Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55756 |
| ensemblid | ENSG00000104299.15 |
| hgncid | 25592 |
| symbol | INTS9 |
| name | integrator complex subunit 9 |
| refseq_nuc | NM_018250.4 |
| refseq_prot | NP_060720.2 |
| ensembl_nuc | ENST00000521022.6 |
| ensembl_prot | ENSP00000429065.1 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28767661 |
| end | 28889969 |
| strand | - |
| ver | v1.2 |
| region | chr8:28767661-28889969 |
| region5000 | chr8:28762661-28894969 |
| regionname0 | INTS9_chr8_28767661_28889969 |
| regionname5000 | INTS9_chr8_28762661_28894969 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 658 | 355 | 90 | 62 | 153 | 12 | 36 | 125 | INTS9_chr8_28762661_28894969 | INTS9 | MKLYC others(653): Show |
chr8 | 28762661 | 28894969 |
| a0002 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | MKLYC others(653): Show |
chr8 | 28762661 | 28894969 |
| a0003 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | MKLYC others(653): Show |
chr8 | 28762661 | 28894969 |
| a0004 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | MKLYC others(653): Show |
chr8 | 28762661 | 28894969 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1974 | 344 | 82 | 61 | 152 | 11 | 36 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0002 | 0/0 | 1974 | 4 | 4 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0003 | 0/0 | 1974 | 3 | 2 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0005 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0007 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0009 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0001c0010 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0002c0004 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0003c0008 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 | ||
| a0004c0006 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | ATGAA others(1969): Show |
chr8 | 28762661 | 28894969 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2549 | 317 | 59 | 59 | 151 | 11 | 35 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0002 | 0/0 | 2549 | 11 | 8 | 2 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0003 | 0/0 | 2549 | 3 | 3 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0004 | 0/0 | 2549 | 8 | 8 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0005 | 0/0 | 2549 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0006 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0007 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0001t0008 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0002t0003 | 0/0 | 2549 | 4 | 4 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0003t0001 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0005t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0007t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0009t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0001c0010t0003 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0002c0004t0002 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0003c0008t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| a0004c0006t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | GGCTG others(2544): Show |
chr8 | 28762661 | 28894969 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0003t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0005t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0001c0010t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0002c0004t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0003c0008t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| a0004c0006t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0009 | t0001 | g0208 | EUR | GBR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | FIN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00621 | hp2 | a0001 | c0007 | t0001 | g0165 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0136 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | IBS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02055 | hp1 | a0001 | c0010 | t0003 | g0348 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CDX | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0316 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0305 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0194 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02809 | hp2 | a0002 | c0004 | t0002 | g0315 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0295 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02965 | hp2 | a0003 | c0008 | t0001 | g0006 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0297 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | ESN | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0296 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | BEB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0351 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CHB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19079 | hp2 | a0004 | c0006 | t0001 | g0325 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ASW | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0294 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0293 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | MSL | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | USA | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | USA | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | LWK | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0086 | REF | REF | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0111 | REF | REF | INTS9_chr8_28762661_28894969 | INTS9 | chr8 | 28762661 | 28894969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28769966 | C | T | 1 | a0004 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.1723G>A | p.Val575Ile | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/17 | 1810/2549 | 1723/1977 | 575/658 | chr8 | 28769966 | |||
| chr8:28813551 | T | C | 1 | a0003 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.550A>G | p.Met184Val | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/17 | 637/2549 | 550/1977 | 184/658 | chr8 | 28813551 | |||
| chr8:28837641 | C | T | 1 | a0002 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.397G>A | p.Gly133Ser | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/17 | 484/2549 | 397/1977 | 133/658 | chr8 | 28837641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28780908 | G | A | 1 | a0001c0002 | 4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.1185C>T | p.Thr395Thr | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1272/2549 | 1185/1977 | 395/658 | chr8 | 28780908 | |||
| chr8:28780938 | G | A | 1 | a0001c0007 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1155C>T | p.Asn385Asn | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1242/2549 | 1155/1977 | 385/658 | chr8 | 28780938 | |||
| chr8:28780986 | C | T | 1 | a0001c0003 | 3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1107G>A | p.Gln369Gln | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/17 | 1194/2549 | 1107/1977 | 369/658 | chr8 | 28780986 | |||
| chr8:28813588 | A | G | 1 | a0001c0005 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.513T>C | p.Asp171Asp | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/17 | 600/2549 | 513/1977 | 171/658 | chr8 | 28813588 | |||
| chr8:28850222 | G | A | 1 | a0001c0009 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.189C>T | p.Phe63Phe | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/17 | 276/2549 | 189/1977 | 63/658 | chr8 | 28850222 | |||
| chr8:28850264 | C | A | 1 | a0001c0010 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.147G>T | p.Leu49Leu | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/17 | 234/2549 | 147/1977 | 49/658 | chr8 | 28850264 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28767912 | A | G | 1 | a0001c0001t0006 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 234 | chr8 | 28767912 | ||||||
| chr8:28767923 | G | A | 1 | a0001c0001t0005 | 2 | HG03516.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*223C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 223 | chr8 | 28767923 | ||||||
| chr8:28767939 | G | T | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0010t0003 |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*207C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 207 | chr8 | 28767939 | ||||||
| chr8:28768016 | T | C | 1 | a0001c0001t0004 | 8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*130A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 130 | chr8 | 28768016 | ||||||
| chr8:28768070 | G | C | 4 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(1): Show |
15 | HG00738.hp2 HG01243.hp2 HG02280.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 76 | chr8 | 28768070 | ||||||
| chr8:28768091 | G | A | 1 | a0001c0001t0007 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 55 | chr8 | 28768091 | ||||||
| chr8:28768123 | G | C | 1 | a0001c0001t0008 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 17/17 | 23 | chr8 | 28768123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28768594 | A | C | 1 | a0001c0001t0008g0194 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1801-272T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768594 | |||||||
| chr8:28768625 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1801-303G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768625 | |||||||
| chr8:28768738 | G | A | 4 | a0001c0001t0002g0075 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG00738.hp2 HG01243.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801-416C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768738 | |||||||
| chr8:28768819 | A | G | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1801-497T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768819 | |||||||
| chr8:28768901 | C | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(123): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1801-579G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768901 | |||||||
| chr8:28768953 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
125 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1801-631C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28768953 | |||||||
| chr8:28769035 | T | A | 15 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(12): Show |
16 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.1801-713A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769035 | |||||||
| chr8:28769116 | C | T | 7 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0001c0001t0002g0312 others(4): Show |
7 | HG02280.hp2 HG02809.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1800+773G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769116 | |||||||
| chr8:28769178 | A | C | 14 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0121 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1800+711T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769178 | |||||||
| chr8:28769189 | C | T | 27 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0121 others(24): Show |
27 | HG00738.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1800+700G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769189 | |||||||
| chr8:28769397 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1800+492A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769397 | |||||||
| chr8:28769582 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1800+307G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 16/16 | chr8 | 28769582 | |||||||
| chr8:28770195 | A | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663-169T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770195 | |||||||
| chr8:28770202 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1663-176G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770202 | |||||||
| chr8:28770279 | A | G | 7 | a0001c0001t0004g0002 a0001c0001t0004g0128 a0001c0001t0004g0153 others(4): Show |
8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663-253T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770279 | |||||||
| chr8:28770307 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | NA18947.hp1 NA19007.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663-281C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770307 | |||||||
| chr8:28770324 | G | C | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(12): Show |
15 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1663-298C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770324 | |||||||
| chr8:28770350 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1663-324G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770350 | |||||||
| chr8:28770457 | T | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0270 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1663-431A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770457 | |||||||
| chr8:28770476 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1663-450G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770476 | |||||||
| chr8:28770477 | G | A | 33 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(30): Show |
33 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1663-451C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770477 | |||||||
| chr8:28770515 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1662+467C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770515 | |||||||
| chr8:28770524 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1662+458C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770524 | |||||||
| chr8:28770651 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1662+331T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770651 | |||||||
| chr8:28770659 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1662+323C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770659 | |||||||
| chr8:28770701 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1662+281G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770701 | |||||||
| chr8:28770720 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1662+262G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770720 | |||||||
| chr8:28770767 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.1662+215G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770767 | |||||||
| chr8:28770776 | G | A | 33 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(30): Show |
33 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1662+206C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770776 | |||||||
| chr8:28770881 | A | G | 8 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+101T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770881 | |||||||
| chr8:28770903 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(193): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1662+79T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 15/16 | chr8 | 28770903 | |||||||
| chr8:28771320 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1564-240C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771320 | |||||||
| chr8:28771323 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1564-243G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771323 | |||||||
| chr8:28771324 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0305 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1564-244C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771324 | |||||||
| chr8:28771636 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1564-556A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771636 | |||||||
| chr8:28771643 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(143): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1564-563C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771643 | |||||||
| chr8:28771656 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1564-576G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771656 | |||||||
| chr8:28771680 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1564-600C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771680 | |||||||
| chr8:28771693 | G | A | 8 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564-613C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771693 | |||||||
| chr8:28771699 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1564-619G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771699 | |||||||
| chr8:28771862 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0305 |
2 | HG02630.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1564-782C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771862 | |||||||
| chr8:28771901 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1564-821G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28771901 | |||||||
| chr8:28772001 | C | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1564-921G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772001 | |||||||
| chr8:28772234 | G | A | 32 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(29): Show |
32 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1564-1154C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772234 | |||||||
| chr8:28772239 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(159): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1564-1159C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772239 | |||||||
| chr8:28772253 | G | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(27): Show |
30 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1564-1173C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772253 | |||||||
| chr8:28772262 | C | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-1182G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772262 | |||||||
| chr8:28772317 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1564-1237G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772317 | |||||||
| chr8:28772407 | G | A | 1 | a0001c0002t0003g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1564-1327C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772407 | |||||||
| chr8:28772530 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1564-1450G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772530 | |||||||
| chr8:28772537 | G | A | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1564-1457C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772537 | |||||||
| chr8:28772632 | CCT | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0287 others(1): Show |
4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564-1554_1564-155 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772632 | |||||||
| chr8:28772794 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG00642.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1564-1714C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772794 | |||||||
| chr8:28772801 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02922.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1564-1721G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772801 | |||||||
| chr8:28772806 | CAAAAAAA others(3): Show |
C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(123): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1564-1736_1564-172 others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772806 | |||||||
| chr8:28772806 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0271 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1564-1737_1564-172 others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772806 | |||||||
| chr8:28772862 | A | G | 7 | a0001c0001t0004g0002 a0001c0001t0004g0128 a0001c0001t0004g0153 others(4): Show |
8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564-1782T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28772862 | |||||||
| chr8:28773058 | T | C | 13 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1564-1978A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773058 | |||||||
| chr8:28773132 | G | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0280 |
2 | NA18962.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1564-2052C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773132 | |||||||
| chr8:28773184 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1564-2104G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773184 | |||||||
| chr8:28773238 | T | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
8 | HG00597.hp1 HG02027.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1564-2158A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773238 | |||||||
| chr8:28773274 | T | C | 14 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1564-2194A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773274 | |||||||
| chr8:28773279 | C | T | 15 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(12): Show |
15 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1564-2199G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773279 | |||||||
| chr8:28773371 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1564-2291C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773371 | |||||||
| chr8:28773395 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0217 a0001c0001t0001g0218 |
4 | HG02818.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-2315G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773395 | |||||||
| chr8:28773463 | C | CA | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0004g0002 others(5): Show |
9 | HG02630.hp1 HG02818.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1563+2295dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | |||||||
| chr8:28773463 | CA | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1563+2295delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | |||||||
| chr8:28773463 | CAA | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(120): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1563+2294_1563+229 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | |||||||
| chr8:28773463 | CAAA | C | 10 | a0001c0001t0001g0217 a0001c0001t0001g0282 a0001c0001t0002g0146 others(7): Show |
10 | HG00738.hp2 HG01243.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1563+2293_1563+229 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773463 | |||||||
| chr8:28773464 | A | C | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1563+2295T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773464 | |||||||
| chr8:28773490 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+2269T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773490 | |||||||
| chr8:28773554 | C | CT | 22 | a0001c0001t0001g0045 a0001c0001t0001g0102 a0001c0001t0001g0120 others(19): Show |
22 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1563+2204dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773554 | |||||||
| chr8:28773598 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1563+2161G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773598 | |||||||
| chr8:28773664 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1563+2095G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773664 | |||||||
| chr8:28773694 | G | GT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(137): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1563+2064dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773694 | |||||||
| chr8:28773694 | G | GTTT | 8 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+2062_1563+206 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773694 | |||||||
| chr8:28773771 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1563+1988C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773771 | |||||||
| chr8:28773845 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0014 |
2 | HG02559.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1563+1914G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773845 | |||||||
| chr8:28773966 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
141 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1563+1793G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28773966 | |||||||
| chr8:28774016 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(184): Show |
189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1563+1743G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774016 | |||||||
| chr8:28774074 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
134 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(131): Show |
intron_variant | MODIFIER | c.1563+1685G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774074 | |||||||
| chr8:28774093 | G | A | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1563+1666C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774093 | |||||||
| chr8:28774111 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1563+1648G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774111 | |||||||
| chr8:28774298 | A | G | 8 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+1461T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774298 | |||||||
| chr8:28774524 | GAA | G | 7 | a0001c0001t0004g0002 a0001c0001t0004g0128 a0001c0001t0004g0153 others(4): Show |
8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1563+1233_1563+123 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774524 | |||||||
| chr8:28774689 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(179): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1563+1070C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28774689 | |||||||
| chr8:28775035 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563+724G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775035 | |||||||
| chr8:28775251 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1563+508G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775251 | |||||||
| chr8:28775428 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1563+331G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775428 | |||||||
| chr8:28775462 | A | G | 13 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(10): Show |
13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563+297T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775462 | |||||||
| chr8:28775581 | A | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1563+178T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775581 | |||||||
| chr8:28775631 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1563+128G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775631 | |||||||
| chr8:28775646 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0287 others(1): Show |
4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1563+113C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775646 | |||||||
| chr8:28775695 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1563+64A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 14/16 | chr8 | 28775695 | |||||||
| chr8:28776029 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1396-103T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776029 | |||||||
| chr8:28776071 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1396-145T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776071 | |||||||
| chr8:28776168 | C | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-242G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776168 | |||||||
| chr8:28776227 | T | G | 4 | a0001c0001t0003g0309 a0001c0001t0003g0310 a0001c0001t0003g0314 others(1): Show |
4 | HG02055.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-301A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776227 | |||||||
| chr8:28776413 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
135 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1396-487C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776413 | |||||||
| chr8:28776427 | G | GT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0052 others(50): Show |
54 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1396-502dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776427 | |||||||
| chr8:28776427 | G | GTT | 18 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0133 others(15): Show |
18 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1396-503_1396-502d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776427 | |||||||
| chr8:28776429 | TTTTTTTT others(4): Show |
T | 12 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(9): Show |
13 | HG00738.hp2 HG01243.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.1396-514_1396-504d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776429 | |||||||
| chr8:28776433 | TTTTTTTG | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0147 others(68): Show |
72 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1396-514_1396-508d others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776433 | |||||||
| chr8:28776436 | T | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
123 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1396-510A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776436 | |||||||
| chr8:28776438 | TTG | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
117 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.1396-514_1396-513d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776438 | |||||||
| chr8:28776439 | TG | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0180 a0001c0001t0003g0309 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1396-514delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776439 | |||||||
| chr8:28776440 | G | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0052 others(74): Show |
78 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1396-514C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776440 | |||||||
| chr8:28776445 | T | G | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1396-519A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28776445 | |||||||
| chr8:28777057 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395+772G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777057 | |||||||
| chr8:28777077 | T | C | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1395+752A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777077 | |||||||
| chr8:28777259 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1395+570C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777259 | |||||||
| chr8:28777283 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1395+546G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777283 | |||||||
| chr8:28777284 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0224 |
2 | NA18944.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1395+545C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777284 | |||||||
| chr8:28777313 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395+516G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777313 | |||||||
| chr8:28777336 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1395+493G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777336 | |||||||
| chr8:28777338 | C | T | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1395+491G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777338 | |||||||
| chr8:28777370 | T | A | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1395+459A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777370 | |||||||
| chr8:28777453 | T | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0156 a0001c0003t0001g0316 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395+376A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777453 | |||||||
| chr8:28777540 | C | CT | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(155): Show |
161 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1395+288dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777540 | |||||||
| chr8:28777639 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1395+190C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777639 | |||||||
| chr8:28777680 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1395+149C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777680 | |||||||
| chr8:28777786 | G | C | 19 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(16): Show |
20 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1395+43C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 13/16 | chr8 | 28777786 | |||||||
| chr8:28778045 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0289 |
2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1271-92T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778045 | |||||||
| chr8:28778199 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1271-246C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778199 | |||||||
| chr8:28778270 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0052 a0001c0001t0001g0064 others(50): Show |
54 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1271-317C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778270 | |||||||
