Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5775 |
| ensemblid | ENSG00000088179.9 |
| hgncid | 9656 |
| symbol | PTPN4 |
| name | protein tyrosine phosphatase non-receptor type 4 |
| refseq_nuc | NM_002830.4 |
| refseq_prot | NP_002821.1 |
| ensembl_nuc | ENST00000263708.7 |
| ensembl_prot | ENSP00000263708.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 119759922 |
| end | 119984899 |
| strand | + |
| ver | v1.2 |
| region | chr2:119759922-119984899 |
| region5000 | chr2:119754922-119989899 |
| regionname0 | PTPN4_chr2_119759922_119984899 |
| regionname5000 | PTPN4_chr2_119754922_119989899 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 926 | 233 | 69 | 48 | 80 | 6 | 28 | 50 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0002 | 0/0 | 926 | 13 | 9 | 4 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0003 | 0/0 | 926 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0004 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0005 | 0/0 | 926 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0006 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| a0007 | 0/0 | 926 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | MTSRF others(921): Show |
chr2 | 119754922 | 119989899 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2778 | 232 | 69 | 48 | 80 | 6 | 27 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0001c0006 | 0/0 | 2778 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0002c0002 | 0/0 | 2778 | 10 | 9 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0002c0003 | 0/0 | 2778 | 3 | 0 | 3 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0003c0004 | 0/0 | 2778 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0004c0005 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0005c0009 | 0/0 | 2778 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0006c0007 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 | ||
| a0007c0008 | 0/0 | 2778 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | ATGAC others(2773): Show |
chr2 | 119754922 | 119989899 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11089 | 72 | 9 | 20 | 30 | 3 | 10 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0002 | 0/0 | 11090 | 61 | 15 | 14 | 23 | 2 | 7 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0003 | 0/0 | 11089 | 17 | 1 | 2 | 8 | 1 | 5 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0004 | 1/0 | 11090 | 7 | 5 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0006 | 0/0 | 11090 | 5 | 4 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0007 | 0/0 | 11090 | 5 | 0 | 0 | 5 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0008 | 0/0 | 11089 | 5 | 4 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0009 | 0/0 | 11089 | 4 | 4 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0010 | 0/0 | 11089 | 4 | 3 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0011 | 0/0 | 11090 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0012 | 0/0 | 11088 | 3 | 3 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11083): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0013 | 0/0 | 11089 | 3 | 1 | 0 | 2 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0014 | 0/0 | 11090 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0017 | 0/0 | 11089 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0018 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0019 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0020 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0021 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0022 | 0/0 | 11058 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11053): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0023 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0024 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0025 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0026 | 0/0 | 11090 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0028 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0029 | 0/0 | 11091 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11086): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0030 | 0/0 | 11091 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11086): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0031 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0032 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0033 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0034 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0036 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0037 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0038 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0039 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0040 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0041 | 0/0 | 11090 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0042 | 0/0 | 11089 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0043 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0044 | 0/0 | 11089 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0045 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0046 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0047 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0048 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0049 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0050 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0051 | 0/1 | 11091 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11086): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0052 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0053 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0054 | 0/0 | 11089 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0055 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0056 | 0/0 | 11089 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0057 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0001t0058 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0001c0006t0003 | 0/0 | 11089 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0002c0002t0005 | 0/0 | 11090 | 7 | 6 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0002c0002t0016 | 0/0 | 11090 | 2 | 2 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0002c0002t0035 | 0/0 | 11074 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11069): Show |
chr2 | 119754922 | 119989899 |
| a0002c0003t0015 | 0/0 | 11090 | 2 | 0 | 2 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0002c0003t0027 | 0/0 | 11090 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0003c0004t0001 | 0/0 | 11089 | 2 | 0 | 0 | 2 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0004c0005t0001 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0005c0009t0001 | 0/0 | 11089 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11084): Show |
chr2 | 119754922 | 119989899 |
| a0006c0007t0002 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| a0007c0008t0004 | 0/0 | 11090 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | AGGAT others(11085): Show |
chr2 | 119754922 | 119989899 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0010g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0010g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0012g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0013g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0014g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0018g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0019g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0020g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0022g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0023g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0024g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0025g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0026g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0028g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0029g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0030g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0031g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0032g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0033g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0034g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0036g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0037g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0038g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0039g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0040g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0041g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0042g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0043g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0044g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0045g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0046g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0047g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0048g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0049g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0050g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0051g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0052g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0053g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0054g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0055g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0056g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0057g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0001t0058g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0001c0006t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0002t0035g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0003t0015g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0003t0015g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0002c0003t0027g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0003c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0004c0005t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0005c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0006c0007t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| a0007c0008t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0041 | EUR | FIN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00544 | hp1 | a0001 | c0001 | t0049 | g0122 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00597 | hp1 | a0004 | c0005 | t0001 | g0029 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00738 | hp1 | a0002 | c0003 | t0015 | g0026 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00738 | hp2 | a0001 | c0001 | t0028 | g0183 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG00741 | hp2 | a0002 | c0003 | t0015 | g0025 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01069 | hp1 | a0001 | c0001 | t0023 | g0147 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01070 | hp1 | a0001 | c0001 | t0022 | g0173 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01175 | hp1 | a0001 | c0001 | t0036 | g0034 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01243 | hp2 | a0002 | c0002 | t0005 | g0243 | AMR | PUR | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01257 | hp2 | a0001 | c0001 | t0056 | g0061 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01346 | hp1 | a0002 | c0003 | t0027 | g0024 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01346 | hp2 | a0001 | c0001 | t0044 | g0144 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01433 | hp1 | a0001 | c0001 | t0042 | g0074 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01496 | hp1 | a0001 | c0001 | t0020 | g0205 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0167 | EUR | IBS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | IBS | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0140 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG01981 | hp2 | a0001 | c0001 | t0019 | g0207 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0235 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02071 | hp1 | a0001 | c0001 | t0057 | g0058 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02080 | hp2 | a0005 | c0009 | t0001 | g0110 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02083 | hp1 | a0001 | c0001 | t0046 | g0090 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CDX | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02165 | hp1 | a0001 | c0001 | t0013 | g0145 | EAS | CDX | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02280 | hp1 | a0001 | c0001 | t0043 | g0108 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | KHV | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02572 | hp1 | a0002 | c0002 | t0016 | g0246 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02615 | hp2 | a0001 | c0001 | t0039 | g0107 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02622 | hp1 | a0001 | c0001 | t0053 | g0040 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0109 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0238 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0222 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02809 | hp2 | a0002 | c0002 | t0005 | g0242 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02818 | hp1 | a0006 | c0007 | t0002 | g0163 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0247 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02886 | hp2 | a0002 | c0002 | t0005 | g0249 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02895 | hp1 | a0002 | c0002 | t0035 | g0248 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02896 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02922 | hp1 | a0001 | c0001 | t0037 | g0019 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0023 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02970 | hp1 | a0007 | c0008 | t0004 | g0035 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03017 | hp1 | a0001 | c0001 | t0055 | g0057 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0012 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03098 | hp2 | a0001 | c0001 | t0054 | g0047 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03195 | hp1 | a0001 | c0001 | t0038 | g0037 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03195 | hp2 | a0001 | c0001 | t0034 | g0032 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03209 | hp2 | a0001 | c0001 | t0021 | g0217 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03239 | hp1 | a0001 | c0001 | t0045 | g0089 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03239 | hp2 | a0001 | c0001 | t0041 | g0210 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03486 | hp1 | a0001 | c0001 | t0030 | g0033 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03490 | hp1 | a0001 | c0001 | t0010 | g0005 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03516 | hp1 | a0002 | c0002 | t0016 | g0241 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03516 | hp2 | a0001 | c0001 | t0031 | g0011 | AFR | ESN | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | GWD | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03579 | hp1 | a0001 | c0001 | t0050 | g0084 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03669 | hp1 | a0001 | c0006 | t0003 | g0105 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | STU | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG04228 | hp2 | a0001 | c0001 | t0058 | g0049 | SAS | STU | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18612 | hp1 | a0001 | c0001 | t0040 | g0142 | EAS | CHB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18939 | hp1 | a0001 | c0001 | t0024 | g0195 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18967 | hp2 | a0001 | c0001 | t0029 | g0197 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18990 | hp2 | a0003 | c0004 | t0001 | g0075 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18999 | hp1 | a0001 | c0001 | t0052 | g0149 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19007 | hp2 | a0001 | c0001 | t0025 | g0199 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19009 | hp2 | a0001 | c0001 | t0018 | g0240 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19030 | hp1 | a0001 | c0001 | t0032 | g0006 | AFR | LWK | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0232 | AFR | LWK | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0182 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19070 | hp1 | a0001 | c0001 | t0013 | g0146 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19074 | hp2 | a0003 | c0004 | t0001 | g0080 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19080 | hp1 | a0001 | c0001 | t0047 | g0097 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19086 | hp1 | a0001 | c0001 | t0026 | g0225 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19086 | hp2 | a0001 | c0001 | t0048 | g0030 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0220 | AFR | YRI | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0245 | AFR | YRI | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | ASW | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ASW | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | GIH | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | GIH | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02109 | hp2 | a0002 | c0002 | t0005 | g0244 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02486 | hp1 | a0001 | c0001 | t0033 | g0007 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0150 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0114 | AFR | ACB | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| HG03471 | hp2 | a0002 | c0002 | t0005 | g0250 | AFR | MSL | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0093 | AFR | LWK | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| NA21309 | hp2 | a0001 | c0001 | t0011 | g0236 | AFR | LWK | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0051 | g0045 | REF | REF | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0020 | REF | REF | PTPN4_chr2_119754922_119989899 | PTPN4 | chr2 | 119754922 | 119989899 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119862630 | C | T | 1 | a0003 | 2 | NA18990.hp2 NA19074.hp2 |
missense_variant | MODERATE | c.233C>T | p.Ser78Phe | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/27 | 713/11090 | 233/2781 | 78/926 | chr2 | 119862630 | |||
| chr2:119932479 | A | C | 1 | a0005 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1126A>C | p.Asn376His | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/27 | 1606/11090 | 1126/2781 | 376/926 | chr2 | 119932479 | |||
| chr2:119934891 | G | A | 1 | a0004 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1288G>A | p.Glu430Lys | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/27 | 1768/11090 | 1288/2781 | 430/926 | chr2 | 119934891 | |||
| chr2:119945173 | C | T | 1 | a0007 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1448C>T | p.Ser483Leu | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/27 | 1928/11090 | 1448/2781 | 483/926 | chr2 | 119945173 | |||
| chr2:119945221 | C | T | 1 | a0006 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1496C>T | p.Ser499Phe | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/27 | 1976/11090 | 1496/2781 | 499/926 | chr2 | 119945221 | |||
| chr2:119977059 | A | T | 1 | a0002 | 13 | HG00738.hp1 HG00741.hp2 HG01243.hp2 others(10): Show |
missense_variant | MODERATE | c.2770A>T | p.Thr924Ser | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3250/11090 | 2770/2781 | 924/926 | chr2 | 119977059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119877498 | A | G | 1 | a0002c0003 | 3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
synonymous_variant | LOW | c.324A>G | p.Lys108Lys | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/27 | 804/11090 | 324/2781 | 108/926 | chr2 | 119877498 | |||
| chr2:119946565 | A | G | 1 | a0001c0006 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1647A>G | p.Pro549Pro | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/27 | 2127/11090 | 1647/2781 | 549/926 | chr2 | 119946565 | |||
| chr2:119956930 | G | A | 2 | a0002c0003 a0003c0004 |
5 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
synonymous_variant | LOW | c.2067G>A | p.Ser689Ser | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 21/27 | 2547/11090 | 2067/2781 | 689/926 | chr2 | 119956930 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119760017 | C | T | 27 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(24): Show |
121 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(118): Show |
5_prime_UTR_variant | MODIFIER | c.-385C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/27 | 49837 | chr2 | 119760017 | ||||||
| chr2:119760030 | T | G | 1 | a0001c0001t0040 | 1 | NA18612.hp1 | 5_prime_UTR_variant | MODIFIER | c.-372T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/27 | 49824 | chr2 | 119760030 | ||||||
| chr2:119760162 | C | T | 1 | a0001c0001t0058 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-240C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/27 | 49692 | chr2 | 119760162 | ||||||
| chr2:119760190 | C | G | 1 | a0001c0001t0039 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/27 | 49664 | chr2 | 119760190 | ||||||
| chr2:119977161 | C | CA | 21 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(18): Show |
93 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*101dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 102 | INFO_REALIGN_3_PRIME | chr2 | 119977161 | |||||
| chr2:119977229 | A | G | 1 | a0001c0001t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 159 | chr2 | 119977229 | ||||||
| chr2:119977514 | T | A | 1 | a0001c0001t0042 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 444 | chr2 | 119977514 | ||||||
| chr2:119978121 | C | T | 1 | a0001c0001t0057 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1051C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 1051 | chr2 | 119978121 | ||||||
| chr2:119978431 | GT | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
238 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*1368delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 1368 | INFO_REALIGN_3_PRIME | chr2 | 119978431 | |||||
| chr2:119978857 | C | T | 1 | a0001c0001t0028 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 1787 | chr2 | 119978857 | ||||||
| chr2:119978940 | A | T | 3 | a0002c0002t0005 a0002c0002t0016 a0002c0002t0035 |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1870A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 1870 | chr2 | 119978940 | ||||||
| chr2:119979189 | CT | C | 1 | a0001c0001t0012 | 3 | HG02896.hp1 HG02897.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2120delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 2120 | chr2 | 119979189 | ||||||
| chr2:119979306 | T | C | 18 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(15): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2236T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 2236 | chr2 | 119979306 | ||||||
| chr2:119979743 | G | T | 1 | a0001c0001t0026 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2673G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 2673 | chr2 | 119979743 | ||||||
| chr2:119979898 | G | A | 1 | a0002c0003t0027 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2828G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 2828 | chr2 | 119979898 | ||||||
| chr2:119979910 | C | T | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG01257.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2840C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 2840 | chr2 | 119979910 | ||||||
| chr2:119980249 | C | A | 27 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(24): Show |
112 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3179C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3179 | chr2 | 119980249 | ||||||
| chr2:119980309 | T | C | 1 | a0001c0001t0055 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3239T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3239 | chr2 | 119980309 | ||||||
| chr2:119980346 | G | A | 3 | a0001c0001t0030 a0001c0001t0036 a0001c0001t0037 |
3 | HG01175.hp1 HG02922.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3276G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3276 | chr2 | 119980346 | ||||||
| chr2:119980578 | T | C | 2 | a0001c0001t0034 a0001c0001t0039 |
2 | HG02615.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3508T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3508 | chr2 | 119980578 | ||||||
| chr2:119980705 | G | A | 2 | a0001c0001t0017 a0001c0001t0043 |
3 | HG01891.hp1 HG02280.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3635G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3635 | chr2 | 119980705 | ||||||
| chr2:119980928 | G | A | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*3858G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3858 | chr2 | 119980928 | ||||||
| chr2:119980972 | T | C | 3 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0031 |
9 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3902T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3902 | chr2 | 119980972 | ||||||
| chr2:119981012 | T | C | 3 | a0001c0001t0044 a0002c0003t0015 a0002c0003t0027 |
4 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3942T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3942 | chr2 | 119981012 | ||||||
| chr2:119981045 | A | G | 1 | a0001c0001t0033 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3975A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 3975 | chr2 | 119981045 | ||||||
| chr2:119981158 | T | C | 3 | a0002c0002t0005 a0002c0002t0016 a0002c0002t0035 |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4088T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4088 | chr2 | 119981158 | ||||||
| chr2:119981308 | G | A | 1 | a0001c0001t0018 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4238G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4238 | chr2 | 119981308 | ||||||
| chr2:119981334 | T | C | 1 | a0001c0001t0017 | 2 | HG01891.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4264T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4264 | chr2 | 119981334 | ||||||
| chr2:119981574 | C | T | 1 | a0001c0001t0038 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4504C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4504 | chr2 | 119981574 | ||||||
| chr2:119981584 | A | G | 1 | a0001c0001t0023 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4514A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4514 | chr2 | 119981584 | ||||||
| chr2:119981660 | T | C | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(40): Show |
151 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*4590T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4590 | chr2 | 119981660 | ||||||
| chr2:119981660 | TGTTTTTT others(25): Show |
T | 1 | a0001c0001t0022 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4591_*4622delGTTT others(28): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4591 | chr2 | 119981660 | ||||||
| chr2:119981691 | C | G | 2 | a0001c0001t0008 a0001c0001t0012 |
8 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4621C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4621 | chr2 | 119981691 | ||||||
| chr2:119981727 | C | T | 1 | a0001c0001t0052 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4657C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4657 | chr2 | 119981727 | ||||||
| chr2:119981747 | T | TA | 3 | a0002c0002t0005 a0002c0002t0016 a0002c0002t0035 |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4683dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4684 | INFO_REALIGN_3_PRIME | chr2 | 119981747 | |||||
| chr2:119981946 | C | T | 1 | a0001c0001t0007 | 5 | HG00609.hp2 HG02523.hp2 NA19065.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4876C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 4876 | chr2 | 119981946 | ||||||
| chr2:119982437 | T | C | 1 | a0001c0001t0045 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5367T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 5367 | chr2 | 119982437 | ||||||
| chr2:119982714 | G | C | 1 | a0001c0001t0046 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5644G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 5644 | chr2 | 119982714 | ||||||
| chr2:119982884 | G | A | 1 | a0001c0001t0009 | 4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5814G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 5814 | chr2 | 119982884 | ||||||
| chr2:119982893 | G | T | 2 | a0001c0001t0006 a0001c0001t0011 |
8 | HG00639.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5823G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 5823 | chr2 | 119982893 | ||||||
| chr2:119982904 | TATATTAA others(9): Show |
T | 1 | a0002c0002t0035 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5836_*5851delTATT others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 5836 | INFO_REALIGN_3_PRIME | chr2 | 119982904 | |||||
| chr2:119983091 | C | G | 3 | a0001c0001t0044 a0002c0003t0015 a0002c0003t0027 |
4 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6021C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6021 | chr2 | 119983091 | ||||||
| chr2:119983235 | C | T | 12 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0032 others(9): Show |
23 | HG00738.hp1 HG00741.hp2 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*6165C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6165 | chr2 | 119983235 | ||||||
| chr2:119983318 | T | C | 1 | a0001c0001t0038 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6248T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6248 | chr2 | 119983318 | ||||||
| chr2:119983507 | T | C | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0008 others(37): Show |
146 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*6437T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6437 | chr2 | 119983507 | ||||||
| chr2:119983538 | A | G | 1 | a0001c0001t0050 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6468A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6468 | chr2 | 119983538 | ||||||
| chr2:119983721 | A | G | 1 | a0002c0002t0016 | 2 | HG02572.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6651A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 6651 | chr2 | 119983721 | ||||||
| chr2:119984187 | G | T | 1 | a0002c0002t0035 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7117G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7117 | chr2 | 119984187 | ||||||
| chr2:119984192 | C | T | 1 | a0001c0001t0049 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7122C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7122 | chr2 | 119984192 | ||||||
| chr2:119984230 | T | C | 1 | a0001c0001t0047 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7160T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7160 | chr2 | 119984230 | ||||||
| chr2:119984405 | A | G | 3 | a0002c0002t0005 a0002c0002t0016 a0002c0002t0035 |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*7335A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7335 | chr2 | 119984405 | ||||||
| chr2:119984422 | G | A | 1 | a0001c0001t0053 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7352G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7352 | chr2 | 119984422 | ||||||
| chr2:119984433 | T | C | 21 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0019 others(18): Show |
94 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*7363T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7363 | chr2 | 119984433 | ||||||
| chr2:119984611 | T | C | 1 | a0001c0001t0048 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7541T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7541 | chr2 | 119984611 | ||||||
| chr2:119984678 | C | A | 1 | a0001c0001t0021 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7608C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7608 | chr2 | 119984678 | ||||||
| chr2:119984758 | T | A | 1 | a0001c0001t0011 | 3 | HG02055.hp1 NA19030.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7688T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7688 | chr2 | 119984758 | ||||||
| chr2:119984834 | C | A | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
237 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*7764C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 27/27 | 7764 | chr2 | 119984834 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:119760451 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-18+67A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119760451 | |||||||
| chr2:119760559 | GCTTT | G | 3 | a0001c0001t0010g0001 a0001c0001t0010g0002 a0001c0001t0010g0003 |
3 | HG02257.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-18+181_-18+184del others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760559 | ||||||
| chr2:119760692 | A | G | 1 | a0001c0001t0003g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-18+308A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119760692 | |||||||
| chr2:119760733 | C | CT | 87 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0042 others(84): Show |
87 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.-18+371dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTT | 43 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0116 others(40): Show |
43 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18+370_-18+371dup others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTTT | 61 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(58): Show |
61 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-18+369_-18+371dup others(3): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTTTT | 21 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0213 others(18): Show |
21 | HG00639.hp2 HG01169.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18+368_-18+371dup others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTTTTT | 9 | a0001c0001t0002g0233 a0001c0001t0002g0234 a0001c0001t0002g0239 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+367_-18+371dup others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTTTTTT | 5 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+366_-18+371dup others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | C | CTTTTTTT | 5 | a0002c0002t0005g0247 a0002c0002t0005g0249 a0002c0002t0005g0250 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+365_-18+371dup others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | CTTTT | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+368_-18+371del others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760733 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0004 a0001c0001t0010g0005 |
2 | HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-18+362_-18+371del others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760733 | ||||||
| chr2:119760815 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+431T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119760815 | |||||||
| chr2:119760838 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+454T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119760838 | |||||||
| chr2:119760871 | CA | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0043 others(207): Show |
210 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.-18+508delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119760871 | ||||||
| chr2:119760901 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+517G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119760901 | |||||||
| chr2:119761128 | T | C | 1 | a0001c0001t0002g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+744T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761128 | |||||||
| chr2:119761329 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+945T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761329 | |||||||
| chr2:119761349 | A | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+965A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761349 | |||||||
| chr2:119761742 | A | G | 1 | a0001c0001t0052g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-18+1358A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761742 | |||||||
| chr2:119761746 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(93): Show |
96 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-18+1362G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761746 | |||||||
| chr2:119761756 | C | G | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.-18+1372C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761756 | |||||||
| chr2:119761887 | C | T | 64 | a0001c0001t0002g0148 a0001c0001t0002g0154 a0001c0001t0002g0155 others(61): Show |
64 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-18+1503C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119761887 | |||||||
| chr2:119762237 | C | T | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-18+1853C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119762237 | |||||||
| chr2:119762341 | C | CT | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+1967dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119762341 | ||||||
| chr2:119762678 | G | A | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-18+2294G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119762678 | |||||||
| chr2:119762795 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2411A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119762795 | |||||||
| chr2:119763321 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-18+2937G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119763321 | |||||||
| chr2:119763779 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+3395A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119763779 | |||||||
| chr2:119763862 | A | C | 3 | a0001c0001t0001g0098 a0001c0001t0003g0113 a0001c0001t0047g0097 |
3 | HG02056.hp1 NA19080.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-18+3478A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119763862 | |||||||
| chr2:119763905 | C | T | 1 | a0001c0001t0004g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-18+3521C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119763905 | |||||||
| chr2:119764099 | A | G | 2 | a0002c0002t0005g0244 a0002c0002t0005g0245 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-18+3715A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764099 | |||||||
| chr2:119764175 | A | G | 5 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0230 others(2): Show |
5 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+3791A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764175 | |||||||
| chr2:119764243 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-18+3859C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764243 | |||||||
| chr2:119764327 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-18+3943G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764327 | |||||||
| chr2:119764345 | C | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.-18+3961C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764345 | |||||||
| chr2:119764488 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-18+4104A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764488 | |||||||
| chr2:119764606 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18+4222G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764606 | |||||||
| chr2:119764747 | G | A | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+4363G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119764747 | |||||||
| chr2:119765019 | C | A | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+4635C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765019 | |||||||
| chr2:119765069 | G | C | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+4685G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765069 | |||||||
| chr2:119765080 | T | A | 1 | a0001c0001t0003g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+4696T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765080 | |||||||
| chr2:119765084 | C | T | 8 | a0001c0001t0006g0023 a0001c0001t0006g0166 a0001c0001t0006g0219 others(5): Show |
8 | HG00639.hp2 HG02055.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+4700C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765084 | |||||||
| chr2:119765354 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(107): Show |
110 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-18+4970C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765354 | |||||||
| chr2:119765455 | A | G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+5071A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765455 | |||||||
| chr2:119765561 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18+5177A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765561 | |||||||
| chr2:119765704 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-18+5320G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765704 | |||||||
| chr2:119765914 | C | CTG | 7 | a0001c0001t0001g0043 a0001c0001t0008g0013 a0001c0001t0008g0016 others(4): Show |
7 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+5549_-18+5550d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765914 | ||||||
| chr2:119765914 | C | CTGTG | 113 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(110): Show |
113 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18+5547_-18+5550d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765914 | ||||||
| chr2:119765914 | C | CTGTGTG | 4 | a0001c0001t0001g0094 a0001c0001t0017g0093 a0001c0001t0017g0140 others(1): Show |
4 | HG01891.hp1 HG01928.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+5545_-18+5550d others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765914 | ||||||
| chr2:119765933 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+5549T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119765933 | |||||||
| chr2:119765933 | T | TGTGC | 89 | a0001c0001t0001g0044 a0001c0001t0002g0148 a0001c0001t0002g0152 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-18+5550_-18+5551i others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765933 | ||||||
| chr2:119765933 | T | TGTGTGTG others(1): Show |
3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+5550_-18+5551i others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765933 | ||||||
| chr2:119765933 | T | TGTGTGTG others(3): Show |
3 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 |
3 | HG02976.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+5550_-18+5551i others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119765933 | ||||||
| chr2:119766156 | G | T | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+5772G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766156 | |||||||
| chr2:119766186 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-18+5802C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766186 | |||||||
| chr2:119766229 | A | C | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18+5845A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766229 | |||||||
| chr2:119766443 | T | TGC | 9 | a0001c0001t0001g0044 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG01109.hp1 HG01169.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+6065_-18+6066d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766443 | ||||||
| chr2:119766443 | T | TGCGC | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6063_-18+6066d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766443 | ||||||
| chr2:119766445 | C | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+6061C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766445 | |||||||
| chr2:119766449 | CGT | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): Show |
27 | HG00609.hp1 HG01175.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+6098_-18+6099d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766449 | ||||||
| chr2:119766449 | CGTGT | C | 34 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(31): Show |
34 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+6096_-18+6099d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766449 | ||||||
| chr2:119766449 | CGTGTGT | C | 15 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0116 others(12): Show |
15 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+6094_-18+6099d others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766449 | ||||||
| chr2:119766451 | T | C | 165 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0044 others(162): Show |
165 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.-18+6067T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766451 | |||||||
| chr2:119766452 | G | T | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+6068G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766452 | |||||||
| chr2:119766453 | T | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(171): Show |
174 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.-18+6069T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766453 | |||||||
| chr2:119766453 | T | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+6069T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766453 | |||||||
| chr2:119766454 | G | C | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18+6070G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766454 | |||||||
| chr2:119766455 | T | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.-18+6071T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766455 | |||||||
| chr2:119766457 | T | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.-18+6073T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766457 | |||||||
| chr2:119766458 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-18+6074G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766458 | |||||||
| chr2:119766458 | GTGTGTGT others(19): Show |
G | 2 | a0002c0003t0015g0025 a0002c0003t0015g0026 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-18+6100_-18+6125d others(28): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766458 | ||||||
| chr2:119766459 | T | A | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-18+6075T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766459 | |||||||
| chr2:119766459 | T | C | 145 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0043 others(142): Show |
145 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.-18+6075T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766459 | |||||||
| chr2:119766460 | GTGTGTGT others(17): Show |
G | 1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18+6100_-18+6123d others(26): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766460 | ||||||
| chr2:119766461 | T | C | 90 | a0001c0001t0001g0046 a0001c0001t0001g0116 a0001c0001t0002g0148 others(87): Show |
90 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.-18+6077T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766461 | |||||||
| chr2:119766462 | G | T | 7 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(4): Show |
7 | HG00735.hp2 HG02486.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+6078G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766462 | |||||||
| chr2:119766463 | T | C | 67 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0002g0155 others(64): Show |
67 | HG00544.hp2 HG00639.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.-18+6079T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766463 | |||||||
| chr2:119766464 | G | T | 4 | a0001c0001t0012g0012 a0001c0001t0012g0015 a0001c0001t0031g0011 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+6080G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766464 | |||||||
| chr2:119766464 | GTGTGTGT others(13): Show |
G | 2 | a0001c0001t0002g0153 a0001c0001t0011g0236 |
2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+6100_-18+6119d others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766464 | ||||||
| chr2:119766465 | T | C | 51 | a0001c0001t0002g0148 a0001c0001t0002g0167 a0001c0001t0002g0168 others(48): Show |
