Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 167153 |
| ensemblid | ENSG00000164329.15 |
| hgncid | 26776 |
| symbol | TENT2 |
| name | terminal nucleotidyltransferase 2 |
| refseq_nuc | NM_001114394.3 |
| refseq_prot | NP_001107866.1 |
| ensembl_nuc | ENST00000453514.6 |
| ensembl_prot | ENSP00000397563.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 79612441 |
| end | 79688246 |
| strand | + |
| ver | v1.2 |
| region | chr5:79612441-79688246 |
| region5000 | chr5:79607441-79693246 |
| regionname0 | TENT2_chr5_79612441_79688246 |
| regionname5000 | TENT2_chr5_79607441_79693246 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 484 | 340 | 87 | 50 | 149 | 12 | 40 | 113 | TENT2_chr5_79607441_79693246 | TENT2 | MFPNS others(479): Show |
chr5 | 79607441 | 79693246 |
| a0002 | 0/0 | 484 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | MFPNS others(479): Show |
chr5 | 79607441 | 79693246 |
| a0003 | 0/0 | 484 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | MFPNS others(479): Show |
chr5 | 79607441 | 79693246 |
| a0004 | 0/0 | 484 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | MFPNS others(479): Show |
chr5 | 79607441 | 79693246 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1452 | 317 | 85 | 40 | 143 | 12 | 35 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0001c0002 | 0/0 | 1452 | 18 | 1 | 10 | 2 | 0 | 5 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0001c0003 | 0/0 | 1452 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0001c0007 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0002c0004 | 0/0 | 1452 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0003c0005 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 | ||
| a0004c0006 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATGTT others(1447): Show |
chr5 | 79607441 | 79693246 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5103 | 146 | 21 | 22 | 87 | 4 | 12 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0002 | 0/0 | 5101 | 20 | 1 | 0 | 18 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0003 | 0/0 | 5098 | 19 | 5 | 1 | 6 | 0 | 7 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0004 | 0/0 | 5101 | 21 | 21 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0005 | 0/0 | 5103 | 17 | 0 | 0 | 13 | 0 | 4 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0006 | 0/0 | 5106 | 16 | 3 | 4 | 5 | 2 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0007 | 0/0 | 5103 | 9 | 0 | 1 | 5 | 2 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0008 | 0/1 | 5103 | 8 | 0 | 0 | 5 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0009 | 0/0 | 5101 | 7 | 6 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0010 | 0/0 | 5098 | 2 | 0 | 0 | 0 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0011 | 0/0 | 5098 | 6 | 5 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0012 | 0/0 | 5101 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0013 | 0/0 | 5103 | 3 | 1 | 1 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0014 | 0/0 | 5106 | 3 | 0 | 0 | 1 | 1 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0015 | 0/0 | 5106 | 3 | 0 | 3 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0016 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0017 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0018 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0019 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0020 | 0/0 | 5103 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0021 | 0/0 | 5106 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0022 | 0/0 | 5098 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0024 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0026 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0027 | 0/0 | 5098 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0028 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0029 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0030 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0031 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0032 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0033 | 0/0 | 5103 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0034 | 1/0 | 5100 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5095): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0035 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0036 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0037 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0038 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0039 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0040 | 0/0 | 5106 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0041 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0042 | 0/0 | 5103 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0043 | 0/0 | 5100 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5095): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0044 | 0/0 | 5106 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5101): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0045 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0046 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0001t0047 | 0/0 | 5103 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5098): Show |
chr5 | 79607441 | 79693246 |
| a0001c0002t0002 | 0/0 | 5101 | 13 | 0 | 10 | 0 | 0 | 3 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0002t0003 | 0/0 | 5098 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0002t0012 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0002t0016 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0001c0002t0023 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0003t0010 | 0/0 | 5098 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0001c0007t0025 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0002c0004t0003 | 0/0 | 5098 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| a0003c0005t0004 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5096): Show |
chr5 | 79607441 | 79693246 |
| a0004c0006t0003 | 0/0 | 5098 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | ATCCG others(5093): Show |
chr5 | 79607441 | 79693246 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0010g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0011g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0011g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0011g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0011g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0013g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0013g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0014g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0015g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0015g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0015g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0016g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0017g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0017g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0018g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0019g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0019g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0021g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0021g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0022g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0026g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0027g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0028g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0029g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0030g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0031g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0032g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0033g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0034g0016 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0035g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0036g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0037g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0038g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0039g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0040g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0041g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0042g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0043g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0044g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0045g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0046g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0001t0047g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0016g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0002t0023g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0003t0010g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0003t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0003t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0003t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0001c0007t0025g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0002c0004t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0002c0004t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0003c0005t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| a0004c0006t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0014 | g0119 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0285 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00140 | hp1 | a0001 | c0001 | t0033 | g0226 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | GBR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0191 | EUR | FIN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0176 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00423 | hp2 | a0001 | c0001 | t0014 | g0148 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00558 | hp2 | a0001 | c0001 | t0032 | g0236 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00741 | hp1 | a0001 | c0001 | t0007 | g0124 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0100 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0294 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01167 | hp1 | a0001 | c0001 | t0043 | g0016 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01167 | hp2 | a0001 | c0001 | t0022 | g0079 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01243 | hp2 | a0001 | c0001 | t0045 | g0018 | AMR | PUR | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01255 | hp2 | a0001 | c0001 | t0013 | g0216 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01257 | hp1 | a0001 | c0001 | t0015 | g0282 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01358 | hp2 | a0001 | c0001 | t0039 | g0264 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | CLM | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01515 | hp1 | a0001 | c0001 | t0007 | g0219 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01515 | hp2 | a0001 | c0001 | t0010 | g0007 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0322 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0007 | EUR | IBS | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01884 | hp1 | a0001 | c0007 | t0025 | g0108 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0039 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0102 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01978 | hp2 | a0001 | c0001 | t0028 | g0313 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01981 | hp1 | a0001 | c0001 | t0030 | g0167 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02004 | hp2 | a0001 | c0001 | t0044 | g0279 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0112 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0085 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CDX | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02258 | hp1 | a0001 | c0001 | t0013 | g0275 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02273 | hp2 | a0001 | c0001 | t0015 | g0284 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0041 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02300 | hp1 | a0001 | c0001 | t0015 | g0280 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02451 | hp1 | a0001 | c0001 | t0018 | g0243 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02572 | hp2 | a0003 | c0005 | t0004 | g0076 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0126 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0078 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02615 | hp2 | a0001 | c0001 | t0018 | g0135 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0131 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02647 | hp1 | a0001 | c0001 | t0041 | g0111 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02683 | hp2 | a0001 | c0001 | t0013 | g0234 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0129 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0114 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02738 | hp1 | a0001 | c0002 | t0023 | g0107 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02738 | hp2 | a0001 | c0001 | t0036 | g0110 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0013 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02818 | hp1 | a0001 | c0001 | t0017 | g0134 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02818 | hp2 | a0001 | c0001 | t0040 | g0142 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02886 | hp1 | a0001 | c0002 | t0012 | g0097 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0272 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0009 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0273 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02965 | hp2 | a0001 | c0001 | t0024 | g0034 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02970 | hp2 | a0001 | c0001 | t0038 | g0218 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0146 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0312 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03098 | hp2 | a0001 | c0001 | t0042 | g0321 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0105 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0140 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03225 | hp1 | a0001 | c0001 | t0031 | g0242 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03239 | hp1 | a0001 | c0001 | t0029 | g0240 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03239 | hp2 | a0001 | c0002 | t0016 | g0109 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03453 | hp1 | a0001 | c0001 | t0020 | g0130 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0125 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0104 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03579 | hp1 | a0001 | c0001 | t0019 | g0128 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03688 | hp1 | a0001 | c0001 | t0014 | g0120 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0004 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03710 | hp1 | a0001 | c0001 | t0009 | g0043 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0144 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0301 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03927 | hp1 | a0001 | c0001 | t0037 | g0147 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0186 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0315 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | STU | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | CHB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0096 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18941 | hp2 | a0002 | c0004 | t0003 | g0049 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18947 | hp1 | a0001 | c0001 | t0046 | g0067 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18947 | hp2 | a0001 | c0003 | t0010 | g0090 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18951 | hp2 | a0002 | c0004 | t0003 | g0008 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18962 | hp2 | a0001 | c0003 | t0010 | g0047 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18964 | hp1 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18965 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18971 | hp2 | a0001 | c0001 | t0047 | g0238 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18984 | hp2 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0115 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0190 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18999 | hp2 | a0001 | c0001 | t0008 | g0202 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19000 | hp1 | a0001 | c0003 | t0010 | g0091 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19009 | hp1 | a0001 | c0001 | t0006 | g0306 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19010 | hp2 | a0001 | c0003 | t0010 | g0089 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19043 | hp1 | a0001 | c0001 | t0026 | g0072 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19074 | hp2 | a0004 | c0006 | t0003 | g0132 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19080 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | YRI | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20129 | hp2 | a0001 | c0001 | t0012 | g0106 | AFR | ASW | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | GIH | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0270 | SAS | GIH | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02486 | hp2 | a0001 | c0001 | t0021 | g0113 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0037 | AFR | USA | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA21309 | hp1 | a0001 | c0001 | t0035 | g0141 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | LWK | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0008 | g0229 | REF | REF | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0034 | g0016 | REF | REF | TENT2_chr5_79607441_79693246 | TENT2 | chr5 | 79607441 | 79693246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79619674 | G | A | 1 | a0002 | 2 | NA18941.hp2 NA18951.hp2 |
missense_variant | MODERATE | c.26G>A | p.Arg9His | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 698/5100 | 26/1455 | 9/484 | chr5 | 79619674 | |||
| chr5:79619770 | A | G | 1 | a0004 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.122A>G | p.Asn41Ser | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 794/5100 | 122/1455 | 41/484 | chr5 | 79619770 | |||
| chr5:79685205 | C | T | 1 | a0003 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1387C>T | p.His463Tyr | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2059/5100 | 1387/1455 | 463/484 | chr5 | 79685205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79619744 | C | T | 1 | a0001c0007 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.96C>T | p.His32His | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/15 | 768/5100 | 96/1455 | 32/484 | chr5 | 79619744 | |||
| chr5:79668906 | T | G | 1 | a0001c0002 | 18 | HG00544.hp2 HG01433.hp2 HG01928.hp2 others(15): Show |
synonymous_variant | LOW | c.1086T>G | p.Pro362Pro | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/15 | 1758/5100 | 1086/1455 | 362/484 | chr5 | 79668906 | |||
| chr5:79682016 | G | A | 1 | a0001c0003 | 4 | NA18947.hp2 NA18962.hp2 NA19000.hp1 others(1): Show |
synonymous_variant | LOW | c.1335G>A | p.Val445Val | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/15 | 2007/5100 | 1335/1455 | 445/484 | chr5 | 79682016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79612460 | T | C | 1 | a0001c0001t0022 | 1 | HG01167.hp2 | 5_prime_UTR_variant | MODIFIER | c.-653T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 7189 | chr5 | 79612460 | ||||||
| chr5:79612529 | A | G | 1 | a0001c0001t0047 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-584A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 7120 | chr5 | 79612529 | ||||||
| chr5:79612702 | C | G | 1 | a0001c0001t0046 | 1 | NA18947.hp1 | 5_prime_UTR_variant | MODIFIER | c.-411C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6947 | chr5 | 79612702 | ||||||
| chr5:79612757 | C | T | 1 | a0001c0001t0045 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-356C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6892 | chr5 | 79612757 | ||||||
| chr5:79612901 | C | T | 2 | a0001c0001t0015 a0001c0001t0044 |
4 | HG01257.hp1 HG02004.hp2 HG02273.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-212C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6748 | chr5 | 79612901 | ||||||
| chr5:79612981 | C | T | 1 | a0001c0001t0043 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/15 | 6668 | chr5 | 79612981 | ||||||
| chr5:79685428 | A | T | 1 | a0001c0001t0021 | 2 | HG02486.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*155A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 155 | chr5 | 79685428 | ||||||
| chr5:79685546 | TAACTG | T | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*277_*281delTGAAC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 277 | INFO_REALIGN_3_PRIME | chr5 | 79685546 | |||||
| chr5:79685606 | T | G | 1 | a0001c0002t0023 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 333 | chr5 | 79685606 | ||||||
| chr5:79685727 | G | T | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
151 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 454 | chr5 | 79685727 | ||||||
| chr5:79686102 | A | G | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*829A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 829 | chr5 | 79686102 | ||||||
| chr5:79686296 | A | C | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1023A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1023 | chr5 | 79686296 | ||||||
| chr5:79686365 | T | G | 9 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0014 others(6): Show |
37 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1092 | chr5 | 79686365 | ||||||
| chr5:79686740 | C | A | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1467C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1467 | chr5 | 79686740 | ||||||