| chr8:28778294 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1271-341T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778294 | |||||||
| chr8:28778353 | G | C | 1 | a0001c0002t0003g0295 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1271-400C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778353 | |||||||
| chr8:28778454 | G | A | 5 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0001c0001t0002g0312 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-501C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778454 | |||||||
| chr8:28778592 | CG | C | 5 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0001c0001t0002g0312 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-640delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778592 | |||||||
| chr8:28778595 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1271-642C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778595 | |||||||
| chr8:28778730 | T | C | 5 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0001c0001t0002g0312 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1271-777A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778730 | |||||||
| chr8:28778759 | G | A | 2 | a0001c0001t0002g0264 a0002c0004t0002g0315 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1271-806C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778759 | |||||||
| chr8:28778771 | T | C | 7 | a0001c0001t0004g0002 a0001c0001t0004g0128 a0001c0001t0004g0153 others(4): Show |
8 | HG02630.hp1 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1271-818A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28778771 | |||||||
| chr8:28779078 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1271-1125A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779078 | |||||||
| chr8:28779165 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1271-1212C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779165 | |||||||
| chr8:28779166 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1271-1213G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779166 | |||||||
| chr8:28779452 | T | G | 2 | a0001c0001t0001g0352 a0001c0003t0001g0136 |
2 | HG01261.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1270+1371A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779452 | |||||||
| chr8:28779510 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1270+1313A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779510 | |||||||
| chr8:28779639 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0343 |
2 | HG01168.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1270+1184C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779639 | |||||||
| chr8:28779669 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0005t0001g0293 |
3 | HG02258.hp2 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1270+1154G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779669 | |||||||
| chr8:28779818 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01884.hp1 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1270+1005T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779818 | |||||||
| chr8:28779887 | C | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1270+936G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28779887 | |||||||
| chr8:28780008 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0352 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1270+815C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780008 | |||||||
| chr8:28780044 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1270+779G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780044 | |||||||
| chr8:28780051 | A | AT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1270+771_1270+772i others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780051 | |||||||
| chr8:28780052 | G | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(138): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1270+771C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780052 | |||||||
| chr8:28780053 | G | GTT | 7 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG00639.hp1 HG01069.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1270+768_1270+769d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780053 | |||||||
| chr8:28780053 | G | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1270+770C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780053 | |||||||
| chr8:28780065 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1270+758A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780065 | |||||||
| chr8:28780069 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+754G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780069 | |||||||
| chr8:28780070 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+753A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780070 | |||||||
| chr8:28780076 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1270+747G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780076 | |||||||
| chr8:28780127 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1270+696G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780127 | |||||||
| chr8:28780129 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1270+694T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780129 | |||||||
| chr8:28780166 | GGAA | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1270+654_1270+656d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780166 | |||||||
| chr8:28780167 | G | T | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1270+656C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780167 | |||||||
| chr8:28780178 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0286 |
2 | NA18999.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1270+645T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780178 | |||||||
| chr8:28780227 | TA | T | 24 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0047 others(21): Show |
24 | HG00408.hp1 HG00621.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1270+595delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAA | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0050 others(28): Show |
31 | HG00280.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1270+594_1270+595d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAA | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0102 others(24): Show |
28 | HG00597.hp1 HG01109.hp2 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.1270+593_1270+595d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAA | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0110 others(12): Show |
15 | HG01070.hp1 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1270+592_1270+595d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(2): Show |
T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0029 others(15): Show |
18 | HG00735.hp2 HG01175.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.1270+587_1270+595d others(11): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(3): Show |
T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
79 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1270+586_1270+595d others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(4): Show |
T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0069 a0001c0001t0001g0156 others(8): Show |
12 | HG01069.hp1 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1270+585_1270+595d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1270+584_1270+595d others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(6): Show |
T | 25 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0152 others(22): Show |
25 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1270+583_1270+595d others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(7): Show |
T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(96): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1270+582_1270+595d others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(8): Show |
T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0277 a0001c0001t0001g0301 |
3 | HG01496.hp1 HG01943.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1270+581_1270+595d others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780227 | TAAAAAAA others(16): Show |
T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0009t0001g0208 |
3 | HG00140.hp1 HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1270+573_1270+595d others(25): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780227 | |||||||
| chr8:28780237 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1270+586T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780237 | |||||||
| chr8:28780341 | C | T | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1270+482G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780341 | |||||||
| chr8:28780356 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0002c0004t0002g0315 |
3 | HG02809.hp2 HG02965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1270+467T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780356 | |||||||
| chr8:28780515 | C | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1270+308G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780515 | |||||||
| chr8:28780554 | G | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1270+269C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780554 | |||||||
| chr8:28780608 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1270+215G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780608 | |||||||
| chr8:28780644 | A | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1270+179T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780644 | |||||||
| chr8:28780664 | C | A | 6 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(3): Show |
6 | HG00738.hp2 HG01243.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1270+159G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780664 | |||||||
| chr8:28780706 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1270+117G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780706 | |||||||
| chr8:28780752 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1270+71A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780752 | |||||||
| chr8:28780796 | A | G | 9 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0128 others(6): Show |
10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1270+27T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 12/16 | chr8 | 28780796 | |||||||
| chr8:28781060 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(61): Show |
65 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1099-66G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781060 | |||||||
| chr8:28781179 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-185G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781179 | |||||||
| chr8:28781223 | G | A | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1099-229C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781223 | |||||||
| chr8:28781296 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-302C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781296 | |||||||
| chr8:28781396 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1099-402C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781396 | |||||||
| chr8:28781587 | C | T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1099-593G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781587 | |||||||
| chr8:28781627 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1099-633G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781627 | |||||||
| chr8:28781752 | G | T | 9 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0128 others(6): Show |
10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-758C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781752 | |||||||
| chr8:28781758 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1099-764G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781758 | |||||||
| chr8:28781851 | G | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1099-857C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781851 | |||||||
| chr8:28781859 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1099-865C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781859 | |||||||
| chr8:28781884 | T | C | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-890A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781884 | |||||||
| chr8:28781927 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1099-933G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781927 | |||||||
| chr8:28781943 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-949G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781943 | |||||||
| chr8:28781944 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1099-950C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781944 | |||||||
| chr8:28781952 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0352 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1099-958C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781952 | |||||||
| chr8:28781953 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1099-959A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781953 | |||||||
| chr8:28781967 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1099-973C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28781967 | |||||||
| chr8:28782019 | T | A | 3 | a0001c0001t0005g0162 a0001c0001t0005g0176 a0003c0008t0001g0006 |
3 | HG02965.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-1025A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782019 | |||||||
| chr8:28782042 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-1048C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782042 | |||||||
| chr8:28782288 | T | A | 13 | a0001c0001t0001g0179 a0001c0001t0001g0222 a0001c0001t0001g0224 others(10): Show |
13 | NA18612.hp2 NA18944.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1099-1294A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782288 | |||||||
| chr8:28782304 | C | G | 15 | a0001c0001t0001g0289 a0001c0001t0001g0345 a0001c0001t0001g0352 others(12): Show |
15 | HG01261.hp1 HG02109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-1310G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782304 | |||||||
| chr8:28782352 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.1099-1358A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782352 | |||||||
| chr8:28782353 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1099-1359G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782353 | |||||||
| chr8:28782507 | T | C | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-1513A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782507 | |||||||
| chr8:28782539 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-1545C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782539 | |||||||
| chr8:28782770 | C | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(231): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1099-1776G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782770 | |||||||
| chr8:28782833 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-1839T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782833 | |||||||
| chr8:28782853 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(118): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1099-1859C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782853 | |||||||
| chr8:28782870 | A | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1099-1876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28782870 | |||||||
| chr8:28783031 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1099-2037C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783031 | |||||||
| chr8:28783093 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1099-2099G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783093 | |||||||
| chr8:28783102 | G | A | 11 | a0001c0001t0001g0289 a0001c0001t0001g0343 a0001c0001t0001g0345 others(8): Show |
11 | HG01261.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2108C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783102 | |||||||
| chr8:28783109 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1099-2115G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783109 | |||||||
| chr8:28783142 | C | CA | 17 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0121 others(14): Show |
17 | HG01261.hp1 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1099-2149dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | C | CAA | 11 | a0001c0001t0001g0045 a0001c0001t0001g0126 a0001c0001t0001g0345 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1099-2150_1099-214 others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CA | C | 54 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0047 others(51): Show |
55 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.1099-2149delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAA | C | 26 | a0001c0001t0001g0156 a0001c0001t0001g0172 a0001c0001t0001g0199 others(23): Show |
27 | HG00597.hp2 HG00738.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.1099-2151_1099-214 others(7): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAAA | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(95): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1099-2152_1099-214 others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAAAA | C | 6 | a0001c0001t0001g0175 a0001c0001t0001g0242 a0001c0001t0001g0246 others(3): Show |
6 | HG02258.hp1 HG02976.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-2153_1099-214 others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAAAAAA others(4): Show |
C | 12 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(9): Show |
12 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1099-2159_1099-214 others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAAAAAA others(5): Show |
C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1099-2160_1099-214 others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783142 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0005g0162 a0001c0001t0005g0176 a0003c0008t0001g0006 |
3 | HG02965.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1099-2161_1099-214 others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783142 | |||||||
| chr8:28783183 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-2189G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783183 | |||||||
| chr8:28783188 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-2194G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783188 | |||||||
| chr8:28783254 | A | G | 24 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(21): Show |
24 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-2260T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783254 | |||||||
| chr8:28783568 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1099-2574C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783568 | |||||||
| chr8:28783658 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1099-2664C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783658 | |||||||
| chr8:28783670 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1099-2676C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783670 | |||||||
| chr8:28783693 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-2699A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783693 | |||||||
| chr8:28783855 | T | C | 9 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0128 others(6): Show |
10 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-2861A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783855 | |||||||
| chr8:28783885 | A | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0302 |
2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1099-2891T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783885 | |||||||
| chr8:28783898 | G | C | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1099-2904C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28783898 | |||||||
| chr8:28784011 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1099-3017A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784011 | |||||||
| chr8:28784132 | T | A | 24 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(21): Show |
24 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1099-3138A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784132 | |||||||
| chr8:28784162 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1099-3168T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784162 | |||||||
| chr8:28784205 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1099-3211G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784205 | |||||||
| chr8:28784207 | A | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1099-3213T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784207 | |||||||
| chr8:28784221 | A | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | NA18947.hp1 NA19007.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-3227T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784221 | |||||||
| chr8:28784704 | G | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0220 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1098+3125C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784704 | |||||||
| chr8:28784705 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(117): Show |
122 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1098+3124C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784705 | |||||||
| chr8:28784758 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1098+3071G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784758 | |||||||
| chr8:28784954 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1098+2875G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28784954 | |||||||
| chr8:28785069 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0040 |
2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1098+2760A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785069 | |||||||
| chr8:28785140 | G | A | 13 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1098+2689C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785140 | |||||||
| chr8:28785188 | C | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1098+2641G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785188 | |||||||
| chr8:28785244 | A | G | 19 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(16): Show |
19 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1098+2585T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785244 | |||||||
| chr8:28785411 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1098+2418G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785411 | |||||||
| chr8:28785502 | T | C | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+2327A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785502 | |||||||
| chr8:28785543 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(185): Show |
191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1098+2286G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785543 | |||||||
| chr8:28785579 | C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1098+2250G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785579 | |||||||
| chr8:28785620 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1098+2209G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785620 | |||||||
| chr8:28785664 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1098+2165G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785664 | |||||||
| chr8:28785709 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1098+2120G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785709 | |||||||
| chr8:28785792 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1098+2037A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785792 | |||||||
| chr8:28785904 | G | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1098+1925C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785904 | |||||||
| chr8:28785940 | G | A | 2 | a0001c0001t0001g0282 a0001c0005t0001g0293 |
2 | HG02559.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1098+1889C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28785940 | |||||||
| chr8:28786205 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1098+1624A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786205 | |||||||
| chr8:28786226 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+1603G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786226 | |||||||
| chr8:28786300 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(63): Show |
67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.1098+1529C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786300 | |||||||
| chr8:28786327 | A | G | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1098+1502T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786327 | |||||||
| chr8:28786352 | T | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1098+1477A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786352 | |||||||
| chr8:28786583 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1098+1246C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786583 | |||||||
| chr8:28786672 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1098+1157G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786672 | |||||||
| chr8:28786729 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+1100A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786729 | |||||||
| chr8:28786766 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1098+1063T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786766 | |||||||
| chr8:28786829 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1098+1000A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786829 | |||||||
| chr8:28786863 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1098+966T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786863 | |||||||
| chr8:28786908 | G | A | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1098+921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786908 | |||||||
| chr8:28786952 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1098+877A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786952 | |||||||
| chr8:28786960 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1098+869T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28786960 | |||||||
| chr8:28787007 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+822C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787007 | |||||||
| chr8:28787013 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1098+816T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787013 | |||||||
| chr8:28787117 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1098+712A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787117 | |||||||
| chr8:28787141 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1098+688G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787141 | |||||||
| chr8:28787154 | TCATAATA others(4): Show |
T | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1098+664_1098+674d others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787154 | |||||||
| chr8:28787254 | A | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1098+575T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787254 | |||||||
| chr8:28787301 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1098+528A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787301 | |||||||
| chr8:28787440 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0055 others(118): Show |
123 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1098+389C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787440 | |||||||
| chr8:28787626 | G | A | 9 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0345 others(6): Show |
9 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1098+203C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787626 | |||||||
| chr8:28787681 | TA | T | 14 | a0001c0001t0001g0289 a0001c0001t0001g0343 a0001c0001t0002g0146 others(11): Show |
14 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1098+147delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787681 | |||||||
| chr8:28787754 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1098+75G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 11/16 | chr8 | 28787754 | |||||||
| chr8:28787971 | T | C | 7 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038-82A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28787971 | |||||||
| chr8:28788048 | G | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1038-159C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788048 | |||||||
| chr8:28788153 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0257 |
2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1038-264T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788153 | |||||||
| chr8:28788156 | G | C | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0070 others(11): Show |
14 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1038-267C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788156 | |||||||
| chr8:28788171 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1038-282G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788171 | |||||||
| chr8:28788217 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1038-328G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788217 | |||||||
| chr8:28788306 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1038-417T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788306 | |||||||
| chr8:28788324 | T | G | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038-435A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788324 | |||||||
| chr8:28788339 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0001g0337 |
2 | NA18963.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1038-450C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788339 | |||||||
| chr8:28788449 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1038-560G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788449 | |||||||
| chr8:28788562 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1038-673C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788562 | |||||||
| chr8:28788691 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
79 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1038-802A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788691 | |||||||
| chr8:28788890 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1038-1001T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788890 | |||||||
| chr8:28788941 | A | T | 3 | a0001c0003t0001g0136 a0001c0003t0001g0316 a0001c0003t0001g0351 |
3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1038-1052T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28788941 | |||||||
| chr8:28789092 | A | C | 14 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(11): Show |
14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1038-1203T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789092 | |||||||
| chr8:28789195 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1038-1306G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789195 | |||||||
| chr8:28789351 | T | C | 22 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0122 others(19): Show |
22 | HG00738.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1038-1462A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789351 | |||||||
| chr8:28789385 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1038-1496G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789385 | |||||||
| chr8:28789456 | AGGAGATC others(49): Show |
A | 4 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG00140.hp1 HG00323.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-1623_1038-156 others(60): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789456 | |||||||
| chr8:28789514 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1038-1625A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789514 | |||||||
| chr8:28789767 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1038-1878T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789767 | |||||||
| chr8:28789880 | AAACCAAC others(1): Show |
A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1038-1999_1038-199 others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789880 | |||||||
| chr8:28789909 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1038-2020T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28789909 | |||||||
| chr8:28790315 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1038-2426T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790315 | |||||||
| chr8:28790475 | G | A | 9 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0253 others(6): Show |
9 | HG01358.hp1 HG01496.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1038-2586C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790475 | |||||||