51 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-18+6081T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766465 | |||||||
| chr2:119766466 | GTGTGTGT others(11): Show |
G | 1 | a0001c0001t0002g0213 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+6100_-18+6117d others(20): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766466 | ||||||
| chr2:119766467 | T | C | 27 | a0001c0001t0002g0170 a0001c0001t0002g0176 a0001c0001t0002g0184 others(24): Show |
27 | HG00735.hp2 HG01069.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18+6083T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766467 | |||||||
| chr2:119766468 | GTGTGTGT others(9): Show |
G | 2 | a0001c0001t0002g0234 a0001c0001t0007g0185 |
2 | HG01891.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-18+6100_-18+6115d others(18): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766468 | ||||||
| chr2:119766469 | T | C | 20 | a0001c0001t0002g0176 a0001c0001t0002g0184 a0001c0001t0002g0186 others(17): Show |
20 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+6085T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766469 | |||||||
| chr2:119766470 | GTGTGTGT others(7): Show |
G | 9 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0215 others(6): Show |
9 | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6113d others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766470 | ||||||
| chr2:119766471 | T | C | 8 | a0001c0001t0002g0184 a0001c0001t0008g0013 a0001c0001t0008g0016 others(5): Show |
8 | HG00735.hp2 HG02698.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+6087T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766471 | |||||||
| chr2:119766472 | GTGTGTGT others(5): Show |
G | 10 | a0001c0001t0002g0154 a0001c0001t0002g0201 a0001c0001t0002g0218 others(7): Show |
10 | HG00639.hp2 HG02155.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6111d others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766472 | ||||||
| chr2:119766473 | T | C | 2 | a0001c0001t0012g0012 a0001c0001t0012g0015 |
2 | HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-18+6089T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766473 | |||||||
| chr2:119766474 | GTGTGTGT others(3): Show |
G | 20 | a0001c0001t0002g0152 a0001c0001t0002g0164 a0001c0001t0002g0174 others(17): Show |
20 | HG00423.hp2 HG01070.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6109d others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766474 | ||||||
| chr2:119766476 | G | C | 1 | a0001c0001t0013g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-18+6092G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766476 | |||||||
| chr2:119766476 | GTGTGTGT others(1): Show |
G | 14 | a0001c0001t0002g0179 a0001c0001t0002g0190 a0001c0001t0002g0198 others(11): Show |
14 | HG00735.hp2 HG01975.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6107d others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766476 | ||||||
| chr2:119766478 | G | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0138 a0001c0001t0001g0143 others(3): Show |
6 | HG01167.hp1 HG01884.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+6094G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766478 | |||||||
| chr2:119766478 | GTGTGTC | G | 23 | a0001c0001t0002g0160 a0001c0001t0002g0162 a0001c0001t0002g0165 others(20): Show |
23 | HG00544.hp2 HG00609.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6105d others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766478 | ||||||
| chr2:119766480 | G | C | 5 | a0001c0001t0001g0087 a0001c0001t0001g0129 a0001c0001t0010g0002 others(2): Show |
5 | HG00621.hp1 HG01346.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+6096G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766480 | |||||||
| chr2:119766480 | GTGTC | G | 21 | a0001c0001t0001g0096 a0001c0001t0001g0138 a0001c0001t0001g0143 others(18): Show |
21 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6103d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766480 | ||||||
| chr2:119766482 | G | C | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18+6098G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766482 | |||||||
| chr2:119766482 | GTC | G | 9 | a0001c0001t0001g0087 a0001c0001t0001g0129 a0001c0001t0002g0186 others(6): Show |
9 | HG00621.hp1 HG01358.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+6100_-18+6101d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766482 | ||||||
| chr2:119766484 | C | CTG | 5 | a0001c0001t0001g0092 a0001c0001t0001g0137 a0001c0001t0030g0033 others(2): Show |
5 | HG01069.hp2 HG01261.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+6125_-18+6126d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119766484 | ||||||
| chr2:119766484 | C | G | 14 | a0001c0001t0001g0130 a0001c0001t0002g0170 a0001c0001t0002g0171 others(11): Show |
14 | HG00738.hp2 HG00741.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18+6100C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766484 | |||||||
| chr2:119766485 | T | C | 2 | a0001c0001t0011g0235 a0001c0001t0011g0236 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+6101T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766485 | |||||||
| chr2:119766486 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0004g0018 |
2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-18+6102G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766486 | |||||||
| chr2:119766487 | T | C | 2 | a0001c0001t0011g0235 a0001c0001t0011g0236 |
2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+6103T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766487 | |||||||
| chr2:119766488 | G | C | 1 | a0001c0001t0050g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18+6104G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766488 | |||||||
| chr2:119766489 | T | C | 1 | a0001c0001t0011g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+6105T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766489 | |||||||
| chr2:119766491 | T | C | 1 | a0001c0001t0011g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-18+6107T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766491 | |||||||
| chr2:119766509 | T | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+6125T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766509 | |||||||
| chr2:119766528 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+6144C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766528 | |||||||
| chr2:119766546 | C | G | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+6162C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766546 | |||||||
| chr2:119766971 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+6587C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119766971 | |||||||
| chr2:119767199 | T | C | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.-18+6815T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119767199 | |||||||
| chr2:119767701 | A | G | 1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18+7317A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119767701 | |||||||
| chr2:119767928 | A | T | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-18+7544A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119767928 | |||||||
| chr2:119768016 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-18+7632T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768016 | |||||||
| chr2:119768147 | A | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-18+7763A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768147 | |||||||
| chr2:119768371 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18+7987G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768371 | |||||||
| chr2:119768598 | C | T | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-18+8214C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768598 | |||||||
| chr2:119768666 | T | C | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18+8282T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768666 | |||||||
| chr2:119768720 | C | T | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-18+8336C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768720 | |||||||
| chr2:119768844 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+8460A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768844 | |||||||
| chr2:119768971 | C | T | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-18+8587C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119768971 | |||||||
| chr2:119769037 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18+8653T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769037 | |||||||
| chr2:119769051 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-18+8667A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769051 | |||||||
| chr2:119769107 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+8723G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769107 | |||||||
| chr2:119769127 | T | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-18+8743T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769127 | |||||||
| chr2:119769256 | T | A | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-18+8872T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769256 | |||||||
| chr2:119769727 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+9343A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119769727 | |||||||
| chr2:119770376 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-18+9992G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119770376 | |||||||
| chr2:119770630 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+10246C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119770630 | |||||||
| chr2:119770728 | GCTAA | G | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+10349_-18+1035 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119770728 | ||||||
| chr2:119770878 | C | CT | 6 | a0001c0001t0001g0156 a0001c0001t0002g0204 a0001c0001t0007g0229 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+10513dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119770878 | ||||||
| chr2:119770878 | CT | C | 11 | a0001c0001t0002g0176 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01167.hp2 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+10513delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119770878 | ||||||
| chr2:119770941 | G | C | 98 | a0001c0001t0001g0085 a0001c0001t0002g0148 a0001c0001t0002g0152 others(95): Show |
98 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18+10557G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119770941 | |||||||
| chr2:119770941 | G | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+10557G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119770941 | |||||||
| chr2:119771101 | C | T | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18+10717C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771101 | |||||||
| chr2:119771206 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+10822C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771206 | |||||||
| chr2:119771446 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18+11062A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771446 | |||||||
| chr2:119771482 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+11098G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771482 | |||||||
| chr2:119771540 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+11156C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771540 | |||||||
| chr2:119771982 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+11598A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119771982 | |||||||
| chr2:119772218 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+11834G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119772218 | |||||||
| chr2:119772244 | T | A | 112 | a0001c0001t0001g0085 a0001c0001t0002g0148 a0001c0001t0002g0152 others(109): Show |
112 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.-18+11860T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119772244 | |||||||
| chr2:119772489 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+12105A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119772489 | |||||||
| chr2:119772725 | G | A | 88 | a0001c0001t0001g0085 a0001c0001t0002g0148 a0001c0001t0002g0152 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18+12341G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119772725 | |||||||
| chr2:119772818 | C | T | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+12434C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119772818 | |||||||
| chr2:119773031 | T | G | 88 | a0001c0001t0001g0085 a0001c0001t0002g0148 a0001c0001t0002g0152 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18+12647T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773031 | |||||||
| chr2:119773275 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0228 |
2 | HG02027.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-18+12891C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773275 | |||||||
| chr2:119773322 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-18+12938T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773322 | |||||||
| chr2:119773533 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-18+13149C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773533 | |||||||
| chr2:119773735 | C | CA | 7 | a0001c0001t0002g0170 a0001c0001t0002g0223 a0001c0001t0002g0230 others(4): Show |
7 | HG00609.hp2 HG01192.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+13368dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119773735 | ||||||
| chr2:119773735 | CA | C | 123 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(120): Show |
123 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-18+13368delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119773735 | ||||||
| chr2:119773788 | A | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+13404A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773788 | |||||||
| chr2:119773977 | G | A | 1 | a0001c0001t0007g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-18+13593G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119773977 | |||||||
| chr2:119774010 | T | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+13626T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774010 | |||||||
| chr2:119774227 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+13843G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774227 | |||||||
| chr2:119774362 | A | G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+13978A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774362 | |||||||
| chr2:119774529 | G | A | 1 | a0001c0001t0058g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-18+14145G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774529 | |||||||
| chr2:119774561 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+14177A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774561 | |||||||
| chr2:119774738 | C | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+14354C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774738 | |||||||
| chr2:119774774 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-18+14390C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119774774 | |||||||
| chr2:119775004 | G | A | 2 | a0001c0001t0003g0104 a0001c0001t0003g0141 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-18+14620G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119775004 | |||||||
| chr2:119775012 | T | A | 88 | a0001c0001t0001g0085 a0001c0001t0002g0148 a0001c0001t0002g0152 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18+14628T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119775012 | |||||||
| chr2:119775096 | G | GA | 6 | a0001c0001t0001g0050 a0001c0001t0001g0127 a0001c0001t0003g0128 others(3): Show |
6 | HG00741.hp2 HG01192.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+14741dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GA | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0028 others(81): Show |
84 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.-18+14741delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GAA | G | 12 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0118 others(9): Show |
12 | HG00323.hp1 HG01069.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+14740_-18+1474 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GAAAAA | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0014 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+14737_-18+1474 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GAAAAAAA others(6): Show |
G | 15 | a0001c0001t0002g0152 a0001c0001t0002g0159 a0001c0001t0002g0160 others(12): Show |
15 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18+14729_-18+1474 others(17): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GAAAAAAA others(7): Show |
G | 71 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0002g0154 others(68): Show |
71 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-18+14728_-18+1474 others(18): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775096 | GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0011g0236 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+14727_-18+1474 others(19): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775096 | ||||||
| chr2:119775097 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0043g0108 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-18+14713A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119775097 | |||||||
| chr2:119775304 | C | T | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+14920C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119775304 | |||||||
| chr2:119775352 | TTGG | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+14970_-18+1497 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775352 | ||||||
| chr2:119775802 | G | GATATCT | 16 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0002g0203 others(13): Show |
16 | HG00323.hp2 HG00597.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+15453_-18+1545 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775802 | ||||||
| chr2:119775802 | GATATCT | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(196): Show |
199 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.-18+15453_-18+1545 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775802 | ||||||
| chr2:119775802 | GATATCTA others(5): Show |
G | 2 | a0001c0001t0001g0118 a0001c0001t0002g0180 |
2 | NA18946.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-18+15447_-18+1545 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775802 | ||||||
| chr2:119775802 | GATATCTA others(11): Show |
G | 2 | a0001c0001t0048g0030 a0001c0001t0056g0061 |
2 | HG01257.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-18+15441_-18+1545 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119775802 | ||||||
| chr2:119776003 | T | C | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-18+15619T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776003 | |||||||
| chr2:119776052 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18+15668G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776052 | |||||||
| chr2:119776271 | G | A | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18+15887G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776271 | |||||||
| chr2:119776425 | C | T | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18+16041C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776425 | |||||||
| chr2:119776541 | G | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+16157G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776541 | |||||||
| chr2:119776607 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+16223A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119776607 | |||||||
| chr2:119777478 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-18+17094A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119777478 | |||||||
| chr2:119777821 | AT | A | 11 | a0001c0001t0047g0097 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+17448delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119777821 | ||||||
| chr2:119777837 | T | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+17453T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119777837 | |||||||
| chr2:119778056 | A | G | 1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-18+17672A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778056 | |||||||
| chr2:119778362 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-18+17978T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778362 | |||||||
| chr2:119778390 | T | A | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-18+18006T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778390 | |||||||
| chr2:119778443 | A | G | 1 | a0001c0001t0044g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-18+18059A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778443 | |||||||
| chr2:119778620 | A | G | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+18236A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778620 | |||||||
| chr2:119778626 | T | C | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-18+18242T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778626 | |||||||
| chr2:119778686 | GT | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+18305delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119778686 | ||||||
| chr2:119778917 | C | CTTT | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.-18+18534_-18+1853 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119778917 | ||||||
| chr2:119778963 | G | C | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+18579G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119778963 | |||||||
| chr2:119779104 | C | G | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18+18720C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779104 | |||||||
| chr2:119779133 | G | A | 2 | a0001c0001t0055g0057 a0001c0001t0056g0061 |
2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-18+18749G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779133 | |||||||
| chr2:119779433 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-18+19049C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779433 | |||||||
| chr2:119779461 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+19077C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779461 | |||||||
| chr2:119779473 | C | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18+19089C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779473 | |||||||
| chr2:119779521 | G | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+19137G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779521 | |||||||
| chr2:119779616 | C | CA | 11 | a0001c0001t0001g0051 a0001c0001t0001g0062 a0001c0001t0001g0121 others(8): Show |
11 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+19250dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119779616 | ||||||
| chr2:119779639 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-18+19255A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779639 | |||||||
| chr2:119779771 | G | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-18+19387G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779771 | |||||||
| chr2:119779901 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0116 |
2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-18+19517C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119779901 | |||||||
| chr2:119780052 | A | AT | 88 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-18+19678dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119780052 | ||||||
| chr2:119780052 | AT | A | 12 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(9): Show |
12 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+19678delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119780052 | ||||||
| chr2:119780097 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18+19713A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780097 | |||||||
| chr2:119780098 | T | C | 1 | a0001c0001t0003g0066 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-18+19714T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780098 | |||||||
| chr2:119780159 | T | A | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-18+19775T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780159 | |||||||
| chr2:119780239 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+19855T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780239 | |||||||
| chr2:119780394 | A | G | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18+20010A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780394 | |||||||
| chr2:119780464 | C | T | 1 | a0001c0001t0003g0104 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-18+20080C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780464 | |||||||
| chr2:119780618 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18+20234T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780618 | |||||||
| chr2:119780641 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-18+20257G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780641 | |||||||
| chr2:119780774 | G | A | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18+20390G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119780774 | |||||||
| chr2:119781009 | G | A | 3 | a0001c0001t0002g0170 a0001c0001t0002g0239 a0001c0001t0028g0183 |
3 | HG00738.hp2 HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-18+20625G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781009 | |||||||
| chr2:119781031 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-18+20647G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781031 | |||||||
| chr2:119781261 | T | C | 6 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+20877T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781261 | |||||||
| chr2:119781330 | A | T | 1 | a0002c0002t0005g0243 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-18+20946A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781330 | |||||||
| chr2:119781371 | T | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(54): Show |
57 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-18+20987T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781371 | |||||||
| chr2:119781534 | C | T | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18+21150C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781534 | |||||||
| chr2:119781763 | C | T | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-18+21379C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781763 | |||||||
| chr2:119781849 | G | A | 245 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.-18+21465G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119781849 | |||||||
| chr2:119782109 | A | G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+21725A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782109 | |||||||
| chr2:119782155 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-18+21771G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782155 | |||||||
| chr2:119782198 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+21814C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782198 | |||||||
| chr2:119782303 | C | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+21919C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782303 | |||||||
| chr2:119782306 | A | C | 120 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0079 others(117): Show |
120 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.-18+21922A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782306 | |||||||
| chr2:119782648 | G | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-18+22264G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782648 | |||||||
| chr2:119782709 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+22325C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782709 | |||||||
| chr2:119782714 | C | CT | 5 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0111 others(2): Show |
5 | HG01517.hp1 HG02615.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+22341dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119782714 | ||||||
| chr2:119782715 | T | C | 12 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(9): Show |
12 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-18+22331T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782715 | |||||||
| chr2:119782874 | T | TA | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-18+22501dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119782874 | ||||||
| chr2:119782874 | T | TAA | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+22500_-18+2250 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119782874 | ||||||
| chr2:119782891 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-18+22507A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119782891 | |||||||
| chr2:119782999 | C | CT | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-18+22628dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119782999 | ||||||
| chr2:119782999 | CT | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+22628delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119782999 | ||||||
| chr2:119783039 | G | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+22655G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783039 | |||||||
| chr2:119783169 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+22785T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783169 | |||||||
| chr2:119783182 | G | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-18+22798G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783182 | |||||||
| chr2:119783352 | T | C | 1 | a0001c0001t0010g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18+22968T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783352 | |||||||
| chr2:119783409 | G | A | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-18+23025G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783409 | |||||||
| chr2:119783756 | G | A | 2 | a0001c0001t0002g0152 a0001c0001t0002g0160 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-18+23372G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119783756 | |||||||
| chr2:119784017 | G | GC | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-18+23634dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784017 | ||||||
| chr2:119784273 | C | CT | 6 | a0001c0001t0001g0131 a0001c0001t0002g0214 a0001c0001t0002g0239 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+23908dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784273 | ||||||
| chr2:119784273 | CT | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0120 a0001c0001t0001g0132 others(5): Show |
8 | HG00323.hp2 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+23908delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784273 | ||||||
| chr2:119784384 | A | AT | 124 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(121): Show |
124 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-18+24020dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784384 | ||||||
| chr2:119784425 | C | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18+24041C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784425 | |||||||
| chr2:119784447 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-18+24063C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784447 | |||||||
| chr2:119784578 | A | G | 11 | a0001c0001t0002g0203 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01243.hp2 HG02083.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+24194A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784578 | |||||||
| chr2:119784585 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+24201C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784585 | |||||||
| chr2:119784696 | A | AT | 94 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0158 others(91): Show |
94 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.-18+24334dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784696 | ||||||
| chr2:119784696 | A | ATT | 8 | a0001c0001t0002g0154 a0001c0001t0002g0160 a0001c0001t0002g0169 others(5): Show |
8 | HG01255.hp2 HG02055.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+24333_-18+2433 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784696 | ||||||
| chr2:119784696 | AT | A | 13 | a0001c0001t0003g0041 a0001c0001t0003g0102 a0001c0001t0008g0008 others(10): Show |
13 | HG00323.hp1 HG00735.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18+24334delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784696 | ||||||
| chr2:119784735 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-18+24351G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784735 | |||||||
| chr2:119784817 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-18+24433C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784817 | |||||||
| chr2:119784958 | C | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-18+24574C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119784958 | |||||||
| chr2:119784959 | TGAG | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-18+24581_-18+2458 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119784959 | ||||||
| chr2:119785239 | G | A | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-17-24598G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785239 | |||||||
| chr2:119785260 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-24577A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785260 | |||||||
| chr2:119785371 | T | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0079 a0001c0001t0001g0125 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-24466T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785371 | |||||||
| chr2:119785514 | T | G | 1 | a0001c0001t0054g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-17-24323T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785514 | |||||||
| chr2:119785727 | GTTTGC | G | 7 | a0002c0002t0005g0244 a0002c0002t0005g0245 a0002c0002t0005g0249 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-24105_-17-2410 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119785727 | ||||||
| chr2:119785746 | G | T | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-24091G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785746 | |||||||
| chr2:119785751 | C | T | 1 | a0001c0001t0058g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-17-24086C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785751 | |||||||
| chr2:119785924 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0001g0131 a0001c0001t0058g0049 |
3 | HG03654.hp1 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-17-23913C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119785924 | |||||||
| chr2:119786751 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-23086G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119786751 | |||||||
| chr2:119786993 | T | C | 2 | a0001c0001t0002g0202 a0001c0001t0020g0205 |
2 | HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-17-22844T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119786993 | |||||||
| chr2:119787062 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-17-22775C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119787062 | |||||||
| chr2:119787152 | C | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-22685C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119787152 | |||||||
| chr2:119787712 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-17-22125G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119787712 | |||||||
| chr2:119787991 | T | A | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-21846T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119787991 | |||||||
| chr2:119788088 | T | A | 2 | a0001c0001t0002g0212 a0001c0001t0002g0228 |
2 | HG02027.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-17-21749T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119788088 | |||||||
| chr2:119788259 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0020g0205 |
2 | HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-17-21578A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119788259 | |||||||
| chr2:119788580 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-21257A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119788580 | |||||||
| chr2:119788701 | A | T | 2 | a0001c0001t0001g0044 a0001c0001t0046g0090 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-17-21136A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119788701 | |||||||
| chr2:119788987 | A | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-20850A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119788987 | |||||||
| chr2:119789091 | CT | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0123 others(3): Show |
6 | HG01069.hp2 HG01975.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-20733delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119789091 | ||||||
| chr2:119789381 | C | G | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-17-20456C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119789381 | |||||||
| chr2:119789764 | T | C | 233 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(230): Show |
233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-17-20073T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119789764 | |||||||
| chr2:119789851 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-19986T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119789851 | |||||||
| chr2:119789889 | A | AT | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-19938dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119789889 | ||||||
| chr2:119789928 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(52): Show |
55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-17-19909A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119789928 | |||||||
| chr2:119790018 | G | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-19819G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119790018 | |||||||
| chr2:119790070 | A | C | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-19767A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119790070 | |||||||
| chr2:119790364 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-19473A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119790364 | |||||||
| chr2:119790555 | T | C | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-17-19282T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119790555 | |||||||
| chr2:119791021 | C | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0044 others(24): Show |
27 | HG00609.hp1 HG00621.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-17-18816C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791021 | |||||||
| chr2:119791036 | C | T | 1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-18801C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791036 | |||||||
| chr2:119791121 | A | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-18716A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791121 | |||||||
| chr2:119791128 | C | CT | 12 | a0001c0001t0001g0076 a0001c0001t0008g0008 a0001c0001t0008g0009 others(9): Show |
12 | HG00735.hp2 HG02080.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17-18690dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119791128 | ||||||
| chr2:119791128 | CT | C | 91 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0068 others(88): Show |
91 | HG00544.hp2 HG00609.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.-17-18690delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119791128 | ||||||
| chr2:119791128 | CTT | C | 11 | a0001c0001t0006g0023 a0001c0001t0006g0166 a0001c0001t0006g0219 others(8): Show |
11 | HG00639.hp2 HG01070.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-18691_-17-1869 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119791128 | ||||||
| chr2:119791354 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-18483A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791354 | |||||||
| chr2:119791558 | A | G | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-17-18279A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791558 | |||||||
| chr2:119791704 | G | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-17-18133G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791704 | |||||||
| chr2:119791774 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0116 |
2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-17-18063G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119791774 | |||||||
| chr2:119791863 | T | TC | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-17973dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119791863 | ||||||
| chr2:119792096 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-17-17741C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119792096 | |||||||
| chr2:119792558 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-17-17279T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119792558 | |||||||
| chr2:119792765 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-17072C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119792765 | |||||||
| chr2:119793186 | C | T | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-16651C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793186 | |||||||
| chr2:119793253 | A | G | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-16584A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793253 | |||||||
| chr2:119793551 | G | C | 1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-17-16286G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793551 | |||||||
| chr2:119793690 | T | C | 1 | a0001c0001t0006g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-17-16147T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793690 | |||||||
| chr2:119793846 | G | GT | 6 | a0001c0001t0004g0022 a0001c0001t0004g0039 a0001c0001t0009g0150 others(3): Show |
6 | HG00741.hp2 HG01192.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-15962dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119793846 | ||||||
| chr2:119793846 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0008g0009 a0001c0001t0008g0010 |
2 | HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-15971_-17-1596 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119793846 | ||||||
| chr2:119793846 | G | GTTTTTTT others(4): Show |
2 | a0001c0001t0032g0006 a0001c0001t0033g0007 |
2 | HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-17-15972_-17-1596 others(15): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119793846 | ||||||
| chr2:119793846 | GT | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0046 a0001c0001t0001g0053 others(52): Show |
55 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.-17-15962delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119793846 | ||||||
| chr2:119793846 | GTT | G | 154 | a0001c0001t0001g0017 a0001c0001t0001g0027 a0001c0001t0001g0028 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.-17-15963_-17-1596 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119793846 | ||||||
| chr2:119793887 | C | A | 2 | a0001c0001t0006g0166 a0001c0001t0006g0219 |
2 | HG00639.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-17-15950C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793887 | |||||||
| chr2:119793962 | C | A | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-17-15875C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793962 | |||||||
| chr2:119793970 | C | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-15867C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793970 | |||||||
| chr2:119793991 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-15846G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119793991 | |||||||
| chr2:119794017 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-15820T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794017 | |||||||
| chr2:119794087 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-15750A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794087 | |||||||
| chr2:119794126 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-15711G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794126 | |||||||
| chr2:119794134 | C | T | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-15703C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794134 | |||||||
| chr2:119794418 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-15419G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794418 | |||||||
| chr2:119794420 | G | A | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-15417G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794420 | |||||||
| chr2:119794534 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-17-15303A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794534 | |||||||
| chr2:119794672 | T | G | 4 | a0001c0001t0001g0069 a0001c0001t0057g0058 a0003c0004t0001g0075 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-15165T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794672 | |||||||
| chr2:119794883 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-14954C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119794883 | |||||||
| chr2:119795371 | C | T | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-14466C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119795371 | |||||||
| chr2:119795531 | T | C | 87 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-17-14306T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119795531 | |||||||
| chr2:119796015 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-17-13822C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796015 | |||||||
| chr2:119796095 | A | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.-17-13742A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796095 | |||||||
| chr2:119796139 | C | CCCACTGC others(2): Show |
245 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.-17-13696_-17-1368 others(13): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119796139 | ||||||
| chr2:119796203 | G | A | 1 | a0001c0001t0032g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-17-13634G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796203 | |||||||
| chr2:119796284 | A | G | 6 | a0001c0001t0001g0088 a0001c0001t0003g0128 a0001c0001t0010g0005 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-13553A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796284 | |||||||
| chr2:119796739 | T | C | 1 | a0001c0001t0003g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-17-13098T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796739 | |||||||
| chr2:119796860 | TTG | T | 25 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0001g0139 others(22): Show |
25 | HG00597.hp1 HG00735.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-12941_-17-1294 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119796860 | ||||||
| chr2:119796860 | TTGTG | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(188): Show |
191 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-17-12943_-17-1294 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119796860 | ||||||
| chr2:119796860 | TTGTGTG | T | 11 | a0001c0001t0001g0017 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01070.hp2 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-12945_-17-1294 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119796860 | ||||||
| chr2:119796860 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0006g0023 a0001c0001t0006g0220 a0001c0001t0006g0237 others(2): Show |
5 | HG02572.hp2 HG02965.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-12949_-17-1294 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119796860 | ||||||
| chr2:119796866 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-17-12971G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796866 | |||||||
