Show |
8 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-47129G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904254 | |||||||
| chr12:65904306 | C | T | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-47077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904306 | |||||||
| chr12:65904368 | A | G | 3 | a0001c0001t0003g0177 a0001c0001t0003g0233 a0001c0001t0050g0218 |
3 | HG02257.hp2 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.250-47015A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904368 | |||||||
| chr12:65904388 | A | G | 1 | a0001c0001t0015g0136 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.250-46995A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904388 | |||||||
| chr12:65904399 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.250-46984C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904399 | |||||||
| chr12:65904762 | A | G | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-46621A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904762 | |||||||
| chr12:65904908 | G | A | 6 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-46475G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904908 | |||||||
| chr12:65904922 | A | G | 37 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(34): Show |
37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.250-46461A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904922 | |||||||
| chr12:65904996 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.250-46387C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904996 | |||||||
| chr12:65904998 | C | T | 1 | a0001c0001t0017g0013 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.250-46385C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65904998 | |||||||
| chr12:65905182 | T | TCA | 8 | a0001c0001t0011g0027 a0001c0001t0021g0067 a0001c0001t0025g0183 others(5): Show |
8 | HG01192.hp2 HG02258.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-46178_250-4617 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | ||||||
| chr12:65905182 | T | TCACA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(35): Show |
38 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.250-46180_250-4617 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | ||||||
| chr12:65905182 | T | TCACACA | 9 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-46182_250-4617 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65905182 | ||||||
| chr12:65905269 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.250-46114T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905269 | |||||||
| chr12:65905362 | C | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-46021C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905362 | |||||||
| chr12:65905966 | AGTCATTA others(8): Show |
A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-45416_250-4540 others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905966 | |||||||
| chr12:65905983 | C | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.250-45400C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65905983 | |||||||
| chr12:65906255 | A | G | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-45128A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906255 | |||||||
| chr12:65906539 | C | A | 37 | a0001c0001t0001g0075 a0001c0001t0004g0024 a0001c0001t0004g0028 others(34): Show |
37 | HG00558.hp1 HG00609.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.250-44844C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906539 | |||||||
| chr12:65906603 | G | A | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-44780G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65906603 | |||||||
| chr12:65907052 | T | A | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-44331T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907052 | |||||||
| chr12:65907163 | G | A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-44220G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907163 | |||||||
| chr12:65907202 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.250-44181C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907202 | |||||||
| chr12:65907411 | C | CA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(36): Show |
39 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.250-43952dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65907411 | ||||||
| chr12:65907411 | CA | C | 10 | a0001c0001t0002g0133 a0001c0001t0002g0145 a0001c0001t0003g0112 others(7): Show |
10 | HG00741.hp1 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-43952delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65907411 | ||||||
| chr12:65907435 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.250-43948G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907435 | |||||||
| chr12:65907436 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.250-43947G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907436 | |||||||
| chr12:65907638 | C | T | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-43745C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907638 | |||||||
| chr12:65907769 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.250-43614C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907769 | |||||||
| chr12:65907831 | A | G | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-43552A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907831 | |||||||
| chr12:65907969 | T | A | 1 | a0001c0001t0034g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-43414T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65907969 | |||||||
| chr12:65908226 | C | T | 1 | a0001c0001t0073g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250-43157C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908226 | |||||||
| chr12:65908230 | C | T | 8 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-43153C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908230 | |||||||
| chr12:65908509 | C | T | 1 | a0001c0001t0019g0117 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.250-42874C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908509 | |||||||
| chr12:65908821 | A | G | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-42562A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65908821 | |||||||
| chr12:65909085 | G | T | 19 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(16): Show |
19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-42298G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909085 | |||||||
| chr12:65909288 | T | G | 1 | a0001c0001t0067g0230 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.250-42095T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909288 | |||||||
| chr12:65909396 | T | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-41987T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909396 | |||||||
| chr12:65909456 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-41927T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909456 | |||||||
| chr12:65909472 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-41911T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909472 | |||||||
| chr12:65909719 | T | C | 1 | a0001c0001t0068g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.250-41664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909719 | |||||||
| chr12:65909754 | G | A | 1 | a0001c0001t0008g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.250-41629G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909754 | |||||||
| chr12:65909900 | C | T | 1 | a0001c0001t0007g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-41483C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909900 | |||||||
| chr12:65909955 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0194 others(99): Show |
102 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.250-41428G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65909955 | |||||||
| chr12:65910056 | G | A | 5 | a0001c0001t0001g0075 a0001c0001t0009g0054 a0001c0001t0009g0074 others(2): Show |
5 | HG02040.hp1 HG02074.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-41327G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910056 | |||||||
| chr12:65910060 | G | A | 1 | a0001c0001t0047g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-41323G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910060 | |||||||
| chr12:65910070 | G | C | 1 | a0001c0001t0047g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-41313G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910070 | |||||||
| chr12:65910546 | A | G | 1 | a0001c0001t0018g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-40837A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910546 | |||||||
| chr12:65910618 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-40765G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910618 | |||||||
| chr12:65910793 | T | C | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-40590T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910793 | |||||||
| chr12:65910864 | G | A | 7 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-40519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910864 | |||||||
| chr12:65910972 | C | G | 9 | a0001c0001t0013g0003 a0001c0001t0013g0004 a0001c0001t0017g0224 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-40411C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65910972 | |||||||
| chr12:65911454 | C | A | 1 | a0001c0001t0004g0025 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.250-39929C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911454 | |||||||
| chr12:65911514 | G | A | 19 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(16): Show |
19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-39869G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911514 | |||||||
| chr12:65911615 | A | T | 1 | a0001c0001t0012g0055 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.250-39768A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911615 | |||||||
| chr12:65911923 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(8): Show |
11 | HG00609.hp2 HG00621.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.250-39460C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65911923 | |||||||