| chr5:79686869 | A | G | 1 | a0001c0001t0035 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1596A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1596 | chr5 | 79686869 | ||||||
| chr5:79686962 | T | C | 2 | a0001c0001t0019 a0001c0001t0020 |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1689T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1689 | chr5 | 79686962 | ||||||
| chr5:79687096 | T | C | 1 | a0001c0001t0029 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1823 | chr5 | 79687096 | ||||||
| chr5:79687133 | G | GCTT | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*1861_*1863dupCTT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 1864 | INFO_REALIGN_3_PRIME | chr5 | 79687133 | |||||
| chr5:79687295 | T | C | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2022T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2022 | chr5 | 79687295 | ||||||
| chr5:79687555 | A | G | 1 | a0001c0001t0033 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2282A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2282 | chr5 | 79687555 | ||||||
| chr5:79687594 | A | G | 10 | a0001c0001t0011 a0001c0001t0012 a0001c0001t0013 others(7): Show |
19 | HG01109.hp1 HG01243.hp2 HG01255.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2321A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2321 | chr5 | 79687594 | ||||||
| chr5:79687614 | C | T | 1 | a0001c0001t0037 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2341 | chr5 | 79687614 | ||||||
| chr5:79687690 | A | G | 7 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(4): Show |
33 | HG00408.hp2 HG00558.hp1 HG01515.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2417A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2417 | chr5 | 79687690 | ||||||
| chr5:79687705 | C | T | 1 | a0001c0001t0032 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2432C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2432 | chr5 | 79687705 | ||||||
| chr5:79687775 | A | C | 11 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0016 others(8): Show |
40 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2502A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2502 | chr5 | 79687775 | ||||||
| chr5:79687876 | G | A | 1 | a0001c0001t0044 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2603G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2603 | chr5 | 79687876 | ||||||
| chr5:79687877 | C | A | 1 | a0001c0007t0025 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2604C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2604 | chr5 | 79687877 | ||||||
| chr5:79687995 | G | GAAT | 24 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(21): Show |
104 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2725_*2727dupTAA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2728 | INFO_REALIGN_3_PRIME | chr5 | 79687995 | |||||
| chr5:79688036 | G | A | 1 | a0001c0001t0030 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2763G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2763 | chr5 | 79688036 | ||||||
| chr5:79688130 | A | G | 1 | a0001c0001t0031 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2857A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2857 | chr5 | 79688130 | ||||||
| chr5:79688223 | A | G | 11 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0018 others(8): Show |
33 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2950A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 15/15 | 2950 | chr5 | 79688223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:79613140 | A | G | 1 | a0001c0001t0006g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+65A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613140 | |||||||
| chr5:79613501 | T | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+426T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613501 | |||||||
| chr5:79613703 | C | T | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+628C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79613703 | |||||||
| chr5:79614091 | C | CT | 34 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.-38+1043dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614091 | CT | C | 18 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(15): Show |
18 | HG01175.hp2 HG01433.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-38+1043delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614091 | CTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(87): Show |
94 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.-38+1042_-38+1043d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614091 | CTTT | C | 96 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(93): Show |
104 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.-38+1041_-38+1043d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614091 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0041g0111 a0001c0001t0045g0018 |
2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-38+1034_-38+1043d others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614091 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0036g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-38+1031_-38+1043d others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614091 | ||||||
| chr5:79614119 | G | T | 1 | a0001c0001t0001g0320 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-38+1044G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614119 | |||||||
| chr5:79614135 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+1060A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614135 | |||||||
| chr5:79614309 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(31): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.-38+1234G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614309 | |||||||
| chr5:79614425 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+1350C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614425 | |||||||
| chr5:79614704 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-38+1629G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614704 | |||||||
| chr5:79614780 | A | T | 1 | a0001c0001t0016g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+1705A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614780 | |||||||
| chr5:79614808 | TTA | T | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1735_-38+1736d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79614808 | ||||||
| chr5:79614952 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+1877G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79614952 | |||||||
| chr5:79615253 | C | T | 1 | a0001c0002t0023g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-38+2178C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615253 | |||||||
| chr5:79615370 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+2295G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615370 | |||||||
| chr5:79615486 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+2411A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615486 | |||||||
| chr5:79615549 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-38+2474C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615549 | |||||||
| chr5:79615641 | G | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+2566G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615641 | |||||||
| chr5:79615709 | C | CT | 100 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(97): Show |
106 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.-38+2646dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79615709 | ||||||
| chr5:79615788 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-38+2713C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615788 | |||||||
| chr5:79615807 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-38+2732G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615807 | |||||||
| chr5:79615815 | C | T | 1 | a0001c0001t0005g0127 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-38+2740C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615815 | |||||||
| chr5:79615991 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+2916C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79615991 | |||||||
| chr5:79616003 | C | G | 1 | a0001c0001t0001g0286 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-38+2928C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616003 | |||||||
| chr5:79616008 | C | T | 5 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0190 others(2): Show |
5 | HG00280.hp1 NA18960.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+2933C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616008 | |||||||
| chr5:79616067 | A | G | 1 | a0001c0001t0006g0285 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+2992A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616067 | |||||||
| chr5:79616076 | G | A | 56 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(53): Show |
61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.-38+3001G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616076 | |||||||
| chr5:79616077 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-38+3002G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616077 | |||||||
| chr5:79616121 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-38+3046A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616121 | |||||||
| chr5:79616140 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-38+3065G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616140 | |||||||
| chr5:79616152 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0212 a0001c0001t0017g0134 |
3 | HG02630.hp1 HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38+3077G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616152 | |||||||
| chr5:79616189 | A | AT | 29 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0209 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.-38+3140dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | ||||||
| chr5:79616189 | AT | A | 15 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
15 | HG01074.hp2 HG01255.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+3140delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | ||||||
| chr5:79616189 | ATT | A | 8 | a0001c0001t0002g0070 a0001c0001t0004g0040 a0001c0001t0004g0086 others(5): Show |
8 | HG01934.hp2 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38+3139_-38+3140d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | ||||||
| chr5:79616189 | ATTT | A | 94 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(91): Show |
101 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.-38+3138_-38+3140d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616189 | ||||||
| chr5:79616262 | G | A | 1 | a0001c0001t0018g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-38+3187G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616262 | |||||||
| chr5:79616285 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-38+3210G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616285 | |||||||
| chr5:79616474 | C | T | 3 | a0001c0002t0002g0069 a0001c0002t0002g0103 a0001c0002t0023g0107 |
3 | HG02738.hp1 HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-37-3138C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616474 | |||||||
| chr5:79616475 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-37-3137G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616475 | |||||||
| chr5:79616557 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-3055A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616557 | |||||||
| chr5:79616671 | T | TTG | 204 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(201): Show |
216 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.-37-2940_-37-2939i others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79616671 | ||||||
| chr5:79616779 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-37-2833T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616779 | |||||||
| chr5:79616889 | A | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-2723A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616889 | |||||||
| chr5:79616916 | A | G | 2 | a0001c0001t0004g0006 a0001c0001t0016g0041 |
3 | HG02280.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-2696A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616916 | |||||||
| chr5:79616970 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-2642A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616970 | |||||||
| chr5:79616973 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-37-2639G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79616973 | |||||||
| chr5:79617016 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2596C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617016 | |||||||
| chr5:79617017 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2595T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617017 | |||||||
| chr5:79617018 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-37-2594C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617018 | |||||||
| chr5:79617020 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-37-2592C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617020 | |||||||
| chr5:79617060 | A | G | 1 | a0001c0001t0005g0123 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-37-2552A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617060 | |||||||
| chr5:79617128 | A | C | 7 | a0001c0001t0005g0002 a0001c0001t0005g0121 a0001c0001t0005g0122 others(4): Show |
8 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-2484A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617128 | |||||||
| chr5:79617482 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-2130A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617482 | |||||||
| chr5:79617514 | A | G | 3 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0312 |
3 | HG02886.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-37-2098A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617514 | |||||||
| chr5:79617530 | A | G | 1 | a0001c0001t0015g0284 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-37-2082A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617530 | |||||||
| chr5:79617530 | A | T | 1 | a0001c0001t0006g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-37-2082A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617530 | |||||||
| chr5:79617597 | C | T | 12 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0004g0013 others(9): Show |
12 | HG01167.hp2 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-2015C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617597 | |||||||
| chr5:79617618 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1994G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617618 | |||||||
| chr5:79617816 | T | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1796T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617816 | |||||||
| chr5:79617926 | T | C | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-37-1686T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79617926 | |||||||
| chr5:79618402 | A | AT | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.-37-1198dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79618402 | ||||||
| chr5:79618412 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-37-1200T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618412 | |||||||
| chr5:79618484 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1128C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618484 | |||||||
| chr5:79618524 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-1088A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618524 | |||||||
| chr5:79618594 | G | GT | 32 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0182 others(29): Show |
33 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-37-1008dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 79618594 | ||||||
| chr5:79618728 | G | A | 7 | a0001c0001t0001g0149 a0001c0001t0019g0128 a0001c0001t0019g0129 others(4): Show |
7 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-884G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618728 | |||||||
| chr5:79618739 | C | T | 1 | a0001c0001t0008g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-37-873C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79618739 | |||||||
| chr5:79619050 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.-37-562A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619050 | |||||||
| chr5:79619082 | C | G | 8 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0087 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-530C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619082 | |||||||
| chr5:79619292 | G | A | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-320G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619292 | |||||||
| chr5:79619308 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-37-304G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619308 | |||||||
| chr5:79619399 | A | G | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37-213A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619399 | |||||||
| chr5:79619461 | C | A | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-151C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 1/14 | chr5 | 79619461 | |||||||
| chr5:79619839 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0028g0313 |
2 | HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.137+54G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/14 | chr5 | 79619839 | |||||||
| chr5:79619870 | A | C | 3 | a0001c0001t0001g0213 a0001c0001t0001g0269 a0001c0001t0001g0311 |
3 | HG01516.hp2 HG01517.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.137+85A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 2/14 | chr5 | 79619870 | |||||||
| chr5:79620169 | A | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(54): Show |
61 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.227+86A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620169 | |||||||
| chr5:79620774 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.227+691G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620774 | |||||||
| chr5:79620895 | A | T | 1 | a0001c0001t0002g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.227+812A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79620895 | |||||||
| chr5:79620924 | CAATT | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.227+846_227+849del others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79620924 | ||||||
| chr5:79621003 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.227+920C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621003 | |||||||
| chr5:79621068 | C | T | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227+985C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621068 | |||||||
| chr5:79621105 | TA | T | 82 | a0001c0001t0001g0211 a0001c0001t0001g0283 a0001c0001t0002g0077 others(79): Show |
85 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.227+1034delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621105 | ||||||
| chr5:79621105 | TAA | T | 55 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(52): Show |
60 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.227+1033_227+1034d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621105 | ||||||
| chr5:79621578 | G | A | 1 | a0001c0001t0005g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.227+1495G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621578 | |||||||
| chr5:79621640 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.227+1557C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621640 | |||||||
| chr5:79621757 | C | CA | 15 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(12): Show |
15 | HG00099.hp2 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.228-1480dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79621757 | ||||||
| chr5:79621765 | A | AC | 100 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(97): Show |
107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.228-1487_228-1486i others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621765 | |||||||
| chr5:79621765 | A | C | 1 | a0001c0001t0004g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.228-1487A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621765 | |||||||
| chr5:79621769 | A | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.228-1483A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621769 | |||||||
| chr5:79621776 | A | AC | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1476_228-1475i others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621776 | |||||||
| chr5:79621780 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1472A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621780 | |||||||
| chr5:79621782 | C | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-1470C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621782 | |||||||
| chr5:79621991 | C | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0080 a0001c0001t0011g0020 |
3 | HG03139.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.228-1261C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79621991 | |||||||
| chr5:79622173 | C | T | 2 | a0001c0001t0042g0321 a0001c0001t0045g0018 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.228-1079C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622173 | |||||||
| chr5:79622194 | A | G | 1 | a0001c0001t0017g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.228-1058A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622194 | |||||||
| chr5:79622261 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-991C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622261 | |||||||
| chr5:79622276 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.228-976C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622276 | |||||||
| chr5:79622293 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-959T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622293 | |||||||