| chr2:119796892 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12945G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796892 | |||||||
| chr2:119796900 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-12937T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796900 | |||||||
| chr2:119796917 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17-12920G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119796917 | |||||||
| chr2:119797342 | G | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-12495G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119797342 | |||||||
| chr2:119797639 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0081 |
3 | HG01952.hp1 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-17-12198G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119797639 | |||||||
| chr2:119797738 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-17-12099G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119797738 | |||||||
| chr2:119797787 | G | C | 1 | a0001c0001t0046g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-17-12050G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119797787 | |||||||
| chr2:119797850 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-11987C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119797850 | |||||||
| chr2:119798325 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-17-11512C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119798325 | |||||||
| chr2:119798531 | C | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.-17-11306C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119798531 | |||||||
| chr2:119798732 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-11105A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119798732 | |||||||
| chr2:119798740 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-17-11097G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119798740 | |||||||
| chr2:119798754 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-17-11083T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119798754 | |||||||
| chr2:119799003 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-17-10834G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799003 | |||||||
| chr2:119799069 | A | G | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-17-10768A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799069 | |||||||
| chr2:119799082 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-10755G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799082 | |||||||
| chr2:119799238 | T | G | 3 | a0001c0001t0002g0215 a0001c0001t0002g0216 a0001c0001t0002g0233 |
3 | HG02559.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-17-10599T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799238 | |||||||
| chr2:119799328 | A | T | 1 | a0001c0001t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-17-10509A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799328 | |||||||
| chr2:119799769 | G | A | 2 | a0001c0001t0010g0002 a0001c0001t0010g0003 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-17-10068G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119799769 | |||||||
| chr2:119800066 | A | T | 1 | a0001c0001t0004g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-17-9771A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119800066 | |||||||
| chr2:119800441 | A | AT | 12 | a0001c0001t0001g0070 a0001c0001t0002g0239 a0002c0002t0005g0242 others(9): Show |
12 | HG01243.hp2 HG01981.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-17-9381dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119800441 | ||||||
| chr2:119800526 | CT | C | 133 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(130): Show |
133 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.-17-9299delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119800526 | ||||||
| chr2:119800575 | A | T | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-17-9262A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119800575 | |||||||
| chr2:119800891 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-8946A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119800891 | |||||||
| chr2:119800917 | C | T | 4 | a0001c0001t0002g0148 a0001c0001t0002g0204 a0001c0001t0002g0224 others(1): Show |
4 | HG01070.hp1 HG01192.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-8920C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119800917 | |||||||
| chr2:119801614 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-17-8223A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119801614 | |||||||
| chr2:119801863 | ATTTC | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-7966_-17-7963d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801863 | ||||||
| chr2:119801879 | G | C | 3 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0081 |
3 | HG01952.hp1 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-17-7958G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119801879 | |||||||
| chr2:119801900 | G | GT | 40 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0054 others(37): Show |
40 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-17-7917dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801900 | ||||||
| chr2:119801900 | G | GTT | 53 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0169 others(50): Show |
53 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-17-7918_-17-7917d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801900 | ||||||
| chr2:119801900 | G | GTTT | 11 | a0001c0001t0002g0148 a0001c0001t0002g0172 a0001c0001t0002g0179 others(8): Show |
11 | HG01261.hp1 HG01433.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-7919_-17-7917d others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801900 | ||||||
| chr2:119801900 | GT | G | 15 | a0001c0001t0001g0067 a0001c0001t0001g0092 a0001c0001t0008g0008 others(12): Show |
15 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-7917delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801900 | ||||||
| chr2:119801900 | GTT | G | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-7918_-17-7917d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119801900 | ||||||
| chr2:119802226 | G | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-17-7611G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119802226 | |||||||
| chr2:119802980 | T | G | 2 | a0002c0003t0015g0025 a0002c0003t0015g0026 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.-17-6857T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119802980 | |||||||
| chr2:119803080 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-17-6757T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119803080 | |||||||
| chr2:119803194 | C | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-6643C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119803194 | |||||||
| chr2:119803304 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-17-6533A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119803304 | |||||||
| chr2:119804062 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-17-5775G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804062 | |||||||
| chr2:119804103 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-17-5734C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804103 | |||||||
| chr2:119804106 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-5731C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804106 | |||||||
| chr2:119804209 | C | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-17-5628C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804209 | |||||||
| chr2:119804362 | G | A | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-17-5475G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804362 | |||||||
| chr2:119804401 | G | A | 2 | a0001c0001t0017g0093 a0001c0001t0017g0140 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-17-5436G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804401 | |||||||
| chr2:119804614 | CT | C | 3 | a0001c0001t0001g0076 a0001c0001t0003g0031 a0001c0001t0003g0100 |
3 | HG03704.hp1 HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-17-5217delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119804614 | ||||||
| chr2:119804697 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-17-5140G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804697 | |||||||
| chr2:119804738 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-17-5099A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119804738 | |||||||
| chr2:119805021 | CATCTCTG | C | 45 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(42): Show |
45 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-17-4813_-17-4807d others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119805021 | ||||||
| chr2:119805130 | GTTGT | G | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-17-4700_-17-4697d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119805130 | ||||||
| chr2:119805145 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-4692C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119805145 | |||||||
| chr2:119805673 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-17-4164G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119805673 | |||||||
| chr2:119805775 | G | A | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.-17-4062G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119805775 | |||||||
| chr2:119805869 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-3968G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119805869 | |||||||
| chr2:119806080 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-3757A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119806080 | |||||||
| chr2:119806480 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-17-3357C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119806480 | |||||||
| chr2:119806564 | G | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.-17-3273G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119806564 | |||||||
| chr2:119806854 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-17-2983A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119806854 | |||||||
| chr2:119807086 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0111 a0001c0001t0058g0049 |
3 | HG01517.hp1 HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-17-2751A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807086 | |||||||
| chr2:119807253 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-17-2584C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807253 | |||||||
| chr2:119807277 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0078 |
2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.-17-2560A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807277 | |||||||
| chr2:119807384 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2453A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807384 | |||||||
| chr2:119807588 | C | G | 1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-17-2249C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807588 | |||||||
| chr2:119807660 | G | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2177G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807660 | |||||||
| chr2:119807663 | C | G | 3 | a0001c0001t0001g0098 a0001c0001t0003g0113 a0001c0001t0047g0097 |
3 | HG02056.hp1 NA19080.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-17-2174C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807663 | |||||||
| chr2:119807685 | A | G | 3 | a0001c0001t0003g0041 a0001c0001t0055g0057 a0001c0001t0056g0061 |
3 | HG00323.hp1 HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-17-2152A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807685 | |||||||
| chr2:119807887 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-17-1950C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119807887 | |||||||
| chr2:119808116 | A | G | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-17-1721A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119808116 | |||||||
| chr2:119808771 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-17-1066C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119808771 | |||||||
| chr2:119808772 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-17-1065A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119808772 | |||||||
| chr2:119808775 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17-1062G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119808775 | |||||||
| chr2:119808957 | A | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-880A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119808957 | |||||||
| chr2:119809041 | G | C | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17-796G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119809041 | |||||||
| chr2:119809134 | T | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-703T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119809134 | |||||||
| chr2:119809249 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-17-588C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119809249 | |||||||
| chr2:119809327 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-17-510A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119809327 | |||||||
| chr2:119809816 | A | AT | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-17-8dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr2 | 119809816 | ||||||
| chr2:119809816 | A | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-21A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 1/26 | chr2 | 119809816 | |||||||
| chr2:119810076 | T | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+85T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810076 | |||||||
| chr2:119810095 | T | C | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.138+104T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810095 | |||||||
| chr2:119810233 | T | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+242T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810233 | |||||||
| chr2:119810304 | T | G | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.138+313T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810304 | |||||||
| chr2:119810664 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.138+673T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810664 | |||||||
| chr2:119810845 | C | CT | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+858dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119810845 | ||||||
| chr2:119810872 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+881C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119810872 | |||||||
| chr2:119811493 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.138+1502G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119811493 | |||||||
| chr2:119811526 | A | G | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+1535A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119811526 | |||||||
| chr2:119811577 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.138+1586A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119811577 | |||||||
| chr2:119811916 | C | T | 1 | a0001c0001t0009g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+1925C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119811916 | |||||||
| chr2:119812185 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+2194T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119812185 | |||||||
| chr2:119812365 | C | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+2374C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119812365 | |||||||
| chr2:119812602 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138+2611G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119812602 | |||||||
| chr2:119812706 | C | A | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.138+2715C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119812706 | |||||||
| chr2:119812975 | A | G | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+2984A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119812975 | |||||||
| chr2:119813239 | G | A | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.138+3248G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813239 | |||||||
| chr2:119813252 | C | CTT | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+3272_138+3273d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119813252 | ||||||
| chr2:119813317 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+3326G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813317 | |||||||
| chr2:119813324 | C | T | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.138+3333C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813324 | |||||||
| chr2:119813723 | G | T | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.138+3732G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813723 | |||||||
| chr2:119813828 | T | TA | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+3838dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119813828 | ||||||
| chr2:119813829 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.138+3838A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813829 | |||||||
| chr2:119813984 | A | C | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.138+3993A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119813984 | |||||||
| chr2:119814233 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.138+4242T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814233 | |||||||
| chr2:119814258 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | NA18986.hp2 NA19009.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.138+4267A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814258 | |||||||
| chr2:119814400 | T | A | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+4409T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814400 | |||||||
| chr2:119814465 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.138+4474C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814465 | |||||||
| chr2:119814511 | A | T | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+4520A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814511 | |||||||
| chr2:119814551 | C | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+4560C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814551 | |||||||
| chr2:119814684 | T | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+4693T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119814684 | |||||||
| chr2:119815109 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.138+5118A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815109 | |||||||
| chr2:119815173 | A | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+5182A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815173 | |||||||
| chr2:119815253 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.138+5262G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815253 | |||||||
| chr2:119815296 | T | A | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+5305T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815296 | |||||||
| chr2:119815342 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.138+5351A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815342 | |||||||
| chr2:119815352 | T | A | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+5361T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815352 | |||||||
| chr2:119815454 | T | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+5463T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815454 | |||||||
| chr2:119815535 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0133 |
3 | HG01496.hp2 HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.138+5544A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815535 | |||||||
| chr2:119815596 | A | T | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.138+5605A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815596 | |||||||
| chr2:119815637 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0003g0113 a0001c0001t0047g0097 |
3 | HG02056.hp1 NA19080.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.138+5646T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815637 | |||||||
| chr2:119815647 | T | C | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.138+5656T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815647 | |||||||
| chr2:119815959 | A | G | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.138+5968A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815959 | |||||||
| chr2:119815963 | C | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.138+5972C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119815963 | |||||||
| chr2:119816115 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.138+6124T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816115 | |||||||
| chr2:119816260 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.138+6269T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816260 | |||||||
| chr2:119816320 | G | A | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+6329G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816320 | |||||||
| chr2:119816564 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.138+6573T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816564 | |||||||
| chr2:119816595 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.138+6604A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816595 | |||||||
| chr2:119816652 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138+6661A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816652 | |||||||
| chr2:119816808 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.138+6817G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816808 | |||||||
| chr2:119816813 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+6822A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119816813 | |||||||
| chr2:119817331 | C | CT | 12 | a0001c0001t0006g0237 a0001c0001t0008g0008 a0001c0001t0008g0009 others(9): Show |
12 | HG00735.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.138+7354dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119817331 | ||||||
| chr2:119817524 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+7533T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119817524 | |||||||
| chr2:119817602 | C | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.138+7611C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119817602 | |||||||
| chr2:119817847 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.138+7856G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119817847 | |||||||
| chr2:119817865 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+7874T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119817865 | |||||||
| chr2:119818015 | T | C | 140 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(137): Show |
140 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.138+8024T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818015 | |||||||
| chr2:119818136 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+8145A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818136 | |||||||
| chr2:119818255 | CT | C | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+8265delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818255 | |||||||
| chr2:119818515 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+8524A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818515 | |||||||
| chr2:119818768 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138+8777A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818768 | |||||||
| chr2:119818879 | A | C | 1 | a0001c0001t0044g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138+8888A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119818879 | |||||||
| chr2:119819238 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0079 a0001c0001t0001g0125 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+9247C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119819238 | |||||||
| chr2:119819294 | A | G | 2 | a0001c0001t0006g0220 a0001c0001t0006g0237 |
2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.138+9303A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119819294 | |||||||
| chr2:119819650 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+9659A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119819650 | |||||||
| chr2:119819689 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+9698A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119819689 | |||||||
| chr2:119819943 | C | G | 1 | a0001c0001t0002g0179 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.138+9952C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119819943 | |||||||
| chr2:119820032 | A | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+10041A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820032 | |||||||
| chr2:119820142 | T | A | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.138+10151T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820142 | |||||||
| chr2:119820151 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.138+10160G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820151 | |||||||
| chr2:119820240 | A | G | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+10249A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820240 | |||||||
| chr2:119820419 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+10428T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820419 | |||||||
| chr2:119820592 | G | T | 2 | a0001c0001t0010g0002 a0001c0001t0010g0003 |
2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.138+10601G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820592 | |||||||
| chr2:119820630 | A | G | 127 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(124): Show |
127 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.138+10639A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820630 | |||||||
| chr2:119820862 | T | C | 2 | a0001c0001t0003g0113 a0001c0001t0047g0097 |
2 | HG02056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.138+10871T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820862 | |||||||
| chr2:119820878 | C | A | 1 | a0001c0001t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.138+10887C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820878 | |||||||
| chr2:119820883 | A | ATG | 86 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(83): Show |
86 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.138+10900_138+1090 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119820883 | ||||||
| chr2:119820926 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.138+10935C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119820926 | |||||||
| chr2:119821093 | AT | A | 95 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0002g0148 others(92): Show |
95 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.138+11122delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119821093 | ||||||
| chr2:119821093 | ATT | A | 8 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(5): Show |
8 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+11121_138+1112 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119821093 | ||||||
| chr2:119821178 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+11187C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821178 | |||||||
| chr2:119821254 | A | C | 2 | a0001c0001t0017g0093 a0001c0001t0017g0140 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.138+11263A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821254 | |||||||
| chr2:119821366 | C | CA | 43 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0170 others(40): Show |
43 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.138+11376dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119821366 | ||||||
| chr2:119821451 | G | A | 1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.138+11460G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821451 | |||||||
| chr2:119821569 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.138+11578G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821569 | |||||||
| chr2:119821579 | A | C | 1 | a0001c0001t0009g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+11588A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821579 | |||||||
| chr2:119821769 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0057g0058 a0003c0004t0001g0075 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+11778T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821769 | |||||||
| chr2:119821774 | C | A | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.138+11783C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821774 | |||||||
| chr2:119821941 | C | T | 1 | a0006c0007t0002g0163 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.138+11950C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119821941 | |||||||
| chr2:119822353 | C | G | 2 | a0001c0001t0013g0109 a0001c0001t0043g0108 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.138+12362C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822353 | |||||||
| chr2:119822361 | C | T | 1 | a0001c0001t0046g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.138+12370C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822361 | |||||||
| chr2:119822364 | C | CT | 15 | a0001c0001t0001g0052 a0001c0001t0001g0158 a0001c0001t0001g0252 others(12): Show |
15 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+12385dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119822364 | ||||||
| chr2:119822364 | CT | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0050 a0001c0001t0001g0053 others(91): Show |
94 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.138+12385delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119822364 | ||||||
| chr2:119822364 | CTT | C | 10 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0227 others(7): Show |
10 | HG00423.hp2 HG00609.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+12384_138+1238 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119822364 | ||||||
| chr2:119822365 | T | C | 3 | a0001c0001t0002g0179 a0001c0001t0002g0198 a0001c0001t0029g0197 |
3 | NA18967.hp2 NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.138+12374T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822365 | |||||||
| chr2:119822366 | T | C | 2 | a0001c0001t0002g0170 a0001c0001t0028g0183 |
2 | HG00738.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.138+12375T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822366 | |||||||
| chr2:119822389 | C | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.138+12398C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822389 | |||||||
| chr2:119822420 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+12429G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822420 | |||||||
| chr2:119822451 | C | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+12460C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822451 | |||||||
| chr2:119822560 | T | C | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.138+12569T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822560 | |||||||
| chr2:119822595 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138+12604G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822595 | |||||||
| chr2:119822608 | C | T | 2 | a0001c0001t0002g0159 a0001c0001t0003g0113 |
2 | HG02056.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.138+12617C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822608 | |||||||
| chr2:119822907 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+12916G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822907 | |||||||
| chr2:119822966 | C | A | 127 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(124): Show |
127 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.138+12975C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119822966 | |||||||
| chr2:119823235 | C | CT | 6 | a0001c0001t0001g0043 a0001c0001t0001g0062 a0001c0001t0001g0079 others(3): Show |
6 | HG01516.hp2 HG02572.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+13260dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119823235 | ||||||
| chr2:119823257 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0127 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.138+13266C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823257 | |||||||
| chr2:119823281 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+13290C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823281 | |||||||
| chr2:119823283 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0116 |
2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.138+13292A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823283 | |||||||
| chr2:119823395 | C | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+13404C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823395 | |||||||
| chr2:119823474 | C | G | 2 | a0002c0003t0015g0025 a0002c0003t0015g0026 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.138+13483C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823474 | |||||||
| chr2:119823492 | T | C | 111 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(108): Show |
111 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.138+13501T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823492 | |||||||
| chr2:119823534 | ATC | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+13545_138+1354 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119823534 | ||||||
| chr2:119823795 | T | C | 1 | a0001c0001t0026g0225 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.138+13804T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823795 | |||||||
| chr2:119823812 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138+13821G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119823812 | |||||||
| chr2:119823995 | CT | C | 4 | a0001c0001t0008g0013 a0001c0001t0012g0012 a0001c0001t0012g0014 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+14008delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119823995 | ||||||
| chr2:119824066 | T | C | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.138+14075T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119824066 | |||||||
| chr2:119824281 | G | T | 1 | a0001c0001t0046g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.138+14290G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119824281 | |||||||
| chr2:119824403 | A | C | 1 | a0001c0001t0004g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.138+14412A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119824403 | |||||||
| chr2:119825025 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+15034A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825025 | |||||||
| chr2:119825117 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.138+15126A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825117 | |||||||
| chr2:119825270 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.138+15279A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825270 | |||||||
| chr2:119825281 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+15290C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825281 | |||||||
| chr2:119825495 | C | CT | 97 | a0001c0001t0001g0060 a0001c0001t0001g0112 a0001c0001t0002g0148 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.138+15522dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119825495 | ||||||
| chr2:119825495 | C | CTT | 17 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0174 others(14): Show |
17 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.138+15521_138+1552 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119825495 | ||||||
| chr2:119825621 | G | A | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.138+15630G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825621 | |||||||
| chr2:119825839 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.138+15848A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825839 | |||||||
| chr2:119825926 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+15935T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119825926 | |||||||
| chr2:119826130 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.138+16139C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826130 | |||||||
| chr2:119826275 | C | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+16284C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826275 | |||||||
| chr2:119826305 | C | G | 1 | a0001c0001t0013g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.138+16314C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826305 | |||||||
| chr2:119826370 | G | C | 11 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0174 others(8): Show |
11 | HG02135.hp1 NA18612.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+16379G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826370 | |||||||
| chr2:119826911 | C | T | 1 | a0001c0001t0009g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.138+16920C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826911 | |||||||
| chr2:119826937 | A | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+16946A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119826937 | |||||||
| chr2:119827129 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+17138T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827129 | |||||||
| chr2:119827145 | C | A | 2 | a0001c0001t0002g0212 a0001c0001t0002g0228 |
2 | HG02027.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.138+17154C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827145 | |||||||
| chr2:119827380 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+17389T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827380 | |||||||
| chr2:119827543 | T | G | 2 | a0001c0001t0002g0202 a0001c0001t0020g0205 |
2 | HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.138+17552T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827543 | |||||||
| chr2:119827560 | T | C | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.138+17569T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827560 | |||||||
| chr2:119827601 | T | G | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.138+17610T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119827601 | |||||||
| chr2:119828055 | A | C | 25 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(22): Show |
25 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.138+18064A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828055 | |||||||
| chr2:119828078 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.138+18087C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828078 | |||||||
| chr2:119828267 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.138+18276A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828267 | |||||||
| chr2:119828277 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.138+18286G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828277 | |||||||
| chr2:119828732 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.138+18741T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828732 | |||||||
| chr2:119828806 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.138+18815C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828806 | |||||||
| chr2:119828816 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.138+18825T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119828816 | |||||||
| chr2:119829091 | A | G | 4 | a0001c0001t0003g0103 a0001c0001t0003g0106 a0001c0001t0003g0251 others(1): Show |
4 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+19100A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829091 | |||||||
| chr2:119829113 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.138+19122G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829113 | |||||||
| chr2:119829292 | T | C | 1 | a0001c0001t0007g0182 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.138+19301T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829292 | |||||||
| chr2:119829527 | T | G | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.138+19536T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829527 | |||||||
| chr2:119829634 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+19643G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829634 | |||||||
| chr2:119829822 | A | C | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+19831A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829822 | |||||||
| chr2:119829826 | T | C | 1 | a0001c0001t0047g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.138+19835T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829826 | |||||||
| chr2:119829999 | T | A | 1 | a0002c0002t0005g0250 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.138+20008T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119829999 | |||||||
| chr2:119830103 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0046g0090 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.138+20112A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830103 | |||||||
| chr2:119830110 | C | T | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.138+20119C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830110 | |||||||
| chr2:119830383 | G | A | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+20392G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830383 | |||||||
| chr2:119830485 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138+20494A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830485 | |||||||
| chr2:119830530 | G | A | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.138+20539G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830530 | |||||||
| chr2:119830626 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+20635G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830626 | |||||||
| chr2:119830688 | G | C | 1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.138+20697G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830688 | |||||||
| chr2:119830764 | C | T | 1 | a0001c0006t0003g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.138+20773C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119830764 | |||||||
| chr2:119831204 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.138+21213T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831204 | |||||||
| chr2:119831219 | C | G | 128 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(125): Show |
128 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.138+21228C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831219 | |||||||
| chr2:119831265 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138+21274G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831265 | |||||||
| chr2:119831421 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.138+21430A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831421 | |||||||
| chr2:119831485 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.138+21494G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831485 | |||||||
| chr2:119831508 | G | A | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+21517G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831508 | |||||||
| chr2:119831522 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+21531A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831522 | |||||||
| chr2:119831638 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.138+21647T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831638 | |||||||
| chr2:119831968 | T | A | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.138+21977T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119831968 | |||||||
| chr2:119832061 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0057g0058 |
2 | HG02071.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.138+22070A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832061 | |||||||
| chr2:119832200 | G | T | 1 | a0001c0001t0055g0057 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.138+22209G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832200 | |||||||
| chr2:119832278 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0141 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.138+22287A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832278 | |||||||
| chr2:119832342 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.138+22351G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832342 | |||||||
| chr2:119832369 | G | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+22378G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832369 | |||||||
| chr2:119832985 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.138+22994A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119832985 | |||||||
| chr2:119833281 | C | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0111 a0001c0001t0001g0120 others(3): Show |
6 | HG01109.hp1 HG01175.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+23290C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119833281 | |||||||
| chr2:119833428 | T | C | 1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+23437T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119833428 | |||||||
| chr2:119833632 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.138+23641C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119833632 | |||||||
| chr2:119834081 | A | G | 128 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(125): Show |
128 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.138+24090A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834081 | |||||||
| chr2:119834161 | C | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0226 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.138+24170C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834161 | |||||||
| chr2:119834173 | A | G | 58 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(55): Show |
58 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.138+24182A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834173 | |||||||
| chr2:119834219 | T | G | 1 | a0001c0001t0025g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.138+24228T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834219 | |||||||
| chr2:119834548 | C | T | 1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.138+24557C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834548 | |||||||
| chr2:119834850 | T | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+24859T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119834850 | |||||||
| chr2:119835004 | A | G | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.138+25013A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835004 | |||||||
| chr2:119835039 | G | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+25048G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835039 | |||||||
| chr2:119835140 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.138+25149T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835140 | |||||||
| chr2:119835223 | C | T | 2 | a0001c0001t0006g0166 a0001c0001t0006g0219 |
2 | HG00639.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.138+25232C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835223 | |||||||
| chr2:119835329 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+25338C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835329 | |||||||
| chr2:119835339 | C | T | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.138+25348C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835339 | |||||||
| chr2:119835407 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138+25416A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835407 | |||||||
| chr2:119835434 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+25443C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835434 | |||||||
| chr2:119835791 | C | T | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+25800C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119835791 | |||||||
| chr2:119836000 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0143 a0001c0001t0010g0001 others(7): Show |