| chr12:65912583 | T | C | 1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-38800T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912583 | |||||||
| chr12:65912602 | G | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-38781G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912602 | |||||||
| chr12:65912661 | A | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(193): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.250-38722A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65912661 | |||||||
| chr12:65913089 | T | C | 19 | a0001c0001t0008g0056 a0001c0001t0008g0057 a0001c0001t0008g0058 others(16): Show |
19 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-38294T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913089 | |||||||
| chr12:65913090 | T | G | 3 | a0001c0001t0008g0057 a0001c0001t0008g0058 a0001c0001t0008g0061 |
3 | HG02132.hp1 NA18959.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.250-38293T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913090 | |||||||
| chr12:65913311 | C | T | 1 | a0001c0001t0051g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250-38072C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913311 | |||||||
| chr12:65913321 | C | T | 1 | a0001c0001t0041g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.250-38062C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913321 | |||||||
| chr12:65913353 | G | A | 7 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.250-38030G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913353 | |||||||
| chr12:65913438 | G | A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-37945G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913438 | |||||||
| chr12:65913567 | G | A | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.250-37816G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913567 | |||||||
| chr12:65913860 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.250-37523C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913860 | |||||||
| chr12:65913900 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.250-37483A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65913900 | |||||||
| chr12:65914050 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0109 others(111): Show |
114 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.250-37333A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914050 | |||||||
| chr12:65914168 | A | T | 2 | a0001c0001t0013g0204 a0001c0001t0027g0191 |
2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.250-37215A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914168 | |||||||
| chr12:65914421 | C | T | 1 | a0001c0001t0072g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.250-36962C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914421 | |||||||
| chr12:65914448 | T | A | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-36935T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914448 | |||||||
| chr12:65914522 | T | C | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-36861T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914522 | |||||||
| chr12:65914545 | A | T | 1 | a0001c0001t0003g0137 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250-36838A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914545 | |||||||
| chr12:65914645 | A | T | 3 | a0001c0001t0003g0122 a0001c0001t0007g0231 a0001c0001t0056g0228 |
3 | HG00741.hp1 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-36738A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914645 | |||||||
| chr12:65914668 | G | T | 1 | a0001c0001t0043g0002 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.250-36715G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914668 | |||||||
| chr12:65914696 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.250-36687C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914696 | |||||||
| chr12:65914745 | G | A | 1 | a0001c0001t0047g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-36638G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914745 | |||||||
| chr12:65914864 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0109 others(111): Show |
114 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.250-36519A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914864 | |||||||
| chr12:65914919 | C | T | 1 | a0001c0001t0011g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-36464C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65914919 | |||||||
| chr12:65915008 | C | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-36375C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915008 | |||||||
| chr12:65915079 | C | G | 1 | a0001c0001t0003g0234 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.250-36304C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915079 | |||||||
| chr12:65915135 | T | C | 2 | a0001c0001t0002g0099 a0001c0001t0028g0144 |
2 | HG00673.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.250-36248T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915135 | |||||||
| chr12:65915416 | G | GT | 20 | a0001c0001t0001g0109 a0001c0001t0008g0056 a0001c0001t0008g0057 others(17): Show |
20 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.250-35966dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65915416 | ||||||
| chr12:65915424 | T | C | 1 | a0001c0001t0011g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.250-35959T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915424 | |||||||
| chr12:65915818 | A | G | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-35565A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915818 | |||||||
| chr12:65915946 | G | C | 1 | a0001c0001t0037g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-35437G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65915946 | |||||||
| chr12:65916146 | A | G | 1 | a0002c0002t0002g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.250-35237A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916146 | |||||||
| chr12:65916217 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-35166C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916217 | |||||||
| chr12:65916218 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0194 a0001c0001t0002g0001 others(23): Show |
26 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-35165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916218 | |||||||
| chr12:65916292 | G | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-35091G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916292 | |||||||
| chr12:65916766 | A | G | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-34617A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916766 | |||||||
| chr12:65916815 | G | T | 1 | a0001c0001t0064g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250-34568G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916815 | |||||||
| chr12:65916888 | T | G | 1 | a0001c0001t0011g0184 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.250-34495T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65916888 | |||||||
| chr12:65917277 | C | T | 1 | a0001c0001t0005g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.250-34106C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917277 | |||||||
| chr12:65917465 | C | G | 1 | a0001c0001t0021g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.250-33918C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917465 | |||||||
| chr12:65917730 | G | C | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.250-33653G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917730 | |||||||
| chr12:65917749 | G | A | 1 | a0001c0001t0016g0045 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.250-33634G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65917749 | |||||||
| chr12:65918240 | T | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-33143T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918240 | |||||||
| chr12:65918476 | T | G | 8 | a0001c0001t0013g0004 a0001c0001t0017g0224 a0001c0001t0033g0227 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-32907T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918476 | |||||||
| chr12:65918658 | G | A | 8 | a0001c0001t0013g0004 a0001c0001t0017g0224 a0001c0001t0033g0227 others(5): Show |
8 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-32725G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918658 | |||||||
| chr12:65918665 | G | A | 1 | a0001c0001t0009g0034 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.250-32718G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918665 | |||||||
| chr12:65918704 | G | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-32679G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918704 | |||||||
| chr12:65918978 | G | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-32405G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65918978 | |||||||
| chr12:65919422 | T | G | 2 | a0001c0001t0001g0150 a0001c0001t0002g0156 |
2 | HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-31961T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65919422 | |||||||
| chr12:65919730 | G | A | 1 | a0001c0001t0070g0210 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.250-31653G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65919730 | |||||||
| chr12:65920186 | G | A | 1 | a0001c0001t0034g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.250-31197G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920186 | |||||||
| chr12:65920568 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30815A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920568 | |||||||
| chr12:65920640 | C | T | 2 | a0001c0001t0023g0047 a0001c0001t0023g0048 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.250-30743C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920640 | |||||||
| chr12:65920685 | C | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-30698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920685 | |||||||
| chr12:65920804 | C | T | 3 | a0001c0001t0017g0224 a0001c0001t0045g0026 a0001c0001t0057g0225 |