| chr5:79622556 | G | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-696G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622556 | |||||||
| chr5:79622622 | G | C | 1 | a0001c0001t0041g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.228-630G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622622 | |||||||
| chr5:79622642 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-610C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622642 | |||||||
| chr5:79622737 | A | G | 1 | a0001c0002t0003g0044 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.228-515A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622737 | |||||||
| chr5:79622772 | G | A | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-480G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622772 | |||||||
| chr5:79622780 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.228-472A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622780 | |||||||
| chr5:79622786 | T | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.228-466T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | chr5 | 79622786 | |||||||
| chr5:79623054 | A | AT | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.228-190dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79623054 | ||||||
| chr5:79623054 | AT | A | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.228-190delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 79623054 | ||||||
| chr5:79623602 | A | G | 1 | a0001c0007t0025g0108 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.465+113A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623602 | |||||||
| chr5:79623779 | G | GA | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+302dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79623779 | ||||||
| chr5:79623947 | C | T | 2 | a0001c0001t0007g0191 a0001c0001t0007g0210 |
2 | HG00280.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.465+458C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623947 | |||||||
| chr5:79623993 | A | T | 1 | a0001c0001t0001g0265 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+504A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79623993 | |||||||
| chr5:79624254 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+765G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624254 | |||||||
| chr5:79624340 | T | C | 1 | a0001c0001t0018g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.465+851T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624340 | |||||||
| chr5:79624374 | A | G | 5 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0308 others(2): Show |
5 | NA18978.hp1 NA18995.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+885A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624374 | |||||||
| chr5:79624380 | G | C | 1 | a0001c0001t0006g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.465+891G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624380 | |||||||
| chr5:79624411 | T | C | 8 | a0001c0001t0001g0137 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | NA18955.hp1 NA18965.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+922T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624411 | |||||||
| chr5:79624427 | T | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+938T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624427 | |||||||
| chr5:79624449 | A | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0195 a0001c0001t0001g0199 others(41): Show |
46 | HG00408.hp1 HG01256.hp1 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.465+960A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624449 | |||||||
| chr5:79624585 | C | T | 2 | a0001c0001t0038g0218 a0001c0001t0041g0111 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.465+1096C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624585 | |||||||
| chr5:79624688 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+1199T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624688 | |||||||
| chr5:79624701 | C | T | 1 | a0001c0001t0046g0067 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.465+1212C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624701 | |||||||
| chr5:79624723 | A | G | 1 | a0001c0001t0026g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.465+1234A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624723 | |||||||
| chr5:79624729 | A | T | 1 | a0001c0001t0001g0307 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.465+1240A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79624729 | |||||||
| chr5:79625224 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.465+1735T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625224 | |||||||
| chr5:79625550 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+2061C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625550 | |||||||
| chr5:79625636 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+2147A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625636 | |||||||
| chr5:79625834 | GT | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.465+2358delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79625834 | ||||||
| chr5:79625946 | C | T | 1 | a0001c0001t0036g0110 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.465+2457C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79625946 | |||||||
| chr5:79626072 | C | CCACTTTG others(7): Show |
1 | a0001c0001t0003g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.465+2596_465+2597i others(16): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626072 | ||||||
| chr5:79626120 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+2631C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626120 | |||||||
| chr5:79626277 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.465+2788C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626277 | |||||||
| chr5:79626306 | A | AT | 18 | a0001c0001t0001g0214 a0001c0001t0001g0220 a0001c0001t0001g0223 others(15): Show |
18 | HG00639.hp2 HG02055.hp1 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.465+2836dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626306 | ||||||
| chr5:79626306 | AT | A | 28 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.465+2836delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626306 | ||||||
| chr5:79626408 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.465+2919C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626408 | |||||||
| chr5:79626489 | A | G | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.465+3000A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626489 | |||||||
| chr5:79626619 | T | C | 2 | a0001c0001t0007g0188 a0001c0001t0007g0190 |
2 | NA18972.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.465+3130T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626619 | |||||||
| chr5:79626625 | A | AT | 144 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(141): Show |
152 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.465+3152dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626625 | ||||||
| chr5:79626625 | A | ATT | 58 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(55): Show |
62 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.465+3151_465+3152d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79626625 | ||||||
| chr5:79626789 | G | GTAATGCC others(2): Show |
103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+3300_465+3301i others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626789 | |||||||
| chr5:79626832 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+3343A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626832 | |||||||
| chr5:79626835 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.465+3346G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79626835 | |||||||
| chr5:79627091 | C | G | 3 | a0001c0001t0001g0286 a0001c0001t0018g0243 a0001c0001t0031g0242 |
3 | HG02451.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.465+3602C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627091 | |||||||
| chr5:79627096 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.465+3607G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627096 | |||||||
| chr5:79627129 | C | CA | 49 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(46): Show |
50 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.465+3655dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | ||||||
| chr5:79627129 | C | CAA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(144): Show |
158 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.465+3654_465+3655d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | ||||||
| chr5:79627129 | C | CAAA | 11 | a0001c0001t0001g0138 a0001c0001t0001g0156 a0001c0001t0001g0157 others(8): Show |
11 | HG00597.hp2 HG01109.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.465+3653_465+3655d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627129 | ||||||
| chr5:79627155 | T | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+3666T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627155 | |||||||
| chr5:79627221 | G | C | 1 | a0001c0001t0004g0036 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.465+3732G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627221 | |||||||
| chr5:79627235 | C | G | 1 | a0001c0002t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.465+3746C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627235 | |||||||
| chr5:79627268 | GAACT | G | 3 | a0001c0001t0009g0038 a0001c0001t0009g0039 a0001c0001t0009g0085 |
3 | HG01891.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.465+3788_465+3791d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79627268 | ||||||
| chr5:79627495 | C | T | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+4006C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627495 | |||||||
| chr5:79627507 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4018C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627507 | |||||||
| chr5:79627735 | T | A | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.465+4246T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627735 | |||||||
| chr5:79627847 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.465+4358G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627847 | |||||||
| chr5:79627895 | C | T | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+4406C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627895 | |||||||
| chr5:79627900 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4411A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627900 | |||||||
| chr5:79627955 | A | G | 1 | a0001c0001t0018g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.465+4466A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79627955 | |||||||
| chr5:79628017 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+4528G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628017 | |||||||
| chr5:79628189 | C | T | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+4700C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628189 | |||||||
| chr5:79628199 | G | A | 56 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(53): Show |
61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.465+4710G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628199 | |||||||
| chr5:79628276 | G | A | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.465+4787G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628276 | |||||||
| chr5:79628465 | C | T | 1 | a0001c0001t0014g0120 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.465+4976C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628465 | |||||||
| chr5:79628490 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+5001T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628490 | |||||||
| chr5:79628682 | T | G | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+5193T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628682 | |||||||
| chr5:79628780 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.465+5291A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628780 | |||||||
| chr5:79628786 | C | T | 1 | a0001c0001t0015g0282 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.465+5297C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79628786 | |||||||
| chr5:79629017 | G | C | 1 | a0001c0001t0033g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.465+5528G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629017 | |||||||
| chr5:79629068 | AG | A | 4 | a0001c0001t0004g0035 a0001c0001t0009g0038 a0001c0001t0009g0039 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+5581delG | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629068 | ||||||
| chr5:79629482 | A | G | 7 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0087 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+5993A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629482 | |||||||
| chr5:79629543 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.465+6054A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629543 | |||||||
| chr5:79629603 | GGATCACG others(4319): Show |
G | 1 | a0001c0001t0001g0268 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.465+6155_466-6882d others(2): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629603 | ||||||
| chr5:79629688 | G | A | 57 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(54): Show |
62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.465+6199G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629688 | |||||||
| chr5:79629817 | ACT | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6331_465+6332d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629817 | ||||||
| chr5:79629887 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6398G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629887 | |||||||
| chr5:79629920 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6431A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79629920 | |||||||
| chr5:79629958 | A | AC | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6473dupC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79629958 | ||||||
| chr5:79630083 | C | G | 69 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(66): Show |
74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.465+6594C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630083 | |||||||
| chr5:79630089 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.465+6600C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630089 | |||||||
| chr5:79630130 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+6641G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630130 | |||||||
| chr5:79630201 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.465+6712G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630201 | |||||||
| chr5:79630253 | G | A | 4 | a0001c0001t0003g0005 a0001c0001t0003g0022 a0001c0001t0003g0024 others(1): Show |
4 | HG03654.hp2 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+6764G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630253 | |||||||
| chr5:79630365 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+6876G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630365 | |||||||
| chr5:79630624 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.465+7135T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630624 | |||||||
| chr5:79630739 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+7250A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630739 | |||||||
| chr5:79630804 | G | A | 3 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0012g0104 |
3 | HG02486.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.465+7315G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79630804 | |||||||
| chr5:79630817 | G | GT | 109 | a0001c0001t0001g0198 a0001c0001t0001g0223 a0001c0001t0001g0231 others(106): Show |
115 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(112): Show |
intron_variant | MODIFIER | c.465+7344dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | ||||||
| chr5:79630817 | G | GTT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(51): Show |
59 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.465+7343_465+7344d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | ||||||
| chr5:79630817 | GT | G | 9 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG02055.hp1 HG02132.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.465+7344delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79630817 | ||||||
| chr5:79631137 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+7648A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631137 | |||||||
| chr5:79631144 | A | G | 1 | a0001c0002t0002g0099 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.465+7655A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631144 | |||||||
| chr5:79631162 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7673C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631162 | |||||||
| chr5:79631195 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+7706A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631195 | |||||||
| chr5:79631230 | T | C | 1 | a0001c0001t0005g0144 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.465+7741T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631230 | |||||||
| chr5:79631260 | G | C | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.465+7771G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631260 | |||||||
| chr5:79631335 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.465+7846G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631335 | |||||||
| chr5:79631519 | T | C | 2 | a0001c0001t0008g0248 a0001c0001t0008g0259 |
2 | NA18965.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.465+8030T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631519 | |||||||
| chr5:79631537 | C | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+8048C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631537 | |||||||
| chr5:79631567 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.465+8078G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631567 | |||||||
| chr5:79631595 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8106G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631595 | |||||||
| chr5:79631657 | G | T | 1 | a0001c0001t0001g0295 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.465+8168G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631657 | |||||||
| chr5:79631818 | A | G | 1 | a0001c0001t0007g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.465+8329A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631818 | |||||||
| chr5:79631837 | G | A | 2 | a0001c0001t0005g0115 a0001c0001t0005g0144 |
2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.465+8348G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631837 | |||||||
| chr5:79631884 | TAGG | T | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.465+8401_465+8403d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79631884 | ||||||
| chr5:79631927 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.465+8438C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631927 | |||||||
| chr5:79631975 | G | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8486G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631975 | |||||||
| chr5:79631986 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.465+8497C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79631986 | |||||||
| chr5:79632166 | A | G | 8 | a0001c0001t0001g0137 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | NA18955.hp1 NA18965.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+8677A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632166 | |||||||
| chr5:79632254 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-8597T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632254 | |||||||
| chr5:79632274 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.466-8577A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632274 | |||||||
| chr5:79632726 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0018g0135 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466-8125G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632726 | |||||||
| chr5:79632731 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-8120G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632731 | |||||||
| chr5:79632753 | G | GACTCT | 5 | a0001c0001t0002g0046 a0001c0001t0002g0068 a0001c0001t0002g0071 others(2): Show |
5 | HG02165.hp1 NA18950.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-8097_466-8093d others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79632753 | ||||||
| chr5:79632801 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-8050C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632801 | |||||||
| chr5:79632806 | A | G | 1 | a0001c0001t0003g0011 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.466-8045A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632806 | |||||||
| chr5:79632926 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.466-7925C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632926 | |||||||
| chr5:79632962 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7889A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79632962 | |||||||
| chr5:79633015 | A | G | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-7836A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633015 | |||||||
| chr5:79633090 | T | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0297 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.466-7761T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633090 | |||||||
| chr5:79633093 | A | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-7758A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633093 | |||||||
| chr5:79633121 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.466-7730G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633121 | |||||||