10 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.138+26009C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836000 | |||||||
| chr2:119836068 | CA | C | 113 | a0001c0001t0001g0060 a0001c0001t0002g0148 a0001c0001t0002g0152 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.138+26091delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119836068 | ||||||
| chr2:119836078 | AAAAAG | A | 12 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(9): Show |
12 | HG00735.hp2 HG01496.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.138+26091_138+2609 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119836078 | ||||||
| chr2:119836358 | T | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-26178T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836358 | |||||||
| chr2:119836455 | C | T | 97 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(94): Show |
97 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.139-26081C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836455 | |||||||
| chr2:119836522 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-26014C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836522 | |||||||
| chr2:119836543 | C | T | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.139-25993C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836543 | |||||||
| chr2:119836552 | G | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-25984G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836552 | |||||||
| chr2:119836668 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-25868C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836668 | |||||||
| chr2:119836969 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-25567C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119836969 | |||||||
| chr2:119837028 | C | T | 1 | a0001c0001t0003g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.139-25508C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837028 | |||||||
| chr2:119837029 | G | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-25507G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837029 | |||||||
| chr2:119837061 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-25475A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837061 | |||||||
| chr2:119837113 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-25423G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837113 | |||||||
| chr2:119837115 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-25421G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837115 | |||||||
| chr2:119837405 | C | T | 111 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(108): Show |
111 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.139-25131C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837405 | |||||||
| chr2:119837462 | G | T | 1 | a0001c0001t0056g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.139-25074G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837462 | |||||||
| chr2:119837493 | ACTC | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-25039_139-2503 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119837493 | ||||||
| chr2:119837593 | G | T | 1 | a0001c0001t0050g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.139-24943G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837593 | |||||||
| chr2:119837644 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.139-24892C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837644 | |||||||
| chr2:119837685 | C | T | 17 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(14): Show |
17 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-24851C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837685 | |||||||
| chr2:119837738 | G | A | 1 | a0001c0001t0056g0061 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.139-24798G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837738 | |||||||
| chr2:119837770 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.139-24766A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119837770 | |||||||
| chr2:119837781 | TC | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-24753delC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119837781 | ||||||
| chr2:119838009 | A | G | 4 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(1): Show |
4 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-24527A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838009 | |||||||
| chr2:119838135 | A | T | 1 | a0001c0001t0046g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.139-24401A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838135 | |||||||
| chr2:119838140 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-24396A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838140 | |||||||
| chr2:119838305 | G | A | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.139-24231G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838305 | |||||||
| chr2:119838307 | G | T | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.139-24229G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838307 | |||||||
| chr2:119838991 | T | C | 1 | a0001c0001t0008g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.139-23545T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119838991 | |||||||
| chr2:119839019 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-23517C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839019 | |||||||
| chr2:119839123 | T | C | 1 | a0001c0001t0003g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.139-23413T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839123 | |||||||
| chr2:119839290 | A | G | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.139-23246A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839290 | |||||||
| chr2:119839344 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.139-23192C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839344 | |||||||
| chr2:119839506 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0078 |
2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.139-23030G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839506 | |||||||
| chr2:119839524 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139-23012T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839524 | |||||||
| chr2:119839570 | A | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-22966A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839570 | |||||||
| chr2:119839649 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-22887G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119839649 | |||||||
| chr2:119840064 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-22472A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119840064 | |||||||
| chr2:119840123 | T | C | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-22413T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119840123 | |||||||
| chr2:119840535 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-22001A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119840535 | |||||||
| chr2:119841033 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.139-21503C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841033 | |||||||
| chr2:119841150 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-21386T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841150 | |||||||
| chr2:119841180 | A | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-21356A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841180 | |||||||
| chr2:119841339 | G | A | 7 | a0002c0002t0005g0244 a0002c0002t0005g0245 a0002c0002t0005g0249 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-21197G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841339 | |||||||
| chr2:119841399 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.139-21137G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841399 | |||||||
| chr2:119841800 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-20736A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841800 | |||||||
| chr2:119841857 | G | C | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.139-20679G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119841857 | |||||||
| chr2:119842090 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-20446A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119842090 | |||||||
| chr2:119842572 | C | T | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.139-19964C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119842572 | |||||||
| chr2:119842756 | A | G | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-19780A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119842756 | |||||||
| chr2:119842858 | T | TTG | 21 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0091 others(18): Show |
21 | HG01175.hp1 HG01192.hp2 HG02148.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-19662_139-1966 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119842858 | ||||||
| chr2:119842858 | T | TTGTG | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-19664_139-1966 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119842858 | ||||||
| chr2:119842948 | A | G | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.139-19588A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119842948 | |||||||
| chr2:119842980 | G | A | 7 | a0002c0002t0005g0244 a0002c0002t0005g0245 a0002c0002t0005g0249 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-19556G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119842980 | |||||||
| chr2:119843021 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-19515T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843021 | |||||||
| chr2:119843121 | T | G | 1 | a0001c0001t0001g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.139-19415T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843121 | |||||||
| chr2:119843218 | C | CT | 14 | a0001c0001t0001g0064 a0001c0001t0001g0143 a0001c0001t0003g0102 others(11): Show |
14 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-19298dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843218 | ||||||
| chr2:119843218 | CT | C | 103 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0078 others(100): Show |
103 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.139-19298delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843218 | ||||||
| chr2:119843243 | C | T | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-19293C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843243 | |||||||
| chr2:119843354 | T | C | 1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.139-19182T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843354 | |||||||
| chr2:119843380 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-19156T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843380 | |||||||
| chr2:119843470 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-19066T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843470 | |||||||
| chr2:119843556 | G | T | 1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-18980G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843556 | |||||||
| chr2:119843626 | C | A | 1 | a0001c0001t0004g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-18910C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843626 | |||||||
| chr2:119843632 | A | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0239 |
2 | HG02738.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.139-18904A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843632 | |||||||
| chr2:119843633 | C | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0239 |
2 | HG02738.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.139-18903C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843633 | |||||||
| chr2:119843634 | CT | C | 110 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(107): Show |
110 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.139-18900delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843634 | ||||||
| chr2:119843635 | T | C | 2 | a0001c0001t0002g0206 a0001c0001t0002g0239 |
2 | HG02738.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.139-18901T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843635 | |||||||
| chr2:119843652 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-18884C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843652 | |||||||
| chr2:119843653 | G | T | 1 | a0001c0001t0007g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.139-18883G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843653 | |||||||
| chr2:119843755 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18781T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843755 | |||||||
| chr2:119843768 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18768T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843768 | |||||||
| chr2:119843772 | C | T | 15 | a0001c0001t0002g0180 a0001c0001t0002g0189 a0001c0001t0002g0190 others(12): Show |
15 | HG00423.hp2 HG00609.hp2 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-18764C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843772 | |||||||
| chr2:119843781 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18755C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843781 | |||||||
| chr2:119843794 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-18742G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843794 | |||||||
| chr2:119843795 | G | C | 1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.139-18741G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843795 | |||||||
| chr2:119843801 | T | TGACCCCC others(471): Show |
1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18732_139-1873 others(482): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843801 | ||||||
| chr2:119843805 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18731A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843805 | |||||||
| chr2:119843826 | G | A | 1 | a0001c0001t0002g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.139-18710G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843826 | |||||||
| chr2:119843839 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18697G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843839 | |||||||
| chr2:119843841 | G | T | 1 | a0001c0001t0004g0022 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.139-18695G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843841 | |||||||
| chr2:119843893 | A | ACCTCCCG others(646): Show |
1 | a0002c0003t0015g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-18616_139-1861 others(657): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(512): Show |
3 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0233 |
3 | HG02895.hp2 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.139-18616_139-1861 others(523): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(513): Show |
1 | a0001c0001t0002g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.139-18616_139-1861 others(524): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(512): Show |
1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.139-18616_139-1861 others(523): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(468): Show |
1 | a0001c0001t0001g0118 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(479): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
27 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0062 others(24): Show |
27 | HG00323.hp1 HG00423.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
4 | a0001c0001t0001g0052 a0001c0001t0001g0129 a0001c0001t0042g0074 others(1): Show |
4 | HG00621.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG03704.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0003g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0125 |
2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
1 | a0001c0001t0001g0059 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
2 | a0001c0001t0001g0064 a0001c0001t0058g0049 |
2 | HG02080.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(472): Show |
1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(483): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(469): Show |
31 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0042 others(28): Show |
31 | HG00621.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(480): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
2 | a0001c0001t0046g0090 a0001c0001t0054g0047 |
2 | HG02083.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
2 | a0001c0001t0001g0055 a0001c0001t0053g0040 |
2 | HG00609.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(610): Show |
1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(621): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(610): Show |
8 | a0002c0002t0005g0243 a0002c0002t0005g0244 a0002c0002t0005g0245 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(621): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
1 | a0002c0002t0016g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(563): Show |
1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(574): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(610): Show |
12 | a0001c0001t0002g0159 a0001c0001t0002g0164 a0001c0001t0002g0165 others(9): Show |
12 | HG00639.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(621): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
19 | a0001c0001t0002g0167 a0001c0001t0002g0171 a0001c0001t0002g0175 others(16): Show |
19 | HG01070.hp1 HG01255.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
2 | a0001c0001t0002g0184 a0001c0001t0007g0182 |
2 | HG02698.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
14 | a0001c0001t0001g0098 a0001c0001t0002g0154 a0001c0001t0002g0168 others(11): Show |
14 | HG00423.hp2 HG00609.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(613): Show |
1 | a0001c0001t0023g0147 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(624): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
1 | a0001c0001t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(613): Show |
1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(624): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
1 | a0001c0001t0002g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
1 | a0001c0001t0021g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(613): Show |
3 | a0001c0001t0002g0179 a0001c0001t0002g0181 a0001c0001t0002g0189 |
3 | HG03669.hp2 NA18952.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(624): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(614): Show |
1 | a0001c0001t0002g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(625): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(614): Show |
1 | a0001c0001t0011g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(625): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(610): Show |
1 | a0002c0002t0005g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(621): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(614): Show |
1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(625): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0001g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
3 | a0001c0001t0002g0170 a0001c0001t0002g0231 a0001c0001t0019g0207 |
3 | HG01358.hp2 HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
4 | a0001c0001t0002g0176 a0001c0001t0002g0188 a0001c0001t0002g0209 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(472): Show |
1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(483): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(470): Show |
1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(481): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(472): Show |
1 | a0001c0001t0003g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(483): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(611): Show |
1 | a0001c0001t0002g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(622): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(613): Show |
3 | a0001c0001t0002g0148 a0001c0001t0002g0201 a0001c0001t0002g0221 |
3 | HG01261.hp1 HG03942.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(624): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(614): Show |
1 | a0001c0001t0002g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(625): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(620): Show |
1 | a0001c0001t0002g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(631): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(613): Show |
1 | a0001c0001t0028g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(624): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(616): Show |
1 | a0001c0001t0002g0212 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(627): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(472): Show |
1 | a0001c0001t0001g0028 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(483): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(472): Show |
1 | a0001c0001t0001g0136 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(483): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(620): Show |
1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(631): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843893 | A | ACCTCCCG others(612): Show |
1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-18621_139-1862 others(623): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843893 | ||||||
| chr2:119843899 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-18637C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843899 | |||||||
| chr2:119843900 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-18636G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843900 | |||||||
| chr2:119843900 | G | GGACGGGG others(648): Show |
1 | a0001c0006t0003g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.139-18628_139-1862 others(659): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(820): Show |
1 | a0002c0003t0015g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.139-18616_139-1861 others(831): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(643): Show |
3 | a0001c0001t0013g0145 a0001c0001t0013g0146 a0005c0009t0001g0110 |
3 | HG02080.hp2 HG02165.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(654): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(820): Show |
1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(831): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(645): Show |
2 | a0001c0001t0055g0057 a0001c0001t0056g0061 |
2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(656): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(646): Show |
1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(657): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(647): Show |
1 | a0001c0001t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(658): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(647): Show |
1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(658): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(647): Show |
1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(658): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(644): Show |
3 | a0001c0001t0010g0001 a0001c0001t0010g0002 a0001c0001t0010g0003 |
3 | HG02257.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(655): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(644): Show |
2 | a0001c0001t0013g0109 a0001c0001t0043g0108 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.139-18614_139-1861 others(655): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(645): Show |
1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(656): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(221): Show |
11 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(8): Show |
11 | HG01192.hp2 HG02486.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(232): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(645): Show |
9 | a0001c0001t0001g0252 a0001c0001t0003g0099 a0001c0001t0003g0100 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(656): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(648): Show |
1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(659): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(646): Show |
1 | a0001c0001t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(657): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(790): Show |
1 | a0001c0001t0002g0187 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(801): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(789): Show |
1 | a0001c0001t0002g0230 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(800): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(789): Show |
1 | a0001c0001t0002g0228 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(800): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(791): Show |
1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(802): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(646): Show |
1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(657): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(647): Show |
1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(658): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(222): Show |
1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(233): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(650): Show |
1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(661): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843900 | G | GGACGGGG others(794): Show |
1 | a0001c0001t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(805): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843900 | ||||||
| chr2:119843908 | C | CGGCTGGC others(282): Show |
1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18614_139-1861 others(293): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843908 | ||||||
| chr2:119843908 | C | CGGCTGGC others(321): Show |
1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18616_139-1861 others(332): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843908 | ||||||
| chr2:119843916 | C | CGGGCGGG others(221): Show |
4 | a0001c0001t0004g0018 a0001c0001t0004g0022 a0001c0001t0030g0033 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-18614_139-1861 others(232): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843916 | ||||||
| chr2:119843916 | C | CGGGCGGG others(222): Show |
1 | a0001c0001t0004g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.139-18614_139-1861 others(233): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843916 | ||||||
| chr2:119843920 | C | CT | 10 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-18616_139-1861 others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843920 | |||||||
| chr2:119843923 | A | G | 10 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-18613A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843923 | |||||||
| chr2:119843928 | T | C | 84 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(81): Show |
84 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.139-18608T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843928 | |||||||
| chr2:119843930 | A | ACCCCCCC others(498): Show |
4 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(1): Show |
4 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-18599_139-1859 others(509): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843930 | ||||||
| chr2:119843930 | A | ACCCCCCC others(498): Show |
3 | a0001c0001t0008g0013 a0001c0001t0012g0014 a0001c0001t0012g0015 |
3 | HG02896.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.139-18599_139-1859 others(509): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843930 | ||||||
| chr2:119843930 | A | ACCCCCCC others(499): Show |
1 | a0001c0001t0012g0012 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.139-18599_139-1859 others(510): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843930 | ||||||
| chr2:119843930 | A | ACCCCCCC others(500): Show |
1 | a0001c0001t0032g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-18599_139-1859 others(511): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843930 | ||||||
| chr2:119843930 | A | ACCCCCCC others(502): Show |
1 | a0001c0001t0008g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.139-18599_139-1859 others(513): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843930 | ||||||
| chr2:119843946 | C | T | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18590C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843946 | |||||||
| chr2:119843949 | G | A | 7 | a0002c0002t0005g0244 a0002c0002t0005g0245 a0002c0002t0005g0249 others(4): Show |
7 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-18587G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843949 | |||||||
| chr2:119843953 | G | A | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-18583G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843953 | |||||||
| chr2:119843958 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0028 others(85): Show |
88 | HG00323.hp1 HG00423.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.139-18578G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119843958 | |||||||
| chr2:119843969 | C | CG | 6 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0155 others(3): Show |
6 | HG00741.hp2 HG01192.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-18561dupG | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119843969 | ||||||
| chr2:119844014 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0031g0011 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.139-18522C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844014 | |||||||
| chr2:119844015 | C | G | 68 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0071 others(65): Show |
68 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.139-18521C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844015 | |||||||
| chr2:119844047 | C | T | 5 | a0001c0001t0002g0187 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG01192.hp1 HG01978.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-18489C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844047 | |||||||
| chr2:119844076 | A | AGACGGGG others(144): Show |
1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18438_139-1843 others(155): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844076 | ||||||
| chr2:119844085 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-18451G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844085 | |||||||
| chr2:119844099 | A | AGGGCTCA others(42): Show |
5 | a0001c0001t0002g0187 a0001c0001t0002g0208 a0001c0001t0002g0224 others(2): Show |
5 | HG01192.hp1 HG01978.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-18432_139-1843 others(53): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTCA others(42): Show |
57 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0096 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.139-18432_139-1843 others(53): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTCA others(42): Show |
1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.139-18432_139-1843 others(53): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTCA others(43): Show |
1 | a0002c0003t0015g0026 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.139-18432_139-1843 others(54): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(218): Show |
10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-18395_139-1839 others(229): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(169): Show |
5 | a0001c0001t0002g0152 a0001c0001t0002g0160 a0001c0001t0002g0164 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-18391_139-1839 others(180): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(218): Show |
66 | a0001c0001t0001g0098 a0001c0001t0002g0153 a0001c0001t0002g0154 others(63): Show |
66 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.139-18380_139-1837 others(229): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(140): Show |
2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.139-18380_139-1837 others(151): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(219): Show |
1 | a0001c0001t0003g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.139-18380_139-1837 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(219): Show |
1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-18380_139-1837 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(219): Show |
3 | a0001c0001t0002g0212 a0001c0001t0011g0232 a0001c0001t0011g0235 |
3 | HG02027.hp1 HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.139-18385_139-1838 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(219): Show |
1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.139-18423_139-1842 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(220): Show |
1 | a0001c0001t0003g0103 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.139-18423_139-1842 others(231): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | AGGGCTGA others(222): Show |
1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.139-18423_139-1842 others(233): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844099 | ||||||
| chr2:119844099 | A | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18437A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844099 | |||||||
| chr2:119844104 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18432T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844104 | |||||||
| chr2:119844105 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.139-18431G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844105 | |||||||
| chr2:119844105 | G | GACCCCCC others(218): Show |
76 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0028 others(73): Show |
76 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.139-18380_139-1837 others(229): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(218): Show |
1 | a0001c0001t0001g0119 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.139-18380_139-1837 others(229): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(219): Show |
4 | a0001c0001t0001g0085 a0001c0001t0001g0112 a0001c0001t0001g0136 others(1): Show |
4 | HG01433.hp1 HG01496.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-18380_139-1837 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(220): Show |
1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-18380_139-1837 others(231): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(219): Show |
1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.139-18385_139-1838 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(219): Show |
1 | a0001c0001t0001g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.139-18423_139-1842 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | GACCCCCC others(220): Show |
1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.139-18423_139-1842 others(231): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844105 | ||||||
| chr2:119844105 | G | T | 9 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0096 others(6): Show |
9 | HG00544.hp1 HG00741.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-18431G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844105 | |||||||
| chr2:119844106 | A | ACCCCCCC others(219): Show |
1 | a0001c0001t0003g0128 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.139-18380_139-1837 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844106 | ||||||
| chr2:119844106 | A | ACCCCCCC others(220): Show |
1 | a0002c0003t0015g0025 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-18385_139-1838 others(231): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844106 | ||||||
| chr2:119844106 | A | ACCCCCCC others(223): Show |
1 | a0001c0001t0002g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.139-18423_139-1842 others(234): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844106 | ||||||
| chr2:119844106 | A | ATCCCCCC others(43): Show |
1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.139-18430_139-1842 others(54): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844106 | |||||||
| chr2:119844145 | C | CGGGGGGC others(219): Show |
4 | a0001c0001t0002g0148 a0001c0001t0002g0172 a0001c0001t0002g0181 others(1): Show |
4 | HG01261.hp1 HG01433.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-18380_139-1837 others(230): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844145 | ||||||
| chr2:119844164 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.139-18372A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844164 | |||||||
| chr2:119844174 | C | G | 2 | a0001c0001t0017g0093 a0001c0001t0017g0140 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.139-18362C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844174 | |||||||
| chr2:119844175 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.139-18361G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844175 | |||||||
| chr2:119844179 | G | A | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.139-18357G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844179 | |||||||
| chr2:119844192 | G | C | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18344G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844192 | |||||||
| chr2:119844209 | A | G | 10 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-18327A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844209 | |||||||
| chr2:119844224 | C | T | 10 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-18312C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844224 | |||||||
| chr2:119844225 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.139-18311G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844225 | |||||||
| chr2:119844227 | G | C | 2 | a0001c0001t0002g0162 a0001c0001t0031g0011 |
2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.139-18309G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844227 | |||||||
| chr2:119844239 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-18297G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844239 | |||||||
| chr2:119844282 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18254C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844282 | |||||||
| chr2:119844284 | C | T | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18252C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844284 | |||||||
| chr2:119844299 | CCCGGACG others(10): Show |
C | 4 | a0001c0001t0030g0033 a0002c0003t0015g0025 a0002c0003t0015g0026 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-18215_139-1819 others(21): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844299 | ||||||
| chr2:119844316 | G | GCCAGGCG others(25): Show |
1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18218_139-1821 others(36): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844316 | ||||||
| chr2:119844316 | G | GCCGGGCA others(329): Show |
1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-18216_139-1821 others(340): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844316 | ||||||
| chr2:119844322 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.139-18214C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844322 | |||||||
| chr2:119844347 | T | C | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18189T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844347 | |||||||
| chr2:119844349 | AC | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0043 others(81): Show |
84 | HG00323.hp1 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.139-18175delC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844349 | ||||||
| chr2:119844349 | ACC | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0069 a0001c0001t0002g0160 others(10): Show |
13 | HG00609.hp2 HG00738.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.139-18176_139-1817 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844349 | ||||||
| chr2:119844349 | ACCC | A | 117 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(114): Show |
117 | HG00423.hp2 HG00544.hp2 HG00639.hp2 others(114): Show |
intron_variant | MODIFIER | c.139-18177_139-1817 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844349 | ||||||
| chr2:119844355 | C | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18181C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844355 | |||||||
| chr2:119844381 | T | C | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18155T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844381 | |||||||
| chr2:119844386 | G | GGCCGGGC others(155): Show |
1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-18150_139-1814 others(166): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844386 | |||||||
| chr2:119844388 | C | T | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-18148C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844388 | |||||||
| chr2:119844433 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-18103G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844433 | |||||||
| chr2:119844517 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139-18019G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844517 | |||||||
| chr2:119844536 | C | T | 2 | a0001c0001t0002g0148 a0001c0001t0002g0204 |
2 | HG01257.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.139-18000C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844536 | |||||||
| chr2:119844542 | G | A | 1 | a0001c0001t0014g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.139-17994G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844542 | |||||||
| chr2:119844555 | C | T | 2 | a0001c0001t0006g0166 a0001c0001t0006g0219 |
2 | HG00639.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.139-17981C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844555 | |||||||
| chr2:119844565 | C | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-17971C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844565 | |||||||
| chr2:119844625 | G | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17911G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844625 | |||||||
| chr2:119844635 | T | G | 2 | a0001c0001t0002g0184 a0001c0001t0023g0147 |
2 | HG01069.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.139-17901T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844635 | |||||||
| chr2:119844636 | C | G | 90 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.139-17900C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844636 | |||||||
| chr2:119844737 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.139-17799C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844737 | |||||||
| chr2:119844845 | C | CG | 3 | a0001c0001t0002g0211 a0001c0001t0002g0239 a0001c0001t0020g0205 |
3 | HG01496.hp1 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.139-17689dupG | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119844845 | ||||||
| chr2:119844848 | T | G | 131 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(128): Show |
131 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.139-17688T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844848 | |||||||
| chr2:119844858 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.139-17678G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844858 | |||||||
| chr2:119844989 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17547A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844989 | |||||||
| chr2:119844992 | T | G | 6 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-17544T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119844992 | |||||||
| chr2:119845065 | A | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-17471A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845065 | |||||||
| chr2:119845072 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-17464G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845072 | |||||||
| chr2:119845083 | T | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | NA18986.hp2 NA19009.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.139-17453T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845083 | |||||||
| chr2:119845125 | A | G | 141 | a0001c0001t0001g0098 a0001c0001t0001g0143 a0001c0001t0002g0148 others(138): Show |
141 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.139-17411A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845125 | |||||||
| chr2:119845206 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.139-17330C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845206 | |||||||
| chr2:119845231 | G | GGGGAGA | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-17295_139-1729 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845231 | ||||||
| chr2:119845231 | G | GGGGAGAG others(5): Show |
10 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-17301_139-1729 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845231 | ||||||
| chr2:119845231 | GGGGAGA | G | 91 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0112 others(88): Show |
91 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.139-17295_139-1729 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845231 | ||||||
| chr2:119845235 | AGAGGGAG others(11): Show |
A | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-17295_139-1727 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845235 | ||||||
| chr2:119845241 | A | AGAGGGG | 53 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0046 others(50): Show |
53 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.139-17271_139-1726 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845241 | ||||||
| chr2:119845241 | A | AGAGGGGG others(5): Show |
1 | a0001c0001t0001g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.139-17277_139-1726 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845241 | ||||||
| chr2:119845241 | AGAGGGG | A | 16 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(13): Show |
16 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.139-17271_139-1726 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845241 | ||||||
| chr2:119845253 | G | A | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-17283G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845253 | |||||||
| chr2:119845253 | G | GGAGGGA | 23 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(20): Show |
23 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.139-17278_139-1727 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGAGGGAG others(5): Show |
10 | a0001c0001t0002g0148 a0001c0001t0002g0171 a0001c0001t0002g0181 others(7): Show |
10 | HG00544.hp2 HG01070.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-17278_139-1727 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGAGGGAG others(11): Show |
22 | a0001c0001t0001g0098 a0001c0001t0002g0155 a0001c0001t0002g0170 others(19): Show |
22 | HG00609.hp2 HG00738.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.139-17278_139-1727 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGAGGGAG others(17): Show |
22 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0172 others(19): Show |
22 | HG00423.hp2 HG01069.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.139-17278_139-1727 others(28): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGAGGGAG others(23): Show |
4 | a0001c0001t0002g0184 a0001c0001t0002g0239 a0001c0001t0014g0238 others(1): Show |
4 | HG02630.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-17278_139-1727 others(34): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGAGGGAG others(29): Show |
1 | a0001c0001t0026g0225 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.139-17278_139-1727 others(40): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845253 | G | GGGAGGGA others(18): Show |
1 | a0001c0001t0002g0211 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-17282_139-1728 others(29): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845253 | ||||||
| chr2:119845259 | G | A | 90 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.139-17277G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845259 | |||||||
| chr2:119845259 | G | GGAGGGA | 12 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(9): Show |