3 | HG02559.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.250-30579C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920804 | |||||||
| chr12:65920879 | T | A | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30504T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920879 | |||||||
| chr12:65920881 | G | A | 21 | a0001c0001t0001g0109 a0001c0001t0003g0130 a0001c0001t0008g0056 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-30502G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920881 | |||||||
| chr12:65920886 | G | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0053g0180 others(2): Show |
5 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-30497G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920886 | |||||||
| chr12:65920979 | A | T | 19 | a0001c0001t0003g0112 a0001c0001t0003g0234 a0001c0001t0005g0094 others(16): Show |
19 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.250-30404A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65920979 | |||||||
| chr12:65921018 | T | C | 3 | a0001c0001t0008g0167 a0001c0001t0009g0168 a0001c0001t0011g0169 |
3 | HG02683.hp1 HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.250-30365T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921018 | |||||||
| chr12:65921040 | G | T | 1 | a0001c0001t0017g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.250-30343G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921040 | |||||||
| chr12:65921127 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0007g0231 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.250-30256T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921127 | |||||||
| chr12:65921164 | T | C | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-30219T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921164 | |||||||
| chr12:65921507 | A | G | 9 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-29876A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921507 | |||||||
| chr12:65921599 | CCTGA | C | 21 | a0001c0001t0001g0109 a0001c0001t0003g0130 a0001c0001t0008g0056 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-29781_250-2977 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65921599 | ||||||
| chr12:65921699 | C | G | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-29684C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921699 | |||||||
| chr12:65921996 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.250-29387A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65921996 | |||||||
| chr12:65922118 | T | C | 101 | a0001c0001t0001g0075 a0001c0001t0001g0107 a0001c0001t0001g0109 others(98): Show |
101 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.250-29265T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922118 | |||||||
| chr12:65922218 | C | T | 10 | a0001c0001t0010g0190 a0001c0001t0010g0208 a0001c0001t0018g0207 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-29165C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922218 | |||||||
| chr12:65922263 | C | G | 3 | a0001c0001t0008g0069 a0001c0001t0009g0076 a0001c0001t0012g0049 |
3 | HG02451.hp1 HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-29120C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922263 | |||||||
| chr12:65922309 | G | A | 1 | a0001c0001t0050g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.250-29074G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922309 | |||||||
| chr12:65922601 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.250-28782G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922601 | |||||||
| chr12:65922704 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(189): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.250-28679G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922704 | |||||||
| chr12:65922891 | G | A | 18 | a0001c0001t0009g0076 a0001c0001t0010g0190 a0001c0001t0013g0003 others(15): Show |
18 | HG01167.hp1 HG01169.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-28492G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65922891 | |||||||
| chr12:65923118 | G | A | 1 | a0001c0001t0008g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.250-28265G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923118 | |||||||
| chr12:65923133 | A | C | 2 | a0001c0001t0002g0176 a0001c0001t0013g0004 |
2 | HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.250-28250A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923133 | |||||||
| chr12:65923359 | C | T | 1 | a0001c0001t0008g0056 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.250-28024C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923359 | |||||||
| chr12:65923425 | T | G | 1 | a0001c0001t0035g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-27958T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923425 | |||||||
| chr12:65923707 | C | A | 6 | a0001c0001t0018g0207 a0001c0001t0018g0209 a0001c0001t0018g0211 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-27676C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923707 | |||||||
| chr12:65923721 | T | A | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-27662T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923721 | |||||||
| chr12:65923757 | C | A | 9 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(6): Show |
9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-27626C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923757 | |||||||
| chr12:65923795 | G | A | 43 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(40): Show |
43 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.250-27588G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923795 | |||||||
| chr12:65923808 | G | A | 1 | a0001c0001t0015g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.250-27575G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65923808 | |||||||
| chr12:65924178 | C | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-27205C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924178 | |||||||
| chr12:65924368 | C | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-27015C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924368 | |||||||
| chr12:65924437 | C | T | 3 | a0001c0001t0006g0078 a0001c0001t0006g0079 a0001c0001t0006g0081 |
3 | HG01074.hp1 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.250-26946C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924437 | |||||||
| chr12:65924450 | T | TAC | 4 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 others(1): Show |
4 | HG01891.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-26917_250-2691 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65924450 | ||||||
| chr12:65924454 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0075g0087 |
2 | HG02027.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.250-26929C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924454 | |||||||
| chr12:65924669 | G | A | 1 | a0001c0001t0009g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.250-26714G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924669 | |||||||
| chr12:65924791 | C | G | 2 | a0001c0001t0008g0056 a0001c0001t0073g0189 |
2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.250-26592C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924791 | |||||||
| chr12:65924929 | T | C | 2 | a0001c0001t0016g0062 a0001c0001t0016g0063 |
2 | NA18970.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.250-26454T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65924929 | |||||||
| chr12:65925404 | A | C | 4 | a0001c0001t0015g0044 a0001c0001t0017g0224 a0001c0001t0024g0046 others(1): Show |
4 | HG02647.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-25979A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925404 | |||||||
| chr12:65925653 | A | G | 6 | a0001c0001t0010g0009 a0001c0001t0046g0216 a0001c0001t0060g0007 others(3): Show |
6 | HG01361.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-25730A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925653 | |||||||
| chr12:65925719 | T | C | 4 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0055g0182 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-25664T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925719 | |||||||
| chr12:65925755 | A | G | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-25628A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925755 | |||||||
| chr12:65925777 | C | CG | 87 | a0001c0001t0001g0194 a0001c0001t0004g0024 a0001c0001t0004g0025 others(84): Show |
87 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.250-25603dupG | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65925777 | ||||||
| chr12:65925905 | T | C | 1 | a0001c0001t0006g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.250-25478T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65925905 | |||||||
| chr12:65926094 | T | A | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-25289T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926094 | |||||||
| chr12:65926095 | A | T | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-25288A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926095 | |||||||
| chr12:65926216 | A | C | 83 | a0001c0001t0001g0194 a0001c0001t0004g0024 a0001c0001t0004g0025 others(80): Show |
83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-25167A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926216 | |||||||
| chr12:65926510 | T | A | 1 | a0001c0001t0030g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.250-24873T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926510 | |||||||
| chr12:65926680 | A | G | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-24703A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926680 | |||||||
| chr12:65926978 | T | C | 1 | a0001c0001t0012g0031 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.250-24405T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65926978 | |||||||
| chr12:65927041 | G | A | 9 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(6): Show |
9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-24342G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927041 | |||||||
| chr12:65927093 | G | A | 83 | a0001c0001t0001g0194 a0001c0001t0004g0024 a0001c0001t0004g0025 others(80): Show |