| chr5:79633122 | G | A | 2 | a0001c0001t0003g0005 a0001c0001t0003g0022 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.466-7729G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633122 | |||||||
| chr5:79633183 | C | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7668C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633183 | |||||||
| chr5:79633212 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7639T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633212 | |||||||
| chr5:79633239 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7612A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633239 | |||||||
| chr5:79633413 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7438C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633413 | |||||||
| chr5:79633432 | G | GT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0152 others(64): Show |
67 | HG00544.hp1 HG00609.hp1 HG01167.hp2 others(64): Show |
intron_variant | MODIFIER | c.466-7394dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | ||||||
| chr5:79633432 | G | GTT | 9 | a0001c0001t0001g0228 a0001c0001t0002g0063 a0001c0001t0002g0077 others(6): Show |
9 | HG00597.hp1 HG02486.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-7395_466-7394d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | ||||||
| chr5:79633432 | G | GTTT | 21 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(18): Show |
21 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-7396_466-7394d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | ||||||
| chr5:79633432 | G | GTTTT | 9 | a0001c0001t0005g0002 a0001c0001t0005g0121 a0001c0001t0005g0122 others(6): Show |
9 | HG02080.hp1 HG02602.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.466-7397_466-7394d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | ||||||
| chr5:79633432 | GT | G | 8 | a0001c0001t0002g0010 a0001c0001t0011g0037 a0001c0001t0019g0128 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-7394delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633432 | ||||||
| chr5:79633458 | G | A | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-7393G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633458 | |||||||
| chr5:79633502 | T | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-7349T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633502 | |||||||
| chr5:79633605 | G | A | 1 | a0001c0001t0007g0189 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.466-7246G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633605 | |||||||
| chr5:79633635 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.466-7216C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633635 | |||||||
| chr5:79633721 | G | GT | 18 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(15): Show |
18 | HG01109.hp2 HG01884.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.466-7112dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633721 | ||||||
| chr5:79633721 | GTTTTTT | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.466-7117_466-7112d others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633721 | ||||||
| chr5:79633935 | C | T | 2 | a0001c0001t0014g0119 a0001c0001t0014g0120 |
2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.466-6916C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633935 | |||||||
| chr5:79633950 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.466-6901G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633950 | |||||||
| chr5:79633953 | A | T | 15 | a0001c0002t0002g0012 a0001c0002t0002g0042 a0001c0002t0002g0057 others(12): Show |
16 | HG00544.hp2 HG01433.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.466-6898A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79633953 | |||||||
| chr5:79633997 | C | CA | 29 | a0001c0001t0001g0136 a0001c0001t0001g0150 a0001c0001t0001g0159 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.466-6832dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | ||||||
| chr5:79633997 | CAAA | C | 9 | a0001c0001t0002g0046 a0001c0001t0002g0063 a0001c0001t0020g0131 others(6): Show |
9 | HG02622.hp2 HG03669.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.466-6834_466-6832d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | ||||||
| chr5:79633997 | CAAAA | C | 93 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(90): Show |
100 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.466-6835_466-6832d others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79633997 | ||||||
| chr5:79634041 | C | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-6810C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634041 | |||||||
| chr5:79634091 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.466-6760G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634091 | |||||||
| chr5:79634092 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.466-6759C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634092 | |||||||
| chr5:79634114 | C | T | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-6737C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634114 | |||||||
| chr5:79634137 | A | G | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-6714A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634137 | |||||||
| chr5:79634154 | C | CA | 21 | a0001c0001t0001g0133 a0001c0001t0001g0161 a0001c0001t0001g0204 others(18): Show |
21 | HG00597.hp1 HG00639.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.466-6678dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634154 | ||||||
| chr5:79634154 | CA | C | 28 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0318 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-6678delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634154 | ||||||
| chr5:79634170 | A | C | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-6681A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634170 | |||||||
| chr5:79634210 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.466-6641T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634210 | |||||||
| chr5:79634237 | A | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6614A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634237 | |||||||
| chr5:79634248 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-6603T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634248 | |||||||
| chr5:79634278 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.466-6573G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634278 | |||||||
| chr5:79634286 | A | T | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.466-6565A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634286 | |||||||
| chr5:79634447 | C | T | 1 | a0001c0001t0041g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.466-6404C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634447 | |||||||
| chr5:79634482 | A | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.466-6369A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634482 | |||||||
| chr5:79634618 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(153): Show |
167 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.466-6233T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634618 | |||||||
| chr5:79634715 | A | G | 57 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(54): Show |
62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.466-6136A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634715 | |||||||
| chr5:79634735 | ATAGCCTA others(34): Show |
A | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-6103_466-6063d others(43): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79634735 | ||||||
| chr5:79634839 | A | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-6012A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634839 | |||||||
| chr5:79634874 | G | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.466-5977G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79634874 | |||||||
| chr5:79635058 | G | A | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466-5793G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635058 | |||||||
| chr5:79635164 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5687C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635164 | |||||||
| chr5:79635215 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5636G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635215 | |||||||
| chr5:79635420 | G | A | 5 | a0001c0001t0001g0214 a0001c0001t0001g0251 a0001c0001t0001g0266 others(2): Show |
5 | NA18940.hp2 NA18952.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-5431G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635420 | |||||||
| chr5:79635624 | G | A | 1 | a0001c0001t0005g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.466-5227G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635624 | |||||||
| chr5:79635636 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-5215C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635636 | |||||||
| chr5:79635678 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.466-5173C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635678 | |||||||
| chr5:79635689 | A | G | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-5162A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635689 | |||||||
| chr5:79635897 | G | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-4954G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79635897 | |||||||
| chr5:79636061 | G | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.466-4790G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636061 | |||||||
| chr5:79636096 | A | G | 1 | a0001c0001t0003g0011 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.466-4755A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636096 | |||||||
| chr5:79636428 | C | T | 3 | a0001c0001t0002g0010 a0001c0001t0002g0066 a0001c0001t0002g0088 |
4 | NA18945.hp2 NA18972.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-4423C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636428 | |||||||
| chr5:79636628 | A | G | 1 | a0001c0001t0012g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.466-4223A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636628 | |||||||
| chr5:79636676 | G | C | 19 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(16): Show |
21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-4175G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636676 | |||||||
| chr5:79636894 | G | A | 1 | a0001c0001t0006g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.466-3957G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79636894 | |||||||
| chr5:79637127 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0018g0135 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.466-3724G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637127 | |||||||
| chr5:79637129 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.466-3722A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637129 | |||||||
| chr5:79637229 | C | CA | 28 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(25): Show |
29 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.466-3610dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | ||||||
| chr5:79637229 | CA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(51): Show |
58 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.466-3610delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | ||||||
| chr5:79637229 | CAA | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-3611_466-3610d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637229 | ||||||
| chr5:79637473 | C | T | 1 | a0001c0001t0006g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.466-3378C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637473 | |||||||
| chr5:79637628 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0225 others(8): Show |
14 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-3223T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637628 | |||||||
| chr5:79637798 | C | CT | 99 | a0001c0001t0001g0177 a0001c0001t0001g0208 a0001c0001t0001g0244 others(96): Show |
106 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(103): Show |
intron_variant | MODIFIER | c.466-3036dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | ||||||
| chr5:79637798 | C | CTT | 8 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0003g0055 others(5): Show |
8 | HG02055.hp2 HG02273.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-3037_466-3036d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | ||||||
| chr5:79637798 | CT | C | 7 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0004g0013 others(4): Show |
7 | HG02486.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-3036delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79637798 | ||||||
| chr5:79637814 | T | G | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.466-3037T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637814 | |||||||
| chr5:79637821 | G | A | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.466-3030G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637821 | |||||||
| chr5:79637827 | G | A | 1 | a0001c0001t0008g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466-3024G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637827 | |||||||
| chr5:79637880 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0310 |
2 | NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.466-2971C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637880 | |||||||
| chr5:79637923 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.466-2928A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79637923 | |||||||
| chr5:79638044 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-2807T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638044 | |||||||
| chr5:79638318 | C | A | 14 | a0001c0001t0004g0023 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.466-2533C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638318 | |||||||
| chr5:79638506 | T | C | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466-2345T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638506 | |||||||
| chr5:79638733 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-2118C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638733 | |||||||
| chr5:79638768 | A | G | 1 | a0001c0001t0029g0240 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.466-2083A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638768 | |||||||
| chr5:79638797 | G | T | 7 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0087 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.466-2054G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638797 | |||||||
| chr5:79638909 | G | C | 1 | a0001c0001t0002g0077 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.466-1942G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638909 | |||||||
| chr5:79638990 | G | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0192 |
2 | HG02074.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.466-1861G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79638990 | |||||||
| chr5:79639012 | A | G | 1 | a0001c0002t0012g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.466-1839A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639012 | |||||||
| chr5:79639047 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-1804T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639047 | |||||||
| chr5:79639119 | C | G | 1 | a0001c0001t0008g0176 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.466-1732C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639119 | |||||||
| chr5:79639330 | A | C | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.466-1521A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639330 | |||||||
| chr5:79639374 | G | T | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.466-1477G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639374 | |||||||
| chr5:79639477 | G | GT | 18 | a0001c0001t0003g0073 a0001c0001t0004g0013 a0001c0001t0004g0074 others(15): Show |
18 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.466-1362dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | ||||||
| chr5:79639477 | G | GTT | 69 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(66): Show |
74 | HG00673.hp2 HG01515.hp2 HG01517.hp2 others(71): Show |
intron_variant | MODIFIER | c.466-1363_466-1362d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | ||||||
| chr5:79639477 | G | GTTT | 21 | a0001c0001t0003g0054 a0001c0001t0011g0009 a0001c0001t0011g0096 others(18): Show |
23 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.466-1364_466-1362d others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79639477 | ||||||
| chr5:79639805 | C | A | 19 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(16): Show |
21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.466-1046C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79639805 | |||||||
| chr5:79640068 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-783G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640068 | |||||||
| chr5:79640170 | C | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-681C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640170 | |||||||
| chr5:79640255 | CA | C | 150 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(147): Show |
158 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.466-580delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79640255 | ||||||
| chr5:79640274 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.466-577T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640274 | |||||||
| chr5:79640306 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.466-545T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640306 | |||||||
| chr5:79640373 | C | T | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.466-478C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640373 | |||||||
| chr5:79640457 | C | T | 5 | a0001c0001t0003g0048 a0001c0001t0003g0054 a0001c0001t0011g0009 others(2): Show |
6 | HG00741.hp2 HG01109.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-394C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640457 | |||||||
| chr5:79640514 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0268 others(1): Show |
4 | HG02080.hp2 HG02165.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-337T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640514 | |||||||
| chr5:79640694 | A | C | 1 | a0001c0002t0002g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.466-157A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640694 | |||||||
| chr5:79640775 | AT | A | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.466-73delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr5 | 79640775 | ||||||
| chr5:79640838 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.466-13C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 4/14 | chr5 | 79640838 | |||||||
| chr5:79641079 | C | T | 7 | a0001c0001t0001g0239 a0001c0001t0001g0283 a0001c0001t0001g0296 others(4): Show |
7 | HG00609.hp1 NA18941.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.581-26C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 5/14 | chr5 | 79641079 | |||||||
| chr5:79641089 | T | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0093 a0001c0001t0002g0101 |
3 | NA18940.hp1 NA19002.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.581-16T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 5/14 | chr5 | 79641089 | |||||||
| chr5:79641437 | GT | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+254delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 79641437 | ||||||
| chr5:79641444 | T | C | 3 | a0001c0001t0004g0026 a0001c0001t0004g0027 a0001c0001t0004g0081 |
3 | HG02559.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.672+248T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641444 | |||||||
| chr5:79641498 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+302C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641498 | |||||||
| chr5:79641539 | T | C | 1 | a0001c0001t0046g0067 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.672+343T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641539 | |||||||
| chr5:79641686 | C | G | 1 | a0001c0001t0012g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.672+490C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641686 | |||||||
| chr5:79641707 | TG | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+512delG | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641707 | |||||||
| chr5:79641786 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.672+590G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79641786 | |||||||
| chr5:79642286 | T | C | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-546T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642286 | |||||||
| chr5:79642379 | C | T | 1 | a0001c0001t0041g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.673-453C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642379 | |||||||
| chr5:79642492 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(206): Show |
221 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.673-340A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 6/14 | chr5 | 79642492 | |||||||
| chr5:79643308 | T | G | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.751+398T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643308 | |||||||
| chr5:79643319 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.751+409T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643319 | |||||||
| chr5:79643518 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+608C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643518 | |||||||
| chr5:79643705 | A | C | 1 | a0001c0001t0003g0019 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.751+795A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643705 | |||||||
| chr5:79643724 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+814C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643724 | |||||||