12 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.139-17272_139-1727 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845259 | ||||||
| chr2:119845259 | G | GGAGGGAG others(11): Show |
1 | a0001c0001t0032g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-17272_139-1727 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845259 | ||||||
| chr2:119845265 | G | A | 108 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(105): Show |
108 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.139-17271G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845265 | |||||||
| chr2:119845265 | G | GGAGGGA | 10 | a0001c0001t0001g0051 a0001c0001t0004g0018 a0001c0001t0004g0021 others(7): Show |
10 | HG02486.hp2 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-17241_139-1723 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845265 | ||||||
| chr2:119845265 | G | GGAGGGAG others(11): Show |
1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-17253_139-1723 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845265 | ||||||
| chr2:119845265 | G | GGAGGGGG others(5): Show |
11 | a0001c0001t0001g0050 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
11 | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-17266_139-1726 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845265 | ||||||
| chr2:119845269 | GGAGAGGG others(3): Show |
G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17265_139-1725 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845269 | ||||||
| chr2:119845271 | A | G | 20 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0077 others(17): Show |
20 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-17265A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845271 | |||||||
| chr2:119845277 | A | G | 2 | a0001c0001t0001g0158 a0001c0006t0003g0105 |
2 | HG02056.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.139-17259A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845277 | |||||||
| chr2:119845285 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17251A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845285 | |||||||
| chr2:119845295 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.139-17241A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845295 | |||||||
| chr2:119845295 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17241A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845295 | |||||||
| chr2:119845357 | C | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-17179C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845357 | |||||||
| chr2:119845662 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.139-16874A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845662 | |||||||
| chr2:119845801 | ATCTTT | A | 6 | a0001c0001t0006g0023 a0001c0001t0006g0220 a0001c0001t0006g0237 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-16728_139-1672 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119845801 | ||||||
| chr2:119845849 | G | A | 114 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-16687G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845849 | |||||||
| chr2:119845864 | A | G | 131 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(128): Show |
131 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.139-16672A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845864 | |||||||
| chr2:119845904 | C | T | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.139-16632C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845904 | |||||||
| chr2:119845905 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0047g0097 |
2 | HG02056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.139-16631G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845905 | |||||||
| chr2:119845977 | C | T | 65 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0154 others(62): Show |
65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.139-16559C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119845977 | |||||||
| chr2:119846021 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-16515C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846021 | |||||||
| chr2:119846135 | T | C | 1 | a0001c0001t0025g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.139-16401T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846135 | |||||||
| chr2:119846208 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.139-16328G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846208 | |||||||
| chr2:119846366 | C | T | 7 | a0001c0001t0002g0152 a0001c0001t0002g0160 a0001c0001t0002g0162 others(4): Show |
7 | HG01884.hp1 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-16170C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846366 | |||||||
| chr2:119846466 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.139-16070G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846466 | |||||||
| chr2:119846552 | A | AT | 21 | a0001c0001t0002g0211 a0001c0001t0003g0048 a0001c0001t0003g0083 others(18): Show |
21 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-15972dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119846552 | ||||||
| chr2:119846553 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.139-15983T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846553 | |||||||
| chr2:119846824 | C | T | 90 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.139-15712C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846824 | |||||||
| chr2:119846834 | ATAACT | A | 25 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(22): Show |
25 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.139-15698_139-1569 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119846834 | ||||||
| chr2:119846878 | TCA | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-15657_139-1565 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846878 | |||||||
| chr2:119846912 | C | A | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.139-15624C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846912 | |||||||
| chr2:119846915 | A | AT | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-15620dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119846915 | ||||||
| chr2:119846927 | A | G | 1 | a0001c0001t0007g0185 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.139-15609A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119846927 | |||||||
| chr2:119847197 | G | GTA | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-15330_139-1532 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847197 | ||||||
| chr2:119847254 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.139-15282A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847254 | |||||||
| chr2:119847270 | C | CTA | 9 | a0001c0001t0001g0143 a0001c0001t0002g0161 a0001c0001t0002g0176 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-15261_139-1526 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847270 | ||||||
| chr2:119847270 | C | CTATA | 6 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(3): Show |
6 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-15263_139-1526 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847270 | ||||||
| chr2:119847275 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0046g0090 |
2 | HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.139-15261T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847275 | |||||||
| chr2:119847275 | T | TAC | 13 | a0001c0001t0001g0055 a0001c0001t0001g0070 a0001c0001t0001g0081 others(10): Show |
13 | HG00323.hp2 HG00609.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.139-15221_139-1522 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | T | TACAC | 4 | a0001c0001t0001g0052 a0001c0001t0001g0071 a0001c0001t0001g0117 others(1): Show |
4 | HG01952.hp1 HG03942.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-15223_139-1522 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | T | TACACAC | 3 | a0001c0001t0001g0017 a0001c0001t0001g0092 a0001c0001t0001g0158 |
3 | HG01069.hp2 HG01070.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.139-15225_139-1522 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | T | TATATACA others(3): Show |
1 | a0001c0001t0030g0033 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.139-15260_139-1525 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | TAC | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0003g0041 others(1): Show |
4 | HG00323.hp1 HG03017.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-15221_139-1522 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | TACAC | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0137 a0001c0001t0009g0150 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-15223_139-1522 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847275 | TACACACA others(1): Show |
T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-15227_139-1522 others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847275 | ||||||
| chr2:119847277 | C | T | 124 | a0001c0001t0001g0098 a0001c0001t0001g0143 a0001c0001t0002g0148 others(121): Show |
124 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.139-15259C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847277 | |||||||
| chr2:119847279 | C | T | 20 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(17): Show |
20 | HG00735.hp2 HG01175.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-15257C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847279 | |||||||
| chr2:119847281 | C | T | 12 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(9): Show |
12 | HG00735.hp2 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.139-15255C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847281 | |||||||
| chr2:119847283 | C | T | 10 | a0001c0001t0008g0010 a0001c0001t0008g0013 a0001c0001t0008g0016 others(7): Show |
10 | HG00735.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-15253C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847283 | |||||||
| chr2:119847285 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-15251C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847285 | |||||||
| chr2:119847307 | C | T | 1 | a0001c0001t0006g0166 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.139-15229C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847307 | |||||||
| chr2:119847309 | C | T | 13 | a0001c0001t0002g0176 a0001c0001t0002g0226 a0001c0001t0006g0023 others(10): Show |
13 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-15227C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847309 | |||||||
| chr2:119847311 | C | T | 86 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0153 others(83): Show |
86 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.139-15225C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847311 | |||||||
| chr2:119847313 | C | T | 101 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(98): Show |
101 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.139-15223C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847313 | |||||||
| chr2:119847315 | C | CACACAT | 5 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0069 others(2): Show |
5 | HG01358.hp1 HG01978.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-15220_139-1521 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847315 | ||||||
| chr2:119847315 | C | CACAT | 12 | a0001c0001t0001g0068 a0001c0001t0001g0096 a0001c0001t0001g0112 others(9): Show |
12 | HG00544.hp1 HG01081.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.139-15220_139-1521 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847315 | ||||||
| chr2:119847315 | C | CAT | 29 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0063 others(26): Show |
29 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.139-15208_139-1520 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847315 | ||||||
| chr2:119847315 | C | T | 135 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(132): Show |
135 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.139-15221C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847315 | |||||||
| chr2:119847317 | T | C | 6 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0113 others(3): Show |
6 | HG00323.hp2 HG01433.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-15219T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847317 | |||||||
| chr2:119847327 | TA | T | 6 | a0001c0001t0006g0219 a0001c0001t0006g0220 a0001c0001t0006g0237 others(3): Show |
6 | HG00639.hp2 HG02055.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-15208delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847327 | |||||||
| chr2:119847328 | A | AT | 20 | a0001c0001t0001g0143 a0001c0001t0002g0153 a0001c0001t0002g0234 others(17): Show |
20 | HG01109.hp2 HG01192.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.139-15192dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847328 | ||||||
| chr2:119847328 | A | ATAT | 47 | a0001c0001t0001g0062 a0001c0001t0002g0152 a0001c0001t0002g0159 others(44): Show |
47 | HG00423.hp2 HG00609.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.139-15207_139-1520 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847328 | ||||||
| chr2:119847328 | A | ATATAT | 12 | a0001c0001t0002g0162 a0001c0001t0002g0203 a0001c0001t0019g0207 others(9): Show |
12 | HG01070.hp1 HG01433.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.139-15207_139-1520 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847328 | ||||||
| chr2:119847328 | A | ATT | 16 | a0001c0001t0001g0098 a0001c0001t0002g0174 a0001c0001t0002g0175 others(13): Show |
16 | HG01346.hp2 HG02135.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-15193_139-1519 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847328 | ||||||
| chr2:119847328 | A | ATTT | 7 | a0001c0001t0002g0170 a0001c0001t0007g0178 a0001c0001t0014g0222 others(4): Show |
7 | HG01358.hp2 HG02523.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-15194_139-1519 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119847328 | ||||||
| chr2:119847328 | A | T | 3 | a0001c0001t0003g0083 a0001c0001t0006g0023 a0001c0001t0036g0034 |
3 | HG01175.hp1 HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.139-15208A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847328 | |||||||
| chr2:119847329 | T | TA | 5 | a0001c0001t0001g0076 a0001c0001t0002g0184 a0001c0001t0003g0113 others(2): Show |
5 | HG01069.hp1 HG02056.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-15207_139-1520 others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847329 | |||||||
| chr2:119847329 | T | TATA | 5 | a0001c0001t0001g0079 a0001c0001t0001g0123 a0001c0001t0002g0209 others(2): Show |
5 | HG01516.hp2 HG01975.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-15207_139-1520 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847329 | |||||||
| chr2:119847330 | T | A | 24 | a0001c0001t0001g0017 a0001c0001t0001g0055 a0001c0001t0001g0065 others(21): Show |
24 | HG00323.hp2 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.139-15206T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847330 | |||||||
| chr2:119847331 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0003g0251 |
2 | HG01516.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.139-15205T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847331 | |||||||
| chr2:119847525 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.139-15011C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847525 | |||||||
| chr2:119847570 | G | A | 3 | a0001c0001t0002g0176 a0001c0001t0002g0188 a0001c0001t0002g0226 |
3 | HG01167.hp2 HG01169.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.139-14966G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847570 | |||||||
| chr2:119847616 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.139-14920A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847616 | |||||||
| chr2:119847807 | A | G | 114 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-14729A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119847807 | |||||||
| chr2:119848179 | C | CT | 5 | a0001c0001t0011g0235 a0001c0001t0034g0032 a0002c0003t0015g0025 others(2): Show |
5 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-14345dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119848179 | ||||||
| chr2:119848204 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-14332C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848204 | |||||||
| chr2:119848243 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.139-14293G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848243 | |||||||
| chr2:119848266 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.139-14270C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848266 | |||||||
| chr2:119848267 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.139-14269G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848267 | |||||||
| chr2:119848281 | C | T | 4 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0216 others(1): Show |
4 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-14255C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848281 | |||||||
| chr2:119848319 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0081 |
3 | HG01952.hp1 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.139-14217G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848319 | |||||||
| chr2:119848575 | A | T | 140 | a0001c0001t0001g0098 a0001c0001t0001g0143 a0001c0001t0002g0148 others(137): Show |
140 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.139-13961A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848575 | |||||||
| chr2:119848755 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-13781C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848755 | |||||||
| chr2:119848789 | C | T | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.139-13747C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848789 | |||||||
| chr2:119848792 | G | A | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-13744G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848792 | |||||||
| chr2:119848851 | G | A | 65 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0154 others(62): Show |
65 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.139-13685G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848851 | |||||||
| chr2:119848890 | C | T | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-13646C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119848890 | |||||||
| chr2:119849039 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.139-13497A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849039 | |||||||
| chr2:119849090 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-13446A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849090 | |||||||
| chr2:119849189 | A | C | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.139-13347A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849189 | |||||||
| chr2:119849204 | C | T | 48 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(45): Show |
48 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.139-13332C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849204 | |||||||
| chr2:119849281 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.139-13255G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849281 | |||||||
| chr2:119849377 | C | T | 100 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(97): Show |
100 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.139-13159C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849377 | |||||||
| chr2:119849851 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.139-12685C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119849851 | |||||||
| chr2:119850121 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0129 a0001c0001t0001g0138 |
3 | HG00621.hp1 HG01167.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.139-12415A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850121 | |||||||
| chr2:119850297 | T | C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0111 a0001c0001t0044g0144 others(1): Show |
4 | HG01346.hp2 HG01517.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-12239T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850297 | |||||||
| chr2:119850312 | T | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0072 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.139-12224T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850312 | |||||||
| chr2:119850346 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.139-12190G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850346 | |||||||
| chr2:119850486 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.139-12050T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850486 | |||||||
| chr2:119850555 | G | A | 114 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-11981G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119850555 | |||||||
| chr2:119851086 | T | C | 2 | a0001c0001t0003g0066 a0001c0001t0003g0072 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.139-11450T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119851086 | |||||||
| chr2:119851651 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-10885A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119851651 | |||||||
| chr2:119851805 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-10731G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119851805 | |||||||
| chr2:119852194 | C | G | 1 | a0001c0001t0013g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.139-10342C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852194 | |||||||
| chr2:119852209 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.139-10327G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852209 | |||||||
| chr2:119852235 | G | A | 1 | a0001c0001t0002g0198 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.139-10301G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852235 | |||||||
| chr2:119852462 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.139-10074G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852462 | |||||||
| chr2:119852478 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-10058C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852478 | |||||||
| chr2:119852482 | A | G | 141 | a0001c0001t0001g0098 a0001c0001t0001g0143 a0001c0001t0002g0148 others(138): Show |
141 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.139-10054A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852482 | |||||||
| chr2:119852572 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.139-9964A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852572 | |||||||
| chr2:119852719 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-9817T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852719 | |||||||
| chr2:119852938 | A | G | 1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.139-9598A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119852938 | |||||||
| chr2:119853484 | G | A | 114 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.139-9052G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119853484 | |||||||
| chr2:119853542 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.139-8994A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119853542 | |||||||
| chr2:119853725 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.139-8811T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119853725 | |||||||
| chr2:119853766 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-8770C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119853766 | |||||||
| chr2:119853959 | G | C | 2 | a0002c0002t0016g0241 a0002c0002t0016g0246 |
2 | HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.139-8577G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119853959 | |||||||
| chr2:119854247 | C | T | 1 | a0007c0008t0004g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-8289C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854247 | |||||||
| chr2:119854391 | C | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0078 a0001c0001t0003g0113 others(1): Show |
4 | HG02056.hp1 NA18939.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-8145C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854391 | |||||||
| chr2:119854439 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-8097C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854439 | |||||||
| chr2:119854456 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.139-8080A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854456 | |||||||
| chr2:119854553 | A | G | 1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.139-7983A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854553 | |||||||
| chr2:119854562 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.139-7974C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854562 | |||||||
| chr2:119854602 | CATGCATG others(3): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-7933_139-7924d others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854602 | |||||||
| chr2:119854607 | A | G | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.139-7929A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854607 | |||||||
| chr2:119854862 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.139-7674G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854862 | |||||||
| chr2:119854953 | C | T | 130 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(127): Show |
130 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.139-7583C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119854953 | |||||||
| chr2:119855142 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.139-7394G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855142 | |||||||
| chr2:119855187 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.139-7349C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855187 | |||||||
| chr2:119855406 | C | T | 14 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(11): Show |
14 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-7130C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855406 | |||||||
| chr2:119855437 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139-7099G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855437 | |||||||
| chr2:119855442 | G | T | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.139-7094G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855442 | |||||||
| chr2:119855550 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-6986T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855550 | |||||||
| chr2:119855808 | T | C | 1 | a0001c0001t0018g0240 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.139-6728T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855808 | |||||||
| chr2:119855812 | A | T | 115 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(112): Show |
115 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.139-6724A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119855812 | |||||||
| chr2:119856056 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.139-6480A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856056 | |||||||
| chr2:119856398 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.139-6138A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856398 | |||||||
| chr2:119856465 | T | G | 89 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.139-6071T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856465 | |||||||
| chr2:119856548 | G | A | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-5988G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856548 | |||||||
| chr2:119856573 | G | C | 6 | a0002c0002t0005g0244 a0002c0002t0005g0245 a0002c0002t0005g0249 others(3): Show |
6 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-5963G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856573 | |||||||
| chr2:119856791 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-5745A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119856791 | |||||||
| chr2:119857107 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.139-5429A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857107 | |||||||
| chr2:119857490 | C | T | 2 | a0001c0001t0003g0113 a0001c0001t0047g0097 |
2 | HG02056.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.139-5046C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857490 | |||||||
| chr2:119857500 | C | T | 1 | a0001c0001t0047g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.139-5036C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857500 | |||||||
| chr2:119857542 | T | A | 1 | a0001c0001t0003g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.139-4994T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857542 | |||||||
| chr2:119857579 | G | GA | 7 | a0001c0001t0001g0068 a0001c0001t0002g0212 a0001c0001t0002g0224 others(4): Show |
7 | HG01192.hp1 HG02027.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-4943dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119857579 | ||||||
| chr2:119857582 | A | G | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-4954A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857582 | |||||||
| chr2:119857644 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-4892T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857644 | |||||||
| chr2:119857979 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.139-4557T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119857979 | |||||||
| chr2:119858168 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.139-4368T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858168 | |||||||
| chr2:119858195 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.139-4341A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858195 | |||||||
| chr2:119858373 | T | A | 1 | a0002c0002t0005g0250 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.139-4163T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858373 | |||||||
| chr2:119858423 | G | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-4113G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858423 | |||||||
| chr2:119858501 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.139-4035A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858501 | |||||||
| chr2:119858680 | G | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.139-3856G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119858680 | |||||||
| chr2:119859871 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.139-2665T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119859871 | |||||||
| chr2:119859912 | C | T | 55 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(52): Show |
55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.139-2624C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119859912 | |||||||
| chr2:119859969 | C | A | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.139-2567C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119859969 | |||||||
| chr2:119860000 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.139-2536T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860000 | |||||||
| chr2:119860241 | G | A | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.139-2295G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860241 | |||||||
| chr2:119860409 | T | C | 137 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.139-2127T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860409 | |||||||
| chr2:119860492 | C | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0079 a0001c0001t0001g0125 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-2044C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860492 | |||||||
| chr2:119860558 | C | A | 2 | a0001c0001t0002g0148 a0001c0001t0002g0204 |
2 | HG01257.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.139-1978C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860558 | |||||||
| chr2:119860900 | G | T | 54 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(51): Show |
54 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.139-1636G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860900 | |||||||
| chr2:119860972 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18986.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.139-1564C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119860972 | |||||||
| chr2:119861046 | C | CA | 87 | a0001c0001t0001g0112 a0001c0001t0002g0148 a0001c0001t0002g0152 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.139-1474dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119861046 | ||||||
| chr2:119861123 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-1413C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119861123 | |||||||
| chr2:119861309 | A | G | 1 | a0001c0001t0003g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.139-1227A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119861309 | |||||||
| chr2:119861496 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-1040C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119861496 | |||||||
| chr2:119861989 | A | ATT | 140 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(137): Show |
140 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.139-546_139-545ins others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr2 | 119861989 | ||||||
| chr2:119862486 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.139-50A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 2/26 | chr2 | 119862486 | |||||||
| chr2:119862929 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.246+286G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119862929 | |||||||
| chr2:119863203 | A | G | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.246+560A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119863203 | |||||||
| chr2:119863215 | G | A | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.246+572G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119863215 | |||||||
| chr2:119863303 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+660G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119863303 | |||||||
| chr2:119863377 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+734G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119863377 | |||||||
| chr2:119864150 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+1507C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119864150 | |||||||
| chr2:119864482 | G | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0138 |
2 | HG00621.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.246+1839G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119864482 | |||||||
| chr2:119864735 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+2092G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119864735 | |||||||
| chr2:119864743 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+2100A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119864743 | |||||||
| chr2:119865616 | G | C | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246+2973G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119865616 | |||||||
| chr2:119865701 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | NA18986.hp2 NA19009.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.246+3058C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119865701 | |||||||
| chr2:119865969 | G | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+3326G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119865969 | |||||||
| chr2:119866035 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.246+3392G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119866035 | |||||||
| chr2:119866277 | C | T | 1 | a0001c0001t0026g0225 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.246+3634C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119866277 | |||||||
| chr2:119866352 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+3709A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119866352 | |||||||
| chr2:119866575 | A | C | 1 | a0001c0006t0003g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.246+3932A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119866575 | |||||||
| chr2:119866865 | G | A | 1 | a0001c0001t0002g0159 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.246+4222G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119866865 | |||||||
| chr2:119867197 | C | T | 1 | a0001c0001t0034g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+4554C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119867197 | |||||||
| chr2:119867313 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.246+4670C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119867313 | |||||||
| chr2:119867941 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+5298G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119867941 | |||||||
| chr2:119868155 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+5512C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868155 | |||||||
| chr2:119868199 | C | T | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.246+5556C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868199 | |||||||
| chr2:119868581 | C | T | 1 | a0003c0004t0001g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.246+5938C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868581 | |||||||
| chr2:119868592 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.246+5949C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868592 | |||||||
| chr2:119868625 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+5982C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868625 | |||||||
| chr2:119868635 | C | A | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246+5992C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868635 | |||||||
| chr2:119868906 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.246+6263T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868906 | |||||||
| chr2:119868944 | C | T | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+6301C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119868944 | |||||||
| chr2:119869124 | A | AC | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+6482dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119869124 | ||||||
| chr2:119869154 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.246+6511T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869154 | |||||||
| chr2:119869251 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.246+6608A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869251 | |||||||
| chr2:119869273 | A | T | 1 | a0001c0001t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.246+6630A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869273 | |||||||
| chr2:119869450 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.246+6807C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869450 | |||||||
| chr2:119869504 | A | G | 2 | a0002c0002t0005g0244 a0002c0002t0005g0245 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.246+6861A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869504 | |||||||
| chr2:119869839 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+7196G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869839 | |||||||
| chr2:119869888 | G | A | 1 | a0001c0001t0032g0006 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.246+7245G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869888 | |||||||
| chr2:119869942 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+7299G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869942 | |||||||
| chr2:119869988 | T | G | 1 | a0001c0001t0003g0251 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.247-7335T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119869988 | |||||||
| chr2:119870887 | C | A | 153 | a0001c0001t0001g0143 a0001c0001t0001g0158 a0001c0001t0001g0252 others(150): Show |
153 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.247-6436C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119870887 | |||||||
| chr2:119871222 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.247-6101G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871222 | |||||||
| chr2:119871235 | T | A | 1 | a0002c0002t0005g0243 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247-6088T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871235 | |||||||
| chr2:119871488 | G | A | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.247-5835G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871488 | |||||||
| chr2:119871741 | T | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.247-5582T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871741 | |||||||
| chr2:119871796 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.247-5527C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871796 | |||||||
| chr2:119871856 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0138 |
2 | HG00621.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.247-5467A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871856 | |||||||
| chr2:119871890 | A | G | 2 | a0001c0001t0003g0031 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.247-5433A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871890 | |||||||
| chr2:119871922 | C | T | 63 | a0001c0001t0002g0148 a0001c0001t0002g0154 a0001c0001t0002g0155 others(60): Show |
63 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.247-5401C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119871922 | |||||||
| chr2:119872182 | A | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-5141A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119872182 | |||||||
| chr2:119872204 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-5119C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119872204 | |||||||
| chr2:119872262 | T | G | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-5061T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119872262 | |||||||
| chr2:119872693 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.247-4630A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119872693 | |||||||
| chr2:119873116 | C | T | 1 | a0001c0001t0025g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.247-4207C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873116 | |||||||
| chr2:119873176 | T | G | 1 | a0001c0001t0003g0102 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.247-4147T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873176 | |||||||
| chr2:119873179 | T | G | 22 | a0001c0001t0001g0070 a0001c0001t0001g0088 a0001c0001t0001g0120 others(19): Show |
22 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.247-4144T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873179 | |||||||
| chr2:119873197 | T | G | 14 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(11): Show |
14 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.247-4126T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873197 | |||||||
| chr2:119873468 | G | A | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.247-3855G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873468 | |||||||
| chr2:119873522 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-3801A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119873522 | |||||||
| chr2:119874008 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247-3315G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119874008 | |||||||
| chr2:119874290 | A | G | 1 | a0001c0001t0047g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.247-3033A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119874290 | |||||||
| chr2:119874492 | T | C | 2 | a0001c0001t0013g0109 a0001c0001t0043g0108 |
2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.247-2831T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119874492 | |||||||
| chr2:119874857 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-2466C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119874857 | |||||||
| chr2:119875082 | T | A | 1 | a0001c0001t0002g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247-2241T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119875082 | |||||||
| chr2:119875139 | G | C | 114 | a0001c0001t0001g0098 a0001c0001t0002g0148 a0001c0001t0002g0152 others(111): Show |
114 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.247-2184G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119875139 | |||||||
| chr2:119875289 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.247-2034T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119875289 | |||||||
| chr2:119875330 | T | G | 1 | a0001c0001t0028g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.247-1993T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119875330 | |||||||
| chr2:119875427 | C | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-1896C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119875427 | |||||||
| chr2:119876064 | A | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-1259A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876064 | |||||||
| chr2:119876189 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.247-1134C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876189 | |||||||
| chr2:119876792 | T | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-531T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876792 | |||||||
| chr2:119876896 | C | CAT | 3 | a0001c0001t0004g0036 a0001c0001t0004g0039 a0001c0001t0038g0037 |
3 | HG01192.hp2 HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.247-426_247-425dup others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876896 | ||||||
| chr2:119876897 | A | ATG | 39 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0044 others(36): Show |
39 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.247-383_247-382dup others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | A | ATGTG | 21 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0082 others(18): Show |
21 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.247-385_247-382dup others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | A | ATGTGTG | 7 | a0001c0001t0001g0087 a0001c0001t0001g0252 a0001c0001t0003g0066 others(4): Show |
7 | HG00323.hp2 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-387_247-382dup others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0062 a0001c0001t0003g0048 a0001c0001t0003g0083 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-391_247-382dup others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.247-426A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876897 | |||||||
| chr2:119876897 | ATG | A | 76 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0076 others(73): Show |
76 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.247-383_247-382del others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | ATGTG | A | 10 | a0001c0001t0001g0117 a0001c0001t0002g0172 a0001c0001t0002g0176 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-385_247-382del others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | ATGTGTGT others(1): Show |
A | 14 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(11): Show |
14 | HG00735.hp2 HG02109.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.247-389_247-382del others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | ATGTGTGT others(3): Show |
A | 2 | a0002c0002t0005g0243 a0002c0002t0005g0247 |
2 | HG01243.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.247-391_247-382del others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876897 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0052g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.247-397_247-382del others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876897 | ||||||
| chr2:119876938 | T | C | 25 | a0001c0001t0001g0143 a0001c0001t0008g0008 a0001c0001t0008g0009 others(22): Show |
25 | HG00735.hp2 HG01884.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.247-385T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876938 | |||||||
| chr2:119876940 | T | C | 89 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0154 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.247-383T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876940 | |||||||