83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-24290G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927093 | |||||||
| chr12:65927111 | A | G | 44 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(41): Show |
44 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.250-24272A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927111 | |||||||
| chr12:65927114 | G | A | 42 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(39): Show |
42 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.250-24269G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927114 | |||||||
| chr12:65927145 | C | T | 1 | a0001c0001t0002g0140 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.250-24238C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927145 | |||||||
| chr12:65927564 | C | G | 83 | a0001c0001t0001g0194 a0001c0001t0004g0024 a0001c0001t0004g0025 others(80): Show |
83 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.250-23819C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927564 | |||||||
| chr12:65927566 | C | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0001g0107 others(14): Show |
17 | HG00423.hp2 HG01192.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.250-23817C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927566 | |||||||
| chr12:65927692 | T | A | 2 | a0001c0001t0012g0049 a0001c0001t0027g0186 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-23691T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927692 | |||||||
| chr12:65927712 | T | C | 87 | a0001c0001t0001g0194 a0001c0001t0004g0024 a0001c0001t0004g0025 others(84): Show |
87 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.250-23671T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927712 | |||||||
| chr12:65927831 | C | CTG | 70 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(67): Show |
70 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.250-23532_250-2353 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | ||||||
| chr12:65927831 | C | CTGTG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0091 a0001c0001t0002g0001 others(12): Show |
15 | HG01361.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.250-23534_250-2353 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | ||||||
| chr12:65927831 | C | CTGTGTG | 75 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(72): Show |
75 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.250-23536_250-2353 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | ||||||
| chr12:65927831 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-23540_250-2353 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927831 | ||||||
| chr12:65927853 | A | G | 87 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(84): Show |
87 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.250-23530A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927853 | |||||||
| chr12:65927891 | G | A | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-23492G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927891 | |||||||
| chr12:65927949 | GTA | G | 16 | a0001c0001t0001g0075 a0001c0001t0003g0118 a0001c0001t0003g0130 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-23418_250-2341 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | ||||||
| chr12:65927949 | GTATA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-23420_250-2341 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | ||||||
| chr12:65927949 | GTATATA | G | 86 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(83): Show |
86 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.250-23422_250-2341 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65927949 | ||||||
| chr12:65927964 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-23419T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65927964 | |||||||
| chr12:65928160 | C | T | 3 | a0001c0001t0015g0044 a0001c0001t0024g0046 a0001c0001t0024g0051 |
3 | HG02647.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.250-23223C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928160 | |||||||
| chr12:65928181 | C | T | 1 | a0001c0001t0047g0011 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.250-23202C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928181 | |||||||
| chr12:65928275 | C | T | 2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-23108C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928275 | |||||||
| chr12:65928319 | T | C | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-23064T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928319 | |||||||
| chr12:65928542 | C | A | 82 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(79): Show |
82 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.250-22841C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65928542 | |||||||
| chr12:65929011 | C | A | 1 | a0001c0001t0007g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-22372C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929011 | |||||||
| chr12:65929061 | G | A | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-22322G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929061 | |||||||
| chr12:65929304 | G | T | 1 | a0001c0001t0060g0007 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250-22079G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929304 | |||||||
| chr12:65929429 | C | G | 1 | a0001c0001t0003g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.250-21954C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929429 | |||||||
| chr12:65929609 | A | G | 1 | a0001c0001t0011g0040 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.250-21774A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929609 | |||||||
| chr12:65929629 | A | C | 1 | a0001c0001t0028g0144 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.250-21754A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929629 | |||||||
| chr12:65929820 | T | C | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.250-21563T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929820 | |||||||
| chr12:65929930 | G | T | 1 | a0001c0001t0023g0048 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.250-21453G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929930 | |||||||
| chr12:65929939 | C | T | 2 | a0001c0001t0009g0076 a0001c0001t0035g0010 |
2 | HG02896.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.250-21444C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65929939 | |||||||
| chr12:65930096 | T | C | 3 | a0001c0001t0003g0125 a0001c0001t0007g0083 a0001c0001t0007g0165 |
3 | HG00741.hp2 HG01433.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.250-21287T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930096 | |||||||
| chr12:65930107 | G | A | 1 | a0001c0001t0006g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.250-21276G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930107 | |||||||
| chr12:65930187 | A | G | 2 | a0001c0001t0010g0213 a0001c0001t0010g0214 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.250-21196A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930187 | |||||||
| chr12:65930327 | C | T | 2 | a0001c0001t0014g0021 a0001c0001t0014g0022 |
2 | HG00733.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.250-21056C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930327 | |||||||
| chr12:65930387 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0002g0145 |
2 | HG03831.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.250-20996C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930387 | |||||||
| chr12:65930749 | G | A | 1 | a0001c0001t0007g0100 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.250-20634G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930749 | |||||||
| chr12:65930810 | C | T | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-20573C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65930810 | |||||||
| chr12:65931099 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0036g0086 |
2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.250-20284C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931099 | |||||||
| chr12:65931106 | A | AT | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-20272dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931106 | ||||||
| chr12:65931523 | G | A | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250-19860G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931523 | |||||||
| chr12:65931528 | C | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0137 |
2 | NA18952.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.250-19855C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931528 | |||||||
| chr12:65931551 | T | TTG | 16 | a0001c0001t0006g0159 a0001c0001t0007g0165 a0001c0001t0008g0035 others(13): Show |
16 | HG00558.hp2 HG01361.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-19794_250-1979 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | T | TTGTG | 29 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(26): Show |
29 | HG00609.hp1 HG00735.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.250-19796_250-1979 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | T | TTGTGTG | 9 | a0001c0001t0004g0041 a0001c0001t0005g0147 a0001c0001t0005g0193 others(6): Show |
9 | HG01891.hp1 HG02738.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-19798_250-1979 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | T | TTGTGTGT others(1): Show |
26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG00558.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-19800_250-1979 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | T | TTGTGTGT others(3): Show |
3 | a0001c0001t0004g0052 a0001c0001t0006g0138 a0001c0001t0012g0055 |
3 | HG01496.hp1 HG04204.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.250-19802_250-1979 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTG | T | 15 | a0001c0001t0001g0123 a0001c0001t0002g0146 a0001c0001t0002g0176 others(12): Show |
15 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.250-19794_250-1979 others(6): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTGTG | T | 8 | a0001c0001t0001g0077 a0001c0001t0003g0122 a0001c0001t0016g0023 others(5): Show |