| chr5:79643728 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.751+818A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643728 | |||||||
| chr5:79643956 | C | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+1046C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79643956 | |||||||
| chr5:79643986 | C | CT | 80 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0203 others(77): Show |
88 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.751+1090dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79643986 | ||||||
| chr5:79643986 | C | CTT | 26 | a0001c0001t0003g0021 a0001c0001t0003g0025 a0001c0001t0003g0080 others(23): Show |
26 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.751+1089_751+1090d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79643986 | ||||||
| chr5:79644019 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.752-1104A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644019 | |||||||
| chr5:79644023 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0018g0135 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.752-1100C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644023 | |||||||
| chr5:79644024 | G | A | 3 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0040g0142 |
3 | HG02486.hp2 HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.752-1099G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644024 | |||||||
| chr5:79644084 | C | A | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.752-1039C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644084 | |||||||
| chr5:79644084 | C | T | 1 | a0001c0001t0020g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.752-1039C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644084 | |||||||
| chr5:79644213 | C | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.752-910C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644213 | |||||||
| chr5:79644316 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-807G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644316 | |||||||
| chr5:79644369 | T | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-754T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644369 | |||||||
| chr5:79644469 | T | G | 1 | a0001c0001t0007g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.752-654T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644469 | |||||||
| chr5:79644525 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.752-598T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644525 | |||||||
| chr5:79644591 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.752-532C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644591 | |||||||
| chr5:79644837 | C | T | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-286C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644837 | |||||||
| chr5:79644960 | C | T | 19 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(16): Show |
21 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.752-163C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644960 | |||||||
| chr5:79644962 | A | C | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.752-161A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79644962 | |||||||
| chr5:79645044 | A | AT | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-73dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | 79645044 | ||||||
| chr5:79645055 | A | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.752-68A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 7/14 | chr5 | 79645055 | |||||||
| chr5:79645526 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.821+334A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645526 | |||||||
| chr5:79645550 | C | T | 1 | a0001c0001t0005g0122 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+358C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645550 | |||||||
| chr5:79645745 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.821+553A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645745 | |||||||
| chr5:79645839 | CCACAAAC others(1): Show |
C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.821+652_821+659del others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 79645839 | ||||||
| chr5:79645858 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.821+666C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645858 | |||||||
| chr5:79645930 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.821+738C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645930 | |||||||
| chr5:79645978 | C | T | 1 | a0001c0001t0026g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.821+786C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79645978 | |||||||
| chr5:79646028 | A | G | 1 | a0001c0001t0006g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.821+836A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646028 | |||||||
| chr5:79646180 | G | A | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+988G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646180 | |||||||
| chr5:79646442 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.821+1250C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646442 | |||||||
| chr5:79646508 | C | T | 1 | a0001c0001t0012g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.821+1316C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646508 | |||||||
| chr5:79646713 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.821+1521G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646713 | |||||||
| chr5:79646769 | CTT | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
109 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(106): Show |
intron_variant | MODIFIER | c.821+1591_821+1592d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr5 | 79646769 | ||||||
| chr5:79646966 | G | A | 1 | a0001c0001t0004g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.822-1651G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79646966 | |||||||
| chr5:79647013 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.822-1604T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647013 | |||||||
| chr5:79647269 | G | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.822-1348G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647269 | |||||||
| chr5:79647336 | A | G | 6 | a0001c0001t0002g0045 a0001c0001t0002g0064 a0001c0001t0002g0092 others(3): Show |
6 | HG04228.hp2 NA18940.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-1281A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647336 | |||||||
| chr5:79647807 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-810C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647807 | |||||||
| chr5:79647825 | G | C | 104 | a0001c0001t0001g0158 a0001c0001t0002g0008 a0001c0001t0002g0010 others(101): Show |
111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.822-792G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79647825 | |||||||
| chr5:79648008 | T | G | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-609T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648008 | |||||||
| chr5:79648009 | A | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.822-608A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648009 | |||||||
| chr5:79648143 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.822-474T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648143 | |||||||
| chr5:79648234 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-383G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648234 | |||||||
| chr5:79648335 | A | T | 1 | a0001c0001t0017g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.822-282A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648335 | |||||||
| chr5:79648356 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-261G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648356 | |||||||
| chr5:79648472 | G | A | 2 | a0001c0001t0003g0080 a0001c0001t0011g0020 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.822-145G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648472 | |||||||
| chr5:79648499 | C | G | 1 | a0001c0001t0040g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.822-118C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648499 | |||||||
| chr5:79648548 | G | C | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.822-69G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648548 | |||||||
| chr5:79648582 | A | G | 1 | a0001c0001t0006g0200 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.822-35A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648582 | |||||||
| chr5:79648611 | A | T | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.822-6A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 8/14 | chr5 | 79648611 | |||||||
| chr5:79648961 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.899-101G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 9/14 | chr5 | 79648961 | |||||||
| chr5:79649266 | A | G | 1 | a0001c0001t0001g0298 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1027+76A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649266 | |||||||
| chr5:79649348 | C | T | 143 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(140): Show |
151 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1027+158C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649348 | |||||||
| chr5:79649386 | G | GT | 92 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(89): Show |
99 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1027+207dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79649386 | ||||||
| chr5:79649386 | G | GTT | 6 | a0001c0001t0003g0021 a0001c0001t0003g0024 a0001c0001t0003g0025 others(3): Show |
6 | HG02451.hp2 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027+206_1027+207d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79649386 | ||||||
| chr5:79649398 | A | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+208A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649398 | |||||||
| chr5:79649505 | G | T | 1 | a0001c0002t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1027+315G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649505 | |||||||
| chr5:79649888 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+698G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649888 | |||||||
| chr5:79649913 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(153): Show |
167 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.1027+723T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79649913 | |||||||
| chr5:79650012 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+822A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650012 | |||||||
| chr5:79650046 | A | C | 69 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(66): Show |
74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1027+856A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650046 | |||||||
| chr5:79650149 | A | G | 1 | a0001c0001t0001g0281 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1027+959A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650149 | |||||||
| chr5:79650182 | A | G | 1 | a0001c0001t0005g0126 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1027+992A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650182 | |||||||
| chr5:79650223 | A | G | 2 | a0001c0001t0004g0087 a0001c0001t0011g0037 |
2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1027+1033A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650223 | |||||||
| chr5:79650243 | T | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1027+1053T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650243 | |||||||
| chr5:79650392 | C | G | 40 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(37): Show |
41 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1027+1202C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650392 | |||||||
| chr5:79650530 | C | T | 1 | a0001c0001t0013g0216 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1027+1340C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650530 | |||||||
| chr5:79650699 | C | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+1509C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650699 | |||||||
| chr5:79650939 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1027+1749G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650939 | |||||||
| chr5:79650979 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1027+1789A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79650979 | |||||||
| chr5:79651031 | C | T | 1 | a0001c0001t0020g0131 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1027+1841C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651031 | |||||||
| chr5:79651032 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1027+1842A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651032 | |||||||
| chr5:79651220 | A | T | 5 | a0001c0001t0006g0017 a0001c0001t0006g0271 a0001c0001t0006g0306 others(2): Show |
6 | HG01358.hp2 HG01943.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+2030A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651220 | |||||||
| chr5:79651227 | G | A | 1 | a0001c0001t0005g0115 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1027+2037G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651227 | |||||||
| chr5:79651395 | C | CA | 10 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0087 others(7): Show |
10 | HG01891.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1027+2215dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79651395 | ||||||
| chr5:79651464 | CA | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+2276delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79651464 | ||||||
| chr5:79651835 | T | C | 5 | a0001c0001t0001g0213 a0001c0001t0001g0233 a0001c0001t0001g0269 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+2645T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651835 | |||||||
| chr5:79651840 | G | A | 57 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(54): Show |
62 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.1027+2650G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651840 | |||||||
| chr5:79651906 | A | G | 14 | a0001c0001t0004g0023 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1027+2716A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79651906 | |||||||
| chr5:79652010 | A | T | 1 | a0001c0001t0018g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1027+2820A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652010 | |||||||
| chr5:79652024 | A | G | 2 | a0001c0001t0004g0028 a0001c0001t0004g0084 |
2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1027+2834A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652024 | |||||||
| chr5:79652131 | C | T | 1 | a0001c0002t0023g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1027+2941C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652131 | |||||||
| chr5:79652353 | C | T | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+3163C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652353 | |||||||
| chr5:79652572 | CA | C | 19 | a0001c0001t0001g0143 a0001c0001t0001g0239 a0001c0001t0001g0283 others(16): Show |
19 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(16): Show |
intron_variant | MODIFIER | c.1027+3386delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79652572 | ||||||
| chr5:79652723 | G | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+3533G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652723 | |||||||
| chr5:79652805 | A | G | 3 | a0001c0001t0001g0213 a0001c0001t0001g0269 a0001c0001t0001g0311 |
3 | HG01516.hp2 HG01517.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1027+3615A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652805 | |||||||
| chr5:79652844 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+3654A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652844 | |||||||
| chr5:79652882 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1027+3692T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79652882 | |||||||
| chr5:79653097 | G | C | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028-3861G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653097 | |||||||
| chr5:79653148 | A | T | 149 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(146): Show |
157 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1028-3810A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653148 | |||||||
| chr5:79653514 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1028-3444T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653514 | |||||||
| chr5:79653590 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-3368A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653590 | |||||||
| chr5:79653641 | C | T | 1 | a0001c0001t0007g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1028-3317C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79653641 | |||||||
| chr5:79654054 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2904A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654054 | |||||||
| chr5:79654085 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2873C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654085 | |||||||
| chr5:79654128 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2830T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654128 | |||||||
| chr5:79654159 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1028-2799C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654159 | |||||||
| chr5:79654212 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1028-2746A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654212 | |||||||
| chr5:79654235 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(207): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1028-2723T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654235 | |||||||
| chr5:79654286 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1028-2672C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654286 | |||||||
| chr5:79654528 | A | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-2430A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654528 | |||||||
| chr5:79654548 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-2410T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654548 | |||||||
| chr5:79654580 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1028-2378G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654580 | |||||||
| chr5:79654584 | C | T | 104 | a0001c0001t0001g0212 a0001c0001t0002g0008 a0001c0001t0002g0010 others(101): Show |
111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1028-2374C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654584 | |||||||
| chr5:79654677 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0164 |
2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1028-2281T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654677 | |||||||
| chr5:79654763 | C | CA | 13 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0004g0013 others(10): Show |
13 | HG01167.hp2 HG02486.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1028-2184dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79654763 | ||||||
| chr5:79654763 | CA | C | 35 | a0001c0001t0001g0175 a0001c0001t0003g0005 a0001c0001t0003g0019 others(32): Show |
37 | HG01256.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.1028-2184delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79654763 | ||||||
| chr5:79654806 | G | A | 3 | a0001c0001t0002g0063 a0001c0001t0003g0055 a0001c0001t0046g0067 |
3 | NA18947.hp1 NA18973.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1028-2152G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654806 | |||||||
| chr5:79654807 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-2151C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654807 | |||||||
| chr5:79654983 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0018g0135 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1028-1975C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79654983 | |||||||
| chr5:79655072 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1886G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655072 | |||||||
| chr5:79655253 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-1705A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655253 | |||||||
| chr5:79655456 | G | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1028-1502G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655456 | |||||||
| chr5:79655536 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-1422T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655536 | |||||||
| chr5:79655566 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1028-1392A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655566 | |||||||
| chr5:79655651 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1307G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655651 | |||||||
| chr5:79655667 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1291G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655667 | |||||||
| chr5:79655744 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-1214G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655744 | |||||||
| chr5:79655746 | GT | G | 100 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(97): Show |
107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1028-1198delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79655746 | ||||||
| chr5:79655891 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-1067C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655891 | |||||||
| chr5:79655895 | G | A | 1 | a0001c0001t0005g0146 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1028-1063G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79655895 | |||||||
| chr5:79656041 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-917A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656041 | |||||||