| chr8:28790513 | A | C | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1038-2624T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790513 | |||||||
| chr8:28790579 | T | C | 4 | a0001c0001t0001g0343 a0001c0001t0002g0349 a0001c0001t0003g0309 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038-2690A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790579 | |||||||
| chr8:28790774 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1038-2885G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790774 | |||||||
| chr8:28790944 | A | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2863T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790944 | |||||||
| chr8:28790969 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2838A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790969 | |||||||
| chr8:28790992 | G | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(111): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1037+2815C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28790992 | |||||||
| chr8:28791081 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+2726C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791081 | |||||||
| chr8:28791184 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1037+2623C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791184 | |||||||
| chr8:28791306 | C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1037+2501G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791306 | |||||||
| chr8:28791437 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+2370A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791437 | |||||||
| chr8:28791466 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1037+2341G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791466 | |||||||
| chr8:28791617 | G | A | 5 | a0001c0001t0001g0223 a0001c0001t0001g0237 a0001c0001t0001g0257 others(2): Show |
5 | NA18747.hp1 NA18944.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.1037+2190C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28791617 | |||||||
| chr8:28792048 | G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1037+1759C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792048 | |||||||
| chr8:28792062 | G | A | 1 | a0001c0009t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1037+1745C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792062 | |||||||
| chr8:28792148 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1037+1659G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792148 | |||||||
| chr8:28792269 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1037+1538T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792269 | |||||||
| chr8:28792336 | A | C | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037+1471T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792336 | |||||||
| chr8:28792552 | C | CA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(124): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1037+1254dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792552 | |||||||
| chr8:28792769 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1037+1038G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792769 | |||||||
| chr8:28792782 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+1025C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792782 | |||||||
| chr8:28792907 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1037+900G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792907 | |||||||
| chr8:28792912 | C | CA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1037+894dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792912 | |||||||
| chr8:28792946 | T | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+861A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792946 | |||||||
| chr8:28792984 | A | AG | 9 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0089 others(6): Show |
9 | HG00423.hp2 HG02071.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.1037+822dupC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792984 | |||||||
| chr8:28792986 | C | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1037+821G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792986 | |||||||
| chr8:28792991 | A | G | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1037+816T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28792991 | |||||||
| chr8:28793341 | G | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0215 others(6): Show |
10 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1037+466C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793341 | |||||||
| chr8:28793412 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1037+395T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793412 | |||||||
| chr8:28793456 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1037+351T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793456 | |||||||
| chr8:28793776 | T | TCA | 8 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0153 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037+29_1037+30dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793776 | |||||||
| chr8:28793779 | C | CA | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1037+27dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793779 | |||||||
| chr8:28793780 | A | AC | 3 | a0001c0001t0001g0241 a0001c0001t0001g0272 a0001c0001t0001g0353 |
3 | HG00733.hp2 HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1037+26_1037+27ins others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793780 | |||||||
| chr8:28793781 | A | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1037+26T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793781 | |||||||
| chr8:28793782 | A | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1037+25T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793782 | |||||||
| chr8:28793783 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
75 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1037+24T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793783 | |||||||
| chr8:28793785 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0150 |
3 | HG01074.hp1 HG03041.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1037+22T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793785 | |||||||
| chr8:28793795 | C | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0180 |
3 | HG02486.hp2 NA19240.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1037+12G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 10/16 | chr8 | 28793795 | |||||||
| chr8:28794040 | TATAAAG | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.857-59_857-54delCT others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794040 | |||||||
| chr8:28794229 | T | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.857-242A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794229 | |||||||
| chr8:28794284 | G | A | 13 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.857-297C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794284 | |||||||
| chr8:28794523 | G | A | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.857-536C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794523 | |||||||
| chr8:28794537 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.857-550A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794537 | |||||||
| chr8:28794730 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.857-743G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794730 | |||||||
| chr8:28794892 | G | GT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0249 a0001c0001t0001g0258 others(1): Show |
5 | HG00597.hp2 HG00673.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-906dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28794892 | |||||||
| chr8:28795092 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.857-1105G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795092 | |||||||
| chr8:28795093 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.857-1106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795093 | |||||||
| chr8:28795210 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.857-1223C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795210 | |||||||
| chr8:28795247 | C | A | 7 | a0001c0001t0001g0166 a0001c0001t0001g0183 a0001c0001t0001g0185 others(4): Show |
7 | HG02027.hp2 NA18941.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.857-1260G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795247 | |||||||
| chr8:28795338 | C | T | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.856+1206G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795338 | |||||||
| chr8:28795407 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(113): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.856+1137G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795407 | |||||||
| chr8:28795512 | C | A | 6 | a0001c0001t0002g0305 a0001c0001t0003g0309 a0001c0001t0003g0310 others(3): Show |
6 | HG01261.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.856+1032G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795512 | |||||||
| chr8:28795554 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.856+990G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795554 | |||||||
| chr8:28795556 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856+988G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795556 | |||||||
| chr8:28795582 | G | C | 7 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+962C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795582 | |||||||
| chr8:28795595 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.856+949C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795595 | |||||||
| chr8:28795614 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856+930A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795614 | |||||||
| chr8:28795639 | C | CA | 13 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0100 others(10): Show |
13 | HG00408.hp1 HG01928.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.856+904dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | |||||||
| chr8:28795639 | CAAA | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): Show |
77 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.856+902_856+904del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | |||||||
| chr8:28795639 | CAAAA | C | 24 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0147 others(21): Show |
24 | HG00323.hp1 HG00738.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.856+901_856+904del others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | |||||||
| chr8:28795639 | CAAAAA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.856+900_856+904del others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | |||||||
| chr8:28795639 | CAAAAAA | C | 7 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(4): Show |
7 | HG01261.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+899_856+904del others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795639 | |||||||
| chr8:28795646 | A | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.856+898T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795646 | |||||||
| chr8:28795742 | GA | G | 3 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.856+801delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795742 | |||||||
| chr8:28795824 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856+720C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28795824 | |||||||
| chr8:28796051 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.856+493C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796051 | |||||||
| chr8:28796080 | C | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0304 a0001c0001t0001g0340 |
3 | HG00558.hp2 NA18993.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.856+464G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796080 | |||||||
| chr8:28796086 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0311 |
2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.856+458C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796086 | |||||||
| chr8:28796087 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.856+457T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796087 | |||||||
| chr8:28796112 | C | T | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+432G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796112 | |||||||
| chr8:28796175 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856+369A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796175 | |||||||
| chr8:28796183 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.856+361C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796183 | |||||||
| chr8:28796237 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.856+307G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796237 | |||||||
| chr8:28796271 | C | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.856+273G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796271 | |||||||
| chr8:28796317 | C | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.856+227G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796317 | |||||||
| chr8:28796335 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.856+209T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796335 | |||||||
| chr8:28796411 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(120): Show |
125 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.856+133T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 9/16 | chr8 | 28796411 | |||||||
| chr8:28796695 | G | A | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-40C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796695 | |||||||
| chr8:28796791 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.745-136T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796791 | |||||||
| chr8:28796953 | A | G | 7 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-298T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796953 | |||||||
| chr8:28796991 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.745-336A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28796991 | |||||||
| chr8:28797088 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-433G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797088 | |||||||
| chr8:28797128 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.745-473C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797128 | |||||||
| chr8:28797188 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-533A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797188 | |||||||
| chr8:28797211 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.745-556T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797211 | |||||||
| chr8:28797289 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.745-634C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797289 | |||||||
| chr8:28797489 | A | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
81 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.745-834T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797489 | |||||||
| chr8:28797563 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.745-908C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797563 | |||||||
| chr8:28797577 | A | ACTCACCA others(119): Show |
1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-1048_745-923du others(127): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797577 | |||||||
| chr8:28797603 | G | T | 4 | a0001c0001t0001g0343 a0001c0003t0001g0136 a0001c0003t0001g0316 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-948C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797603 | |||||||
| chr8:28797724 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.745-1069C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797724 | |||||||
| chr8:28797898 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.745-1243A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797898 | |||||||
| chr8:28797915 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.745-1260G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797915 | |||||||
| chr8:28797924 | C | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1269G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28797924 | |||||||
| chr8:28798009 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.745-1354C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798009 | |||||||
| chr8:28798267 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1612C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798267 | |||||||
| chr8:28798414 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.745-1759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798414 | |||||||
| chr8:28798519 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.745-1864A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798519 | |||||||
| chr8:28798615 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1960G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798615 | |||||||
| chr8:28798784 | C | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.745-2129G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798784 | |||||||
| chr8:28798825 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.745-2170T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798825 | |||||||
| chr8:28798849 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.745-2194T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798849 | |||||||
| chr8:28798982 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-2327C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798982 | |||||||
| chr8:28798986 | T | C | 3 | a0001c0001t0001g0318 a0001c0001t0001g0328 a0004c0006t0001g0325 |
3 | NA18962.hp1 NA19067.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.745-2331A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28798986 | |||||||
| chr8:28799007 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.745-2352T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799007 | |||||||
| chr8:28799021 | G | C | 4 | a0001c0001t0001g0343 a0001c0003t0001g0136 a0001c0003t0001g0316 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-2366C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799021 | |||||||
| chr8:28799160 | C | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.745-2505G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799160 | |||||||
| chr8:28799189 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.745-2534C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799189 | |||||||
| chr8:28799193 | G | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-2538C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799193 | |||||||
| chr8:28799283 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.745-2628G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799283 | |||||||
| chr8:28799296 | C | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(113): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.745-2641G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799296 | |||||||
| chr8:28799323 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.745-2668C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799323 | |||||||
| chr8:28799342 | T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.745-2687A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799342 | |||||||
| chr8:28799594 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-2939G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799594 | |||||||
| chr8:28799662 | A | C | 4 | a0001c0001t0001g0343 a0001c0003t0001g0136 a0001c0003t0001g0316 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-3007T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799662 | |||||||
| chr8:28799676 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-3021G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799676 | |||||||
| chr8:28799677 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0259 |
2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.745-3022C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799677 | |||||||
| chr8:28799984 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.745-3329C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28799984 | |||||||
| chr8:28800064 | G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-3409C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800064 | |||||||
| chr8:28800093 | T | C | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.745-3438A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800093 | |||||||
| chr8:28800244 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.745-3589C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800244 | |||||||
| chr8:28800481 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.745-3826T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800481 | |||||||
| chr8:28800559 | T | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.745-3904A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800559 | |||||||
| chr8:28800559 | T | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.745-3904A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800559 | |||||||
| chr8:28800704 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.745-4049G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800704 | |||||||
| chr8:28800860 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4205G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800860 | |||||||
| chr8:28800998 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0187 |
2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.745-4343T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28800998 | |||||||
| chr8:28801047 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.745-4392G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801047 | |||||||
| chr8:28801134 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-4479C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801134 | |||||||
| chr8:28801173 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-4518A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801173 | |||||||
| chr8:28801315 | C | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-4660G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801315 | |||||||
| chr8:28801339 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.745-4684T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801339 | |||||||
| chr8:28801340 | A | G | 4 | a0001c0001t0001g0343 a0001c0003t0001g0136 a0001c0003t0001g0316 others(1): Show |
4 | HG01261.hp1 HG02451.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-4685T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801340 | |||||||
| chr8:28801348 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.745-4693C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801348 | |||||||
| chr8:28801505 | AC | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.745-4851delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801505 | |||||||
| chr8:28801506 | C | A | 19 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0088 others(16): Show |
19 | HG01070.hp2 HG01261.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.745-4851G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801506 | |||||||
| chr8:28801506 | CA | C | 7 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4852delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801506 | |||||||
| chr8:28801513 | A | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0005g0162 others(1): Show |
4 | HG02055.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-4858T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801513 | |||||||
| chr8:28801514 | C | A | 3 | a0001c0001t0001g0271 a0001c0001t0005g0162 a0001c0001t0005g0176 |
3 | HG03516.hp2 NA18522.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.745-4859G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801514 | |||||||
| chr8:28801531 | A | C | 7 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-4876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801531 | |||||||
| chr8:28801540 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.745-4885A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801540 | |||||||
| chr8:28801983 | G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.745-5328C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28801983 | |||||||
| chr8:28802002 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.745-5347A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802002 | |||||||
| chr8:28802047 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-5392G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802047 | |||||||
| chr8:28802217 | G | C | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-5562C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802217 | |||||||
| chr8:28802238 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(113): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.745-5583T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802238 | |||||||
| chr8:28802370 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.745-5715G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802370 | |||||||
| chr8:28802385 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.745-5730C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802385 | |||||||
| chr8:28802446 | C | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.745-5791G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802446 | |||||||
| chr8:28802693 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(119): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.745-6038T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802693 | |||||||
| chr8:28802946 | C | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.745-6291G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | |||||||
| chr8:28802946 | C | CA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0021 others(21): Show |
25 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.745-6292dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | |||||||
| chr8:28802946 | C | CAA | 7 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(4): Show |
7 | HG02572.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.745-6293_745-6292d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802946 | |||||||
| chr8:28802975 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.745-6320A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28802975 | |||||||
| chr8:28803378 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.745-6723G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803378 | |||||||
| chr8:28803379 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.745-6724T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803379 | |||||||
| chr8:28803491 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.745-6836C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803491 | |||||||
| chr8:28803679 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0070 |
2 | HG00323.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.745-7024A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803679 | |||||||
| chr8:28803769 | G | C | 3 | a0001c0003t0001g0136 a0001c0003t0001g0316 a0001c0003t0001g0351 |
3 | HG01261.hp1 HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.745-7114C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803769 | |||||||
| chr8:28803855 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-7200A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803855 | |||||||
| chr8:28803986 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745-7331G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28803986 | |||||||
| chr8:28804011 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-7356G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804011 | |||||||
| chr8:28804026 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.745-7371G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804026 | |||||||
| chr8:28804246 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.745-7591C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804246 | |||||||
| chr8:28804260 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.745-7605C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804260 | |||||||
| chr8:28804273 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.745-7618C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804273 | |||||||
| chr8:28804294 | A | T | 2 | a0001c0001t0002g0350 a0001c0005t0001g0293 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.745-7639T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804294 | |||||||
| chr8:28804467 | G | A | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.745-7812C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804467 | |||||||
| chr8:28804530 | A | C | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.744+7797T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804530 | |||||||
| chr8:28804559 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.744+7768C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804559 | |||||||
| chr8:28804583 | G | A | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.744+7744C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804583 | |||||||
| chr8:28804650 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0232 |
3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.744+7677C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804650 | |||||||
| chr8:28804682 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.744+7645C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804682 | |||||||
| chr8:28804901 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.744+7426T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28804901 | |||||||
| chr8:28805016 | T | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+7311A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805016 | |||||||
| chr8:28805121 | A | G | 8 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0153 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+7206T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805121 | |||||||
| chr8:28805161 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.744+7166T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805161 | |||||||
| chr8:28805229 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.744+7098C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805229 | |||||||
| chr8:28805373 | C | CT | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+6953dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805373 | |||||||
| chr8:28805497 | A | G | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+6830T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805497 | |||||||
| chr8:28805575 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(111): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.744+6752A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805575 | |||||||
| chr8:28805807 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.744+6520G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805807 | |||||||
| chr8:28805838 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.744+6489T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805838 | |||||||
| chr8:28805906 | G | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(107): Show |
112 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.744+6421C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28805906 | |||||||
| chr8:28806026 | T | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+6301A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806026 | |||||||
| chr8:28806086 | C | CA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.744+6240dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806086 | |||||||
| chr8:28806222 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+6105G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806222 | |||||||
| chr8:28806437 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.744+5890G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806437 | |||||||
| chr8:28806480 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.744+5847G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806480 | |||||||
| chr8:28806506 | TAA | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+5819_744+5820d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806506 | |||||||
| chr8:28806538 | A | G | 1 | a0004c0006t0001g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.744+5789T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806538 | |||||||
| chr8:28806587 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.744+5740G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806587 | |||||||
| chr8:28806721 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.744+5606A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806721 | |||||||