| chr2:119876940 | T | TGC | 17 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0155 others(14): Show |
17 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-381_247-380dup others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119876940 | ||||||
| chr2:119876943 | G | A | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.247-380G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119876943 | |||||||
| chr2:119877069 | G | A | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.247-254G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119877069 | |||||||
| chr2:119877191 | A | AT | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.247-125dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr2 | 119877191 | ||||||
| chr2:119877269 | A | C | 1 | a0001c0001t0001g0063 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.247-54A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 3/26 | chr2 | 119877269 | |||||||
| chr2:119877403 | C | T | 1 | a0001c0001t0007g0185 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.289+38C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 4/26 | chr2 | 119877403 | |||||||
| chr2:119877629 | G | A | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.368+87G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119877629 | |||||||
| chr2:119877890 | TG | T | 9 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(6): Show |
9 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.368+351delG | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119877890 | ||||||
| chr2:119877893 | G | GT | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+361dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119877893 | ||||||
| chr2:119877893 | GT | G | 104 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(101): Show |
104 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.368+361delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119877893 | ||||||
| chr2:119877927 | A | T | 1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.368+385A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119877927 | |||||||
| chr2:119878183 | G | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.368+641G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878183 | |||||||
| chr2:119878373 | C | G | 1 | a0001c0001t0034g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.368+831C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878373 | |||||||
| chr2:119878385 | C | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.368+843C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878385 | |||||||
| chr2:119878689 | C | CT | 44 | a0001c0001t0001g0143 a0001c0001t0001g0158 a0001c0001t0002g0176 others(41): Show |
44 | HG00597.hp2 HG00639.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.368+1166dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119878689 | ||||||
| chr2:119878689 | C | CTT | 92 | a0001c0001t0001g0098 a0001c0001t0001g0127 a0001c0001t0002g0148 others(89): Show |
92 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.368+1165_368+1166d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119878689 | ||||||
| chr2:119878819 | T | C | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.368+1277T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878819 | |||||||
| chr2:119878821 | C | T | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.368+1279C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878821 | |||||||
| chr2:119878822 | A | G | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.368+1280A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878822 | |||||||
| chr2:119878838 | A | C | 1 | a0001c0001t0034g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.368+1296A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878838 | |||||||
| chr2:119878890 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0055g0057 |
2 | HG00609.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.368+1348A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878890 | |||||||
| chr2:119878894 | A | C | 2 | a0001c0001t0001g0055 a0001c0001t0055g0057 |
2 | HG00609.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.368+1352A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878894 | |||||||
| chr2:119878950 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.368+1408G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878950 | |||||||
| chr2:119878962 | A | G | 1 | a0001c0001t0044g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.368+1420A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878962 | |||||||
| chr2:119878971 | T | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.368+1429T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119878971 | |||||||
| chr2:119879010 | A | G | 2 | a0001c0001t0004g0036 a0001c0001t0038g0037 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.368+1468A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879010 | |||||||
| chr2:119879017 | C | T | 5 | a0001c0001t0002g0184 a0001c0001t0023g0147 a0002c0003t0015g0025 others(2): Show |
5 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.368+1475C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879017 | |||||||
| chr2:119879050 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.368+1508G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879050 | |||||||
| chr2:119879092 | G | GA | 105 | a0001c0001t0001g0062 a0001c0001t0001g0098 a0001c0001t0001g0121 others(102): Show |
105 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.368+1564dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119879092 | ||||||
| chr2:119879126 | C | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0003g0128 |
3 | HG02698.hp1 HG03490.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.368+1584C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879126 | |||||||
| chr2:119879373 | A | G | 1 | a0001c0001t0057g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.368+1831A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879373 | |||||||
| chr2:119879415 | T | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0188 a0001c0001t0002g0226 |
3 | HG01167.hp2 HG01169.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.368+1873T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879415 | |||||||
| chr2:119879449 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.368+1907G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879449 | |||||||
| chr2:119879550 | T | A | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.368+2008T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879550 | |||||||
| chr2:119879654 | G | T | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.368+2112G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879654 | |||||||
| chr2:119879893 | C | T | 1 | a0001c0001t0044g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.369-1893C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119879893 | |||||||
| chr2:119880191 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.369-1595T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119880191 | |||||||
| chr2:119880208 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.369-1578A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119880208 | |||||||
| chr2:119880426 | AT | A | 15 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0004g0018 others(12): Show |
15 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.369-1347delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr2 | 119880426 | ||||||
| chr2:119880845 | G | T | 2 | a0001c0001t0002g0228 a0001c0001t0011g0235 |
2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.369-941G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119880845 | |||||||
| chr2:119881029 | G | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.369-757G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119881029 | |||||||
| chr2:119881120 | G | C | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.369-666G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119881120 | |||||||
| chr2:119881695 | G | A | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.369-91G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 5/26 | chr2 | 119881695 | |||||||
| chr2:119881866 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.413+36A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 6/26 | chr2 | 119881866 | |||||||
| chr2:119882663 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.587+40T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119882663 | |||||||
| chr2:119883044 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.587+421T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119883044 | |||||||
| chr2:119883656 | ATTAC | A | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.587+1039_587+1042d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 119883656 | ||||||
| chr2:119883683 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587+1060A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119883683 | |||||||
| chr2:119883719 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.587+1096G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119883719 | |||||||
| chr2:119883724 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.587+1101C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119883724 | |||||||
| chr2:119883923 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.587+1300G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119883923 | |||||||
| chr2:119884115 | G | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.587+1492G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884115 | |||||||
| chr2:119884542 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.588-1253G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884542 | |||||||
| chr2:119884606 | A | G | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.588-1189A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884606 | |||||||
| chr2:119884634 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.588-1161A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884634 | |||||||
| chr2:119884681 | TATA | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.588-1113_588-1111d others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884681 | |||||||
| chr2:119884769 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.588-1026A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884769 | |||||||
| chr2:119884814 | A | T | 1 | a0002c0002t0016g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588-981A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884814 | |||||||
| chr2:119884815 | G | T | 1 | a0002c0002t0016g0241 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.588-980G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884815 | |||||||
| chr2:119884968 | T | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0216 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.588-827T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119884968 | |||||||
| chr2:119885441 | T | C | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.588-354T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | chr2 | 119885441 | |||||||
| chr2:119885704 | G | GT | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.588-85dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr2 | 119885704 | ||||||
| chr2:119886128 | G | A | 1 | a0001c0001t0014g0238 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.675+246G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119886128 | |||||||
| chr2:119886206 | A | G | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.675+324A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119886206 | |||||||
| chr2:119886290 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.675+408C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119886290 | |||||||
| chr2:119886397 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+515C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119886397 | |||||||
| chr2:119886876 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+994A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119886876 | |||||||
| chr2:119887420 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.675+1538A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887420 | |||||||
| chr2:119887460 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+1578T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887460 | |||||||
| chr2:119887545 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.675+1663A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887545 | |||||||
| chr2:119887847 | A | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+1965A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887847 | |||||||
| chr2:119887871 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+1989A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887871 | |||||||
| chr2:119887949 | A | C | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.675+2067A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119887949 | |||||||
| chr2:119888133 | A | T | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.675+2251A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888133 | |||||||
| chr2:119888232 | C | G | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.675+2350C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888232 | |||||||
| chr2:119888261 | T | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+2379T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888261 | |||||||
| chr2:119888346 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.675+2464C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888346 | |||||||
| chr2:119888364 | C | T | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.675+2482C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888364 | |||||||
| chr2:119888379 | C | T | 1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.675+2497C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888379 | |||||||
| chr2:119888521 | T | G | 1 | a0001c0001t0008g0016 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.675+2639T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888521 | |||||||
| chr2:119888651 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.675+2769A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119888651 | |||||||
| chr2:119889121 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.675+3239C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889121 | |||||||
| chr2:119889148 | A | G | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.675+3266A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889148 | |||||||
| chr2:119889194 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675+3312C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889194 | |||||||
| chr2:119889279 | T | G | 140 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(137): Show |
140 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.675+3397T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889279 | |||||||
| chr2:119889286 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0156 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.675+3404G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889286 | |||||||
| chr2:119889313 | G | A | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.675+3431G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889313 | |||||||
| chr2:119889376 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0023g0147 |
2 | HG01069.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.675+3494C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889376 | |||||||
| chr2:119889377 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.675+3495G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889377 | |||||||
| chr2:119889381 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+3499C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889381 | |||||||
| chr2:119889406 | A | C | 102 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(99): Show |
102 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.675+3524A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889406 | |||||||
| chr2:119889474 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+3592G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889474 | |||||||
| chr2:119889595 | T | TA | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+3713_675+3714i others(3): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889595 | |||||||
| chr2:119889606 | A | G | 130 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(127): Show |
130 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.675+3724A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889606 | |||||||
| chr2:119889738 | T | C | 1 | a0001c0001t0044g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.675+3856T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119889738 | |||||||
| chr2:119890084 | T | C | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.675+4202T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890084 | |||||||
| chr2:119890272 | C | CTTT | 107 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(104): Show |
107 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.675+4398_675+4400d others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119890272 | ||||||
| chr2:119890272 | C | CTTTT | 23 | a0001c0001t0002g0188 a0001c0001t0004g0018 a0001c0001t0004g0021 others(20): Show |
23 | HG01175.hp1 HG01192.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.675+4397_675+4400d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119890272 | ||||||
| chr2:119890343 | T | C | 1 | a0001c0001t0002g0203 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+4461T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890343 | |||||||
| chr2:119890416 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.675+4534G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890416 | |||||||
| chr2:119890601 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.675+4719C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890601 | |||||||
| chr2:119890818 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0085 a0001c0001t0001g0094 others(2): Show |
5 | HG01261.hp2 HG01496.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+4936T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890818 | |||||||
| chr2:119890963 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.675+5081C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119890963 | |||||||
| chr2:119891262 | G | A | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.675+5380G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891262 | |||||||
| chr2:119891345 | C | T | 10 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0174 others(7): Show |
10 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.675+5463C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891345 | |||||||
| chr2:119891433 | G | A | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.675+5551G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891433 | |||||||
| chr2:119891467 | C | T | 2 | a0003c0004t0001g0075 a0003c0004t0001g0080 |
2 | NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.675+5585C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891467 | |||||||
| chr2:119891527 | G | A | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.675+5645G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891527 | |||||||
| chr2:119891756 | T | C | 12 | a0001c0001t0002g0170 a0001c0001t0002g0176 a0001c0001t0002g0188 others(9): Show |
12 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.675+5874T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119891756 | |||||||
| chr2:119892071 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.675+6189C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119892071 | |||||||
| chr2:119892888 | A | AT | 6 | a0001c0001t0001g0087 a0001c0001t0004g0036 a0001c0001t0004g0038 others(3): Show |
6 | HG01192.hp2 HG01358.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+7024dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119892888 | ||||||
| chr2:119892888 | AT | A | 114 | a0001c0001t0001g0086 a0001c0001t0001g0156 a0001c0001t0002g0148 others(111): Show |
114 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.675+7024delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119892888 | ||||||
| chr2:119893087 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0156 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.675+7205G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119893087 | |||||||
| chr2:119893341 | T | C | 58 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(55): Show |
58 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.676-7377T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119893341 | |||||||
| chr2:119893459 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.676-7259A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119893459 | |||||||
| chr2:119894115 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.676-6603A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119894115 | |||||||
| chr2:119894291 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.676-6427T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119894291 | |||||||
| chr2:119894541 | A | G | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.676-6177A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119894541 | |||||||
| chr2:119894971 | G | C | 2 | a0002c0003t0015g0025 a0002c0003t0015g0026 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.676-5747G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119894971 | |||||||
| chr2:119894972 | C | A | 2 | a0002c0003t0015g0025 a0002c0003t0015g0026 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.676-5746C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119894972 | |||||||
| chr2:119895624 | C | CA | 6 | a0001c0001t0002g0152 a0001c0001t0002g0160 a0001c0001t0002g0162 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-5085dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119895624 | ||||||
| chr2:119895634 | G | A | 5 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0230 others(2): Show |
5 | HG01928.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-5084G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119895634 | |||||||
| chr2:119895680 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-5038G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119895680 | |||||||
| chr2:119895896 | A | G | 140 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(137): Show |
140 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.676-4822A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119895896 | |||||||
| chr2:119895916 | C | CA | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-4787dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119895916 | ||||||
| chr2:119895916 | C | CAA | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0154 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.676-4788_676-4787d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr2 | 119895916 | ||||||
| chr2:119896218 | A | T | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.676-4500A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896218 | |||||||
| chr2:119896230 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.676-4488T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896230 | |||||||
| chr2:119896471 | G | A | 1 | a0001c0001t0053g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.676-4247G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896471 | |||||||
| chr2:119896904 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-3814G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896904 | |||||||
| chr2:119896989 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-3729C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896989 | |||||||
| chr2:119896990 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.676-3728G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119896990 | |||||||
| chr2:119897121 | C | T | 2 | a0001c0001t0055g0057 a0001c0001t0056g0061 |
2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.676-3597C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897121 | |||||||
| chr2:119897307 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.676-3411G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897307 | |||||||
| chr2:119897320 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-3398A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897320 | |||||||
| chr2:119897466 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-3252A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897466 | |||||||
| chr2:119897563 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.676-3155C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897563 | |||||||
| chr2:119897863 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-2855C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119897863 | |||||||
| chr2:119898014 | T | G | 26 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(23): Show |
26 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.676-2704T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898014 | |||||||
| chr2:119898070 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-2648T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898070 | |||||||
| chr2:119898135 | C | T | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.676-2583C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898135 | |||||||
| chr2:119898374 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.676-2344G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898374 | |||||||
| chr2:119898586 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.676-2132A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898586 | |||||||
| chr2:119898587 | C | A | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.676-2131C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898587 | |||||||
| chr2:119898887 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.676-1831A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119898887 | |||||||
| chr2:119899293 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-1425C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119899293 | |||||||
| chr2:119899295 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-1423C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119899295 | |||||||
| chr2:119899967 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.676-751G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119899967 | |||||||
| chr2:119900280 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.676-438T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900280 | |||||||
| chr2:119900311 | C | A | 136 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(133): Show |
136 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.676-407C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900311 | |||||||
| chr2:119900412 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-306C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900412 | |||||||
| chr2:119900567 | G | T | 139 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(136): Show |
139 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.676-151G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900567 | |||||||
| chr2:119900616 | A | C | 5 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0216 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-102A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900616 | |||||||
| chr2:119900690 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.676-28A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 9/26 | chr2 | 119900690 | |||||||
| chr2:119900956 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.764+150C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119900956 | |||||||
| chr2:119900969 | A | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+163A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119900969 | |||||||
| chr2:119901118 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0078 |
2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.764+312G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901118 | |||||||
| chr2:119901443 | C | T | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.764+637C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901443 | |||||||
| chr2:119901459 | C | T | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.764+653C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901459 | |||||||
| chr2:119901539 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.764+733C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901539 | |||||||
| chr2:119901543 | C | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+737C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901543 | |||||||
| chr2:119901718 | A | G | 1 | a0001c0001t0004g0021 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.764+912A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901718 | |||||||
| chr2:119901845 | T | C | 11 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0174 others(8): Show |
11 | HG02135.hp1 NA18612.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+1039T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901845 | |||||||
| chr2:119901899 | G | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+1093G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119901899 | |||||||
| chr2:119902070 | T | C | 1 | a0001c0001t0002g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.764+1264T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119902070 | |||||||
| chr2:119902147 | A | G | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.764+1341A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119902147 | |||||||
| chr2:119902189 | C | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1383C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119902189 | |||||||
| chr2:119902244 | T | A | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.764+1438T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119902244 | |||||||
| chr2:119902362 | TCACA | T | 4 | a0001c0001t0002g0180 a0001c0001t0002g0189 a0001c0001t0002g0190 others(1): Show |
4 | NA18946.hp2 NA18952.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+1563_764+1566d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119902362 | ||||||
| chr2:119902479 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.764+1673C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119902479 | |||||||
| chr2:119903057 | C | T | 2 | a0001c0001t0002g0170 a0001c0001t0028g0183 |
2 | HG00738.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.764+2251C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903057 | |||||||
| chr2:119903215 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.764+2409C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903215 | |||||||
| chr2:119903341 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.764+2535C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903341 | |||||||
| chr2:119903342 | G | A | 1 | a0001c0001t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.764+2536G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903342 | |||||||
| chr2:119903425 | T | C | 136 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(133): Show |
136 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.764+2619T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903425 | |||||||
| chr2:119903490 | G | C | 1 | a0001c0001t0002g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.764+2684G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903490 | |||||||
| chr2:119903516 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+2710G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903516 | |||||||
| chr2:119903556 | G | GAC | 94 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0088 others(91): Show |
94 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.764+2777_764+2778d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119903556 | ||||||
| chr2:119903556 | G | GACAC | 6 | a0001c0001t0001g0046 a0001c0001t0001g0116 a0001c0001t0002g0184 others(3): Show |
6 | HG00423.hp1 HG01069.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.764+2775_764+2778d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119903556 | ||||||
| chr2:119903556 | GAC | G | 38 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(35): Show |
38 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.764+2777_764+2778d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119903556 | ||||||
| chr2:119903615 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.764+2809G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903615 | |||||||
| chr2:119903643 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+2837C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903643 | |||||||
| chr2:119903665 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.764+2859G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119903665 | |||||||
| chr2:119904026 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0092 a0001c0001t0001g0136 |
3 | HG01069.hp2 HG01070.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.764+3220C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904026 | |||||||
| chr2:119904079 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.764+3273C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904079 | |||||||
| chr2:119904224 | A | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.764+3418A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904224 | |||||||
| chr2:119904248 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+3442G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904248 | |||||||
| chr2:119904363 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.764+3557A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904363 | |||||||
| chr2:119904387 | C | T | 26 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(23): Show |
26 | HG01175.hp1 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.764+3581C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904387 | |||||||
| chr2:119904413 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.764+3607G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904413 | |||||||
| chr2:119904529 | G | A | 139 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(136): Show |
139 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.764+3723G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904529 | |||||||
| chr2:119904739 | A | C | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.764+3933A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904739 | |||||||
| chr2:119904758 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+3952A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904758 | |||||||
| chr2:119904793 | A | G | 3 | a0001c0001t0002g0153 a0001c0001t0002g0165 a0001c0001t0002g0218 |
3 | HG01109.hp2 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.764+3987A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904793 | |||||||
| chr2:119904813 | G | A | 233 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(230): Show |
233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.764+4007G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119904813 | |||||||
| chr2:119905035 | C | CA | 6 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.764+4243dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119905035 | ||||||
| chr2:119905035 | CA | C | 87 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(84): Show |
87 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.764+4243delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119905035 | ||||||
| chr2:119905047 | A | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.764+4241A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905047 | |||||||
| chr2:119905049 | A | AC | 76 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0044 others(73): Show |
76 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.764+4244dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119905049 | ||||||
| chr2:119905049 | A | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0042 others(30): Show |
33 | HG00621.hp2 HG01069.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.764+4243A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905049 | |||||||
| chr2:119905163 | A | T | 1 | a0001c0001t0003g0101 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.764+4357A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905163 | |||||||
| chr2:119905180 | G | A | 26 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(23): Show |
26 | HG01175.hp1 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.764+4374G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905180 | |||||||
| chr2:119905235 | C | G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.764+4429C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905235 | |||||||
| chr2:119905249 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0081 |
3 | HG01952.hp1 HG01975.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.764+4443C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905249 | |||||||
| chr2:119905254 | C | T | 1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.764+4448C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905254 | |||||||
| chr2:119905420 | G | A | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.764+4614G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905420 | |||||||
| chr2:119905685 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+4879A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905685 | |||||||
| chr2:119905780 | G | T | 26 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(23): Show |
26 | HG01175.hp1 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.764+4974G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905780 | |||||||
| chr2:119905847 | A | G | 1 | a0002c0002t0005g0250 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.764+5041A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905847 | |||||||
| chr2:119905874 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.764+5068G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905874 | |||||||
| chr2:119905918 | A | G | 3 | a0001c0001t0003g0041 a0001c0001t0055g0057 a0001c0001t0056g0061 |
3 | HG00323.hp1 HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.764+5112A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905918 | |||||||
| chr2:119905994 | A | C | 1 | a0001c0001t0002g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.764+5188A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119905994 | |||||||
| chr2:119906037 | G | T | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.764+5231G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906037 | |||||||
| chr2:119906041 | C | G | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.764+5235C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906041 | |||||||
| chr2:119906147 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+5341A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906147 | |||||||
| chr2:119906266 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+5460G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906266 | |||||||
| chr2:119906296 | G | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+5490G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906296 | |||||||
| chr2:119906408 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.764+5602C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906408 | |||||||
| chr2:119906939 | G | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+6133G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906939 | |||||||
| chr2:119906997 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.764+6191T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119906997 | |||||||
| chr2:119907232 | A | G | 2 | a0001c0001t0003g0104 a0001c0001t0003g0141 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.764+6426A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907232 | |||||||
| chr2:119907436 | T | TA | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.764+6636dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119907436 | ||||||
| chr2:119907445 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.764+6639T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907445 | |||||||
| chr2:119907457 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.764+6651A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907457 | |||||||
| chr2:119907514 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+6708G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907514 | |||||||
| chr2:119907611 | GA | G | 224 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(221): Show |
224 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.764+6816delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119907611 | ||||||
| chr2:119907638 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.764+6832T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907638 | |||||||
| chr2:119907843 | T | C | 1 | a0001c0001t0002g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.764+7037T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907843 | |||||||
| chr2:119907972 | C | T | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+7166C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119907972 | |||||||
| chr2:119908079 | G | A | 137 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(134): Show |
137 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.765-7100G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119908079 | |||||||
| chr2:119908285 | G | GA | 7 | a0001c0001t0001g0059 a0001c0001t0003g0066 a0001c0001t0003g0072 others(4): Show |
7 | HG00597.hp2 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.765-6888dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119908285 | ||||||
| chr2:119908342 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0091 others(2): Show |
5 | HG02148.hp2 HG03239.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-6837C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119908342 | |||||||
| chr2:119908384 | G | A | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.765-6795G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119908384 | |||||||
| chr2:119908609 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.765-6570C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119908609 | |||||||
| chr2:119909059 | T | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | NA18986.hp2 NA19009.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.765-6120T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909059 | |||||||
| chr2:119909215 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.765-5964A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909215 | |||||||
| chr2:119909389 | A | T | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.765-5790A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909389 | |||||||
| chr2:119909451 | A | G | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.765-5728A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909451 | |||||||
| chr2:119909655 | C | G | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.765-5524C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909655 | |||||||
| chr2:119909790 | C | G | 1 | a0001c0001t0003g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.765-5389C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119909790 | |||||||
| chr2:119910198 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.765-4981C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910198 | |||||||
| chr2:119910255 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.765-4924A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910255 | |||||||
| chr2:119910299 | A | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-4880A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910299 | |||||||
| chr2:119910631 | T | C | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.765-4548T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910631 | |||||||
| chr2:119910719 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0010g0005 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.765-4460C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910719 | |||||||
| chr2:119910785 | A | G | 1 | a0001c0001t0019g0207 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.765-4394A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119910785 | |||||||
| chr2:119911080 | A | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-4099A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911080 | |||||||
| chr2:119911189 | CT | C | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.765-3988delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119911189 | ||||||
| chr2:119911230 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-3949A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911230 | |||||||
| chr2:119911274 | C | T | 1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.765-3905C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911274 | |||||||
| chr2:119911357 | A | G | 3 | a0001c0001t0002g0174 a0001c0001t0002g0175 a0001c0001t0002g0179 |
3 | NA18972.hp2 NA18986.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.765-3822A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911357 | |||||||
| chr2:119911371 | A | G | 1 | a0001c0001t0023g0147 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.765-3808A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911371 | |||||||
| chr2:119911433 | TTTGACAA others(2): Show |
T | 3 | a0001c0001t0001g0051 a0001c0001t0003g0031 a0001c0001t0003g0100 |
3 | HG03704.hp2 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.765-3740_765-3732d others(11): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119911433 | ||||||
| chr2:119911559 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.765-3620G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911559 | |||||||
| chr2:119911975 | CAT | C | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.765-3203_765-3202d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119911975 | |||||||
| chr2:119912124 | AAC | A | 6 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.765-3051_765-3050d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119912124 | ||||||
| chr2:119912157 | C | T | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.765-3022C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912157 | |||||||
| chr2:119912266 | G | A | 27 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(24): Show |
27 | HG01175.hp1 HG01192.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.765-2913G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912266 | |||||||
| chr2:119912313 | G | A | 140 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(137): Show |
140 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.765-2866G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912313 | |||||||
| chr2:119912529 | T | C | 4 | a0001c0001t0002g0180 a0001c0001t0002g0189 a0001c0001t0002g0190 others(1): Show |
4 | NA18946.hp2 NA18952.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-2650T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912529 | |||||||
| chr2:119912539 | A | G | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.765-2640A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912539 | |||||||
| chr2:119912650 | T | G | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.765-2529T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912650 | |||||||
| chr2:119912878 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-2301T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912878 | |||||||
| chr2:119912941 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.765-2238A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912941 | |||||||