8 | HG01884.hp2 HG02300.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-19796_250-1979 others(8): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTGTGTG | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0091 others(71): Show |
74 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.250-19798_250-1979 others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0085 a0001c0001t0040g0217 a0001c0001t0046g0216 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-19800_250-1979 others(12): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.250-19802_250-1979 others(14): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931551 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0007g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.250-19806_250-1979 others(18): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65931551 | ||||||
| chr12:65931730 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.250-19653C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931730 | |||||||
| chr12:65931909 | T | C | 33 | a0001c0001t0003g0016 a0001c0001t0003g0110 a0001c0001t0003g0112 others(30): Show |
33 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.250-19474T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65931909 | |||||||
| chr12:65932063 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.250-19320T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932063 | |||||||
| chr12:65932113 | G | T | 3 | a0001c0001t0012g0060 a0001c0001t0027g0191 a0001c0001t0048g0020 |
3 | NA18952.hp1 NA18972.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.250-19270G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932113 | |||||||
| chr12:65932224 | T | C | 1 | a0001c0001t0012g0014 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.250-19159T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932224 | |||||||
| chr12:65932359 | G | A | 57 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0089 others(54): Show |
57 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.250-19024G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932359 | |||||||
| chr12:65932479 | C | T | 1 | a0001c0001t0006g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.250-18904C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932479 | |||||||
| chr12:65932536 | T | C | 1 | a0001c0001t0076g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.250-18847T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932536 | |||||||
| chr12:65932573 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.250-18810T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932573 | |||||||
| chr12:65932763 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0002g0156 |
2 | HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-18620A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65932763 | |||||||
| chr12:65933154 | A | G | 4 | a0001c0001t0008g0069 a0001c0001t0014g0017 a0001c0001t0022g0018 others(1): Show |
4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-18229A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933154 | |||||||
| chr12:65933163 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(154): Show |
157 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.250-18220A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933163 | |||||||
| chr12:65933248 | C | T | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-18135C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933248 | |||||||
| chr12:65933367 | C | T | 1 | a0001c0001t0009g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250-18016C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933367 | |||||||
| chr12:65933403 | C | T | 2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-17980C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933403 | |||||||
| chr12:65933474 | A | G | 16 | a0001c0001t0001g0075 a0001c0001t0003g0118 a0001c0001t0003g0130 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.250-17909A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933474 | |||||||
| chr12:65933801 | A | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0139 others(1): Show |
4 | HG00621.hp2 NA18941.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-17582A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933801 | |||||||
| chr12:65933852 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(163): Show |
166 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250-17531A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933852 | |||||||
| chr12:65933875 | T | C | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0031g0195 |
3 | HG00621.hp1 HG02165.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.250-17508T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65933875 | |||||||
| chr12:65934198 | T | C | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-17185T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934198 | |||||||
| chr12:65934233 | A | G | 2 | a0001c0001t0012g0049 a0001c0001t0027g0186 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-17150A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934233 | |||||||
| chr12:65934247 | C | T | 82 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(79): Show |
82 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.250-17136C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934247 | |||||||
| chr12:65934374 | T | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-17009T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934374 | |||||||
| chr12:65934466 | C | T | 1 | a0001c0001t0076g0113 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.250-16917C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934466 | |||||||
| chr12:65934607 | C | T | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-16776C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934607 | |||||||
| chr12:65934647 | T | C | 2 | a0001c0001t0013g0003 a0001c0001t0043g0002 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.250-16736T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934647 | |||||||
| chr12:65934851 | C | G | 1 | a0001c0001t0037g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-16532C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65934851 | |||||||
| chr12:65935086 | C | T | 12 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(9): Show |
12 | HG00423.hp1 NA18952.hp1 NA18961.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-16297C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935086 | |||||||
| chr12:65935464 | G | A | 1 | a0001c0001t0008g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.250-15919G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935464 | |||||||
| chr12:65935585 | A | G | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-15798A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935585 | |||||||
| chr12:65935889 | A | T | 1 | a0001c0001t0009g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.250-15494A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65935889 | |||||||
| chr12:65936212 | A | AT | 107 | a0001c0001t0001g0075 a0001c0001t0002g0176 a0001c0001t0003g0016 others(104): Show |
107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.250-15157dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65936212 | ||||||
| chr12:65936212 | AT | A | 12 | a0001c0001t0002g0133 a0001c0001t0005g0173 a0001c0001t0005g0174 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.250-15157delT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65936212 | ||||||
| chr12:65936421 | A | C | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-14962A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936421 | |||||||
| chr12:65936564 | T | G | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-14819T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936564 | |||||||
| chr12:65936565 | C | T | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.250-14818C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936565 | |||||||
| chr12:65936938 | A | T | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.250-14445A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65936938 | |||||||
| chr12:65937284 | C | G | 2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.250-14099C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937284 | |||||||
| chr12:65937480 | G | A | 1 | a0001c0001t0003g0112 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.250-13903G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937480 | |||||||
| chr12:65937585 | G | C | 82 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(79): Show |
82 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.250-13798G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937585 | |||||||
| chr12:65937883 | C | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-13500C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937883 | |||||||
| chr12:65937908 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.250-13475C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937908 | |||||||
| chr12:65937912 | G | A | 1 | a0001c0001t0051g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.250-13471G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65937912 | |||||||
| chr12:65938939 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0109 |
2 | HG01978.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.250-12444C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65938939 | |||||||
| chr12:65939029 | G | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-12354G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939029 | |||||||
| chr12:65939166 | C | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-12217C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939166 | |||||||
| chr12:65939375 | A | T | 1 | a0001c0001t0011g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.250-12008A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939375 | |||||||
| chr12:65939419 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.250-11964G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939419 | |||||||