| chr8:28806789 | C | T | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0070 others(11): Show |
14 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.744+5538G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806789 | |||||||
| chr8:28806843 | G | A | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+5484C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806843 | |||||||
| chr8:28806960 | G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+5367C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28806960 | |||||||
| chr8:28807072 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744+5255A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807072 | |||||||
| chr8:28807073 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
81 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.744+5254C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807073 | |||||||
| chr8:28807102 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.744+5225A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807102 | |||||||
| chr8:28807602 | T | G | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+4725A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807602 | |||||||
| chr8:28807706 | T | C | 8 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0153 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+4621A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807706 | |||||||
| chr8:28807744 | C | A | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+4583G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807744 | |||||||
| chr8:28807958 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.744+4369A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807958 | |||||||
| chr8:28807991 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.744+4336T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28807991 | |||||||
| chr8:28808193 | AT | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0085 a0001c0001t0001g0238 others(4): Show |
7 | HG02572.hp2 HG02886.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+4133delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808193 | |||||||
| chr8:28808193 | ATT | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.744+4132_744+4133d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808193 | |||||||
| chr8:28808251 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.744+4076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808251 | |||||||
| chr8:28808378 | A | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.744+3949T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808378 | |||||||
| chr8:28808420 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.744+3907C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808420 | |||||||
| chr8:28808480 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.744+3847C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808480 | |||||||
| chr8:28808496 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.744+3831G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808496 | |||||||
| chr8:28808528 | C | A | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.744+3799G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808528 | |||||||
| chr8:28808752 | G | A | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+3575C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808752 | |||||||
| chr8:28808765 | G | A | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3562C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808765 | |||||||
| chr8:28808812 | C | G | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3515G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808812 | |||||||
| chr8:28808929 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.744+3398T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808929 | |||||||
| chr8:28808952 | C | CT | 9 | a0001c0001t0001g0078 a0001c0001t0001g0116 a0001c0001t0001g0118 others(6): Show |
9 | HG01069.hp1 HG01346.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.744+3374dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808952 | |||||||
| chr8:28808952 | CT | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.744+3374delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28808952 | |||||||
| chr8:28809023 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.744+3304G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809023 | |||||||
| chr8:28809024 | AC | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.744+3302delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809024 | |||||||
| chr8:28809026 | T | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.744+3301A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809026 | |||||||
| chr8:28809118 | T | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.744+3209A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809118 | |||||||
| chr8:28809121 | T | A | 17 | a0001c0001t0001g0156 a0001c0001t0002g0167 a0001c0001t0002g0168 others(14): Show |
18 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.744+3206A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809121 | |||||||
| chr8:28809143 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(109): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.744+3184C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809143 | |||||||
| chr8:28809198 | A | G | 1 | a0001c0001t0001g0323 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.744+3129T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809198 | |||||||
| chr8:28809265 | G | A | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+3062C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809265 | |||||||
| chr8:28809312 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.744+3015A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809312 | |||||||
| chr8:28809455 | C | G | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+2872G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809455 | |||||||
| chr8:28809658 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.744+2669G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809658 | |||||||
| chr8:28809820 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.744+2507G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809820 | |||||||
| chr8:28809849 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(114): Show |
119 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.744+2478G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809849 | |||||||
| chr8:28809978 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.744+2349A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28809978 | |||||||
| chr8:28810104 | T | C | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+2223A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810104 | |||||||
| chr8:28810331 | A | T | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.744+1996T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810331 | |||||||
| chr8:28810352 | T | TA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.744+1974dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810352 | |||||||
| chr8:28810422 | C | T | 4 | a0001c0001t0001g0170 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG00733.hp2 HG01074.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.744+1905G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810422 | |||||||
| chr8:28810429 | G | C | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.744+1898C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810429 | |||||||
| chr8:28810520 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.744+1807G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810520 | |||||||
| chr8:28810600 | TTCTCTC | T | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1721_744+1726d others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810600 | |||||||
| chr8:28810604 | C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+1723G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810604 | |||||||
| chr8:28810781 | C | CT | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(119): Show |
124 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.744+1545_744+1546i others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810781 | |||||||
| chr8:28810866 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+1461G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28810866 | |||||||
| chr8:28811099 | TTC | T | 21 | a0001c0001t0001g0156 a0001c0001t0002g0167 a0001c0001t0002g0168 others(18): Show |
22 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.744+1226_744+1227d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811099 | |||||||
| chr8:28811128 | CT | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(22): Show |
26 | HG00738.hp2 HG01243.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.744+1198delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811128 | |||||||
| chr8:28811128 | CTT | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(113): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.744+1197_744+1198d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811128 | |||||||
| chr8:28811221 | G | A | 9 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0068 others(6): Show |
9 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+1106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811221 | |||||||
| chr8:28811251 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.744+1076G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811251 | |||||||
| chr8:28811308 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.744+1019C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811308 | |||||||
| chr8:28811406 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.744+921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811406 | |||||||
| chr8:28811423 | CT | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.744+903delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811423 | |||||||
| chr8:28811465 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.744+862C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811465 | |||||||
| chr8:28811475 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.744+852T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811475 | |||||||
| chr8:28811940 | C | T | 1 | a0001c0002t0003g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.744+387G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811940 | |||||||
| chr8:28811941 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0271 |
2 | NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.744+386C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28811941 | |||||||
| chr8:28812219 | A | G | 10 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(7): Show |
10 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.744+108T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28812219 | |||||||
| chr8:28812223 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.744+104G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 8/16 | chr8 | 28812223 | |||||||
| chr8:28812493 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0267 |
2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.610-32C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812493 | |||||||
| chr8:28812779 | A | C | 1 | a0001c0001t0001g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.610-318T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812779 | |||||||
| chr8:28812804 | T | G | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-343A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812804 | |||||||
| chr8:28812827 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.610-366T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812827 | |||||||
| chr8:28812907 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
94 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.610-446C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28812907 | |||||||
| chr8:28813022 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.609+470C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813022 | |||||||
| chr8:28813229 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.609+263A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813229 | |||||||
| chr8:28813245 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.609+247G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813245 | |||||||
| chr8:28813266 | G | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.609+226C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813266 | |||||||
| chr8:28813278 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.609+214G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813278 | |||||||
| chr8:28813321 | G | A | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.609+171C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 7/16 | chr8 | 28813321 | |||||||
| chr8:28813679 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489-67T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813679 | |||||||
| chr8:28813705 | G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-93C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813705 | |||||||
| chr8:28813730 | T | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-118A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813730 | |||||||
| chr8:28813785 | A | G | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-173T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813785 | |||||||
| chr8:28813813 | T | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-201A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813813 | |||||||
| chr8:28813821 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.489-209G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813821 | |||||||
| chr8:28813830 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489-218C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813830 | |||||||
| chr8:28813868 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.489-256G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28813868 | |||||||
| chr8:28814060 | T | A | 2 | a0001c0003t0001g0136 a0001c0003t0001g0351 |
2 | HG01261.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.489-448A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814060 | |||||||
| chr8:28814070 | T | A | 17 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0066 others(14): Show |
17 | HG01261.hp1 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.489-458A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | |||||||
| chr8:28814070 | T | TA | 9 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0215 others(6): Show |
10 | HG02165.hp2 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-459dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | |||||||
| chr8:28814070 | TA | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0112 others(20): Show |
24 | HG01069.hp1 HG01081.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.489-459delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814070 | |||||||
| chr8:28814238 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.489-626G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814238 | |||||||
| chr8:28814282 | TCTCACAC others(5): Show |
T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-682_489-671del others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814282 | |||||||
| chr8:28814284 | T | A | 3 | a0001c0001t0002g0146 a0001c0001t0002g0264 a0002c0004t0002g0315 |
3 | HG02809.hp2 HG02965.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.489-672A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | T | TCA | 29 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0103 others(26): Show |
30 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.489-674_489-673dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | T | TCACA | 18 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0117 others(15): Show |
18 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.489-676_489-673dup others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | T | TCACACA | 6 | a0001c0001t0001g0065 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG00738.hp1 HG01255.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-678_489-673dup others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0130 a0001c0001t0001g0175 |
3 | HG01070.hp1 HG02258.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.489-682_489-673dup others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCA | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0023 others(46): Show |
52 | HG01168.hp1 HG01256.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.489-674_489-673del others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACA | T | 37 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0067 others(34): Show |
37 | HG00280.hp2 HG00733.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.489-676_489-673del others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACA | T | 87 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(84): Show |
87 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.489-678_489-673del others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(1): Show |
T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(36): Show |
40 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.489-680_489-673del others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(3): Show |
T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0098 a0001c0001t0001g0192 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.489-682_489-673del others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(5): Show |
T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0184 a0001c0001t0002g0168 others(2): Show |
5 | HG01243.hp2 HG01358.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.489-684_489-673del others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(9): Show |
T | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489-688_489-673del others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(11): Show |
T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0347 |
3 | HG01069.hp1 HG01167.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.489-690_489-673del others(18): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(13): Show |
T | 10 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0204 others(7): Show |
10 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.489-692_489-673del others(20): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814284 | TCACACAC others(15): Show |
T | 2 | a0001c0001t0001g0007 a0001c0001t0008g0194 |
2 | HG02451.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.489-694_489-673del others(22): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814284 | |||||||
| chr8:28814288 | A | T | 6 | a0001c0001t0004g0002 a0001c0001t0004g0153 a0001c0001t0004g0154 others(3): Show |
7 | HG02630.hp1 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.489-676T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814288 | |||||||
| chr8:28814290 | A | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489-678T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814290 | |||||||
| chr8:28814296 | A | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.489-684T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814296 | |||||||
| chr8:28814334 | A | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489-722T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814334 | |||||||
| chr8:28814341 | C | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(21): Show |
24 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.489-729G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814341 | |||||||
| chr8:28814547 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-935A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814547 | |||||||
| chr8:28814591 | C | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489-979G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814591 | |||||||
| chr8:28814703 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.489-1091C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814703 | |||||||
| chr8:28814756 | T | C | 1 | a0001c0001t0001g0327 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.489-1144A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814756 | |||||||
| chr8:28814844 | G | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(109): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-1232C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814844 | |||||||
| chr8:28814938 | T | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.489-1326A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28814938 | |||||||
| chr8:28815019 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-1407G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815019 | |||||||
| chr8:28815071 | G | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-1459C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815071 | |||||||
| chr8:28815146 | C | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-1534G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815146 | |||||||
| chr8:28815162 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-1550A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815162 | |||||||
| chr8:28815325 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.489-1713C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815325 | |||||||
| chr8:28815325 | G | T | 11 | a0001c0001t0001g0156 a0001c0001t0002g0349 a0001c0001t0003g0309 others(8): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.489-1713C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815325 | |||||||
| chr8:28815380 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.489-1768G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815380 | |||||||
| chr8:28815594 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-1982C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815594 | |||||||
| chr8:28815723 | C | T | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-2111G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815723 | |||||||
| chr8:28815863 | C | T | 8 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(5): Show |
8 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.489-2251G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815863 | |||||||
| chr8:28815872 | A | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-2260T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815872 | |||||||
| chr8:28815929 | A | T | 1 | a0001c0009t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489-2317T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28815929 | |||||||
| chr8:28816155 | A | C | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-2543T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816155 | |||||||
| chr8:28816230 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.489-2618C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816230 | |||||||
| chr8:28816260 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.489-2648C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816260 | |||||||
| chr8:28816449 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.489-2837G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816449 | |||||||
| chr8:28816456 | G | A | 10 | a0001c0001t0001g0156 a0001c0001t0003g0309 a0001c0001t0003g0310 others(7): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-2844C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816456 | |||||||
| chr8:28816458 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0071 |
3 | HG00639.hp1 HG01069.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.489-2846G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816458 | |||||||
| chr8:28816462 | G | A | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(109): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-2850C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816462 | |||||||
| chr8:28816527 | C | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(77): Show |
81 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.489-2915G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816527 | |||||||
| chr8:28816602 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.489-2990G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816602 | |||||||
| chr8:28816604 | C | G | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489-2992G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816604 | |||||||
| chr8:28816633 | T | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-3021A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816633 | |||||||
| chr8:28816640 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-3028T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816640 | |||||||
| chr8:28816644 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-3032G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816644 | |||||||
| chr8:28816723 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.489-3111G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816723 | |||||||
| chr8:28816724 | G | A | 10 | a0001c0001t0001g0156 a0001c0001t0003g0309 a0001c0001t0003g0310 others(7): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-3112C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816724 | |||||||
| chr8:28816814 | T | C | 2 | a0001c0001t0002g0264 a0002c0004t0002g0315 |
2 | HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.489-3202A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816814 | |||||||
| chr8:28816921 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(109): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-3309A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28816921 | |||||||
| chr8:28817052 | T | C | 8 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0153 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.489-3440A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817052 | |||||||
| chr8:28817078 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.489-3466G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817078 | |||||||
| chr8:28817419 | C | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-3807G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817419 | |||||||
| chr8:28817476 | G | A | 2 | a0001c0001t0002g0349 a0001c0001t0004g0128 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.489-3864C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817476 | |||||||
| chr8:28817563 | C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489-3951G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817563 | |||||||
| chr8:28817586 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-3974G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817586 | |||||||
| chr8:28817629 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.489-4017C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817629 | |||||||
| chr8:28817723 | TGAATCTA others(61): Show |
T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(109): Show |
114 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.489-4179_489-4112d others(70): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817723 | |||||||
| chr8:28817805 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4193A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817805 | |||||||
| chr8:28817838 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-4226A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817838 | |||||||
| chr8:28817882 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.489-4270C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28817882 | |||||||
| chr8:28818222 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.489-4610G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818222 | |||||||
| chr8:28818253 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4641C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818253 | |||||||
| chr8:28818275 | A | G | 5 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-4663T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818275 | |||||||
| chr8:28818434 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-4822C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818434 | |||||||
| chr8:28818483 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.489-4871A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818483 | |||||||
| chr8:28818564 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489-4952A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818564 | |||||||
| chr8:28818581 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-4969T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818581 | |||||||
| chr8:28818613 | C | G | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-5001G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818613 | |||||||
| chr8:28818635 | C | A | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.489-5023G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818635 | |||||||
| chr8:28818694 | T | C | 11 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-5082A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818694 | |||||||
| chr8:28818737 | C | T | 1 | a0001c0009t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.489-5125G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818737 | |||||||
| chr8:28818791 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.489-5179A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28818791 | |||||||
| chr8:28819159 | C | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-5547G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819159 | |||||||
| chr8:28819172 | A | T | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489-5560T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819172 | |||||||
| chr8:28819247 | G | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.489-5635C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819247 | |||||||
| chr8:28819485 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.489-5873T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819485 | |||||||
| chr8:28819503 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0251 a0001c0001t0001g0300 |
3 | NA18949.hp2 NA18960.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.489-5891G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819503 | |||||||
| chr8:28819628 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.489-6016A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819628 | |||||||
| chr8:28819670 | T | C | 2 | a0001c0001t0001g0352 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.489-6058A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819670 | |||||||
| chr8:28819688 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.489-6076C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819688 | |||||||
| chr8:28819867 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-6255A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819867 | |||||||
| chr8:28819966 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0273 |
2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.489-6354C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819966 | |||||||
| chr8:28819996 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-6384T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28819996 | |||||||
| chr8:28820251 | T | C | 2 | a0001c0003t0001g0136 a0001c0003t0001g0351 |
2 | HG01261.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.489-6639A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820251 | |||||||
| chr8:28820410 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.489-6798A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820410 | |||||||
| chr8:28820430 | A | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.489-6818T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820430 | |||||||
| chr8:28820582 | G | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-6970C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820582 | |||||||
| chr8:28820607 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.489-6995C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820607 | |||||||
| chr8:28820657 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.489-7045T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820657 | |||||||
| chr8:28820815 | T | C | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-7203A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820815 | |||||||
| chr8:28820849 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-7237C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820849 | |||||||
| chr8:28820850 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.489-7238C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820850 | |||||||
| chr8:28820916 | TA | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(114): Show |