| chr2:119912989 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-2190G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119912989 | |||||||
| chr2:119913611 | G | A | 5 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(2): Show |
5 | HG01192.hp2 HG02647.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.765-1568G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119913611 | |||||||
| chr2:119913821 | C | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.765-1358C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119913821 | |||||||
| chr2:119913914 | AT | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-1260delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119913914 | ||||||
| chr2:119914248 | A | AT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0062 others(13): Show |
16 | HG00544.hp1 HG00735.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.765-903dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATT | 5 | a0001c0001t0004g0018 a0001c0001t0004g0022 a0001c0001t0009g0114 others(2): Show |
5 | HG02559.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-904_765-903dup others(2): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTT | 5 | a0001c0001t0004g0021 a0001c0001t0004g0036 a0001c0001t0004g0038 others(2): Show |
5 | HG02647.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.765-905_765-903dup others(3): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT | 5 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0245 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-909_765-903dup others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0153 a0001c0001t0021g0217 a0006c0007t0002g0163 |
3 | HG01109.hp2 HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.765-912_765-903dup others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(4): Show |
12 | a0001c0001t0002g0160 a0001c0001t0002g0162 a0001c0001t0002g0164 others(9): Show |
12 | HG00639.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.765-913_765-903dup others(11): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0002g0214 a0001c0001t0002g0234 a0001c0001t0014g0222 others(1): Show |
4 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-914_765-903dup others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(6): Show |
4 | a0001c0001t0002g0152 a0001c0001t0002g0159 a0001c0001t0002g0161 others(1): Show |
4 | HG01884.hp1 HG02451.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.765-915_765-903dup others(13): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0006g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.765-916_765-903dup others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0011g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.765-917_765-903dup others(15): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0006g0237 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.765-920_765-903dup others(18): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | AT | A | 17 | a0001c0001t0001g0028 a0001c0001t0001g0043 a0001c0001t0001g0092 others(14): Show |
17 | HG01069.hp2 HG01081.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.765-903delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0002g0200 a0001c0001t0002g0223 |
2 | HG00423.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.765-912_765-903del others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | ATTTTTTT others(4): Show |
A | 70 | a0001c0001t0002g0148 a0001c0001t0002g0154 a0001c0001t0002g0155 others(67): Show |
70 | HG00544.hp2 HG00609.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.765-913_765-903del others(11): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | ATTTTTTT others(5): Show |
A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.765-914_765-903del others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914248 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0039g0107 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.765-916_765-903del others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr2 | 119914248 | ||||||
| chr2:119914391 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765-788C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119914391 | |||||||
| chr2:119914679 | T | A | 110 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(107): Show |
110 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.765-500T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119914679 | |||||||
| chr2:119914870 | C | A | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.765-309C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119914870 | |||||||
| chr2:119914907 | A | G | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765-272A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119914907 | |||||||
| chr2:119915100 | A | G | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.765-79A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 10/26 | chr2 | 119915100 | |||||||
| chr2:119915363 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.828+121C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915363 | |||||||
| chr2:119915525 | T | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.828+283T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915525 | |||||||
| chr2:119915582 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.828+340A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915582 | |||||||
| chr2:119915813 | A | C | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+571A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915813 | |||||||
| chr2:119915935 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.828+693A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915935 | |||||||
| chr2:119915949 | G | A | 1 | a0001c0001t0009g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.828+707G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119915949 | |||||||
| chr2:119916108 | G | A | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.828+866G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916108 | |||||||
| chr2:119916152 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0116 |
2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.828+910A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916152 | |||||||
| chr2:119916177 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.828+935A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916177 | |||||||
| chr2:119916220 | C | G | 2 | a0001c0001t0017g0093 a0001c0001t0017g0140 |
2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.828+978C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916220 | |||||||
| chr2:119916326 | G | A | 1 | a0001c0001t0028g0183 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.828+1084G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916326 | |||||||
| chr2:119916760 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.828+1518A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916760 | |||||||
| chr2:119916763 | C | T | 5 | a0001c0001t0002g0155 a0001c0001t0002g0171 a0001c0001t0002g0174 others(2): Show |
5 | NA18954.hp1 NA18972.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.828+1521C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119916763 | |||||||
| chr2:119917515 | C | T | 136 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(133): Show |
136 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.828+2273C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119917515 | |||||||
| chr2:119917673 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.829-2396G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119917673 | |||||||
| chr2:119917887 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0137 |
2 | HG01261.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.829-2182T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119917887 | |||||||
| chr2:119917919 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.829-2150A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119917919 | |||||||
| chr2:119917952 | C | T | 17 | a0001c0001t0001g0158 a0001c0001t0001g0252 a0001c0001t0003g0031 others(14): Show |
17 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-2117C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119917952 | |||||||
| chr2:119918768 | C | A | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.829-1301C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119918768 | |||||||
| chr2:119918908 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.829-1161C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119918908 | |||||||
| chr2:119919102 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.829-967T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119919102 | |||||||
| chr2:119919456 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 |
3 | HG02630.hp1 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.829-613G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119919456 | |||||||
| chr2:119919658 | A | C | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.829-411A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119919658 | |||||||
| chr2:119919823 | C | CA | 13 | a0001c0001t0001g0071 a0001c0001t0001g0094 a0001c0001t0001g0116 others(10): Show |
13 | HG00639.hp2 HG01255.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.829-225dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 119919823 | ||||||
| chr2:119919823 | CA | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0079 a0001c0001t0001g0129 others(12): Show |
15 | HG00621.hp1 HG00735.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.829-225delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr2 | 119919823 | ||||||
| chr2:119919947 | C | G | 90 | a0001c0001t0001g0121 a0001c0001t0002g0148 a0001c0001t0002g0152 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.829-122C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119919947 | |||||||
| chr2:119920021 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.829-48G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 11/26 | chr2 | 119920021 | |||||||
| chr2:119920306 | T | A | 1 | a0001c0001t0003g0072 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1001+65T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119920306 | |||||||
| chr2:119920831 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001+590T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119920831 | |||||||
| chr2:119920895 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001+654T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119920895 | |||||||
| chr2:119921155 | T | C | 139 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(136): Show |
139 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1001+914T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921155 | |||||||
| chr2:119921164 | G | T | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+923G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921164 | |||||||
| chr2:119921190 | G | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0091 others(1): Show |
4 | HG02148.hp2 NA18954.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1001+949G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921190 | |||||||
| chr2:119921408 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1001+1167A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921408 | |||||||
| chr2:119921620 | C | CT | 55 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0046 others(52): Show |
55 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1001+1392dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119921620 | ||||||
| chr2:119921620 | CT | C | 7 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(4): Show |
7 | HG01884.hp2 HG02080.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1001+1392delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119921620 | ||||||
| chr2:119921683 | T | G | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001+1442T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921683 | |||||||
| chr2:119921696 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1001+1455A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921696 | |||||||
| chr2:119921704 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0023g0147 |
2 | HG01069.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1001+1463G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921704 | |||||||
| chr2:119921706 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1001+1465A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921706 | |||||||
| chr2:119921788 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1001+1547G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119921788 | |||||||
| chr2:119921880 | T | TTA | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1001+1642_1001+164 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119921880 | ||||||
| chr2:119922096 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1001+1855A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119922096 | |||||||
| chr2:119922189 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1001+1948A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119922189 | |||||||
| chr2:119922218 | TA | T | 8 | a0001c0001t0001g0060 a0001c0001t0003g0101 a0001c0001t0003g0102 others(5): Show |
8 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1001+1999delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119922218 | ||||||
| chr2:119922218 | TAA | T | 81 | a0001c0001t0002g0148 a0001c0001t0002g0154 a0001c0001t0002g0167 others(78): Show |
81 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.1001+1998_1001+199 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119922218 | ||||||
| chr2:119922218 | TAAA | T | 38 | a0001c0001t0001g0120 a0001c0001t0001g0143 a0001c0001t0001g0156 others(35): Show |
38 | HG00735.hp2 HG01109.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.1001+1997_1001+199 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119922218 | ||||||
| chr2:119922218 | TAAAAAAA others(6): Show |
T | 17 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(14): Show |
17 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1001+1987_1001+199 others(17): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119922218 | ||||||
| chr2:119922243 | TCGGC | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1001+2006_1001+200 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119922243 | ||||||
| chr2:119922642 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0003g0099 a0001c0001t0003g0101 others(1): Show |
4 | HG00323.hp2 HG00639.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001+2401T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119922642 | |||||||
| chr2:119922698 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1001+2457G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119922698 | |||||||
| chr2:119923008 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1001+2767C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119923008 | |||||||
| chr2:119923084 | T | A | 1 | a0001c0001t0013g0109 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1001+2843T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119923084 | |||||||
| chr2:119923575 | G | A | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1002-3023G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119923575 | |||||||
| chr2:119923645 | T | TTAAAAAA others(18): Show |
1 | a0001c0001t0008g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1002-2921_1002-289 others(29): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119923645 | ||||||
| chr2:119923928 | C | G | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1002-2670C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119923928 | |||||||
| chr2:119923964 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1002-2634T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119923964 | |||||||
| chr2:119924056 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1002-2542G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924056 | |||||||
| chr2:119924086 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002-2512G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924086 | |||||||
| chr2:119924136 | C | CA | 5 | a0001c0001t0001g0121 a0001c0001t0001g0156 a0001c0001t0003g0141 others(2): Show |
5 | HG01175.hp2 HG02027.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002-2442dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924136 | ||||||
| chr2:119924136 | CA | C | 109 | a0001c0001t0001g0079 a0001c0001t0002g0148 a0001c0001t0002g0152 others(106): Show |
109 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.1002-2442delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924136 | ||||||
| chr2:119924136 | CAA | C | 6 | a0001c0001t0002g0159 a0001c0001t0002g0201 a0001c0001t0002g0206 others(3): Show |
6 | HG02922.hp1 HG03041.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1002-2443_1002-244 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924136 | ||||||
| chr2:119924478 | A | AT | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002-2113dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924478 | ||||||
| chr2:119924478 | ATT | A | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01175.hp1 HG01192.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1002-2114_1002-211 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924478 | ||||||
| chr2:119924660 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002-1938C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924660 | |||||||
| chr2:119924668 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1002-1930T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924668 | |||||||
| chr2:119924715 | TA | T | 14 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(11): Show |
14 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1002-1875delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119924715 | ||||||
| chr2:119924722 | AATTGT | A | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1002-1875_1002-187 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924722 | |||||||
| chr2:119924730 | C | G | 99 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(96): Show |
99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.1002-1868C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924730 | |||||||
| chr2:119924949 | A | C | 218 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0043 others(215): Show |
218 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1002-1649A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119924949 | |||||||
| chr2:119925053 | C | T | 89 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1002-1545C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925053 | |||||||
| chr2:119925212 | G | A | 113 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(110): Show |
113 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1002-1386G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925212 | |||||||
| chr2:119925361 | C | T | 2 | a0002c0002t0005g0244 a0002c0002t0005g0245 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1002-1237C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925361 | |||||||
| chr2:119925485 | GGTTA | G | 20 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0059 others(17): Show |
20 | HG00323.hp1 HG00544.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.1002-1111_1002-110 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | INFO_REALIGN_3_PRIME | chr2 | 119925485 | ||||||
| chr2:119925571 | C | T | 2 | a0001c0001t0002g0212 a0001c0001t0002g0228 |
2 | HG02027.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1002-1027C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925571 | |||||||
| chr2:119925844 | T | C | 3 | a0001c0001t0010g0001 a0001c0001t0010g0002 a0001c0001t0010g0003 |
3 | HG02257.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1002-754T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925844 | |||||||
| chr2:119925943 | G | A | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-655G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925943 | |||||||
| chr2:119925969 | G | A | 1 | a0001c0001t0042g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1002-629G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119925969 | |||||||
| chr2:119926109 | G | T | 1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1002-489G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926109 | |||||||
| chr2:119926246 | T | A | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-352T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926246 | |||||||
| chr2:119926255 | A | T | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-343A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926255 | |||||||
| chr2:119926257 | T | G | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-341T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926257 | |||||||
| chr2:119926258 | T | A | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-340T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926258 | |||||||
| chr2:119926261 | C | G | 1 | a0001c0001t0029g0197 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1002-337C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926261 | |||||||
| chr2:119926349 | T | G | 1 | a0001c0001t0017g0093 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1002-249T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926349 | |||||||
| chr2:119926478 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1002-120C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 12/26 | chr2 | 119926478 | |||||||
| chr2:119926834 | T | A | 1 | a0001c0001t0006g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1070+168T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119926834 | |||||||
| chr2:119927113 | C | CT | 22 | a0001c0001t0001g0064 a0001c0001t0001g0112 a0001c0001t0001g0158 others(19): Show |
22 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1070+465dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119927113 | ||||||
| chr2:119927113 | C | CTT | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1070+464_1070+465d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119927113 | ||||||
| chr2:119927113 | CT | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0098 a0001c0001t0001g0138 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1070+465delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119927113 | ||||||
| chr2:119927351 | T | TC | 90 | a0001c0001t0001g0117 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
90 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1070+692dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119927351 | ||||||
| chr2:119927357 | C | T | 6 | a0001c0001t0003g0066 a0001c0001t0003g0072 a0001c0001t0003g0103 others(3): Show |
6 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070+691C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119927357 | |||||||
| chr2:119927383 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0003c0004t0001g0075 others(1): Show |
4 | HG02165.hp2 NA18967.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070+717A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119927383 | |||||||
| chr2:119927514 | C | T | 136 | a0001c0001t0001g0143 a0001c0001t0002g0148 a0001c0001t0002g0152 others(133): Show |
136 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.1070+848C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119927514 | |||||||
| chr2:119927558 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1070+892A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119927558 | |||||||
| chr2:119927740 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1070+1074T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119927740 | |||||||
| chr2:119928231 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1070+1565C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119928231 | |||||||
| chr2:119928671 | A | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1070+2005A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119928671 | |||||||
| chr2:119928853 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1070+2187C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119928853 | |||||||
| chr2:119928933 | T | C | 2 | a0001c0001t0002g0184 a0001c0001t0023g0147 |
2 | HG01069.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1070+2267T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119928933 | |||||||
| chr2:119929098 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2432T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929098 | |||||||
| chr2:119929101 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2435C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929101 | |||||||
| chr2:119929102 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2436T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929102 | |||||||
| chr2:119929103 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2437T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929103 | |||||||
| chr2:119929104 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2438C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929104 | |||||||
| chr2:119929106 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2440T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929106 | |||||||
| chr2:119929107 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2441T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929107 | |||||||
| chr2:119929108 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1070+2442T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929108 | |||||||
| chr2:119929148 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1070+2482G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929148 | |||||||
| chr2:119929271 | A | G | 137 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1070+2605A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929271 | |||||||
| chr2:119929571 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1071-2853T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929571 | |||||||
| chr2:119929838 | G | A | 2 | a0001c0001t0030g0033 a0001c0001t0037g0019 |
2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1071-2586G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929838 | |||||||
| chr2:119929884 | A | G | 3 | a0001c0001t0001g0252 a0001c0001t0003g0099 a0001c0001t0003g0101 |
3 | HG00323.hp2 HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1071-2540A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929884 | |||||||
| chr2:119929895 | T | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071-2529T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929895 | |||||||
| chr2:119929941 | C | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1071-2483C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119929941 | |||||||
| chr2:119930524 | A | G | 1 | a0001c0001t0013g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1071-1900A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119930524 | |||||||
| chr2:119930762 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1071-1662T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119930762 | |||||||
| chr2:119931341 | C | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1071-1083C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119931341 | |||||||
| chr2:119931377 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1071-1047A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119931377 | |||||||
| chr2:119931393 | A | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1071-1031A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119931393 | |||||||
| chr2:119931415 | ATCTTTCT others(1): Show |
A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071-995_1071-988d others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119931415 | ||||||
| chr2:119931433 | C | CT | 13 | a0001c0001t0001g0046 a0001c0001t0001g0070 a0001c0001t0001g0079 others(10): Show |
13 | HG00423.hp1 HG00621.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1071-965dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119931433 | ||||||
| chr2:119931433 | CT | C | 25 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0060 others(22): Show |
25 | HG00735.hp2 HG01070.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.1071-965delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119931433 | ||||||
| chr2:119931433 | CTT | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071-966_1071-965d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | INFO_REALIGN_3_PRIME | chr2 | 119931433 | ||||||
| chr2:119931562 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0211 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1071-862G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119931562 | |||||||
| chr2:119932002 | A | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1071-422A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119932002 | |||||||
| chr2:119932078 | G | A | 1 | a0001c0001t0058g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1071-346G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119932078 | |||||||
| chr2:119932162 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0124 a0001c0001t0042g0074 |
3 | HG01081.hp2 HG01433.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1071-262T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119932162 | |||||||
| chr2:119932329 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1071-95A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119932329 | |||||||
| chr2:119932358 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1071-66G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 13/26 | chr2 | 119932358 | |||||||
| chr2:119932641 | G | A | 27 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(24): Show |
27 | HG01175.hp1 HG01192.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.1196+92G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119932641 | |||||||
| chr2:119932774 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196+225C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119932774 | |||||||
| chr2:119933110 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1196+561C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933110 | |||||||
| chr2:119933166 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1196+617T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933166 | |||||||
| chr2:119933235 | T | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(107): Show |
110 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1196+686T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933235 | |||||||
| chr2:119933319 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1196+770T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933319 | |||||||
| chr2:119933356 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1196+807A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933356 | |||||||
| chr2:119933381 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0053 |
2 | HG01517.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1196+832A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933381 | |||||||
| chr2:119933540 | C | A | 2 | a0001c0001t0003g0031 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1196+991C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933540 | |||||||
| chr2:119933547 | G | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(107): Show |
110 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1196+998G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933547 | |||||||
| chr2:119933662 | C | CA | 28 | a0001c0001t0001g0082 a0001c0001t0001g0094 a0001c0001t0001g0143 others(25): Show |
28 | HG01175.hp1 HG01175.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.1197-1119dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 119933662 | ||||||
| chr2:119933662 | C | CAA | 8 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(5): Show |
8 | HG01192.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197-1120_1197-111 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 119933662 | ||||||
| chr2:119933662 | CA | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0123 a0001c0001t0002g0201 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197-1119delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr2 | 119933662 | ||||||
| chr2:119933881 | A | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1197-919A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933881 | |||||||
| chr2:119933900 | T | A | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197-900T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119933900 | |||||||
| chr2:119934193 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1197-607G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119934193 | |||||||
| chr2:119934204 | T | C | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1197-596T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119934204 | |||||||
| chr2:119934305 | C | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1197-495C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119934305 | |||||||
| chr2:119934525 | A | G | 151 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(148): Show |
151 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1197-275A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119934525 | |||||||
| chr2:119934697 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1197-103C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 14/26 | chr2 | 119934697 | |||||||
| chr2:119935044 | C | T | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1355+86C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935044 | |||||||
| chr2:119935073 | C | G | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1355+115C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935073 | |||||||
| chr2:119935138 | G | C | 248 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(245): Show |
248 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1355+180G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935138 | |||||||
| chr2:119935613 | T | C | 2 | a0001c0001t0003g0066 a0001c0001t0003g0072 |
2 | NA18952.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1355+655T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935613 | |||||||
| chr2:119935797 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355+839A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935797 | |||||||
| chr2:119935900 | C | T | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1355+942C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935900 | |||||||
| chr2:119935909 | A | G | 1 | a0001c0001t0013g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1355+951A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119935909 | |||||||
| chr2:119936072 | G | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1355+1114G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119936072 | |||||||
| chr2:119936224 | G | A | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1355+1266G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119936224 | |||||||
| chr2:119936421 | G | A | 1 | a0001c0001t0010g0005 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1355+1463G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119936421 | |||||||
| chr2:119936635 | T | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0062 others(8): Show |
11 | HG00423.hp1 HG01081.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1355+1677T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119936635 | |||||||
| chr2:119937302 | T | C | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1355+2344T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119937302 | |||||||
| chr2:119937523 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1355+2565A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119937523 | |||||||
| chr2:119937691 | G | C | 1 | a0001c0001t0043g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1355+2733G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119937691 | |||||||
| chr2:119937764 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1355+2806C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119937764 | |||||||
| chr2:119937888 | T | C | 151 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(148): Show |
151 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1355+2930T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119937888 | |||||||
| chr2:119938079 | A | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1355+3121A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938079 | |||||||
| chr2:119938124 | A | AT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(96): Show |
99 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1355+3187dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119938124 | ||||||
| chr2:119938124 | A | ATT | 11 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0073 others(8): Show |
11 | HG01175.hp2 HG01243.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1355+3186_1355+318 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119938124 | ||||||
| chr2:119938124 | AT | A | 9 | a0001c0001t0002g0148 a0001c0001t0002g0201 a0001c0001t0002g0204 others(6): Show |
9 | HG00735.hp2 HG01192.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1355+3187delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119938124 | ||||||
| chr2:119938124 | ATT | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1355+3186_1355+318 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119938124 | ||||||
| chr2:119938378 | C | T | 1 | a0001c0001t0002g0196 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1355+3420C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938378 | |||||||
| chr2:119938389 | A | G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355+3431A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938389 | |||||||
| chr2:119938407 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1355+3449A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938407 | |||||||
| chr2:119938434 | G | A | 6 | a0001c0001t0003g0066 a0001c0001t0003g0072 a0001c0001t0003g0103 others(3): Show |
6 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1355+3476G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938434 | |||||||
| chr2:119938493 | C | G | 1 | a0001c0001t0034g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1355+3535C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938493 | |||||||
| chr2:119938518 | T | C | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355+3560T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938518 | |||||||
| chr2:119938617 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1355+3659G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938617 | |||||||
| chr2:119938634 | T | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0211 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1355+3676T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938634 | |||||||
| chr2:119938766 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0168 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1355+3808G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938766 | |||||||
| chr2:119938940 | C | T | 36 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(33): Show |
36 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1355+3982C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938940 | |||||||
| chr2:119938976 | G | A | 1 | a0001c0006t0003g0105 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1355+4018G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119938976 | |||||||
| chr2:119939479 | C | A | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1355+4521C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119939479 | |||||||
| chr2:119939545 | C | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1355+4587C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119939545 | |||||||
| chr2:119939886 | C | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1355+4928C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119939886 | |||||||
| chr2:119940174 | A | C | 1 | a0001c0001t0002g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1356-4907A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940174 | |||||||
| chr2:119940227 | C | T | 1 | a0001c0001t0046g0090 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1356-4854C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940227 | |||||||
| chr2:119940247 | GA | G | 6 | a0001c0001t0001g0143 a0001c0001t0013g0109 a0001c0001t0013g0145 others(3): Show |
6 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.1356-4832delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119940247 | ||||||
| chr2:119940274 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1356-4807C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940274 | |||||||
| chr2:119940413 | G | T | 3 | a0001c0001t0010g0001 a0001c0001t0010g0002 a0001c0001t0010g0003 |
3 | HG02257.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1356-4668G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940413 | |||||||
| chr2:119940426 | T | C | 1 | a0001c0001t0013g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1356-4655T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940426 | |||||||
| chr2:119940451 | A | C | 1 | a0001c0001t0002g0189 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1356-4630A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940451 | |||||||
| chr2:119940629 | T | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-4452T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940629 | |||||||
| chr2:119940630 | A | T | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1356-4451A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940630 | |||||||
| chr2:119940820 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1356-4261G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940820 | |||||||
| chr2:119940837 | C | G | 1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1356-4244C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940837 | |||||||
| chr2:119940954 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1356-4127G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119940954 | |||||||
| chr2:119941196 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-3885G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941196 | |||||||
| chr2:119941412 | A | AGT | 10 | a0001c0001t0002g0152 a0001c0001t0002g0224 a0001c0001t0006g0023 others(7): Show |
10 | HG00639.hp2 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-3644_1356-364 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119941412 | ||||||
| chr2:119941412 | A | AGTGT | 116 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(113): Show |
116 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1356-3646_1356-364 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119941412 | ||||||
| chr2:119941412 | A | AGTGTGT | 4 | a0001c0001t0001g0158 a0001c0001t0003g0113 a0001c0001t0009g0150 others(1): Show |
4 | HG01891.hp1 HG02056.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1356-3648_1356-364 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119941412 | ||||||
| chr2:119941412 | AGT | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-3644_1356-364 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119941412 | ||||||
| chr2:119941412 | AGTGT | A | 3 | a0001c0001t0010g0001 a0001c0001t0010g0002 a0001c0001t0010g0003 |
3 | HG02257.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1356-3646_1356-364 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119941412 | ||||||
| chr2:119941644 | C | T | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1356-3437C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941644 | |||||||
| chr2:119941899 | T | C | 1 | a0002c0003t0027g0024 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1356-3182T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941899 | |||||||
| chr2:119941908 | T | C | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1356-3173T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941908 | |||||||
| chr2:119941948 | A | C | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356-3133A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941948 | |||||||
| chr2:119941955 | G | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-3126G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119941955 | |||||||
| chr2:119942166 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1356-2915C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119942166 | |||||||
| chr2:119942387 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-2694G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119942387 | |||||||
| chr2:119942580 | C | CA | 13 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(10): Show |
13 | HG00738.hp1 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1356-2498dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119942580 | ||||||
| chr2:119942861 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-2220G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119942861 | |||||||
| chr2:119942873 | G | T | 1 | a0001c0001t0004g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1356-2208G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119942873 | |||||||
| chr2:119942955 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1356-2126A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119942955 | |||||||
| chr2:119943058 | C | G | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1356-2023C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943058 | |||||||
| chr2:119943140 | A | T | 1 | a0001c0001t0052g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1356-1941A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943140 | |||||||
| chr2:119943494 | G | C | 1 | a0001c0001t0024g0195 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1356-1587G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943494 | |||||||
| chr2:119943578 | T | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1356-1503T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943578 | |||||||
| chr2:119943580 | C | CT | 124 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(121): Show |
124 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1356-1478dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119943580 | ||||||
| chr2:119943580 | C | CTT | 14 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0053 others(11): Show |
14 | HG00597.hp1 HG01175.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.1356-1479_1356-147 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119943580 | ||||||
| chr2:119943580 | C | CTTT | 10 | a0001c0001t0001g0073 a0002c0002t0005g0242 a0002c0002t0005g0243 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-1480_1356-147 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119943580 | ||||||
| chr2:119943586 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1356-1495T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943586 | |||||||
| chr2:119943586 | T | TC | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-1495_1356-149 others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943586 | |||||||
| chr2:119943625 | G | C | 1 | a0001c0001t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1356-1456G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943625 | |||||||
| chr2:119943692 | T | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-1389T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943692 | |||||||
| chr2:119943835 | G | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0079 others(4): Show |
7 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1356-1246G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119943835 | |||||||
| chr2:119944227 | C | T | 26 | a0001c0001t0001g0143 a0001c0001t0004g0018 a0001c0001t0004g0021 others(23): Show |
26 | HG01175.hp1 HG01192.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.1356-854C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944227 | |||||||