| chr12:65939673 | G | A | 1 | a0001c0001t0074g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-11710G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939673 | |||||||
| chr12:65939725 | T | C | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-11658T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939725 | |||||||
| chr12:65939847 | G | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-11536G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939847 | |||||||
| chr12:65939884 | G | C | 5 | a0001c0001t0008g0057 a0001c0001t0008g0058 a0001c0001t0008g0061 others(2): Show |
5 | HG02132.hp1 NA18951.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-11499G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939884 | |||||||
| chr12:65939995 | T | G | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-11388T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65939995 | |||||||
| chr12:65940113 | G | GA | 11 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-11261dupA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65940113 | ||||||
| chr12:65940246 | T | C | 5 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(2): Show |
5 | HG01243.hp1 HG02717.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-11137T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65940246 | |||||||
| chr12:65940964 | C | T | 2 | a0001c0001t0003g0112 a0001c0001t0003g0234 |
2 | HG00280.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.250-10419C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65940964 | |||||||
| chr12:65941428 | C | T | 1 | a0001c0001t0007g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.250-9955C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941428 | |||||||
| chr12:65941923 | T | C | 11 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-9460T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941923 | |||||||
| chr12:65941958 | A | T | 9 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(6): Show |
9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-9425A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65941958 | |||||||
| chr12:65942322 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.250-9061T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942322 | |||||||
| chr12:65942912 | C | T | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-8471C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942912 | |||||||
| chr12:65942986 | G | A | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-8397G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65942986 | |||||||
| chr12:65943232 | T | G | 1 | a0001c0001t0021g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.250-8151T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943232 | |||||||
| chr12:65943246 | A | G | 1 | a0001c0001t0036g0086 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.250-8137A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943246 | |||||||
| chr12:65943413 | A | G | 1 | a0001c0001t0073g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.250-7970A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943413 | |||||||
| chr12:65943436 | A | T | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.250-7947A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943436 | |||||||
| chr12:65943462 | G | C | 3 | a0001c0001t0001g0150 a0001c0001t0002g0156 a0002c0002t0002g0098 |
3 | HG02027.hp1 HG02083.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.250-7921G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943462 | |||||||
| chr12:65943864 | G | A | 1 | a0001c0001t0019g0117 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.250-7519G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943864 | |||||||
| chr12:65943902 | C | T | 1 | a0001c0001t0005g0114 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-7481C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65943902 | |||||||
| chr12:65944422 | G | T | 77 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(74): Show |
77 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.250-6961G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944422 | |||||||
| chr12:65944651 | A | AC | 82 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(79): Show |
82 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.250-6730dupC | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65944651 | ||||||
| chr12:65944698 | CA | C | 2 | a0001c0001t0001g0152 a0001c0001t0001g0155 |
2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.250-6684delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944698 | |||||||
| chr12:65944710 | C | T | 1 | a0001c0001t0054g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250-6673C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944710 | |||||||
| chr12:65944802 | C | T | 2 | a0001c0001t0009g0168 a0001c0001t0011g0169 |
2 | HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.250-6581C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65944802 | |||||||
| chr12:65944898 | T | TTGCCCAT others(10): Show |
5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-6484_250-6468d others(19): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65944898 | ||||||
| chr12:65945126 | G | A | 1 | a0001c0001t0024g0046 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.250-6257G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65945126 | |||||||
| chr12:65945235 | TA | T | 9 | a0001c0001t0005g0174 a0001c0001t0005g0229 a0001c0001t0008g0167 others(6): Show |
9 | HG00733.hp1 HG01070.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-6134delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr12 | 65945235 | ||||||
| chr12:65945354 | C | A | 5 | a0001c0001t0015g0044 a0001c0001t0017g0224 a0001c0001t0024g0046 others(2): Show |
5 | HG02647.hp1 HG03041.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-6029C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65945354 | |||||||
| chr12:65946087 | G | A | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-5296G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946087 | |||||||
| chr12:65946228 | A | G | 1 | a0001c0001t0010g0208 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.250-5155A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946228 | |||||||
| chr12:65946506 | T | A | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.250-4877T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946506 | |||||||
| chr12:65946588 | G | C | 1 | a0001c0001t0042g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-4795G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946588 | |||||||
| chr12:65946923 | A | C | 81 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(78): Show |
81 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.250-4460A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946923 | |||||||
| chr12:65946993 | T | C | 11 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.250-4390T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65946993 | |||||||
| chr12:65947124 | T | C | 1 | a0001c0001t0005g0114 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.250-4259T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947124 | |||||||
| chr12:65947144 | G | A | 1 | a0001c0001t0005g0205 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.250-4239G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947144 | |||||||
| chr12:65947209 | T | G | 1 | a0001c0001t0007g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.250-4174T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947209 | |||||||
| chr12:65947255 | G | A | 10 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(7): Show |
10 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-4128G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947255 | |||||||
| chr12:65947269 | G | A | 2 | a0001c0001t0026g0199 a0001c0001t0026g0215 |
2 | NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.250-4114G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947269 | |||||||
| chr12:65947542 | T | C | 1 | a0001c0001t0040g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.250-3841T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947542 | |||||||
| chr12:65947546 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.250-3837A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947546 | |||||||
| chr12:65947729 | A | G | 1 | a0001c0001t0042g0121 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-3654A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947729 | |||||||
| chr12:65947804 | G | A | 1 | a0001c0001t0011g0040 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.250-3579G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947804 | |||||||
| chr12:65947822 | G | A | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-3561G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947822 | |||||||
| chr12:65947944 | A | G | 1 | a0001c0001t0026g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.250-3439A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65947944 | |||||||
| chr12:65948093 | C | T | 16 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(13): Show |
16 | HG00423.hp1 HG04204.hp1 NA18952.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-3290C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948093 | |||||||
| chr12:65948333 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.250-3050A>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948333 | |||||||
| chr12:65948337 | G | A | 16 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(13): Show |
16 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-3046G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948337 | |||||||
| chr12:65948447 | G | A | 2 | a0001c0001t0005g0221 a0001c0001t0049g0039 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-2936G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948447 | |||||||
| chr12:65948481 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.250-2902T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948481 | |||||||
| chr12:65948824 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.250-2559G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65948824 | |||||||