119 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.489-7305delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28820916 | |||||||
| chr8:28821094 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7482A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821094 | |||||||
| chr8:28821217 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7605C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821217 | |||||||
| chr8:28821246 | C | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(64): Show |
68 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.489-7634G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821246 | |||||||
| chr8:28821255 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.489-7643G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821255 | |||||||
| chr8:28821303 | T | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489-7691A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821303 | |||||||
| chr8:28821348 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.489-7736C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821348 | |||||||
| chr8:28821456 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(110): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.489-7844G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821456 | |||||||
| chr8:28821575 | A | AAAC | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.489-7966_489-7964d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821575 | |||||||
| chr8:28821591 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0302 |
2 | NA18941.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.489-7979G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821591 | |||||||
| chr8:28821759 | G | GT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0211 a0001c0001t0001g0212 others(5): Show |
8 | HG01981.hp1 HG03471.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.489-8148dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821759 | |||||||
| chr8:28821794 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.489-8182T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28821794 | |||||||
| chr8:28822016 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.489-8404G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822016 | |||||||
| chr8:28822292 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.489-8680C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822292 | |||||||
| chr8:28822303 | CT | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(111): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.489-8692delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822303 | |||||||
| chr8:28822348 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.489-8736C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822348 | |||||||
| chr8:28822437 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489-8825G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822437 | |||||||
| chr8:28822574 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-8962T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822574 | |||||||
| chr8:28822600 | C | T | 10 | a0001c0001t0001g0156 a0001c0001t0003g0309 a0001c0001t0003g0310 others(7): Show |
11 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489-8988G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822600 | |||||||
| chr8:28822815 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.489-9203C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28822815 | |||||||
| chr8:28823012 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.489-9400G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823012 | |||||||
| chr8:28823049 | T | C | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-9437A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823049 | |||||||
| chr8:28823252 | C | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.489-9640G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823252 | |||||||
| chr8:28823349 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.489-9737C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823349 | |||||||
| chr8:28823482 | T | A | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-9870A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823482 | |||||||
| chr8:28823499 | G | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(62): Show |
66 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.489-9887C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823499 | |||||||
| chr8:28823500 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.489-9888A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823500 | |||||||
| chr8:28823540 | T | A | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-9928A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823540 | |||||||
| chr8:28823595 | AC | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(112): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.489-9984delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823595 | |||||||
| chr8:28823727 | A | G | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489-10115T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823727 | |||||||
| chr8:28823757 | TAACTC | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(63): Show |
67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.489-10150_489-1014 others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823757 | |||||||
| chr8:28823789 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.489-10177A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823789 | |||||||
| chr8:28823811 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.489-10199G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823811 | |||||||
| chr8:28823860 | T | G | 1 | a0001c0001t0001g0223 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.489-10248A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28823860 | |||||||
| chr8:28824072 | C | G | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489-10460G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824072 | |||||||
| chr8:28824164 | T | C | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.489-10552A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824164 | |||||||
| chr8:28824195 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.489-10583C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824195 | |||||||
| chr8:28824247 | A | G | 68 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(65): Show |
69 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.489-10635T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824247 | |||||||
| chr8:28824447 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.489-10835G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824447 | |||||||
| chr8:28824705 | T | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+10587A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824705 | |||||||
| chr8:28824712 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.488+10580G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824712 | |||||||
| chr8:28824791 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.488+10501C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824791 | |||||||
| chr8:28824919 | T | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+10373A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28824919 | |||||||
| chr8:28825033 | C | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.488+10259G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825033 | |||||||
| chr8:28825077 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
82 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.488+10215C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825077 | |||||||
| chr8:28825190 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.488+10102A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825190 | |||||||
| chr8:28825204 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.488+10088A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825204 | |||||||
| chr8:28825304 | G | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.488+9988C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825304 | |||||||
| chr8:28825511 | C | T | 11 | a0001c0001t0001g0156 a0001c0001t0002g0349 a0001c0001t0003g0309 others(8): Show |
12 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.488+9781G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825511 | |||||||
| chr8:28825734 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.488+9558A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825734 | |||||||
| chr8:28825783 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(111): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.488+9509G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825783 | |||||||
| chr8:28825846 | G | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.488+9446C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825846 | |||||||
| chr8:28825852 | C | A | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+9440G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825852 | |||||||
| chr8:28825963 | C | G | 11 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0070 others(8): Show |
11 | HG00280.hp2 HG00323.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.488+9329G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28825963 | |||||||
| chr8:28826045 | A | G | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(112): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.488+9247T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826045 | |||||||
| chr8:28826079 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | NA18973.hp1 NA18999.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.488+9213G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826079 | |||||||
| chr8:28826111 | A | G | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+9181T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826111 | |||||||
| chr8:28826114 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.488+9178C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826114 | |||||||
| chr8:28826311 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.488+8981T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826311 | |||||||
| chr8:28826312 | T | C | 65 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0016 others(62): Show |
66 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.488+8980A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826312 | |||||||
| chr8:28826356 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+8936G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826356 | |||||||
| chr8:28826445 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.488+8847C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826445 | |||||||
| chr8:28826451 | G | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+8841C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826451 | |||||||
| chr8:28826463 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0352 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.488+8829G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826463 | |||||||
| chr8:28826497 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+8795C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826497 | |||||||
| chr8:28826689 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0352 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.488+8603G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28826689 | |||||||
| chr8:28827090 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.488+8202C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827090 | |||||||
| chr8:28827354 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.488+7938C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827354 | |||||||
| chr8:28827356 | G | GT | 8 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(5): Show |
8 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.488+7935dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827356 | |||||||
| chr8:28827466 | G | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(121): Show |
127 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.488+7826C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827466 | |||||||
| chr8:28827511 | G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+7781C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827511 | |||||||
| chr8:28827643 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.488+7649C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827643 | |||||||
| chr8:28827656 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488+7636G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827656 | |||||||
| chr8:28827675 | C | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(120): Show |
126 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.488+7617G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827675 | |||||||
| chr8:28827704 | G | T | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.488+7588C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827704 | |||||||
| chr8:28827812 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.488+7480A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827812 | |||||||
| chr8:28827865 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.488+7427A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827865 | |||||||
| chr8:28827962 | G | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.488+7330C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827962 | |||||||
| chr8:28827968 | G | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.488+7324C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827968 | |||||||
| chr8:28827970 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA19004.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.488+7322T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28827970 | |||||||
| chr8:28828058 | G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+7234C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828058 | |||||||
| chr8:28828099 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7193G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828099 | |||||||
| chr8:28828100 | T | G | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7192A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828100 | |||||||
| chr8:28828101 | C | G | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7191G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828101 | |||||||
| chr8:28828102 | T | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.488+7190A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828102 | |||||||
| chr8:28828123 | T | G | 8 | a0001c0001t0001g0156 a0001c0001t0004g0002 a0001c0001t0004g0153 others(5): Show |
9 | HG02055.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.488+7169A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828123 | |||||||
| chr8:28828541 | C | A | 5 | a0001c0001t0001g0289 a0001c0001t0002g0146 a0001c0001t0002g0264 others(2): Show |
5 | HG02809.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+6751G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828541 | |||||||
| chr8:28828571 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG00621.hp2 HG02165.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.488+6721C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828571 | |||||||
| chr8:28828706 | T | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+6586A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28828706 | |||||||
| chr8:28829084 | T | G | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01884.hp1 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+6208A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829084 | |||||||
| chr8:28829154 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.488+6138G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829154 | |||||||
| chr8:28829379 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.488+5913C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829379 | |||||||
| chr8:28829450 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.488+5842T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829450 | |||||||
| chr8:28829667 | A | G | 4 | a0001c0001t0001g0345 a0001c0001t0002g0270 a0001c0001t0002g0305 others(1): Show |
4 | HG02630.hp2 HG03209.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+5625T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829667 | |||||||
| chr8:28829757 | G | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0186 others(2): Show |
5 | HG03041.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.488+5535C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829757 | |||||||
| chr8:28829780 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.488+5512G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829780 | |||||||
| chr8:28829838 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.488+5454A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829838 | |||||||
| chr8:28829919 | A | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+5373T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829919 | |||||||
| chr8:28829954 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.488+5338G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28829954 | |||||||
| chr8:28830052 | G | GA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
86 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.488+5239dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830052 | |||||||
| chr8:28830096 | G | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.488+5196C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830096 | |||||||
| chr8:28830208 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0088 a0001c0001t0002g0075 |
3 | HG02717.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.488+5084T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830208 | |||||||
| chr8:28830525 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(112): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.488+4767C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830525 | |||||||
| chr8:28830632 | T | TA | 9 | a0001c0001t0001g0185 a0001c0001t0001g0289 a0001c0001t0001g0290 others(6): Show |
9 | HG00621.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.488+4659dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830632 | |||||||
| chr8:28830632 | TA | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0047 others(4): Show |
7 | HG00639.hp1 HG02615.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+4659delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830632 | |||||||
| chr8:28830655 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.488+4637A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830655 | |||||||
| chr8:28830870 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.488+4422T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830870 | |||||||
| chr8:28830896 | C | A | 5 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(2): Show |
5 | HG02630.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.488+4396G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830896 | |||||||
| chr8:28830897 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.488+4395G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28830897 | |||||||
| chr8:28831050 | G | A | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.488+4242C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831050 | |||||||
| chr8:28831184 | T | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+4108A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831184 | |||||||
| chr8:28831314 | C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+3978G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831314 | |||||||
| chr8:28831371 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3921C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831371 | |||||||
| chr8:28831462 | A | T | 10 | a0001c0001t0001g0343 a0001c0001t0002g0167 a0001c0001t0002g0168 others(7): Show |
10 | HG00738.hp2 HG01243.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.488+3830T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831462 | |||||||
| chr8:28831499 | G | A | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.488+3793C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831499 | |||||||
| chr8:28831589 | A | T | 1 | a0001c0001t0001g0324 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.488+3703T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831589 | |||||||
| chr8:28831637 | G | A | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0345 others(4): Show |
7 | HG02055.hp1 HG02630.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+3655C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831637 | |||||||
| chr8:28831687 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.488+3605A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831687 | |||||||
| chr8:28831704 | T | C | 1 | a0001c0001t0001g0339 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.488+3588A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831704 | |||||||
| chr8:28831729 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0010t0003g0348 |
3 | HG02055.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.488+3563G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831729 | |||||||
| chr8:28831746 | T | G | 1 | a0001c0001t0007g0036 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.488+3546A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831746 | |||||||
| chr8:28831759 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.488+3533G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831759 | |||||||
| chr8:28831848 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.488+3444T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831848 | |||||||
| chr8:28831855 | C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+3437G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28831855 | |||||||
| chr8:28832232 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.488+3060G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832232 | |||||||
| chr8:28832460 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.488+2832C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832460 | |||||||
| chr8:28832617 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.488+2675C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832617 | |||||||
| chr8:28832651 | G | C | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.488+2641C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832651 | |||||||
| chr8:28832674 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.488+2618T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832674 | |||||||
| chr8:28832768 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.488+2524A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832768 | |||||||
| chr8:28832935 | C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.488+2357G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28832935 | |||||||
| chr8:28833065 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.488+2227T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833065 | |||||||
| chr8:28833101 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.488+2191C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833101 | |||||||
| chr8:28833109 | C | T | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.488+2183G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833109 | |||||||
| chr8:28833124 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.488+2168G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833124 | |||||||
| chr8:28833125 | G | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0098 |
2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.488+2167C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833125 | |||||||
| chr8:28833216 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.488+2076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833216 | |||||||
| chr8:28833425 | TC | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1866delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833425 | |||||||
| chr8:28833438 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.488+1854C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833438 | |||||||
| chr8:28833451 | C | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0097 |
3 | NA18961.hp1 NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.488+1841G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833451 | |||||||
| chr8:28833480 | T | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1812A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833480 | |||||||
| chr8:28833618 | TCAAAAAC others(5): Show |
T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.488+1662_488+1673d others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833618 | |||||||
| chr8:28833620 | A | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(115): Show |
120 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.488+1672T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833620 | |||||||
| chr8:28833638 | A | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.488+1654T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833638 | |||||||
| chr8:28833642 | ACAAAAAC | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1643_488+1649d others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833642 | |||||||
| chr8:28833650 | C | A | 7 | a0001c0001t0003g0314 a0001c0002t0003g0294 a0001c0002t0003g0295 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.488+1642G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833650 | |||||||
| chr8:28833651 | A | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1641T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833651 | |||||||
| chr8:28833678 | G | GA | 10 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0279 others(7): Show |
11 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.488+1613dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28833678 | |||||||
| chr8:28834189 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.488+1103G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834189 | |||||||
| chr8:28834215 | G | T | 1 | a0001c0001t0001g0109 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.488+1077C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834215 | |||||||
| chr8:28834288 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+1004G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834288 | |||||||
| chr8:28834321 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+971G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834321 | |||||||
| chr8:28834328 | A | C | 1 | a0001c0001t0004g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.488+964T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834328 | |||||||
| chr8:28834359 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0098 |
2 | HG01070.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.488+933G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834359 | |||||||
| chr8:28834546 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0001g0304 |
2 | HG00558.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.488+746G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834546 | |||||||
| chr8:28834663 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.488+629C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834663 | |||||||
| chr8:28834676 | G | GT | 66 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0047 others(63): Show |
67 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.488+615dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834676 | |||||||
| chr8:28834676 | GT | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(125): Show |
131 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.488+615delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834676 | |||||||
| chr8:28834885 | C | G | 1 | a0001c0001t0006g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.488+407G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834885 | |||||||
| chr8:28834968 | C | T | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.488+324G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834968 | |||||||
| chr8:28834971 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0058 |
2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.488+321G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28834971 | |||||||
| chr8:28835134 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.488+158A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835134 | |||||||
| chr8:28835155 | C | G | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.488+137G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835155 | |||||||
| chr8:28835266 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.488+26G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 6/16 | chr8 | 28835266 | |||||||
| chr8:28835421 | T | G | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-43A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835421 | |||||||
| chr8:28835598 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.402-220T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835598 | |||||||
| chr8:28835667 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(99): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.402-289G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835667 | |||||||
| chr8:28835698 | T | G | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.402-320A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835698 | |||||||
| chr8:28835797 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.402-419C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835797 | |||||||
| chr8:28835808 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-430C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835808 | |||||||
| chr8:28835873 | A | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.402-495T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28835873 | |||||||
| chr8:28836057 | G | A | 1 | a0001c0001t0004g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.402-679C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836057 | |||||||
| chr8:28836061 | C | T | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.402-683G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836061 | |||||||
| chr8:28836195 | A | C | 1 | a0001c0001t0001g0334 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.402-817T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836195 | |||||||
| chr8:28836250 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-872G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836250 | |||||||
| chr8:28836251 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.402-873C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836251 | |||||||
| chr8:28836289 | G | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.402-911C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836289 | |||||||
| chr8:28836294 | G | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.402-916C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836294 | |||||||
| chr8:28836312 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
83 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.402-934C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836312 | |||||||
| chr8:28836358 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.402-980A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836358 | |||||||
| chr8:28836576 | A | C | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(6): Show |
10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.401+1061T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836576 | |||||||
| chr8:28836698 | G | A | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(8): Show |
12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.401+939C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836698 | |||||||
| chr8:28836727 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
107 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.401+910A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836727 | |||||||
| chr8:28836770 | A | G | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.401+867T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836770 | |||||||
| chr8:28836857 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.401+780G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836857 | |||||||
| chr8:28836890 | C | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401+747G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836890 | |||||||
| chr8:28836906 | C | T | 2 | a0001c0001t0001g0311 a0001c0001t0001g0340 |
2 | HG00558.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.401+731G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28836906 | |||||||