| chr5:79656117 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1028-841A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656117 | |||||||
| chr5:79656241 | A | ATTAAT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
214 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1028-716_1028-712d others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 79656241 | ||||||
| chr5:79656329 | T | G | 11 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0165 others(8): Show |
11 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1028-629T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656329 | |||||||
| chr5:79656467 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-491T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656467 | |||||||
| chr5:79656841 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-117T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656841 | |||||||
| chr5:79656843 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-115G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656843 | |||||||
| chr5:79656844 | T | G | 1 | a0001c0001t0001g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1028-114T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656844 | |||||||
| chr5:79656868 | G | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1028-90G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656868 | |||||||
| chr5:79656871 | C | T | 3 | a0001c0001t0003g0021 a0001c0001t0003g0080 a0001c0001t0011g0020 |
3 | HG03139.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1028-87C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 10/14 | chr5 | 79656871 | |||||||
| chr5:79657120 | A | G | 1 | a0001c0001t0012g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1071+119A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657120 | |||||||
| chr5:79657197 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1071+196A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657197 | |||||||
| chr5:79657460 | AATACACC others(6625): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0241 |
5 | HG00544.hp1 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+463_1072-4797 others(3): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79657460 | ||||||
| chr5:79657651 | T | G | 1 | a0001c0001t0007g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1071+650T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657651 | |||||||
| chr5:79657789 | A | C | 1 | a0001c0001t0001g0163 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1071+788A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657789 | |||||||
| chr5:79657962 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+961A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79657962 | |||||||
| chr5:79658014 | G | T | 56 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(53): Show |
61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1071+1013G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658014 | |||||||
| chr5:79658267 | T | G | 69 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(66): Show |
74 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.1071+1266T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658267 | |||||||
| chr5:79658298 | A | T | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1297A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658298 | |||||||
| chr5:79658358 | CT | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1071+1371delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79658358 | ||||||
| chr5:79658429 | G | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+1428G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658429 | |||||||
| chr5:79658503 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1502T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658503 | |||||||
| chr5:79658677 | T | C | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1071+1676T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658677 | |||||||
| chr5:79658758 | C | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1757C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658758 | |||||||
| chr5:79658837 | A | C | 3 | a0001c0001t0004g0013 a0001c0001t0004g0075 a0001c0001t0027g0013 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1071+1836A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79658837 | |||||||
| chr5:79658860 | T | TTATC | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+1861_1071+186 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79658860 | ||||||
| chr5:79659016 | G | T | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+2015G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659016 | |||||||
| chr5:79659172 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2171G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659172 | |||||||
| chr5:79659494 | T | G | 20 | a0001c0001t0001g0143 a0001c0001t0001g0239 a0001c0001t0001g0283 others(17): Show |
20 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2493T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659494 | |||||||
| chr5:79659496 | T | C | 20 | a0001c0001t0001g0143 a0001c0001t0001g0239 a0001c0001t0001g0283 others(17): Show |
20 | HG00423.hp1 HG00609.hp1 NA18941.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2495T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659496 | |||||||
| chr5:79659507 | C | T | 1 | a0001c0001t0005g0125 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1071+2506C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659507 | |||||||
| chr5:79659531 | C | CA | 10 | a0001c0001t0001g0153 a0001c0001t0001g0223 a0001c0001t0001g0257 others(7): Show |
10 | HG02647.hp1 HG02970.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.1071+2553dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659531 | ||||||
| chr5:79659552 | AAATGTAT others(4): Show |
A | 1 | a0001c0001t0001g0277 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+256 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659552 | ||||||
| chr5:79659553 | A | AAAATGTA others(3): Show |
1 | a0001c0001t0001g0256 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0251 a0001c0001t0001g0268 others(6): Show |
9 | HG00423.hp1 HG01175.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT | 15 | a0001c0001t0001g0156 a0001c0001t0001g0217 a0001c0001t0001g0253 others(12): Show |
15 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(2): Show |
6 | a0001c0001t0001g0203 a0001c0001t0001g0222 a0001c0001t0001g0307 others(3): Show |
6 | HG02004.hp2 HG02922.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(4): Show |
4 | a0001c0001t0001g0182 a0001c0001t0001g0293 a0001c0001t0001g0302 others(1): Show |
4 | HG00673.hp1 HG01257.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(6): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0158 |
2 | HG01934.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(8): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0303 a0001c0001t0001g0304 |
3 | HG03490.hp1 HG03492.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(19): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(10): Show |
1 | a0001c0001t0001g0015 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(12): Show |
2 | a0001c0001t0001g0195 a0001c0001t0001g0254 |
2 | NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(23): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(14): Show |
1 | a0001c0001t0001g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(25): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(16): Show |
1 | a0001c0001t0001g0255 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(27): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | AAATGTAT others(24): Show |
1 | a0001c0001t0001g0274 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1071+2553_1071+255 others(35): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | A | ATGTAT | 3 | a0001c0001t0001g0184 a0001c0001t0001g0211 a0001c0001t0013g0234 |
3 | HG02258.hp2 HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1071+2552_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | |||||||
| chr5:79659553 | A | ATGTATAT | 4 | a0001c0001t0001g0170 a0001c0001t0001g0183 a0001c0001t0001g0208 others(1): Show |
4 | HG01884.hp2 HG02004.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2552_1071+255 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | |||||||
| chr5:79659553 | A | ATGTATAT others(4): Show |
1 | a0001c0001t0001g0185 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1071+2552_1071+255 others(15): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | |||||||
| chr5:79659553 | A | ATGTATAT others(10): Show |
1 | a0001c0001t0001g0212 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1071+2552_1071+255 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659553 | |||||||
| chr5:79659553 | AATGTAT | A | 7 | a0001c0001t0002g0008 a0001c0001t0003g0005 a0001c0001t0009g0038 others(4): Show |
7 | HG01167.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2555_1071+256 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | AATGTATA others(1): Show |
A | 49 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0046 others(46): Show |
53 | HG00673.hp2 HG01109.hp1 HG01433.hp2 others(50): Show |
intron_variant | MODIFIER | c.1071+2555_1071+256 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659553 | AATGTATA others(9): Show |
A | 3 | a0001c0001t0003g0095 a0001c0003t0010g0047 a0001c0003t0010g0089 |
3 | NA18962.hp2 NA19010.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1071+2555_1071+257 others(20): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659553 | ||||||
| chr5:79659554 | A | AATG | 25 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0001g0213 others(22): Show |
26 | HG00408.hp1 HG01358.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.1071+2553_1071+255 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | AT | A | 5 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0009g0105 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+2554delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGT | A | 7 | a0001c0001t0001g0201 a0001c0001t0004g0074 a0001c0001t0005g0002 others(4): Show |
7 | HG01243.hp2 HG02615.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1071+2554_1071+255 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTAT | A | 4 | a0001c0001t0004g0013 a0001c0001t0004g0075 a0001c0001t0020g0131 others(1): Show |
4 | HG02622.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2554_1071+255 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTATAT | A | 19 | a0001c0001t0002g0066 a0001c0001t0003g0005 a0001c0001t0003g0019 others(16): Show |
20 | HG00544.hp2 HG00741.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.1071+2554_1071+256 others(11): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTATAT others(2): Show |
A | 16 | a0001c0001t0002g0071 a0001c0001t0004g0023 a0001c0001t0004g0026 others(13): Show |
17 | HG01515.hp2 HG01517.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1071+2554_1071+256 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTATAT others(6): Show |
A | 1 | a0001c0001t0001g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1071+2554_1071+256 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTATAT others(8): Show |
A | 1 | a0001c0003t0010g0091 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1071+2554_1071+256 others(19): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659554 | ATGTATAT others(10): Show |
A | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1071+2554_1071+257 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659554 | |||||||
| chr5:79659556 | G | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0143 others(87): Show |
93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1071+2555G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659556 | |||||||
| chr5:79659556 | G | GTA | 15 | a0001c0001t0001g0137 a0001c0001t0001g0221 a0001c0001t0001g0231 others(12): Show |
15 | HG00140.hp1 HG01109.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2592_1071+259 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTATA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0161 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1071+2590_1071+259 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTATATA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(13): Show |
17 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1071+2588_1071+259 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTATATAT others(1): Show |
7 | a0001c0001t0001g0139 a0001c0001t0001g0150 a0001c0001t0001g0163 others(4): Show |
7 | HG01243.hp1 HG01975.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2586_1071+259 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0175 others(1): Show |
4 | HG01175.hp2 HG01256.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2584_1071+259 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0173 a0001c0001t0001g0204 a0001c0001t0008g0202 others(2): Show |
5 | HG01074.hp1 HG01255.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+2582_1071+259 others(16): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1071+2556_1071+255 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | GTA | G | 13 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0152 others(10): Show |
13 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071+2592_1071+259 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | GTATA | G | 15 | a0001c0001t0001g0230 a0001c0001t0001g0286 a0001c0001t0005g0002 others(12): Show |
15 | HG00423.hp2 HG00558.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.1071+2590_1071+259 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | GTATATA | G | 7 | a0001c0001t0001g0138 a0001c0001t0005g0117 a0001c0001t0005g0118 others(4): Show |
7 | HG02602.hp1 HG02602.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2588_1071+259 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0005g0112 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1071+2584_1071+259 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659556 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1071+2578_1071+259 others(20): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659556 | ||||||
| chr5:79659557 | T | A | 4 | a0001c0001t0003g0073 a0001c0001t0009g0105 a0001c0001t0026g0072 others(1): Show |
4 | HG02486.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+2556T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659557 | |||||||
| chr5:79659558 | A | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0249 a0001c0001t0001g0250 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2557A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659558 | |||||||
| chr5:79659559 | T | A | 9 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0004g0074 others(6): Show |
9 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2558T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659559 | |||||||
| chr5:79659560 | A | G | 9 | a0001c0001t0001g0194 a0001c0001t0001g0201 a0001c0001t0005g0002 others(6): Show |
9 | HG01243.hp2 HG02080.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1071+2559A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659560 | |||||||
| chr5:79659561 | T | A | 13 | a0001c0001t0002g0008 a0001c0001t0002g0077 a0001c0001t0003g0005 others(10): Show |
13 | HG01167.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1071+2560T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659561 | |||||||
| chr5:79659562 | A | G | 9 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0003g0073 others(6): Show |
9 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1071+2561A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659562 | |||||||
| chr5:79659563 | T | A | 70 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0046 others(67): Show |
76 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.1071+2562T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659563 | |||||||
| chr5:79659564 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0077 a0001c0001t0004g0013 others(8): Show |
11 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1071+2563A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659564 | |||||||
| chr5:79659565 | T | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(28): Show |
33 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1071+2564T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659565 | |||||||
| chr5:79659566 | A | G | 59 | a0001c0001t0001g0277 a0001c0001t0002g0010 a0001c0001t0002g0045 others(56): Show |
64 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1071+2565A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659566 | |||||||
| chr5:79659568 | A | G | 30 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(27): Show |
32 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.1071+2567A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659568 | |||||||
| chr5:79659570 | A | G | 7 | a0001c0001t0001g0214 a0001c0001t0003g0073 a0001c0001t0004g0074 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1071+2569A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659570 | |||||||
| chr5:79659571 | T | A | 4 | a0001c0001t0003g0095 a0001c0003t0010g0047 a0001c0003t0010g0089 others(1): Show |
4 | NA18962.hp2 NA19000.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+2570T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659571 | |||||||
| chr5:79659572 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0077 a0001c0001t0004g0013 others(5): Show |
8 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1071+2571A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659572 | |||||||
| chr5:79659574 | A | G | 60 | a0001c0001t0002g0010 a0001c0001t0002g0045 a0001c0001t0002g0046 others(57): Show |
65 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1071+2573A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659574 | |||||||
| chr5:79659576 | A | G | 30 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(27): Show |
32 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(29): Show |
intron_variant | MODIFIER | c.1071+2575A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659576 | |||||||
| chr5:79659595 | A | G | 1 | a0001c0001t0006g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1071+2594A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659595 | |||||||
| chr5:79659597 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1071+2596A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659597 | |||||||
| chr5:79659604 | G | A | 1 | a0001c0001t0012g0106 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1071+2603G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659604 | |||||||
| chr5:79659687 | G | A | 1 | a0001c0001t0030g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1071+2686G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659687 | |||||||
| chr5:79659735 | A | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2734A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659735 | |||||||
| chr5:79659739 | T | G | 1 | a0001c0001t0006g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1071+2738T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659739 | |||||||
| chr5:79659880 | A | AT | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+2880dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79659880 | ||||||
| chr5:79659954 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(205): Show |
219 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1071+2953G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659954 | |||||||
| chr5:79659987 | C | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+2986C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659987 | |||||||
| chr5:79659993 | G | T | 1 | a0001c0002t0016g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1071+2992G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79659993 | |||||||
| chr5:79660016 | C | G | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+3015C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660016 | |||||||
| chr5:79660216 | CTG | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+3217_1071+321 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79660216 | ||||||
| chr5:79660249 | A | G | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+3248A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660249 | |||||||
| chr5:79660268 | G | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+3267G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660268 | |||||||
| chr5:79660369 | A | G | 1 | a0001c0007t0025g0108 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1071+3368A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660369 | |||||||
| chr5:79660482 | CATTT | C | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+3484_1071+348 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79660482 | ||||||
| chr5:79660588 | A | G | 1 | a0001c0001t0005g0002 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1071+3587A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660588 | |||||||
| chr5:79660650 | C | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0075 a0001c0001t0027g0013 |
3 | HG02809.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1071+3649C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660650 | |||||||
| chr5:79660796 | G | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1071+3795G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79660796 | |||||||
| chr5:79661005 | A | G | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1071+4004A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661005 | |||||||
| chr5:79661009 | A | T | 3 | a0001c0001t0004g0074 a0001c0001t0009g0078 a0001c0001t0009g0105 |
3 | HG02615.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1071+4008A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661009 | |||||||
| chr5:79661055 | T | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0197 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1071+4054T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661055 | |||||||