| chr2:119944232 | A | G | 6 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1356-849A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944232 | |||||||
| chr2:119944266 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-815C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944266 | |||||||
| chr2:119944407 | T | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356-674T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944407 | |||||||
| chr2:119944798 | AT | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1356-276delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr2 | 119944798 | ||||||
| chr2:119944880 | A | T | 1 | a0001c0001t0007g0185 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1356-201A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944880 | |||||||
| chr2:119944893 | A | C | 1 | a0001c0001t0052g0149 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1356-188A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 15/26 | chr2 | 119944893 | |||||||
| chr2:119945303 | C | G | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1515+63C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945303 | |||||||
| chr2:119945396 | T | A | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1515+156T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945396 | |||||||
| chr2:119945461 | G | C | 1 | a0001c0001t0002g0188 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1515+221G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945461 | |||||||
| chr2:119945605 | AAAAATT | A | 137 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1515+370_1515+375d others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr2 | 119945605 | ||||||
| chr2:119945644 | A | G | 6 | a0001c0001t0003g0066 a0001c0001t0003g0072 a0001c0001t0003g0103 others(3): Show |
6 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+404A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945644 | |||||||
| chr2:119945715 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1515+475A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945715 | |||||||
| chr2:119945787 | C | T | 1 | a0001c0001t0055g0057 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1515+547C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945787 | |||||||
| chr2:119945905 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516-436A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945905 | |||||||
| chr2:119945910 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516-431G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119945910 | |||||||
| chr2:119946243 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516-98T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119946243 | |||||||
| chr2:119946266 | A | G | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1516-75A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 16/26 | chr2 | 119946266 | |||||||
| chr2:119946588 | A | AT | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1656+15dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119946588 | ||||||
| chr2:119946590 | G | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1656+16G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119946590 | |||||||
| chr2:119946631 | A | G | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1656+57A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119946631 | |||||||
| chr2:119947068 | C | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1656+494C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947068 | |||||||
| chr2:119947090 | T | C | 2 | a0001c0001t0004g0038 a0007c0008t0004g0035 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1656+516T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947090 | |||||||
| chr2:119947762 | C | CCA | 29 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0002g0152 others(26): Show |
29 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1656+1217_1656+121 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947762 | C | CCACA | 18 | a0001c0001t0001g0054 a0001c0001t0001g0139 a0001c0001t0003g0031 others(15): Show |
18 | HG01081.hp1 HG01175.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1656+1215_1656+121 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947762 | C | CCACACA | 101 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1656+1213_1656+121 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947762 | C | CCACACAC others(1): Show |
6 | a0001c0001t0001g0042 a0001c0001t0001g0060 a0001c0001t0001g0091 others(3): Show |
6 | HG00741.hp1 HG02148.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1656+1211_1656+121 others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947762 | C | CCACACAC others(3): Show |
4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1656+1209_1656+121 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947762 | CCA | C | 7 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0010g0001 others(4): Show |
7 | HG02257.hp2 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1656+1217_1656+121 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947762 | ||||||
| chr2:119947789 | C | CACACAT | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1656+1218_1656+121 others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947789 | ||||||
| chr2:119947791 | C | CACACACA others(3): Show |
1 | a0001c0001t0001g0157 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1656+1218_1656+121 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119947791 | ||||||
| chr2:119947791 | C | T | 1 | a0001c0001t0008g0010 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1656+1217C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947791 | |||||||
| chr2:119947842 | T | A | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1656+1268T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947842 | |||||||
| chr2:119947843 | A | G | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1656+1269A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947843 | |||||||
| chr2:119947844 | C | T | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1656+1270C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947844 | |||||||
| chr2:119947845 | T | A | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1656+1271T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947845 | |||||||
| chr2:119947847 | C | G | 1 | a0001c0001t0048g0030 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1656+1273C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947847 | |||||||
| chr2:119947864 | C | T | 1 | a0001c0001t0002g0234 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1656+1290C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119947864 | |||||||
| chr2:119948026 | T | A | 1 | a0005c0009t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1656+1452T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119948026 | |||||||
| chr2:119948726 | T | C | 4 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1656+2152T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119948726 | |||||||
| chr2:119948755 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1656+2181G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119948755 | |||||||
| chr2:119949027 | G | T | 1 | a0001c0001t0045g0089 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1656+2453G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949027 | |||||||
| chr2:119949029 | A | G | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1656+2455A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949029 | |||||||
| chr2:119949168 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1656+2594T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949168 | |||||||
| chr2:119949448 | ATCT | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-2521_1657-251 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | INFO_REALIGN_3_PRIME | chr2 | 119949448 | ||||||
| chr2:119949543 | T | C | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1657-2430T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949543 | |||||||
| chr2:119949692 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1657-2281A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949692 | |||||||
| chr2:119949934 | T | G | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1657-2039T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119949934 | |||||||
| chr2:119950068 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1657-1905A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950068 | |||||||
| chr2:119950175 | A | T | 1 | a0001c0001t0010g0005 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1657-1798A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950175 | |||||||
| chr2:119950357 | T | C | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-1616T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950357 | |||||||
| chr2:119950395 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1657-1578G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950395 | |||||||
| chr2:119950447 | T | C | 5 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(2): Show |
5 | HG02630.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1657-1526T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950447 | |||||||
| chr2:119950763 | A | G | 5 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0002c0003t0015g0025 others(2): Show |
5 | HG00423.hp2 HG00738.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.1657-1210A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119950763 | |||||||
| chr2:119951460 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1657-513G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119951460 | |||||||
| chr2:119951555 | G | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1657-418G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119951555 | |||||||
| chr2:119951741 | G | T | 161 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1657-232G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 18/26 | chr2 | 119951741 | |||||||
| chr2:119952184 | C | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1813+55C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952184 | |||||||
| chr2:119952189 | C | T | 1 | a0002c0002t0005g0245 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1813+60C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952189 | |||||||
| chr2:119952289 | G | T | 1 | a0001c0001t0058g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1813+160G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952289 | |||||||
| chr2:119952364 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1813+235G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952364 | |||||||
| chr2:119952834 | C | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1813+705C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952834 | |||||||
| chr2:119952980 | A | G | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1813+851A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119952980 | |||||||
| chr2:119953129 | T | G | 1 | a0001c0001t0002g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1813+1000T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119953129 | |||||||
| chr2:119953299 | A | G | 3 | a0001c0001t0002g0170 a0001c0001t0002g0239 a0001c0001t0028g0183 |
3 | HG00738.hp2 HG01358.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1813+1170A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119953299 | |||||||
| chr2:119953325 | C | T | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1813+1196C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119953325 | |||||||
| chr2:119953864 | T | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1814-1293T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119953864 | |||||||
| chr2:119953941 | A | G | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01346.hp2 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.1814-1216A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119953941 | |||||||
| chr2:119954019 | C | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1814-1138C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954019 | |||||||
| chr2:119954037 | A | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18986.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1814-1120A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954037 | |||||||
| chr2:119954345 | G | A | 13 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(10): Show |
13 | HG00738.hp1 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1814-812G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954345 | |||||||
| chr2:119954400 | G | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1814-757G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954400 | |||||||
| chr2:119954401 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0127 |
2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1814-756A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954401 | |||||||
| chr2:119954443 | C | G | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1814-714C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954443 | |||||||
| chr2:119954529 | T | A | 1 | a0001c0001t0002g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1814-628T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954529 | |||||||
| chr2:119954831 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0111 |
3 | HG01517.hp1 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1814-326C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119954831 | |||||||
| chr2:119955125 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1814-32G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 19/26 | chr2 | 119955125 | |||||||
| chr2:119955441 | A | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1980+118A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955441 | |||||||
| chr2:119955444 | G | GT | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1980+124dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119955444 | ||||||
| chr2:119955633 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1980+310A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955633 | |||||||
| chr2:119955651 | A | G | 6 | a0001c0001t0002g0186 a0001c0001t0002g0192 a0001c0001t0002g0193 others(3): Show |
6 | HG02135.hp1 NA18612.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+328A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955651 | |||||||
| chr2:119955733 | C | A | 2 | a0001c0001t0003g0104 a0001c0001t0003g0141 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1980+410C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955733 | |||||||
| chr2:119955765 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1980+442G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955765 | |||||||
| chr2:119955923 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1980+600T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119955923 | |||||||
| chr2:119955944 | T | TAATA | 7 | a0001c0001t0002g0208 a0001c0001t0002g0213 a0001c0001t0002g0231 others(4): Show |
7 | HG00639.hp2 HG00738.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+660_1980+663d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119955944 | ||||||
| chr2:119955944 | TAATA | T | 38 | a0001c0001t0001g0143 a0001c0001t0002g0180 a0001c0001t0002g0189 others(35): Show |
38 | HG00423.hp2 HG00609.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.1980+660_1980+663d others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119955944 | ||||||
| chr2:119955944 | TAATAAAT others(1): Show |
T | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1980+656_1980+663d others(10): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119955944 | ||||||
| chr2:119955944 | TAATAAAT others(9): Show |
T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(108): Show |
111 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1980+648_1980+663d others(18): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119955944 | ||||||
| chr2:119956193 | A | G | 1 | a0001c0001t0058g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1981-651A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956193 | |||||||
| chr2:119956232 | C | T | 1 | a0001c0001t0014g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1981-612C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956232 | |||||||
| chr2:119956237 | A | AT | 24 | a0001c0001t0001g0017 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
24 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.1981-584dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956237 | A | ATT | 89 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(86): Show |
89 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1981-585_1981-584d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956237 | A | ATTT | 8 | a0001c0001t0001g0076 a0001c0001t0001g0088 a0001c0001t0001g0117 others(5): Show |
8 | HG01261.hp2 HG02698.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1981-586_1981-584d others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956237 | AT | A | 20 | a0001c0001t0001g0143 a0001c0001t0002g0159 a0001c0001t0002g0160 others(17): Show |
20 | HG01167.hp2 HG01257.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1981-584delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956237 | ATT | A | 20 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(17): Show |
20 | HG00738.hp1 HG00741.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1981-585_1981-584d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956237 | ATTT | A | 11 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(8): Show |
11 | HG01192.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1981-586_1981-584d others(5): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956237 | ||||||
| chr2:119956267 | C | T | 17 | a0001c0001t0004g0018 a0001c0001t0004g0021 a0001c0001t0004g0022 others(14): Show |
17 | HG01175.hp1 HG01192.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1981-577C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956267 | |||||||
| chr2:119956323 | C | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.1981-521C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956323 | |||||||
| chr2:119956503 | T | C | 17 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0159 others(14): Show |
17 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1981-341T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956503 | |||||||
| chr2:119956589 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1981-255C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956589 | |||||||
| chr2:119956653 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1981-191G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956653 | |||||||
| chr2:119956703 | G | C | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1981-141G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956703 | |||||||
| chr2:119956724 | A | G | 6 | a0001c0001t0004g0036 a0001c0001t0004g0038 a0001c0001t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01192.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-120A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | chr2 | 119956724 | |||||||
| chr2:119956825 | C | CT | 11 | a0001c0001t0002g0234 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(8): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1981-3dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr2 | 119956825 | ||||||
| chr2:119957241 | A | G | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2133+164A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957241 | |||||||
| chr2:119957422 | T | C | 13 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(10): Show |
13 | HG00738.hp1 HG00741.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2133+345T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957422 | |||||||
| chr2:119957441 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2133+364T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957441 | |||||||
| chr2:119957663 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2133+586G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957663 | |||||||
| chr2:119957897 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2133+820A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957897 | |||||||
| chr2:119957968 | T | A | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2133+891T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119957968 | |||||||
| chr2:119958097 | A | G | 2 | a0001c0001t0002g0152 a0001c0001t0002g0160 |
2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2133+1020A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119958097 | |||||||
| chr2:119958328 | T | TA | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2133+1265dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 119958328 | ||||||
| chr2:119958328 | TA | T | 17 | a0001c0001t0002g0180 a0001c0001t0002g0226 a0001c0001t0008g0008 others(14): Show |
17 | HG01169.hp1 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.2133+1265delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 119958328 | ||||||
| chr2:119958336 | A | T | 10 | a0001c0001t0001g0143 a0001c0001t0002g0161 a0001c0001t0010g0001 others(7): Show |
10 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.2133+1259A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119958336 | |||||||
| chr2:119958441 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2133+1364A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119958441 | |||||||
| chr2:119958445 | TAGAG | T | 14 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(11): Show |
14 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2133+1372_2133+137 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 119958445 | ||||||
| chr2:119959241 | C | CT | 107 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(104): Show |
107 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2134-1555dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr2 | 119959241 | ||||||
| chr2:119959289 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2134-1518A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119959289 | |||||||
| chr2:119959473 | C | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2134-1334C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119959473 | |||||||
| chr2:119959869 | C | T | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2134-938C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119959869 | |||||||
| chr2:119959893 | C | A | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2134-914C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119959893 | |||||||
| chr2:119960055 | A | G | 1 | a0004c0005t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2134-752A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960055 | |||||||
| chr2:119960065 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2134-742A>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960065 | |||||||
| chr2:119960068 | T | C | 88 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.2134-739T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960068 | |||||||
| chr2:119960417 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2134-390A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960417 | |||||||
| chr2:119960500 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2134-307C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960500 | |||||||
| chr2:119960746 | A | G | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2134-61A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 22/26 | chr2 | 119960746 | |||||||
| chr2:119961006 | G | A | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2280+53G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119961006 | |||||||
| chr2:119961096 | T | G | 233 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(230): Show |
233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.2280+143T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119961096 | |||||||
| chr2:119961221 | G | GAACTCTT others(3): Show |
239 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(236): Show |
239 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.2280+274_2280+275i others(12): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr2 | 119961221 | ||||||
| chr2:119961529 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2280+576G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119961529 | |||||||
| chr2:119961803 | T | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(88): Show |
91 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2281-813T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119961803 | |||||||
| chr2:119962025 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2281-591T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119962025 | |||||||
| chr2:119962173 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2281-443G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119962173 | |||||||
| chr2:119962219 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0111 |
3 | HG01517.hp1 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2281-397C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119962219 | |||||||
| chr2:119962220 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2281-396G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 23/26 | chr2 | 119962220 | |||||||
| chr2:119962808 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2409+64A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119962808 | |||||||
| chr2:119963092 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2409+348G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119963092 | |||||||
| chr2:119963258 | T | C | 1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2409+514T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119963258 | |||||||
| chr2:119963596 | A | T | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2409+852A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119963596 | |||||||
| chr2:119963875 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2409+1131A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119963875 | |||||||
| chr2:119964103 | C | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2409+1359C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119964103 | |||||||
| chr2:119964753 | G | A | 1 | a0001c0001t0050g0084 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2410-744G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119964753 | |||||||
| chr2:119964958 | C | T | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2410-539C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119964958 | |||||||
| chr2:119964999 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2410-498C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119964999 | |||||||
| chr2:119965032 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2410-465T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119965032 | |||||||
| chr2:119965074 | A | G | 3 | a0001c0001t0046g0090 a0001c0001t0048g0030 a0001c0001t0057g0058 |
3 | HG02071.hp1 HG02083.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.2410-423A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119965074 | |||||||
| chr2:119965248 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2410-249T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119965248 | |||||||
| chr2:119965462 | T | G | 1 | a0001c0001t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2410-35T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 24/26 | chr2 | 119965462 | |||||||
| chr2:119965865 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2558+220G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119965865 | |||||||
| chr2:119965917 | A | G | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2558+272A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119965917 | |||||||
| chr2:119966133 | G | T | 5 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(2): Show |
5 | HG02486.hp1 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2558+488G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119966133 | |||||||
| chr2:119966211 | G | A | 21 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0053 others(18): Show |
21 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2558+566G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119966211 | |||||||
| chr2:119966357 | C | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2558+712C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119966357 | |||||||
| chr2:119966905 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2559-932C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119966905 | |||||||
| chr2:119967080 | G | C | 1 | a0001c0001t0002g0223 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2559-757G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119967080 | |||||||
| chr2:119967322 | G | A | 88 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.2559-515G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119967322 | |||||||
| chr2:119967375 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2559-462G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119967375 | |||||||
| chr2:119967446 | CA | C | 11 | a0001c0001t0022g0173 a0002c0002t0005g0242 a0002c0002t0005g0243 others(8): Show |
11 | HG01070.hp1 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2559-379delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr2 | 119967446 | ||||||
| chr2:119967820 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2559-17A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 25/26 | chr2 | 119967820 | |||||||
| chr2:119967980 | C | T | 1 | a0002c0002t0016g0241 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.2694+8C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119967980 | |||||||
| chr2:119968128 | A | G | 245 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(242): Show |
245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.2694+156A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119968128 | |||||||
| chr2:119968438 | G | A | 1 | a0001c0001t0009g0150 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2694+466G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119968438 | |||||||
| chr2:119968509 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18986.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2694+537C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119968509 | |||||||
| chr2:119968538 | T | TC | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2694+569dupC | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119968538 | ||||||
| chr2:119968624 | T | C | 1 | a0002c0002t0005g0249 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2694+652T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119968624 | |||||||
| chr2:119969104 | G | C | 4 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0111 others(1): Show |
4 | HG01346.hp2 HG01517.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.2694+1132G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969104 | |||||||
| chr2:119969460 | G | C | 3 | a0001c0001t0003g0048 a0001c0001t0003g0083 a0001c0001t0054g0047 |
3 | HG01243.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2694+1488G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969460 | |||||||
| chr2:119969492 | A | G | 2 | a0001c0001t0014g0222 a0001c0001t0014g0238 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2694+1520A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969492 | |||||||
| chr2:119969552 | C | CT | 109 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(106): Show |
109 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.2694+1604dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119969552 | ||||||
| chr2:119969552 | C | CTT | 21 | a0001c0001t0001g0053 a0001c0001t0001g0082 a0001c0001t0001g0111 others(18): Show |
21 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2694+1603_2694+160 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119969552 | ||||||
| chr2:119969552 | C | CTTT | 10 | a0001c0001t0001g0064 a0001c0001t0031g0011 a0001c0001t0036g0034 others(7): Show |
10 | HG01175.hp1 HG02080.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2694+1602_2694+160 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119969552 | ||||||
| chr2:119969552 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0191 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2694+1593_2694+160 others(16): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119969552 | ||||||
| chr2:119969552 | CTTTTTTT others(6): Show |
C | 86 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(83): Show |
86 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.2694+1592_2694+160 others(17): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119969552 | ||||||
| chr2:119969597 | C | T | 1 | a0001c0001t0057g0058 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2694+1625C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969597 | |||||||
| chr2:119969598 | G | A | 1 | a0002c0002t0005g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2694+1626G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969598 | |||||||
| chr2:119969652 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2694+1680G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969652 | |||||||
| chr2:119969750 | G | A | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2694+1778G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969750 | |||||||
| chr2:119969838 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2694+1866G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969838 | |||||||
| chr2:119969853 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2694+1881C>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969853 | |||||||
| chr2:119969980 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2694+2008G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119969980 | |||||||
| chr2:119970163 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2694+2191G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119970163 | |||||||
| chr2:119970209 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2694+2237G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119970209 | |||||||
| chr2:119970499 | A | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2694+2527A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119970499 | |||||||
| chr2:119970520 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2694+2548A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119970520 | |||||||
| chr2:119971123 | A | T | 1 | a0001c0001t0020g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2694+3151A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971123 | |||||||
| chr2:119971206 | C | G | 1 | a0001c0001t0001g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2694+3234C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971206 | |||||||
| chr2:119971226 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2694+3254G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971226 | |||||||
| chr2:119971508 | G | C | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2694+3536G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971508 | |||||||
| chr2:119971538 | G | A | 1 | a0001c0001t0022g0173 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2694+3566G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971538 | |||||||
| chr2:119971538 | G | T | 1 | a0001c0001t0031g0011 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2694+3566G>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971538 | |||||||
| chr2:119971645 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2694+3673G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971645 | |||||||
| chr2:119971929 | C | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0065 a0001c0001t0001g0079 others(4): Show |
7 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.2694+3957C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119971929 | |||||||
| chr2:119972121 | A | G | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2694+4149A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119972121 | |||||||
| chr2:119972175 | T | TA | 112 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(109): Show |
112 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.2694+4213dupA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119972175 | ||||||
| chr2:119972175 | T | TAA | 112 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(109): Show |
112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2694+4212_2694+421 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119972175 | ||||||
| chr2:119972449 | A | G | 2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2694+4477A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119972449 | |||||||
| chr2:119972747 | G | A | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695-4237G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119972747 | |||||||
| chr2:119972981 | C | T | 2 | a0001c0001t0003g0031 a0001c0001t0003g0100 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2695-4003C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119972981 | |||||||
| chr2:119973242 | G | A | 1 | a0001c0001t0034g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2695-3742G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119973242 | |||||||
| chr2:119973258 | A | G | 1 | a0001c0001t0041g0210 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2695-3726A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119973258 | |||||||
| chr2:119973458 | G | C | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2695-3526G>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119973458 | |||||||
| chr2:119973625 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2695-3359T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119973625 | |||||||
| chr2:119973655 | G | GT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0055 others(27): Show |
30 | HG00609.hp1 HG01069.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2695-3302dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTT | 33 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0060 others(30): Show |
33 | HG00621.hp2 HG00735.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.2695-3303_2695-330 others(6): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTT | 41 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(38): Show |
41 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.2695-3304_2695-330 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTT | 18 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0053 others(15): Show |
18 | HG00544.hp1 HG00639.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.2695-3305_2695-330 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(3): Show |
6 | a0001c0001t0002g0159 a0001c0001t0002g0213 a0001c0001t0002g0215 others(3): Show |
6 | HG02559.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695-3311_2695-330 others(14): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0233 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2695-3312_2695-330 others(15): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(10): Show |
2 | a0001c0001t0002g0153 a0001c0001t0004g0039 |
2 | HG01109.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2695-3318_2695-330 others(21): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0002g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2695-3319_2695-330 others(22): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(12): Show |
3 | a0001c0001t0002g0162 a0001c0001t0021g0217 a0006c0007t0002g0163 |
3 | HG02818.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2695-3320_2695-330 others(23): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(15): Show |
1 | a0001c0001t0036g0034 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2695-3323_2695-330 others(26): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(18): Show |
1 | a0007c0008t0004g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2695-3326_2695-330 others(29): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(19): Show |
2 | a0001c0001t0002g0218 a0001c0001t0004g0038 |
2 | HG02257.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2695-3327_2695-330 others(30): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(20): Show |
1 | a0001c0001t0002g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2695-3328_2695-330 others(31): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(21): Show |
2 | a0001c0001t0034g0032 a0001c0001t0039g0107 |
2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2695-3302_2695-330 others(32): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | G | GTTTTTTT others(30): Show |
2 | a0001c0001t0004g0036 a0001c0001t0038g0037 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2695-3302_2695-330 others(41): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | GTTT | G | 6 | a0001c0001t0012g0012 a0001c0001t0012g0014 a0001c0001t0012g0015 others(3): Show |
6 | HG00738.hp1 HG00741.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2695-3304_2695-330 others(7): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | GTTTT | G | 5 | a0001c0001t0002g0160 a0001c0001t0002g0181 a0001c0001t0002g0209 others(2): Show |
5 | HG01975.hp1 HG02148.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695-3305_2695-330 others(8): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | GTTTTT | G | 59 | a0001c0001t0002g0148 a0001c0001t0002g0154 a0001c0001t0002g0155 others(56): Show |
59 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.2695-3306_2695-330 others(9): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119973655 | GTTTTTTT others(8): Show |
G | 4 | a0001c0001t0009g0114 a0001c0001t0009g0115 a0001c0001t0009g0150 others(1): Show |
4 | HG02486.hp2 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695-3316_2695-330 others(19): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119973655 | ||||||
| chr2:119974085 | T | C | 1 | a0001c0001t0049g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2695-2899T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974085 | |||||||
| chr2:119974272 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2695-2712C>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974272 | |||||||
| chr2:119974351 | G | A | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2695-2633G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974351 | |||||||
| chr2:119974444 | G | A | 88 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0153 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.2695-2540G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974444 | |||||||
| chr2:119974487 | G | A | 1 | a0001c0001t0011g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2695-2497G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974487 | |||||||
| chr2:119974499 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2695-2485G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974499 | |||||||
| chr2:119974926 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2695-2058G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119974926 | |||||||
| chr2:119975028 | CT | C | 6 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(3): Show |
6 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2695-1949delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119975028 | ||||||
| chr2:119975458 | T | A | 5 | a0001c0001t0008g0013 a0001c0001t0008g0016 a0001c0001t0012g0012 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2695-1526T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975458 | |||||||
| chr2:119975461 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2695-1523C>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975461 | |||||||
| chr2:119975543 | T | G | 1 | a0001c0001t0025g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2695-1441T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975543 | |||||||
| chr2:119975682 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2695-1302G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975682 | |||||||
| chr2:119975795 | T | G | 5 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0095 others(2): Show |
5 | HG02109.hp1 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2695-1189T>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975795 | |||||||
| chr2:119975961 | A | G | 3 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0247 |
3 | HG01243.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2695-1023A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975961 | |||||||
| chr2:119975981 | A | AT | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2695-998dupT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119975981 | ||||||
| chr2:119975981 | A | T | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2695-1003A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975981 | |||||||
| chr2:119975987 | A | T | 3 | a0002c0003t0015g0025 a0002c0003t0015g0026 a0002c0003t0027g0024 |
3 | HG00738.hp1 HG00741.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2695-997A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975987 | |||||||
| chr2:119975993 | TTA | T | 7 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(4): Show |
7 | HG01884.hp2 HG02165.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2695-989_2695-988d others(4): Show |
PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119975993 | ||||||
| chr2:119975998 | TA | T | 11 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0087 others(8): Show |
11 | HG01243.hp2 HG01257.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695-985delA | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975998 | |||||||
| chr2:119975999 | A | T | 10 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(7): Show |
10 | HG01884.hp2 HG02165.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2695-985A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119975999 | |||||||
| chr2:119975999 | AT | A | 210 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0028 others(207): Show |
210 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.2695-971delT | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr2 | 119975999 | ||||||
| chr2:119976004 | T | A | 14 | a0001c0001t0001g0091 a0001c0001t0006g0219 a0001c0001t0008g0010 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2695-980T>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976004 | |||||||
| chr2:119976211 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0078 |
2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2695-773A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976211 | |||||||
| chr2:119976226 | T | C | 2 | a0001c0001t0003g0104 a0001c0001t0003g0141 |
2 | NA18946.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2695-758T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976226 | |||||||
| chr2:119976293 | G | A | 9 | a0001c0001t0001g0143 a0001c0001t0010g0001 a0001c0001t0010g0002 others(6): Show |
9 | HG01884.hp2 HG02080.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2695-691G>A | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976293 | |||||||
| chr2:119976329 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2695-655A>G | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976329 | |||||||
| chr2:119976342 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2695-642T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976342 | |||||||
| chr2:119976653 | T | C | 10 | a0002c0002t0005g0242 a0002c0002t0005g0243 a0002c0002t0005g0244 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2695-331T>C | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976653 | |||||||
| chr2:119976699 | A | T | 11 | a0001c0001t0008g0008 a0001c0001t0008g0009 a0001c0001t0008g0010 others(8): Show |
11 | HG00735.hp2 HG02486.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2695-285A>T | PTPN4 | ENSG00000088179.9 | transcript | ENST00000263708.7 | protein_coding | 26/26 | chr2 | 119976699 |