| chr8:28837032 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.401+605G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837032 | |||||||
| chr8:28837248 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.401+389C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837248 | |||||||
| chr8:28837277 | TTTC | T | 13 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.401+357_401+359del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837277 | |||||||
| chr8:28837392 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0220 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.401+245C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837392 | |||||||
| chr8:28837437 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.401+200G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837437 | |||||||
| chr8:28837574 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401+63G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 5/16 | chr8 | 28837574 | |||||||
| chr8:28837844 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(112): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.262-68G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837844 | |||||||
| chr8:28837860 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.262-84G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837860 | |||||||
| chr8:28837941 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.262-165T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837941 | |||||||
| chr8:28837966 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-190G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28837966 | |||||||
| chr8:28838071 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.262-295G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838071 | |||||||
| chr8:28838163 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.262-387A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838163 | |||||||
| chr8:28838177 | T | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-401A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838177 | |||||||
| chr8:28838191 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0040 |
2 | HG01074.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.262-415C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838191 | |||||||
| chr8:28838300 | G | C | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-524C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838300 | |||||||
| chr8:28838355 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.262-579G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838355 | |||||||
| chr8:28838446 | T | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0232 |
3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.262-670A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838446 | |||||||
| chr8:28838521 | C | T | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(8): Show |
12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.262-745G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838521 | |||||||
| chr8:28838582 | C | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0234 a0001c0001t0001g0280 others(1): Show |
4 | HG02071.hp2 HG02602.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-806G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838582 | |||||||
| chr8:28838878 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.262-1102C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838878 | |||||||
| chr8:28838892 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.262-1116G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28838892 | |||||||
| chr8:28839042 | G | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-1266C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839042 | |||||||
| chr8:28839131 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1355C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839131 | |||||||
| chr8:28839203 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262-1427T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839203 | |||||||
| chr8:28839211 | T | C | 9 | a0001c0001t0001g0344 a0001c0001t0002g0350 a0001c0001t0003g0314 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.262-1435A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839211 | |||||||
| chr8:28839279 | T | G | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.262-1503A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839279 | |||||||
| chr8:28839328 | GT | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0088 others(1): Show |
4 | HG02723.hp1 HG03098.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1553delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839328 | |||||||
| chr8:28839345 | C | T | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1569G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839345 | |||||||
| chr8:28839346 | A | G | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1570T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839346 | |||||||
| chr8:28839472 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0047 others(60): Show |
64 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.262-1696G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839472 | |||||||
| chr8:28839477 | C | T | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-1701G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839477 | |||||||
| chr8:28839578 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(112): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.262-1802C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839578 | |||||||
| chr8:28839632 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0117 others(2): Show |
5 | HG00597.hp1 NA18951.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-1856G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839632 | |||||||
| chr8:28839638 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.262-1862T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839638 | |||||||
| chr8:28839741 | T | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG02145.hp1 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-1965A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839741 | |||||||
| chr8:28839821 | C | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2045G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839821 | |||||||
| chr8:28839916 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.262-2140C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839916 | |||||||
| chr8:28839933 | T | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | HG00733.hp2 HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.262-2157A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839933 | |||||||
| chr8:28839955 | C | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-2179G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28839955 | |||||||
| chr8:28840029 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0047 others(60): Show |
64 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.262-2253G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840029 | |||||||
| chr8:28840221 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2445C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840221 | |||||||
| chr8:28840270 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.262-2494T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840270 | |||||||
| chr8:28840294 | G | A | 1 | a0001c0001t0006g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.262-2518C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840294 | |||||||
| chr8:28840384 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.262-2608A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840384 | |||||||
| chr8:28840475 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.262-2699T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840475 | |||||||
| chr8:28840505 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.262-2729A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840505 | |||||||
| chr8:28840506 | G | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.262-2730C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840506 | |||||||
| chr8:28840581 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.262-2805C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840581 | |||||||
| chr8:28840665 | C | A | 14 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(11): Show |
14 | HG00735.hp1 HG01975.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-2889G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840665 | |||||||
| chr8:28840685 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2909G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840685 | |||||||
| chr8:28840686 | A | G | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2910T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840686 | |||||||
| chr8:28840731 | G | T | 1 | a0001c0001t0001g0038 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.262-2955C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840731 | |||||||
| chr8:28840734 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.262-2958G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840734 | |||||||
| chr8:28840797 | T | TG | 43 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0029 others(40): Show |
43 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.262-3022dupC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840797 | |||||||
| chr8:28840844 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-3068A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840844 | |||||||
| chr8:28840959 | T | TA | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0081 others(6): Show |
9 | HG02109.hp2 HG02723.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-3184dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840959 | |||||||
| chr8:28840967 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.262-3191T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840967 | |||||||
| chr8:28840970 | AG | A | 4 | a0001c0001t0001g0200 a0001c0001t0001g0328 a0001c0001t0002g0169 others(1): Show |
4 | HG02922.hp1 NA18522.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-3195delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840970 | |||||||
| chr8:28840971 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.262-3195C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840971 | |||||||
| chr8:28840988 | A | AGCAGATC others(4): Show |
4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3213_262-3212i others(13): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840988 | |||||||
| chr8:28840989 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3213G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840989 | |||||||
| chr8:28840992 | A | G | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3216T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28840992 | |||||||
| chr8:28841051 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.262-3275A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841051 | |||||||
| chr8:28841071 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(307): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(312): Show |
intron_variant | MODIFIER | c.262-3295G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841071 | |||||||
| chr8:28841257 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.262-3481G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841257 | |||||||
| chr8:28841386 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.262-3610T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841386 | |||||||
| chr8:28841703 | GA | G | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-3928delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841703 | |||||||
| chr8:28841782 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0066 |
2 | NA18978.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.262-4006G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841782 | |||||||
| chr8:28841866 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-4090C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841866 | |||||||
| chr8:28841867 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.262-4091G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841867 | |||||||
| chr8:28841944 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-4168G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28841944 | |||||||
| chr8:28842065 | G | C | 1 | a0001c0001t0001g0331 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.262-4289C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842065 | |||||||
| chr8:28842087 | C | CA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG01884.hp2 HG01981.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-4312dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842087 | |||||||
| chr8:28842096 | T | A | 1 | a0002c0004t0002g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.262-4320A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842096 | |||||||
| chr8:28842103 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0082 |
2 | HG01884.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.262-4327C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842103 | |||||||
| chr8:28842988 | C | T | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+3759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28842988 | |||||||
| chr8:28843027 | G | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | NA18974.hp2 NA18988.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.261+3720C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843027 | |||||||
| chr8:28843037 | T | G | 15 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(12): Show |
16 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.261+3710A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843037 | |||||||
| chr8:28843045 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.261+3702G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843045 | |||||||
| chr8:28843220 | G | A | 4 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+3527C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843220 | |||||||
| chr8:28843310 | G | A | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0047 others(57): Show |
61 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.261+3437C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843310 | |||||||
| chr8:28843348 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.261+3399C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843348 | |||||||
| chr8:28843636 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+3111C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843636 | |||||||
| chr8:28843663 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.261+3084A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843663 | |||||||
| chr8:28843753 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.261+2994C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843753 | |||||||
| chr8:28843834 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.261+2913G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843834 | |||||||
| chr8:28843835 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.261+2912T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843835 | |||||||
| chr8:28843908 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(99): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.261+2839A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28843908 | |||||||
| chr8:28844066 | G | C | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(8): Show |
12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2681C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844066 | |||||||
| chr8:28844077 | G | A | 14 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.261+2670C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844077 | |||||||
| chr8:28844105 | A | G | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.261+2642T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844105 | |||||||
| chr8:28844147 | C | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0047 others(57): Show |
61 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.261+2600G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844147 | |||||||
| chr8:28844187 | CTTTT | C | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(8): Show |
12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2556_261+2559d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844187 | |||||||
| chr8:28844214 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0064 others(116): Show |
121 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.261+2533A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844214 | |||||||
| chr8:28844216 | G | T | 22 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0001c0001t0001g0048 others(19): Show |
22 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+2531C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844216 | |||||||
| chr8:28844368 | C | G | 1 | a0001c0001t0001g0280 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.261+2379G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844368 | |||||||
| chr8:28844564 | G | A | 11 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(8): Show |
12 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.261+2183C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844564 | |||||||
| chr8:28844862 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.261+1885C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28844862 | |||||||
| chr8:28845011 | G | A | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1736C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845011 | |||||||
| chr8:28845095 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.261+1652G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845095 | |||||||
| chr8:28845282 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.261+1465G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845282 | |||||||
| chr8:28845426 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.261+1321C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845426 | |||||||
| chr8:28845525 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.261+1222A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28845525 | |||||||
| chr8:28846039 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.261+708G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846039 | |||||||
| chr8:28846369 | C | CTGGCACT others(10): Show |
1 | a0001c0001t0001g0260 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | |||||||
| chr8:28846369 | C | CTGGCATT others(10): Show |
237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | |||||||
| chr8:28846369 | C | CTGGCATT others(10): Show |
9 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(6): Show |
9 | HG02109.hp2 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+377_261+378ins others(17): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846369 | |||||||
| chr8:28846393 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.261+354A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846393 | |||||||
| chr8:28846475 | T | C | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.261+272A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 4/16 | chr8 | 28846475 | |||||||
| chr8:28846912 | C | G | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.199-103G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28846912 | |||||||
| chr8:28846984 | G | T | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-175C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28846984 | |||||||
| chr8:28847063 | C | A | 1 | a0001c0001t0004g0128 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.199-254G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847063 | |||||||
| chr8:28847132 | C | T | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.199-323G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847132 | |||||||
| chr8:28847268 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-459A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847268 | |||||||
| chr8:28847329 | C | T | 4 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0270 others(1): Show |
4 | HG02630.hp2 HG03225.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-520G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847329 | |||||||
| chr8:28847454 | TCCACCAC others(2): Show |
T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG00735.hp1 HG01975.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.199-654_199-646del others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847454 | |||||||
| chr8:28847468 | C | CACCACTA others(20): Show |
4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-686_199-660dup others(27): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847468 | |||||||
| chr8:28847603 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-794A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847603 | |||||||
| chr8:28847684 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-875T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847684 | |||||||
| chr8:28847794 | G | C | 4 | a0001c0001t0001g0289 a0001c0001t0001g0343 a0001c0001t0002g0146 others(1): Show |
4 | HG02809.hp2 HG06807.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-985C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28847794 | |||||||
| chr8:28848186 | A | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0071 |
3 | HG00639.hp1 HG01069.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.199-1377T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848186 | |||||||
| chr8:28848200 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-1391C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848200 | |||||||
| chr8:28848304 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.199-1495A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848304 | |||||||
| chr8:28848371 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-1562C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848371 | |||||||
| chr8:28848439 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
114 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.199-1630A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848439 | |||||||
| chr8:28848463 | T | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.199-1654A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848463 | |||||||
| chr8:28848483 | A | G | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1674T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848483 | |||||||
| chr8:28848548 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(111): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.198+1665A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848548 | |||||||
| chr8:28848555 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+1658C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848555 | |||||||
| chr8:28848645 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+1568A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848645 | |||||||
| chr8:28848750 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+1463A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848750 | |||||||
| chr8:28848758 | C | T | 14 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.198+1455G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848758 | |||||||
| chr8:28848897 | G | A | 2 | a0001c0001t0001g0335 a0001c0001t0001g0336 |
2 | NA18945.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.198+1316C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28848897 | |||||||
| chr8:28849046 | G | C | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.198+1167C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849046 | |||||||
| chr8:28849308 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198+905A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849308 | |||||||
| chr8:28849472 | T | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.198+741A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849472 | |||||||
| chr8:28849528 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.198+685A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849528 | |||||||
| chr8:28849541 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.198+672C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849541 | |||||||
| chr8:28849544 | A | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0235 a0001c0001t0001g0271 |
3 | NA18943.hp1 NA18978.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.198+669T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849544 | |||||||
| chr8:28849604 | G | A | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.198+609C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849604 | |||||||
| chr8:28849646 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+567G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849646 | |||||||
| chr8:28849663 | G | A | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+550C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849663 | |||||||
| chr8:28849984 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.198+229A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28849984 | |||||||
| chr8:28850053 | C | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
114 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.198+160G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850053 | |||||||
| chr8:28850105 | G | GA | 6 | a0001c0001t0001g0085 a0001c0001t0001g0248 a0001c0001t0002g0349 others(3): Show |
6 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+107dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850105 | |||||||
| chr8:28850105 | GA | G | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(6): Show |
10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+107delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850105 | |||||||
| chr8:28850126 | G | GTCACACT others(4): Show |
1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+76_198+86dupTA others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850126 | |||||||
| chr8:28850150 | G | C | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+63C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 3/16 | chr8 | 28850150 | |||||||
| chr8:28850408 | T | TAAAAAAT others(323): Show |
1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138-136_138-135ins others(330): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850408 | |||||||
| chr8:28850504 | A | G | 2 | a0001c0001t0001g0147 a0001c0001t0001g0281 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.138-231T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850504 | |||||||
| chr8:28850531 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.138-258T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850531 | |||||||
| chr8:28850702 | G | A | 19 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0113 others(16): Show |
19 | HG00597.hp1 HG00738.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.138-429C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850702 | |||||||
| chr8:28850735 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.138-462T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850735 | |||||||
| chr8:28850836 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.138-563T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850836 | |||||||
| chr8:28850867 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.138-594G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28850867 | |||||||
| chr8:28851129 | AGGATTTC others(370): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.138-1233_138-857de others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851129 | |||||||
| chr8:28851195 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.138-922C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851195 | |||||||
| chr8:28851315 | A | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
90 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.138-1042T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851315 | |||||||
| chr8:28851322 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.138-1049C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851322 | |||||||
| chr8:28851437 | G | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0214 a0001c0001t0001g0251 |
3 | NA18946.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.138-1164C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851437 | |||||||
| chr8:28851586 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(108): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.138-1313G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851586 | |||||||
| chr8:28851698 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
5 | HG02886.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-1425T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851698 | |||||||
| chr8:28851863 | T | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.138-1590A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851863 | |||||||
| chr8:28851946 | T | C | 4 | a0001c0001t0002g0349 a0001c0001t0003g0309 a0001c0001t0003g0310 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.138-1673A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851946 | |||||||
| chr8:28851958 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.138-1685G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28851958 | |||||||
| chr8:28852028 | G | A | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1755C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852028 | |||||||
| chr8:28852091 | CGCTT | C | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(6): Show |
10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.138-1822_138-1819d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852091 | |||||||
| chr8:28852130 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.138-1857C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852130 | |||||||
| chr8:28852294 | CT | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(126): Show |
132 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.138-2022delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852294 | |||||||
| chr8:28852294 | CTT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
111 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.138-2023_138-2022d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852294 | |||||||
| chr8:28852328 | A | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG01346.hp1 HG01928.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.138-2055T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852328 | |||||||
| chr8:28852350 | C | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-2077G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852350 | |||||||
| chr8:28852993 | T | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-2720A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852993 | |||||||
| chr8:28852995 | A | G | 7 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.138-2722T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28852995 | |||||||
| chr8:28853023 | A | G | 1 | a0001c0001t0006g0015 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.138-2750T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853023 | |||||||
| chr8:28853073 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.138-2800G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853073 | |||||||
| chr8:28853266 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG00642.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.138-2993T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853266 | |||||||
| chr8:28853296 | C | T | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.138-3023G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853296 | |||||||
| chr8:28853413 | C | CAAA | 17 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(14): Show |
18 | HG01261.hp1 HG02055.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.138-3143_138-3141d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853413 | |||||||
| chr8:28853527 | C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.138-3254G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853527 | |||||||
| chr8:28853675 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.138-3402G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853675 | |||||||
| chr8:28853692 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.138-3419T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853692 | |||||||
| chr8:28853770 | CT | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0215 others(6): Show |
10 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.138-3498delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853770 | |||||||
| chr8:28853777 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0093 |