| chr12:65949088 | C | T | 17 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(14): Show |
17 | HG00423.hp1 HG03017.hp2 HG04204.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-2295C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949088 | |||||||
| chr12:65949452 | G | T | 1 | a0001c0001t0003g0130 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.250-1931G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949452 | |||||||
| chr12:65949620 | G | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(163): Show |
166 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.250-1763G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65949620 | |||||||
| chr12:65950030 | C | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0085 others(162): Show |
165 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.250-1353C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950030 | |||||||
| chr12:65950070 | C | T | 2 | a0001c0001t0012g0049 a0001c0001t0027g0186 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.250-1313C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950070 | |||||||
| chr12:65950114 | C | A | 3 | a0001c0001t0003g0142 a0001c0001t0007g0111 a0001c0001t0007g0141 |
3 | HG01167.hp2 HG01261.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.250-1269C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950114 | |||||||
| chr12:65950926 | A | G | 6 | a0001c0001t0018g0207 a0001c0001t0018g0209 a0001c0001t0018g0211 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-457A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65950926 | |||||||
| chr12:65951262 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.250-121T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 3/4 | chr12 | 65951262 | |||||||
| chr12:65951424 | T | C | 1 | a0001c0001t0065g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.282+9T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65951424 | |||||||
| chr12:65951605 | C | G | 1 | a0001c0001t0021g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282+190C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65951605 | |||||||
| chr12:65952341 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(81): Show |
84 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.282+926A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952341 | |||||||
| chr12:65952427 | T | C | 2 | a0001c0001t0015g0170 a0001c0001t0015g0171 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.282+1012T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952427 | |||||||
| chr12:65952589 | TA | T | 5 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+1182delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65952589 | ||||||
| chr12:65952844 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(150): Show |
153 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.282+1429T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952844 | |||||||
| chr12:65952934 | T | C | 16 | a0001c0001t0003g0118 a0001c0001t0003g0130 a0001c0001t0003g0235 others(13): Show |
16 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.282+1519T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65952934 | |||||||
| chr12:65953080 | A | G | 1 | a0001c0001t0074g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+1665A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953080 | |||||||
| chr12:65953149 | C | A | 1 | a0001c0001t0017g0226 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.282+1734C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953149 | |||||||
| chr12:65953239 | T | C | 1 | a0001c0001t0017g0224 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.282+1824T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953239 | |||||||
| chr12:65953257 | T | C | 1 | a0001c0001t0041g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282+1842T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953257 | |||||||
| chr12:65953270 | G | A | 1 | a0001c0001t0025g0183 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.282+1855G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953270 | |||||||
| chr12:65953384 | T | G | 7 | a0001c0001t0001g0077 a0001c0001t0001g0109 a0001c0001t0001g0194 others(4): Show |
7 | HG00609.hp2 HG00735.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1969T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953384 | |||||||
| chr12:65953422 | C | T | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+2007C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953422 | |||||||
| chr12:65953458 | G | A | 2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.282+2043G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953458 | |||||||
| chr12:65953588 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(161): Show |
164 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.282+2173G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953588 | |||||||
| chr12:65953593 | T | C | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+2178T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953593 | |||||||
| chr12:65953657 | C | G | 10 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0001g0103 others(7): Show |
10 | HG01361.hp1 HG01496.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.282+2242C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953657 | |||||||
| chr12:65953914 | T | C | 2 | a0001c0001t0016g0023 a0001c0001t0016g0045 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.282+2499T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65953914 | |||||||
| chr12:65954090 | A | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(80): Show |
83 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+2675A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954090 | |||||||
| chr12:65954157 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.282+2742C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954157 | |||||||
| chr12:65954354 | T | A | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.282+2939T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954354 | |||||||
| chr12:65954600 | C | A | 5 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+3185C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954600 | |||||||
| chr12:65954889 | T | C | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+3474T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954889 | |||||||
| chr12:65954943 | A | G | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+3528A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65954943 | |||||||
| chr12:65955010 | A | G | 44 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(41): Show |
44 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.282+3595A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955010 | |||||||
| chr12:65955022 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.282+3607T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955022 | |||||||
| chr12:65955041 | C | T | 1 | a0001c0001t0053g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.282+3626C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955041 | |||||||
| chr12:65955046 | C | T | 4 | a0001c0001t0008g0069 a0001c0001t0014g0017 a0001c0001t0022g0018 others(1): Show |
4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+3631C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955046 | |||||||
| chr12:65955251 | A | G | 1 | a0001c0001t0006g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.282+3836A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955251 | |||||||
| chr12:65955306 | TA | T | 3 | a0001c0001t0005g0088 a0001c0001t0012g0055 a0001c0001t0025g0185 |
3 | NA18991.hp2 NA19030.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.282+3898delA | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65955306 | ||||||
| chr12:65955315 | A | C | 1 | a0001c0001t0005g0094 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.282+3900A>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955315 | |||||||
| chr12:65955655 | A | G | 1 | a0001c0001t0031g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.282+4240A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955655 | |||||||
| chr12:65955679 | A | G | 1 | a0001c0001t0061g0219 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.282+4264A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955679 | |||||||
| chr12:65955726 | G | A | 1 | a0001c0001t0074g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+4311G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65955726 | |||||||
| chr12:65956012 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0002g0201 others(1): Show |
4 | HG02027.hp2 NA18943.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+4597G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956012 | |||||||
| chr12:65956032 | A | G | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.282+4617A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956032 | |||||||
| chr12:65956063 | TCACTCTA others(1): Show |
T | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+4654_282+4661d others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65956063 | ||||||
| chr12:65956146 | C | T | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4731C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956146 | |||||||
| chr12:65956320 | C | T | 3 | a0001c0001t0010g0009 a0001c0001t0060g0007 a0001c0001t0064g0008 |
3 | HG02615.hp2 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.282+4905C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956320 | |||||||
| chr12:65956691 | C | T | 5 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+5276C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956691 | |||||||
| chr12:65956744 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.282+5329G>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956744 | |||||||
| chr12:65956850 | G | A | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+5435G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956850 | |||||||
| chr12:65956938 | G | A | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282+5523G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65956938 | |||||||
| chr12:65957337 | G | A | 26 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(23): Show |