| chr5:79661088 | G | A | 1 | a0001c0001t0045g0018 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1071+4087G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661088 | |||||||
| chr5:79661720 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+4719G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79661720 | |||||||
| chr5:79662021 | A | G | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1071+5020A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662021 | |||||||
| chr5:79662163 | G | A | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1071+5162G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662163 | |||||||
| chr5:79662165 | T | G | 5 | a0001c0001t0002g0008 a0001c0001t0002g0050 a0001c0001t0002g0051 others(2): Show |
5 | HG00673.hp2 HG02083.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.1071+5164T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662165 | |||||||
| chr5:79662168 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1071+5167A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662168 | |||||||
| chr5:79662396 | C | T | 1 | a0001c0001t0003g0055 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1071+5395C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662396 | |||||||
| chr5:79662543 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+5542G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662543 | |||||||
| chr5:79662667 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1071+5666G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662667 | |||||||
| chr5:79662726 | G | A | 4 | a0001c0001t0003g0005 a0001c0001t0003g0022 a0001c0001t0003g0024 others(1): Show |
4 | HG03654.hp2 HG03927.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+5725G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662726 | |||||||
| chr5:79662905 | C | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0022 |
2 | HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1071+5904C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79662905 | |||||||
| chr5:79663230 | G | C | 2 | a0001c0001t0042g0321 a0001c0001t0045g0018 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1072-5662G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663230 | |||||||
| chr5:79663256 | G | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-5636G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663256 | |||||||
| chr5:79663279 | A | T | 1 | a0001c0001t0030g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1072-5613A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663279 | |||||||
| chr5:79663282 | C | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5610C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663282 | |||||||
| chr5:79663296 | G | C | 14 | a0001c0001t0004g0023 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-5596G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663296 | |||||||
| chr5:79663307 | A | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5585A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663307 | |||||||
| chr5:79663335 | G | A | 2 | a0001c0001t0020g0130 a0001c0001t0020g0131 |
2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1072-5557G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663335 | |||||||
| chr5:79663559 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(198): Show |
212 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1072-5333T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663559 | |||||||
| chr5:79663820 | C | T | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-5072C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663820 | |||||||
| chr5:79663894 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0017g0134 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1072-4998C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663894 | |||||||
| chr5:79663917 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(198): Show |
212 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1072-4975G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663917 | |||||||
| chr5:79663923 | G | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4969G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663923 | |||||||
| chr5:79663931 | T | C | 2 | a0001c0001t0038g0218 a0001c0001t0041g0111 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1072-4961T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79663931 | |||||||
| chr5:79664207 | A | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072-4685A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664207 | |||||||
| chr5:79664392 | C | T | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4500C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664392 | |||||||
| chr5:79664488 | C | T | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072-4404C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664488 | |||||||
| chr5:79664551 | C | T | 12 | a0001c0001t0001g0199 a0001c0001t0001g0214 a0001c0001t0001g0251 others(9): Show |
12 | HG00408.hp1 NA18940.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-4341C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664551 | |||||||
| chr5:79664594 | C | CA | 30 | a0001c0001t0001g0317 a0001c0001t0005g0002 a0001c0001t0005g0112 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1072-4282dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79664594 | ||||||
| chr5:79664594 | CA | C | 102 | a0001c0001t0001g0198 a0001c0001t0002g0008 a0001c0001t0002g0010 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-4282delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79664594 | ||||||
| chr5:79664919 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1072-3973C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79664919 | |||||||
| chr5:79665129 | A | G | 1 | a0001c0001t0022g0079 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1072-3763A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665129 | |||||||
| chr5:79665270 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1072-3622G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665270 | |||||||
| chr5:79665451 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0244 |
2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1072-3441T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665451 | |||||||
| chr5:79665790 | G | A | 1 | a0001c0001t0003g0011 | 2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1072-3102G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665790 | |||||||
| chr5:79665849 | G | T | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-3043G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665849 | |||||||
| chr5:79665896 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1072-2996C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665896 | |||||||
| chr5:79665941 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1072-2951T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79665941 | |||||||
| chr5:79666050 | G | T | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1072-2842G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666050 | |||||||
| chr5:79666069 | A | G | 30 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1072-2823A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666069 | |||||||
| chr5:79666091 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0018g0135 |
2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1072-2801C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666091 | |||||||
| chr5:79666188 | C | T | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2704C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666188 | |||||||
| chr5:79666208 | C | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072-2684C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666208 | |||||||
| chr5:79666240 | C | T | 4 | a0001c0001t0004g0074 a0001c0001t0009g0078 a0001c0001t0009g0105 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072-2652C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666240 | |||||||
| chr5:79666242 | G | T | 1 | a0001c0001t0003g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1072-2650G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666242 | |||||||
| chr5:79666245 | T | TC | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2645dupC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666245 | ||||||
| chr5:79666331 | C | G | 7 | a0001c0001t0005g0002 a0001c0001t0005g0121 a0001c0001t0005g0122 others(4): Show |
8 | HG00423.hp2 HG00558.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1072-2561C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666331 | |||||||
| chr5:79666351 | A | C | 1 | a0001c0001t0001g0319 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1072-2541A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666351 | |||||||
| chr5:79666484 | A | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-2408A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666484 | |||||||
| chr5:79666495 | TCATCACC others(37): Show |
T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0066 a0001c0001t0002g0088 others(1): Show |
5 | HG02155.hp2 NA18945.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072-2352_1072-230 others(48): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666495 | ||||||
| chr5:79666611 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1072-2281C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666611 | |||||||
| chr5:79666655 | A | ATTATAC | 209 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(206): Show |
220 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1072-2234_1072-223 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79666655 | ||||||
| chr5:79666769 | A | G | 1 | a0001c0001t0007g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1072-2123A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666769 | |||||||
| chr5:79666984 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1072-1908A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79666984 | |||||||
| chr5:79667156 | G | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-1736G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667156 | |||||||
| chr5:79667168 | A | G | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-1724A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667168 | |||||||
| chr5:79667233 | T | C | 14 | a0001c0001t0004g0023 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-1659T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667233 | |||||||
| chr5:79667290 | G | A | 101 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(98): Show |
107 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(104): Show |
intron_variant | MODIFIER | c.1072-1602G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667290 | |||||||
| chr5:79667292 | G | C | 33 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(30): Show |
35 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.1072-1600G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667292 | |||||||
| chr5:79667390 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(153): Show |
166 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.1072-1502A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667390 | |||||||
| chr5:79667500 | C | A | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1072-1392C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667500 | |||||||
| chr5:79667528 | T | C | 1 | a0001c0001t0003g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1072-1364T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667528 | |||||||
| chr5:79667882 | G | GT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1072-1010_1072-100 others(5): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667882 | |||||||
| chr5:79667899 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0225 a0001c0001t0001g0231 others(4): Show |
9 | HG00544.hp1 HG02015.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072-993C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667899 | |||||||
| chr5:79667931 | CT | C | 8 | a0001c0001t0002g0063 a0001c0001t0019g0128 a0001c0001t0019g0129 others(5): Show |
8 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1072-947delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79667931 | ||||||
| chr5:79667957 | A | C | 102 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(99): Show |
108 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(105): Show |
intron_variant | MODIFIER | c.1072-935A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79667957 | |||||||
| chr5:79668176 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(199): Show |
213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1072-716G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | chr5 | 79668176 | |||||||
| chr5:79668766 | C | CCAAATTG others(20): Show |
3 | a0001c0001t0006g0260 a0001c0001t0008g0248 a0001c0001t0008g0259 |
3 | NA18965.hp2 NA18979.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1072-124_1072-98du others(28): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 79668766 | ||||||
| chr5:79669064 | A | ATG | 45 | a0001c0001t0001g0198 a0001c0001t0004g0074 a0001c0001t0005g0002 others(42): Show |
46 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.1208+50_1208+51dup others(2): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79669064 | ||||||
| chr5:79669239 | T | G | 1 | a0001c0001t0003g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1208+211T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669239 | |||||||
| chr5:79669425 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1208+397G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669425 | |||||||
| chr5:79669520 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0169 |
2 | HG00597.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1208+492A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669520 | |||||||
| chr5:79669640 | G | T | 1 | a0001c0001t0006g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1208+612G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669640 | |||||||
| chr5:79669770 | A | G | 2 | a0001c0001t0005g0115 a0001c0001t0005g0144 |
2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1208+742A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669770 | |||||||
| chr5:79669869 | C | G | 7 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1208+841C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79669869 | |||||||
| chr5:79670061 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1208+1033A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670061 | |||||||
| chr5:79670189 | A | G | 5 | a0001c0001t0003g0095 a0001c0003t0010g0047 a0001c0003t0010g0089 others(2): Show |
5 | NA18947.hp2 NA18962.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1161A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670189 | |||||||
| chr5:79670226 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1208+1198A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670226 | |||||||
| chr5:79670236 | A | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0225 others(13): Show |
20 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1208+1208A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670236 | |||||||
| chr5:79670285 | C | T | 11 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0165 others(8): Show |
11 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1208+1257C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670285 | |||||||
| chr5:79670311 | T | TTTTA | 5 | a0001c0001t0014g0120 a0001c0001t0019g0128 a0001c0001t0019g0129 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208+1307_1208+131 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79670311 | ||||||
| chr5:79670394 | G | A | 1 | a0001c0001t0006g0271 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1208+1366G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670394 | |||||||
| chr5:79670481 | C | T | 1 | a0001c0001t0007g0186 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1208+1453C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670481 | |||||||
| chr5:79670613 | G | A | 1 | a0001c0001t0038g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1208+1585G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670613 | |||||||
| chr5:79670618 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1208+1590C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670618 | |||||||
| chr5:79670673 | A | G | 1 | a0001c0002t0012g0097 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1208+1645A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670673 | |||||||
| chr5:79670695 | G | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0244 others(1): Show |
4 | HG02040.hp1 HG02132.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+1667G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670695 | |||||||
| chr5:79670733 | T | C | 1 | a0002c0004t0003g0049 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1208+1705T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670733 | |||||||
| chr5:79670867 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1208+1839C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670867 | |||||||
| chr5:79670992 | G | C | 1 | a0001c0001t0018g0243 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1208+1964G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79670992 | |||||||
| chr5:79671049 | T | C | 1 | a0001c0001t0026g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1208+2021T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671049 | |||||||
| chr5:79671120 | G | T | 3 | a0001c0002t0002g0012 a0001c0002t0002g0062 a0001c0002t0002g0102 |
4 | HG01433.hp2 HG01934.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1208+2092G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671120 | |||||||
| chr5:79671222 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1208+2194A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671222 | |||||||
| chr5:79671249 | G | C | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1208+2221G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671249 | |||||||
| chr5:79671700 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0208 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1208+2672C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79671700 | |||||||
| chr5:79672011 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0269 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1208+2983A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672011 | |||||||
| chr5:79672084 | T | C | 8 | a0001c0001t0001g0136 a0001c0001t0001g0183 a0001c0001t0001g0184 others(5): Show |
8 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1208+3056T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672084 | |||||||
| chr5:79672102 | C | CA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(158): Show |
171 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.1208+3085dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79672102 | ||||||
| chr5:79672118 | A | C | 1 | a0001c0001t0004g0006 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1208+3090A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672118 | |||||||
| chr5:79672549 | C | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(31): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208+3521C>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672549 | |||||||
| chr5:79672607 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1208+3579A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672607 | |||||||
| chr5:79672642 | T | G | 2 | a0001c0001t0019g0128 a0001c0001t0019g0129 |
2 | HG02717.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1208+3614T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672642 | |||||||
| chr5:79672652 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1208+3624T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672652 | |||||||
| chr5:79672667 | C | G | 56 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(53): Show |
61 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.1208+3639C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672667 | |||||||
| chr5:79672784 | T | C | 30 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1208+3756T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672784 | |||||||
| chr5:79672837 | C | G | 2 | a0001c0001t0001g0225 a0001c0001t0001g0244 |
2 | NA19078.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1208+3809C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672837 | |||||||
| chr5:79672945 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1208+3917G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672945 | |||||||
| chr5:79672986 | T | G | 1 | a0001c0001t0035g0141 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1208+3958T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79672986 | |||||||
| chr5:79673167 | T | A | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4139T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673167 | |||||||
| chr5:79673391 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4363T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673391 | |||||||
| chr5:79673449 | A | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1208+4421A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673449 | |||||||
| chr5:79673534 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1208+4506A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673534 | |||||||
| chr5:79673564 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0021 others(31): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1208+4536G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673564 | |||||||
| chr5:79673568 | G | GT | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208+4541dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79673568 | ||||||
| chr5:79673846 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1208+4818C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79673846 | |||||||