3 | HG01243.hp1 HG01978.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.138-3504A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853777 | |||||||
| chr8:28853778 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.138-3505A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853778 | |||||||
| chr8:28853966 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.138-3693C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28853966 | |||||||
| chr8:28854012 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(88): Show |
92 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.138-3739G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854012 | |||||||
| chr8:28854230 | G | A | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138-3957C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854230 | |||||||
| chr8:28854394 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(105): Show |
110 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.138-4121C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854394 | |||||||
| chr8:28854493 | A | C | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-4220T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854493 | |||||||
| chr8:28854578 | T | C | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138-4305A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854578 | |||||||
| chr8:28854897 | T | C | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.137+4539A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28854897 | |||||||
| chr8:28855084 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.137+4352T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855084 | |||||||
| chr8:28855087 | C | T | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.137+4349G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855087 | |||||||
| chr8:28855097 | C | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | NA18943.hp2 NA18959.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+4339G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855097 | |||||||
| chr8:28855284 | A | G | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.137+4152T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855284 | |||||||
| chr8:28855819 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.137+3617C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855819 | |||||||
| chr8:28855984 | A | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0232 |
3 | NA18947.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.137+3452T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28855984 | |||||||
| chr8:28856097 | G | A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+3339C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856097 | |||||||
| chr8:28856120 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137+3316T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856120 | |||||||
| chr8:28856135 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.137+3301A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856135 | |||||||
| chr8:28856289 | G | T | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137+3147C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856289 | |||||||
| chr8:28856423 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.137+3013C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856423 | |||||||
| chr8:28856442 | G | GTCTC | 8 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(5): Show |
8 | HG02280.hp2 HG02886.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+2990_137+2993d others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856442 | |||||||
| chr8:28856456 | C | G | 1 | a0001c0001t0004g0291 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137+2980G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856456 | |||||||
| chr8:28856476 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG00323.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.137+2960G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856476 | |||||||
| chr8:28856661 | C | T | 2 | a0001c0001t0002g0146 a0002c0004t0002g0315 |
2 | HG02809.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.137+2775G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856661 | |||||||
| chr8:28856680 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.137+2756A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28856680 | |||||||
| chr8:28857121 | G | A | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.137+2315C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857121 | |||||||
| chr8:28857241 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.137+2195G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857241 | |||||||
| chr8:28857261 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0171 others(7): Show |
11 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.137+2175T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857261 | |||||||
| chr8:28857360 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
95 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.137+2076A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857360 | |||||||
| chr8:28857484 | G | GA | 3 | a0001c0001t0001g0102 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.137+1951dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857484 | |||||||
| chr8:28857560 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.137+1876T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857560 | |||||||
| chr8:28857622 | A | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137+1814T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857622 | |||||||
| chr8:28857657 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1779A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857657 | |||||||
| chr8:28857676 | T | A | 1 | a0001c0001t0001g0013 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.137+1760A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857676 | |||||||
| chr8:28857722 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1714T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857722 | |||||||
| chr8:28857836 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.137+1600G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857836 | |||||||
| chr8:28857935 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1501T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28857935 | |||||||
| chr8:28858009 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0017 others(1): Show |
4 | HG00673.hp2 HG02523.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+1427G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858009 | |||||||
| chr8:28858079 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.137+1357C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858079 | |||||||
| chr8:28858115 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.137+1321T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858115 | |||||||
| chr8:28858155 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137+1281C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858155 | |||||||
| chr8:28858160 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1276C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858160 | |||||||
| chr8:28858592 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+844A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858592 | |||||||
| chr8:28858790 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.137+646G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858790 | |||||||
| chr8:28858974 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0187 |
2 | HG02040.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.137+462A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28858974 | |||||||
| chr8:28859021 | T | TGAAAATA others(2874): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0308 |
2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.137+414_137+415ins others(2881): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859021 | |||||||
| chr8:28859080 | C | G | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.137+356G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859080 | |||||||
| chr8:28859192 | T | C | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(6): Show |
10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.137+244A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859192 | |||||||
| chr8:28859208 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.137+228C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859208 | |||||||
| chr8:28859267 | G | C | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(5): Show |
9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.137+169C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859267 | |||||||
| chr8:28859423 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.137+13G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 2/16 | chr8 | 28859423 | |||||||
| chr8:28859638 | T | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-75A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859638 | |||||||
| chr8:28859830 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG03704.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.10-267A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859830 | |||||||
| chr8:28859845 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-282G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28859845 | |||||||
| chr8:28860018 | C | T | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.10-455G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860018 | |||||||
| chr8:28860021 | GT | G | 9 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(6): Show |
10 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-459delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860021 | |||||||
| chr8:28860031 | TTAAC | T | 3 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0003t0001g0351 |
3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-472_10-469delGT others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860031 | |||||||
| chr8:28860121 | T | G | 1 | a0001c0001t0003g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.10-558A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860121 | |||||||
| chr8:28860147 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.10-584G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860147 | |||||||
| chr8:28860211 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0131 others(1): Show |
4 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-648T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860211 | |||||||
| chr8:28860300 | A | T | 3 | a0001c0001t0001g0318 a0001c0001t0001g0328 a0004c0006t0001g0325 |
3 | NA18962.hp1 NA19067.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.10-737T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860300 | |||||||
| chr8:28860323 | C | A | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-760G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860323 | |||||||
| chr8:28860475 | C | CT | 6 | a0001c0001t0001g0070 a0001c0001t0001g0150 a0001c0001t0001g0151 others(3): Show |
6 | HG00323.hp2 HG02280.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-913dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860475 | |||||||
| chr8:28860664 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10-1101T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860664 | |||||||
| chr8:28860843 | C | T | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-1280G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28860843 | |||||||
| chr8:28861120 | A | C | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.10-1557T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861120 | |||||||
| chr8:28861313 | C | A | 10 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
10 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-1750G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861313 | |||||||
| chr8:28861417 | C | T | 1 | a0002c0004t0002g0315 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.10-1854G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861417 | |||||||
| chr8:28861500 | T | C | 2 | a0001c0001t0001g0352 a0001c0001t0003g0314 |
2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-1937A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861500 | |||||||
| chr8:28861527 | G | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10-1964C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861527 | |||||||
| chr8:28861596 | C | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.10-2033G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861596 | |||||||
| chr8:28861767 | T | G | 24 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0170 others(21): Show |
25 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-2204A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861767 | |||||||
| chr8:28861770 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.10-2207C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28861770 | |||||||
| chr8:28862003 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.10-2440T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862003 | |||||||
| chr8:28862054 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-2491C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862054 | |||||||
| chr8:28862119 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-2556G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862119 | |||||||
| chr8:28862162 | G | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-2599C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862162 | |||||||
| chr8:28862520 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-2957A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862520 | |||||||
| chr8:28862522 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.10-2959G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862522 | |||||||
| chr8:28862547 | A | C | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-2984T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862547 | |||||||
| chr8:28862675 | T | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3112A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862675 | |||||||
| chr8:28862793 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3230G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862793 | |||||||
| chr8:28862902 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-3339G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28862902 | |||||||
| chr8:28863020 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02165.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.10-3457T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863020 | |||||||
| chr8:28863174 | A | AAGTGAAT others(270): Show |
1 | a0001c0001t0001g0045 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.10-3612_10-3611ins others(277): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863174 | |||||||
| chr8:28863212 | T | A | 1 | a0001c0001t0001g0332 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.10-3649A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863212 | |||||||
| chr8:28863530 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-3967G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863530 | |||||||
| chr8:28863547 | G | A | 24 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0170 others(21): Show |
25 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-3984C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863547 | |||||||
| chr8:28863593 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10-4030G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863593 | |||||||
| chr8:28863610 | T | C | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.10-4047A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863610 | |||||||
| chr8:28863611 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(110): Show |
115 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.10-4048T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863611 | |||||||
| chr8:28863612 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-4049G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863612 | |||||||
| chr8:28863677 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4114T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863677 | |||||||
| chr8:28863782 | A | AAAAAAC | 12 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0042 others(9): Show |
12 | HG01167.hp1 HG01346.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.10-4225_10-4220dup others(6): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863782 | |||||||
| chr8:28863856 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG02886.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-4293C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863856 | |||||||
| chr8:28863937 | T | C | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4374A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28863937 | |||||||
| chr8:28864076 | C | T | 9 | a0001c0001t0001g0193 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00280.hp2 HG00733.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-4513G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864076 | |||||||
| chr8:28864080 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-4517A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864080 | |||||||
| chr8:28864164 | G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-4601C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864164 | |||||||
| chr8:28864444 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-4881C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864444 | |||||||
| chr8:28864700 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0151 others(2): Show |
6 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-5137G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864700 | |||||||
| chr8:28864703 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-5140C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864703 | |||||||
| chr8:28864784 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.10-5221G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864784 | |||||||
| chr8:28864818 | A | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5255T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864818 | |||||||
| chr8:28864972 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5409A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864972 | |||||||
| chr8:28864985 | C | CA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0024 others(19): Show |
23 | HG01168.hp1 HG01346.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.10-5423dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864985 | |||||||
| chr8:28864995 | A | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01175.hp1 HG01516.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5432T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28864995 | |||||||
| chr8:28865249 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.10-5686T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865249 | |||||||
| chr8:28865259 | T | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
111 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.10-5696A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865259 | |||||||
| chr8:28865260 | A | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-5697T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865260 | |||||||
| chr8:28865472 | T | TA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0150 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-5910dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865472 | |||||||
| chr8:28865539 | T | C | 1 | a0001c0009t0001g0208 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.10-5976A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865539 | |||||||
| chr8:28865818 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.10-6255A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28865818 | |||||||
| chr8:28866237 | T | C | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-6674A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866237 | |||||||
| chr8:28866243 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.10-6680A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866243 | |||||||
| chr8:28866244 | A | G | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-6681T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866244 | |||||||
| chr8:28866283 | A | G | 38 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(35): Show |
39 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.10-6720T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866283 | |||||||
| chr8:28866402 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.10-6839A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866402 | |||||||
| chr8:28866492 | C | T | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-6929G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866492 | |||||||
| chr8:28866515 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-6952C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866515 | |||||||
| chr8:28866526 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.10-6963C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866526 | |||||||
| chr8:28866568 | T | G | 1 | a0001c0001t0001g0302 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.10-7005A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866568 | |||||||
| chr8:28866751 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.10-7188G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866751 | |||||||
| chr8:28866848 | G | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-7285C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866848 | |||||||
| chr8:28866970 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0343 a0001c0001t0001g0344 a0001c0001t0002g0350 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-7408_10-7407ins others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | |||||||
| chr8:28866970 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0342 |
3 | HG02886.hp1 HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.10-7408_10-7407ins others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | |||||||
| chr8:28866970 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.10-7408_10-7407ins others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28866970 | |||||||
| chr8:28867030 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0003t0001g0351 |
3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-7467A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867030 | |||||||
| chr8:28867052 | C | T | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-7489G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867052 | |||||||
| chr8:28867264 | A | AAAAC | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-7702_10-7701ins others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867264 | |||||||
| chr8:28867440 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10-7877A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867440 | |||||||
| chr8:28867450 | A | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-7887T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867450 | |||||||
| chr8:28867459 | C | T | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-7896G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867459 | |||||||
| chr8:28867526 | G | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-7963C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867526 | |||||||
| chr8:28867531 | T | TA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0091 a0001c0001t0001g0144 others(4): Show |
7 | HG01081.hp2 HG02300.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-7969dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867531 | |||||||
| chr8:28867531 | TA | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0021 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.10-7969delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867531 | |||||||
| chr8:28867532 | A | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(108): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.10-7969T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867532 | |||||||
| chr8:28867577 | AACT | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.10-8017_10-8015del others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867577 | |||||||
| chr8:28867606 | A | G | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-8043T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867606 | |||||||
| chr8:28867665 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10-8102T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867665 | |||||||
| chr8:28867677 | G | A | 2 | a0001c0001t0001g0267 a0001c0003t0001g0316 |
2 | HG02451.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.10-8114C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867677 | |||||||
| chr8:28867719 | G | GT | 21 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(18): Show |
21 | HG00741.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.10-8157dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867719 | |||||||
| chr8:28867764 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.10-8201T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867764 | |||||||
| chr8:28867897 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
95 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.10-8334C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867897 | |||||||
| chr8:28867948 | T | C | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-8385A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28867948 | |||||||
| chr8:28868070 | A | G | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0003g0309 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-8507T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868070 | |||||||
| chr8:28868106 | T | C | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0003g0309 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-8543A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868106 | |||||||
| chr8:28868516 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0007g0036 |
2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.10-8953C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868516 | |||||||
| chr8:28868556 | G | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-8993C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868556 | |||||||
| chr8:28868795 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.10-9232A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868795 | |||||||
| chr8:28868840 | T | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0344 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-9277A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868840 | |||||||
| chr8:28868841 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.10-9278C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868841 | |||||||
| chr8:28868869 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-9306C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868869 | |||||||
| chr8:28868881 | CT | C | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0003g0309 others(2): Show |
5 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-9319delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868881 | |||||||
| chr8:28868916 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.10-9353A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868916 | |||||||
| chr8:28868919 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.10-9356G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868919 | |||||||
| chr8:28868942 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(112): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.10-9379A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28868942 | |||||||
| chr8:28869012 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-9449A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869012 | |||||||
| chr8:28869525 | A | G | 10 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
10 | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-9962T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869525 | |||||||
| chr8:28869543 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-9980T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869543 | |||||||
| chr8:28869644 | A | G | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-10081T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869644 | |||||||
| chr8:28869650 | G | A | 9 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-10087C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869650 | |||||||
| chr8:28869997 | T | C | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-10434A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28869997 | |||||||
| chr8:28870117 | A | C | 1 | a0001c0001t0001g0333 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.10-10554T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870117 | |||||||
| chr8:28870135 | C | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | NA18943.hp2 NA18959.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-10572G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870135 | |||||||
| chr8:28870145 | T | C | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.10-10582A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870145 | |||||||
| chr8:28870319 | A | AT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.10-10757dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870319 | |||||||
| chr8:28870319 | A | ATT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0342 a0001c0001t0001g0343 others(3): Show |
6 | HG00738.hp2 HG01243.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-10758_10-10757d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870319 | |||||||
| chr8:28870349 | CT | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0019 others(77): Show |
81 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.10-10787delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | |||||||
| chr8:28870349 | CTT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.10-10788_10-10787d others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | |||||||
| chr8:28870349 | CTTT | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0283 others(8): Show |
11 | HG01516.hp1 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.10-10789_10-10787d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | |||||||
| chr8:28870349 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0352 a0001c0003t0001g0351 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.10-10799_10-10787d others(15): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870349 | |||||||
| chr8:28870357 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.10-10794A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870357 | |||||||
| chr8:28870358 | T | C | 2 | a0001c0001t0001g0344 a0001c0001t0002g0350 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.10-10795A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870358 | |||||||
| chr8:28870408 | C | A | 2 | a0001c0001t0003g0314 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.10-10845G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28870408 | |||||||
| chr8:28871151 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-11588T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871151 | |||||||
| chr8:28871161 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10-11598G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871161 | |||||||
| chr8:28871354 | A | G | 2 | a0001c0001t0003g0309 a0001c0001t0003g0310 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.10-11791T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871354 | |||||||
| chr8:28871474 | G | A | 2 | a0001c0001t0005g0162 a0001c0001t0005g0176 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.10-11911C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871474 | |||||||
| chr8:28871610 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.10-12047A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871610 | |||||||
| chr8:28871658 | G | A | 1 | a0001c0005t0001g0293 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.10-12095C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871658 | |||||||
| chr8:28871748 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0281 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.10-12185C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871748 | |||||||
| chr8:28871754 | A | C | 2 | a0001c0002t0003g0294 a0001c0002t0003g0297 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.10-12191T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871754 | |||||||