26 | HG00423.hp1 HG02647.hp1 HG02922.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-5908G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957337 | |||||||
| chr12:65957361 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0151 a0001c0001t0001g0153 others(3): Show |
6 | HG00621.hp1 HG02165.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5884C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957361 | |||||||
| chr12:65957515 | T | C | 1 | a0001c0001t0033g0227 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283-5730T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957515 | |||||||
| chr12:65957609 | C | T | 5 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-5636C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957609 | |||||||
| chr12:65957688 | C | G | 2 | a0001c0001t0015g0170 a0001c0001t0015g0171 |
2 | HG02615.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.283-5557C>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957688 | |||||||
| chr12:65957725 | C | T | 2 | a0001c0001t0023g0047 a0001c0001t0023g0048 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283-5520C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957725 | |||||||
| chr12:65957763 | A | G | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-5482A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957763 | |||||||
| chr12:65957932 | A | G | 1 | a0001c0001t0056g0228 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.283-5313A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65957932 | |||||||
| chr12:65958000 | C | CT | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-5245_283-5244i others(3): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958000 | |||||||
| chr12:65958038 | T | C | 44 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(41): Show |
44 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.283-5207T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958038 | |||||||
| chr12:65958046 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(172): Show |
175 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.283-5199T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958046 | |||||||
| chr12:65958371 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0091 others(15): Show |
18 | HG00423.hp2 HG01192.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-4874G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958371 | |||||||
| chr12:65958406 | A | G | 1 | a0001c0001t0006g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.283-4839A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958406 | |||||||
| chr12:65958792 | C | T | 31 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(28): Show |
31 | HG00423.hp1 HG01884.hp2 HG02559.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-4453C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958792 | |||||||
| chr12:65958914 | G | A | 1 | a0001c0001t0009g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283-4331G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958914 | |||||||
| chr12:65958981 | G | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0097 others(6): Show |
9 | HG00621.hp2 HG00673.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-4264G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65958981 | |||||||
| chr12:65959496 | C | T | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-3749C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959496 | |||||||
| chr12:65959507 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283-3738T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959507 | |||||||
| chr12:65959893 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.283-3352T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959893 | |||||||
| chr12:65959959 | G | A | 1 | a0001c0001t0041g0172 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.283-3286G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65959959 | |||||||
| chr12:65960075 | G | C | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-3170G>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960075 | |||||||
| chr12:65960111 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(110): Show |
113 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.283-3134G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960111 | |||||||
| chr12:65960131 | C | T | 1 | a0001c0001t0020g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.283-3114C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960131 | |||||||
| chr12:65960220 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283-3025T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960220 | |||||||
| chr12:65960278 | G | A | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-2967G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960278 | |||||||
| chr12:65960375 | A | G | 1 | a0001c0001t0008g0069 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.283-2870A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960375 | |||||||
| chr12:65960442 | T | C | 3 | a0001c0001t0004g0029 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | NA18948.hp2 NA18957.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.283-2803T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960442 | |||||||
| chr12:65960632 | T | A | 2 | a0001c0001t0012g0049 a0001c0001t0027g0186 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.283-2613T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960632 | |||||||
| chr12:65960845 | T | A | 1 | a0001c0001t0025g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283-2400T>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65960845 | |||||||
| chr12:65961118 | C | T | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-2127C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961118 | |||||||
| chr12:65961131 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(132): Show |
135 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.283-2114G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961131 | |||||||
| chr12:65961168 | C | T | 30 | a0001c0001t0005g0088 a0001c0001t0005g0094 a0001c0001t0005g0114 others(27): Show |
30 | HG00423.hp1 HG01884.hp2 HG02559.hp2 others(27): Show |
intron_variant | MODIFIER | c.283-2077C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961168 | |||||||
| chr12:65961169 | G | A | 9 | a0001c0001t0010g0190 a0001c0001t0018g0207 a0001c0001t0018g0209 others(6): Show |
9 | HG00733.hp2 HG01069.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-2076G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961169 | |||||||
| chr12:65961206 | C | T | 1 | a0001c0001t0009g0074 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283-2039C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961206 | |||||||
| chr12:65961238 | C | A | 4 | a0001c0001t0008g0069 a0001c0001t0014g0017 a0001c0001t0022g0018 others(1): Show |
4 | HG01074.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2007C>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961238 | |||||||
| chr12:65961511 | G | A | 1 | a0001c0001t0003g0016 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.283-1734G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961511 | |||||||
| chr12:65961547 | C | T | 1 | a0001c0001t0010g0190 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.283-1698C>T | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961547 | |||||||
| chr12:65961567 | A | G | 13 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(10): Show |
13 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.283-1678A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65961567 | |||||||
| chr12:65961738 | A | AGT | 4 | a0001c0001t0001g0085 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-1488_283-1487d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | ||||||
| chr12:65961738 | AGT | A | 31 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0028 others(28): Show |
31 | HG00558.hp1 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.283-1488_283-1487d others(4): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | ||||||
| chr12:65961738 | AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0025g0183 a0001c0001t0025g0185 a0001c0001t0040g0217 others(4): Show |
7 | HG01361.hp2 HG02258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1494_283-1487d others(10): Show |
HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65961738 | ||||||
| chr12:65962235 | T | C | 1 | a0001c0001t0012g0055 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.283-1010T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962235 | |||||||
| chr12:65962320 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0077 others(72): Show |
75 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.283-925G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962320 | |||||||
| chr12:65962352 | A | G | 8 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-893A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962352 | |||||||
| chr12:65962428 | T | G | 1 | a0001c0001t0046g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-817T>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962428 | |||||||
| chr12:65962807 | G | A | 4 | a0001c0001t0033g0227 a0001c0001t0037g0223 a0001c0001t0045g0026 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-438G>A | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65962807 | |||||||
| chr12:65962859 | A | AT | 8 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-381dupT | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr12 | 65962859 | ||||||
| chr12:65963033 | A | G | 1 | a0001c0001t0035g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.283-212A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963033 | |||||||
| chr12:65963102 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.283-143A>G | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963102 | |||||||
| chr12:65963220 | T | C | 11 | a0001c0001t0005g0173 a0001c0001t0005g0174 a0001c0001t0005g0175 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-25T>C | HMGA2 | ENSG00000149948.14 | transcript | ENST00000403681.7 | protein_coding | 4/4 | chr12 | 65963220 |