| chr5:79674018 | G | C | 12 | a0001c0001t0002g0077 a0001c0001t0003g0073 a0001c0001t0004g0013 others(9): Show |
12 | HG02486.hp1 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1208+4990G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674018 | |||||||
| chr5:79674144 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1208+5116G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674144 | |||||||
| chr5:79674158 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0241 |
5 | HG00544.hp1 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208+5130C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674158 | |||||||
| chr5:79674267 | A | G | 3 | a0001c0001t0002g0064 a0001c0001t0002g0093 a0001c0001t0002g0101 |
3 | NA18940.hp1 NA19002.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1208+5239A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674267 | |||||||
| chr5:79674312 | T | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(194): Show |
209 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1209-5267T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674312 | |||||||
| chr5:79674380 | C | T | 1 | a0001c0001t0006g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1209-5199C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674380 | |||||||
| chr5:79674483 | A | C | 4 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0244 others(1): Show |
4 | HG02040.hp1 HG02132.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-5096A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674483 | |||||||
| chr5:79674535 | A | G | 3 | a0001c0001t0001g0235 a0001c0001t0008g0301 a0001c0001t0013g0216 |
3 | HG01255.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1209-5044A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674535 | |||||||
| chr5:79674655 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1209-4924A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674655 | |||||||
| chr5:79674780 | A | G | 104 | a0001c0001t0001g0169 a0001c0001t0002g0008 a0001c0001t0002g0010 others(101): Show |
111 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1209-4799A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674780 | |||||||
| chr5:79674966 | C | G | 2 | a0001c0001t0014g0119 a0001c0001t0014g0120 |
2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1209-4613C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79674966 | |||||||
| chr5:79675106 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1209-4473A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675106 | |||||||
| chr5:79675265 | G | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-4314G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675265 | |||||||
| chr5:79675337 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0228 a0001c0001t0001g0230 others(1): Show |
5 | HG00597.hp1 HG00673.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1209-4242G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675337 | |||||||
| chr5:79675984 | C | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-3595C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79675984 | |||||||
| chr5:79676111 | T | G | 14 | a0001c0001t0004g0023 a0001c0001t0004g0026 a0001c0001t0004g0027 others(11): Show |
14 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209-3468T>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676111 | |||||||
| chr5:79676152 | A | C | 1 | a0001c0001t0006g0322 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1209-3427A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676152 | |||||||
| chr5:79676163 | T | TAC | 7 | a0001c0001t0001g0139 a0001c0001t0001g0232 a0001c0001t0001g0241 others(4): Show |
7 | HG00544.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-3390_1209-338 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | T | TACAC | 7 | a0001c0001t0005g0125 a0001c0001t0019g0128 a0001c0001t0019g0129 others(4): Show |
7 | HG02486.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209-3392_1209-338 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | T | TACACAC | 29 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.1209-3394_1209-338 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1209-3396_1209-338 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | TAC | T | 3 | a0001c0001t0001g0302 a0001c0001t0013g0234 a0001c0001t0015g0282 |
3 | HG01257.hp1 HG02148.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1209-3390_1209-338 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | TACAC | T | 4 | a0001c0001t0001g0136 a0001c0001t0001g0257 a0001c0001t0001g0263 others(1): Show |
4 | HG01891.hp2 HG02071.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209-3392_1209-338 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | TACACAC | T | 5 | a0001c0001t0001g0258 a0001c0001t0001g0262 a0001c0001t0002g0046 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-3394_1209-338 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | TACACACA others(1): Show |
T | 99 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(96): Show |
105 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(102): Show |
intron_variant | MODIFIER | c.1209-3396_1209-338 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676163 | TACACACA others(3): Show |
T | 1 | a0001c0001t0022g0079 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1209-3398_1209-338 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79676163 | ||||||
| chr5:79676180 | A | G | 1 | a0001c0001t0012g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1209-3399A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676180 | |||||||
| chr5:79676337 | G | T | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-3242G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676337 | |||||||
| chr5:79676434 | A | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(50): Show |
57 | HG00408.hp2 HG00597.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1209-3145A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676434 | |||||||
| chr5:79676631 | G | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-2948G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79676631 | |||||||
| chr5:79677417 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1209-2162T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677417 | |||||||
| chr5:79677709 | T | C | 32 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(29): Show |
34 | HG00673.hp2 HG02083.hp1 HG02155.hp2 others(31): Show |
intron_variant | MODIFIER | c.1209-1870T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677709 | |||||||
| chr5:79677726 | A | G | 1 | a0001c0001t0021g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209-1853A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677726 | |||||||
| chr5:79677735 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1209-1844C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677735 | |||||||
| chr5:79677764 | T | A | 1 | a0001c0001t0003g0053 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1209-1815T>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677764 | |||||||
| chr5:79677863 | G | C | 1 | a0001c0001t0026g0072 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1209-1716G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79677863 | |||||||
| chr5:79678166 | C | T | 1 | a0001c0001t0040g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1209-1413C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678166 | |||||||
| chr5:79678178 | G | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-1401G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678178 | |||||||
| chr5:79678281 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1209-1298A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678281 | |||||||
| chr5:79678511 | G | GA | 41 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(38): Show |
42 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1209-1060dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79678511 | ||||||
| chr5:79678556 | A | T | 3 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0006g0312 |
3 | HG03041.hp1 NA18955.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1209-1023A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678556 | |||||||
| chr5:79678643 | C | T | 41 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(38): Show |
42 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.1209-936C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678643 | |||||||
| chr5:79678738 | T | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1209-841T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678738 | |||||||
| chr5:79678986 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1209-593A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79678986 | |||||||
| chr5:79679083 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1209-496T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679083 | |||||||
| chr5:79679085 | T | C | 30 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1209-494T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679085 | |||||||
| chr5:79679273 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209-306T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679273 | |||||||
| chr5:79679374 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1209-205G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | chr5 | 79679374 | |||||||
| chr5:79679411 | GA | G | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-159delA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr5 | 79679411 | ||||||
| chr5:79679836 | A | G | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1300+166A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79679836 | |||||||
| chr5:79680487 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1300+817C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680487 | |||||||
| chr5:79680573 | G | A | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300+903G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680573 | |||||||
| chr5:79680633 | G | A | 196 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(193): Show |
208 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.1300+963G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680633 | |||||||
| chr5:79680772 | A | G | 2 | a0001c0001t0014g0119 a0001c0001t0014g0120 |
2 | HG00099.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1300+1102A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680772 | |||||||
| chr5:79680926 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1301-1056G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680926 | |||||||
| chr5:79680986 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1301-996T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79680986 | |||||||
| chr5:79681150 | A | AT | 131 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0154 others(128): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.1301-804dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | ||||||
| chr5:79681150 | A | ATT | 41 | a0001c0001t0001g0223 a0001c0001t0001g0283 a0001c0001t0001g0288 others(38): Show |
42 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1301-805_1301-804d others(4): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | ||||||
| chr5:79681150 | AT | A | 10 | a0001c0001t0001g0151 a0001c0001t0001g0297 a0001c0001t0006g0017 others(7): Show |
11 | HG01243.hp2 HG01943.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.1301-804delT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | ||||||
| chr5:79681150 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0024g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1301-814_1301-804d others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 79681150 | ||||||
| chr5:79681246 | A | G | 2 | a0001c0001t0038g0218 a0001c0001t0041g0111 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1301-736A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681246 | |||||||
| chr5:79681365 | G | A | 2 | a0001c0001t0004g0087 a0001c0001t0011g0037 |
2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1301-617G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681365 | |||||||
| chr5:79681418 | A | G | 30 | a0001c0001t0005g0002 a0001c0001t0005g0112 a0001c0001t0005g0115 others(27): Show |
31 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.1301-564A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681418 | |||||||
| chr5:79681456 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1301-526C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681456 | |||||||
| chr5:79681649 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0164 others(1): Show |
4 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301-333C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681649 | |||||||
| chr5:79681838 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1301-144A>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681838 | |||||||
| chr5:79681961 | C | T | 2 | a0001c0001t0005g0125 a0001c0001t0005g0146 |
2 | HG03017.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1301-21C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 13/14 | chr5 | 79681961 | |||||||
| chr5:79682430 | C | T | 6 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(3): Show |
6 | HG01243.hp2 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1380+369C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682430 | |||||||
| chr5:79682446 | A | AT | 27 | a0001c0001t0001g0172 a0001c0001t0001g0192 a0001c0001t0001g0209 others(24): Show |
28 | HG00609.hp2 HG00741.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.1380+404dupT | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79682446 | ||||||
| chr5:79682566 | T | C | 2 | a0001c0001t0005g0115 a0001c0001t0005g0144 |
2 | HG03831.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1380+505T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682566 | |||||||
| chr5:79682683 | G | A | 2 | a0001c0001t0005g0123 a0001c0001t0005g0145 |
2 | NA18949.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1380+622G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682683 | |||||||
| chr5:79682744 | C | T | 3 | a0001c0001t0006g0272 a0001c0001t0006g0273 a0001c0001t0006g0312 |
3 | HG02886.hp2 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1380+683C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682744 | |||||||
| chr5:79682775 | A | G | 103 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(100): Show |
110 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1380+714A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682775 | |||||||
| chr5:79682806 | T | C | 4 | a0001c0001t0019g0128 a0001c0001t0019g0129 a0001c0001t0020g0130 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+745T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682806 | |||||||
| chr5:79682903 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1380+842A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682903 | |||||||
| chr5:79682904 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1380+843T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682904 | |||||||
| chr5:79682966 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0205 |
2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1380+905A>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79682966 | |||||||
| chr5:79683115 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0172 |
2 | HG00609.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1380+1054A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683115 | |||||||
| chr5:79683313 | T | TCA | 17 | a0001c0001t0001g0192 a0001c0001t0001g0220 a0001c0001t0005g0125 others(14): Show |
18 | HG00099.hp2 HG00639.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1380+1280_1380+128 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | ||||||
| chr5:79683313 | T | TCACA | 7 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
7 | HG01884.hp2 HG02258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380+1278_1380+128 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | ||||||
| chr5:79683313 | TCA | T | 53 | a0001c0001t0002g0077 a0001c0001t0003g0005 a0001c0001t0003g0019 others(50): Show |
56 | HG01167.hp2 HG01433.hp2 HG01891.hp1 others(53): Show |
intron_variant | MODIFIER | c.1380+1280_1380+128 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | ||||||
| chr5:79683313 | TCACA | T | 12 | a0001c0001t0001g0289 a0001c0001t0003g0025 a0001c0001t0003g0080 others(9): Show |
12 | HG00140.hp2 HG01928.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.1380+1278_1380+128 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | ||||||
| chr5:79683313 | TCACACA | T | 51 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0244 others(48): Show |
55 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.1380+1276_1380+128 others(10): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683313 | ||||||
| chr5:79683437 | G | C | 1 | a0001c0001t0028g0313 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1380+1376G>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683437 | |||||||
| chr5:79683541 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1380+1480A>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683541 | |||||||
| chr5:79683565 | G | A | 34 | a0001c0001t0002g0068 a0001c0001t0003g0005 a0001c0001t0003g0019 others(31): Show |
36 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.1380+1504G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683565 | |||||||
| chr5:79683706 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1381-1493G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79683706 | |||||||
| chr5:79683923 | C | CA | 40 | a0001c0001t0001g0143 a0001c0001t0001g0237 a0001c0001t0001g0246 others(37): Show |
40 | HG00673.hp1 HG01109.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1381-1247dupA | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | C | CAA | 7 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0164 others(4): Show |
7 | HG01074.hp1 HG01255.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1381-1248_1381-124 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | C | CAAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0137 others(25): Show |
32 | HG00408.hp2 HG00597.hp2 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.1381-1249_1381-124 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | C | CAAAA | 20 | a0001c0001t0001g0139 a0001c0001t0001g0153 a0001c0001t0001g0158 others(17): Show |
20 | HG00639.hp1 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1381-1250_1381-124 others(8): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | C | CAAAAA | 6 | a0001c0001t0001g0133 a0001c0001t0001g0150 a0001c0001t0001g0174 others(3): Show |
6 | HG01243.hp1 HG02074.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1381-1251_1381-124 others(9): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAA | C | 28 | a0001c0001t0002g0064 a0001c0001t0002g0077 a0001c0001t0002g0088 others(25): Show |
28 | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1381-1248_1381-124 others(6): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAA | C | 72 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0045 others(69): Show |
79 | HG00544.hp2 HG00673.hp2 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.1381-1249_1381-124 others(7): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0005g0002 a0001c0001t0005g0115 a0001c0001t0005g0121 others(6): Show |
10 | HG00423.hp2 HG00558.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.1381-1254_1381-124 others(12): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAAAAAA others(2): Show |
C | 24 | a0001c0001t0005g0112 a0001c0001t0005g0116 a0001c0001t0005g0117 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1381-1255_1381-124 others(13): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0039g0264 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1381-1256_1381-124 others(14): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0258 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1381-1259_1381-124 others(17): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79683923 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0006g0312 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1381-1263_1381-124 others(21): Show |
TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr5 | 79683923 | ||||||
| chr5:79684335 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1381-864G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684335 | |||||||
| chr5:79684420 | C | G | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1381-779C>G | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684420 | |||||||
| chr5:79684565 | T | C | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-634T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684565 | |||||||
| chr5:79684670 | C | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0133 others(198): Show |
213 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.1381-529C>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684670 | |||||||
| chr5:79684857 | T | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(287): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1381-342T>C | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684857 | |||||||
| chr5:79684869 | GC | G | 5 | a0001c0001t0021g0113 a0001c0001t0021g0114 a0001c0001t0038g0218 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1381-329delC | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684869 | |||||||
| chr5:79684931 | G | A | 1 | a0001c0001t0042g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1381-268G>A | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684931 | |||||||
| chr5:79684953 | G | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0208 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1381-246G>T | TENT2 | ENSG00000164329.15 | transcript | ENST00000453514.6 | protein_coding | 14/14 | chr5 | 79684953 |