| chr8:28871763 | T | C | 2 | a0001c0002t0003g0294 a0001c0002t0003g0297 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.10-12200A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871763 | |||||||
| chr8:28871810 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0304 |
2 | HG00558.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.10-12247A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871810 | |||||||
| chr8:28871825 | G | T | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.10-12262C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871825 | |||||||
| chr8:28871849 | T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.10-12286A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871849 | |||||||
| chr8:28871943 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0311 a0001c0001t0001g0340 |
3 | HG00558.hp1 NA18993.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.10-12380T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28871943 | |||||||
| chr8:28872060 | C | G | 5 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.10-12497G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872060 | |||||||
| chr8:28872122 | A | G | 3 | a0001c0001t0001g0345 a0001c0001t0001g0346 a0001c0001t0002g0305 |
3 | HG02630.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-12559T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872122 | |||||||
| chr8:28872129 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.10-12566T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872129 | |||||||
| chr8:28872223 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.10-12660A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872223 | |||||||
| chr8:28872375 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10-12812A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872375 | |||||||
| chr8:28872408 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.10-12845C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28872408 | |||||||
| chr8:28873007 | T | G | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.10-13444A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873007 | |||||||
| chr8:28873051 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0087 |
2 | HG01243.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.10-13488C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873051 | |||||||
| chr8:28873101 | TA | T | 4 | a0001c0002t0003g0294 a0001c0002t0003g0295 a0001c0002t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-13539delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873101 | |||||||
| chr8:28873714 | T | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG01167.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.10-14151A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873714 | |||||||
| chr8:28873801 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.10-14238A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873801 | |||||||
| chr8:28873905 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.10-14342A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873905 | |||||||
| chr8:28873931 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10-14368T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873931 | |||||||
| chr8:28873997 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.10-14434A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28873997 | |||||||
| chr8:28874048 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.10-14485A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874048 | |||||||
| chr8:28874100 | ATTC | A | 3 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0003t0001g0351 |
3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.10-14540_10-14538d others(5): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874100 | |||||||
| chr8:28874289 | G | GT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0083 others(3): Show |
6 | HG01109.hp1 HG02109.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-14727dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874289 | |||||||
| chr8:28874322 | C | T | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(5): Show |
9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-14759G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874322 | |||||||
| chr8:28874450 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.10-14887G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874450 | |||||||
| chr8:28874451 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.10-14888C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874451 | |||||||
| chr8:28874606 | A | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.10-15043T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874606 | |||||||
| chr8:28874814 | A | C | 1 | a0001c0001t0001g0231 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.9+15060T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874814 | |||||||
| chr8:28874890 | G | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0164 others(41): Show |
45 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.9+14984C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28874890 | |||||||
| chr8:28875111 | C | A | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+14763G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875111 | |||||||
| chr8:28875155 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0084 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+14719C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875155 | |||||||
| chr8:28875172 | G | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0286 |
2 | NA18970.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.9+14702C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875172 | |||||||
| chr8:28875249 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+14625C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875249 | |||||||
| chr8:28875289 | C | CA | 13 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(10): Show |
13 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+14584dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875289 | |||||||
| chr8:28875371 | T | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0137 others(112): Show |
117 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.9+14503A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875371 | |||||||
| chr8:28875432 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0076 a0001c0001t0001g0077 others(4): Show |
7 | HG01167.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+14442C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875432 | |||||||
| chr8:28875624 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.9+14250C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875624 | |||||||
| chr8:28875709 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9+14165A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875709 | |||||||
| chr8:28875827 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.9+14047C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875827 | |||||||
| chr8:28875939 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02056.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.9+13935G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28875939 | |||||||
| chr8:28876001 | C | T | 4 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+13873G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876001 | |||||||
| chr8:28876098 | C | T | 12 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+13776G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876098 | |||||||
| chr8:28876569 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.9+13305A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28876569 | |||||||
| chr8:28877057 | A | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0043 others(1): Show |
5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+12817T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877057 | |||||||
| chr8:28877254 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.9+12620T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877254 | |||||||
| chr8:28877353 | A | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG01975.hp2 HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.9+12521T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877353 | |||||||
| chr8:28877534 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9+12340G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877534 | |||||||
| chr8:28877577 | T | A | 1 | a0001c0001t0001g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.9+12297A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877577 | |||||||
| chr8:28877644 | T | A | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.9+12230A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877644 | |||||||
| chr8:28877668 | A | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
6 | HG00735.hp2 HG01175.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.9+12206T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877668 | |||||||
| chr8:28877742 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+12132C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877742 | |||||||
| chr8:28877854 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+12020C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877854 | |||||||
| chr8:28877908 | C | A | 12 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+11966G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28877908 | |||||||
| chr8:28878208 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.9+11666A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878208 | |||||||
| chr8:28878278 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0043 others(1): Show |
5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11596C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878278 | |||||||
| chr8:28878338 | G | A | 5 | a0001c0001t0001g0352 a0001c0001t0002g0312 a0001c0001t0002g0349 others(2): Show |
5 | HG02280.hp2 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11536C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878338 | |||||||
| chr8:28878477 | T | TA | 26 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0138 others(23): Show |
27 | HG01175.hp2 HG01261.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.9+11396dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878477 | |||||||
| chr8:28878518 | G | T | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+11356C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878518 | |||||||
| chr8:28878549 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+11325G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878549 | |||||||
| chr8:28878590 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.9+11284C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878590 | |||||||
| chr8:28878606 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.9+11268C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878606 | |||||||
| chr8:28878628 | G | GT | 8 | a0001c0001t0001g0102 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG01261.hp1 HG02559.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+11245dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878628 | |||||||
| chr8:28878628 | G | GTT | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(3): Show |
7 | HG02622.hp1 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+11244_9+11245dup others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878628 | |||||||
| chr8:28878641 | T | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0279 others(2): Show |
5 | HG00738.hp1 HG01070.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.9+11233A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878641 | |||||||
| chr8:28878641 | T | TA | 12 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+11232dupT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878641 | |||||||
| chr8:28878642 | A | T | 16 | a0001c0001t0001g0047 a0001c0001t0001g0102 a0001c0001t0001g0150 others(13): Show |
16 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.9+11232T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878642 | |||||||
| chr8:28878643 | A | T | 4 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11231T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878643 | |||||||
| chr8:28878644 | A | T | 4 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+11230T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878644 | |||||||
| chr8:28878647 | A | C | 6 | a0001c0001t0001g0353 a0001c0002t0003g0294 a0001c0002t0003g0295 others(3): Show |
6 | HG00741.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.9+11227T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878647 | |||||||
| chr8:28878652 | C | A | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+11222G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878652 | |||||||
| chr8:28878670 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18747.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.9+11204A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878670 | |||||||
| chr8:28878766 | G | C | 8 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0276 others(5): Show |
8 | HG01358.hp1 HG01496.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+11108C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878766 | |||||||
| chr8:28878767 | G | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0043 others(1): Show |
5 | HG00140.hp2 HG01884.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+11107C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878767 | |||||||
| chr8:28878791 | C | T | 10 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0181 others(7): Show |
11 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.9+11083G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878791 | |||||||
| chr8:28878890 | G | C | 1 | a0001c0001t0002g0305 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.9+10984C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878890 | |||||||
| chr8:28878978 | CA | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(308): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.9+10895delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28878978 | |||||||
| chr8:28879045 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0281 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.9+10829C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879045 | |||||||
| chr8:28879250 | CAGGAATG others(890): Show |
C | 1 | a0001c0001t0001g0307 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.9+9727_9+10623del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879250 | |||||||
| chr8:28879338 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.9+10536A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879338 | |||||||
| chr8:28879399 | G | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0137 others(108): Show |
113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.9+10475C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879399 | |||||||
| chr8:28879606 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.9+10268A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879606 | |||||||
| chr8:28879712 | G | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | HG02165.hp2 NA18963.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+10162C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879712 | |||||||
| chr8:28879809 | T | A | 12 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+10065A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879809 | |||||||
| chr8:28879823 | C | A | 1 | a0004c0006t0001g0325 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.9+10051G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879823 | |||||||
| chr8:28879981 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9+9893A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28879981 | |||||||
| chr8:28880034 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.9+9840A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880034 | |||||||
| chr8:28880131 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.9+9743T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880131 | |||||||
| chr8:28880225 | G | GCTCTCC | 9 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0083 others(6): Show |
9 | HG01109.hp1 HG02723.hp1 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+9643_9+9648dupGG others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880225 | G | GCTCTCCC others(11): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0166 |
2 | HG02486.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.9+9631_9+9648dupGG others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880225 | GCTCTCC | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(65): Show |
69 | HG00735.hp1 HG00735.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.9+9643_9+9648delGG others(4): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880225 | GCTCTCCC others(5): Show |
G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0027 others(130): Show |
135 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.9+9637_9+9648delGG others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880225 | GCTCTCCC others(11): Show |
G | 4 | a0001c0001t0001g0227 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+9631_9+9648delGG others(16): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880225 | GCTCTCCC others(17): Show |
G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0171 a0001c0001t0001g0342 others(1): Show |
4 | HG02886.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+9625_9+9648delGG others(22): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880225 | |||||||
| chr8:28880249 | CCTCTCCC others(7): Show |
C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9611_9+9624delAG others(12): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880249 | |||||||
| chr8:28880275 | T | A | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9599A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880275 | |||||||
| chr8:28880277 | T | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9597A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | |||||||
| chr8:28880277 | T | TCCCTCTC others(223): Show |
1 | a0001c0001t0001g0150 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.9+9596_9+9597insGG others(228): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | |||||||
| chr8:28880277 | T | TCCCTCTC others(265): Show |
1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.9+9596_9+9597insGG others(270): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880277 | |||||||
| chr8:28880278 | C | G | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+9596G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880278 | |||||||
| chr8:28880385 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.9+9489T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880385 | |||||||
| chr8:28880419 | T | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+9455A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880419 | |||||||
| chr8:28880422 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02040.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.9+9452G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880422 | |||||||
| chr8:28880431 | G | GT | 24 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
24 | HG00423.hp2 HG01175.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.9+9442dupA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880431 | |||||||
| chr8:28880469 | C | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0164 others(46): Show |
50 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.9+9405G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880469 | |||||||
| chr8:28880506 | C | T | 7 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG02572.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+9368G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880506 | |||||||
| chr8:28880521 | G | A | 9 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+9353C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880521 | |||||||
| chr8:28880589 | G | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0343 |
2 | HG01975.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9+9285C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880589 | |||||||
| chr8:28880775 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
215 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.9+9099C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880775 | |||||||
| chr8:28880865 | G | A | 14 | a0001c0001t0001g0170 a0001c0001t0001g0202 a0001c0001t0001g0203 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.9+9009C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880865 | |||||||
| chr8:28880876 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8998C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28880876 | |||||||
| chr8:28881007 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.9+8867T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881007 | |||||||
| chr8:28881029 | C | T | 3 | a0001c0001t0001g0344 a0001c0001t0003g0309 a0001c0001t0003g0310 |
3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+8845G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881029 | |||||||
| chr8:28881035 | AGAAGTGA others(33): Show |
A | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9+8799_9+8838delCC others(38): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881035 | |||||||
| chr8:28881055 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.9+8819A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881055 | |||||||
| chr8:28881100 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | NA18944.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.9+8774G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881100 | |||||||
| chr8:28881131 | G | C | 4 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8743C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881131 | |||||||
| chr8:28881135 | GC | G | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8738delG | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881135 | |||||||
| chr8:28881173 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.9+8701C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881173 | |||||||
| chr8:28881175 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.9+8699C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881175 | |||||||
| chr8:28881206 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.9+8668A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881206 | |||||||
| chr8:28881215 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
222 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.9+8659G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881215 | |||||||
| chr8:28881219 | TGCCCGGC others(42): Show |
T | 1 | a0001c0001t0001g0106 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.9+8606_9+8654delGG others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881219 | |||||||
| chr8:28881252 | G | T | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+8622C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881252 | |||||||
| chr8:28881285 | AGTCCGGG others(269): Show |
A | 8 | a0001c0001t0001g0179 a0001c0001t0001g0284 a0001c0001t0001g0285 others(5): Show |
8 | HG02109.hp2 HG02896.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.9+8313_9+8588del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881285 | |||||||
| chr8:28881316 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.9+8558G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881316 | |||||||
| chr8:28881330 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.9+8544C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881330 | |||||||
| chr8:28881363 | G | A | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+8511C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881363 | |||||||
| chr8:28881398 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG00738.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.9+8476G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881398 | |||||||
| chr8:28881416 | C | T | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+8458G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881416 | |||||||
| chr8:28881444 | C | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0281 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.9+8430G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881444 | |||||||
| chr8:28881444 | C | T | 11 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+8430G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881444 | |||||||
| chr8:28881464 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.9+8410G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881464 | |||||||
| chr8:28881465 | C | T | 3 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00738.hp2 HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.9+8409G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881465 | |||||||
| chr8:28881476 | A | AGGGGGGG others(42): Show |
1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.9+8397_9+8398insAC others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | |||||||
| chr8:28881476 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0108 |
2 | HG02602.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+8398T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | |||||||
| chr8:28881476 | AG | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(291): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.9+8397delC | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | |||||||
| chr8:28881476 | AGGGGGGG others(43): Show |
A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0287 others(1): Show |
4 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+8348_9+8397delAC others(48): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881476 | |||||||
| chr8:28881477 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0339 |
2 | NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.9+8397C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881477 | |||||||
| chr8:28881588 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.9+8286G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881588 | |||||||
| chr8:28881602 | AGCCGCCC others(120): Show |
A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
11 | HG02056.hp1 HG02809.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+8145_9+8271del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881602 | |||||||
| chr8:28881639 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.9+8235C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881639 | |||||||
| chr8:28881654 | G | T | 3 | a0001c0001t0001g0344 a0001c0001t0003g0309 a0001c0001t0003g0310 |
3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+8220C>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881654 | |||||||
| chr8:28881666 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 |
3 | HG02165.hp1 NA18954.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.9+8208G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881666 | |||||||
| chr8:28881674 | C | CCGGCCAG others(42): Show |
1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(47): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | |||||||
| chr8:28881674 | C | CCGGCCAG others(40): Show |
2 | a0001c0001t0002g0349 a0001c0003t0001g0351 |
2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.9+8199_9+8200insAC others(45): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | |||||||
| chr8:28881674 | C | CCGGCCAG others(39): Show |
1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(44): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | |||||||
| chr8:28881674 | C | CCGGCCAG others(37): Show |
1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8199_9+8200insAC others(42): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881674 | |||||||
| chr8:28881700 | AGGTGGGG others(120): Show |
A | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.9+8047_9+8173del | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881700 | |||||||
| chr8:28881738 | G | A | 1 | a0001c0001t0004g0002 | 2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+8136C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881738 | |||||||
| chr8:28881832 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+8042C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881832 | |||||||
| chr8:28881834 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9+8040C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881834 | |||||||
| chr8:28881848 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.9+8026C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881848 | |||||||
| chr8:28881851 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.9+8023G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881851 | |||||||
| chr8:28881872 | A | T | 1 | a0001c0001t0002g0146 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.9+8002T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881872 | |||||||
| chr8:28881873 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+8001C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881873 | |||||||
| chr8:28881892 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | NA18944.hp1 NA18985.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.9+7982G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881892 | |||||||
| chr8:28881897 | G | A | 1 | a0001c0003t0001g0351 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.9+7977C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881897 | |||||||
| chr8:28881919 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+7955G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881919 | |||||||
| chr8:28881929 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0148 a0001c0001t0001g0215 others(7): Show |
11 | HG02257.hp1 HG02280.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.9+7945G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881929 | |||||||
| chr8:28881985 | T | C | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+7889A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28881985 | |||||||
| chr8:28882088 | C | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+7786G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882088 | |||||||
| chr8:28882109 | C | A | 12 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+7765G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882109 | |||||||
| chr8:28882136 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0003t0001g0351 |
3 | HG03195.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.9+7738A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882136 | |||||||
| chr8:28882244 | T | C | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+7630A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882244 | |||||||
| chr8:28882328 | AGGCCG | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.9+7541_9+7545delCG others(3): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882328 | |||||||
| chr8:28882334 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
98 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.9+7540G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882334 | |||||||
| chr8:28882459 | A | T | 3 | a0001c0001t0001g0344 a0001c0001t0003g0309 a0001c0001t0003g0310 |
3 | HG02572.hp2 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.9+7415T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882459 | |||||||
| chr8:28882475 | G | A | 12 | a0001c0001t0001g0102 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | HG02280.hp2 HG02572.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.9+7399C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882475 | |||||||
| chr8:28882494 | TA | T | 12 | a0001c0001t0001g0103 a0001c0001t0001g0156 a0001c0001t0001g0157 others(9): Show |
13 | HG01261.hp1 HG02027.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.9+7379delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882494 | |||||||
| chr8:28882499 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
235 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.9+7375T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882499 | |||||||
| chr8:28882532 | TA | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.9+7341delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882532 | |||||||
| chr8:28882547 | A | G | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+7327T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882547 | |||||||
| chr8:28882548 | G | A | 1 | a0001c0001t0002g0350 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.9+7326C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882548 | |||||||
| chr8:28882548 | GA | G | 22 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0031 others(19): Show |
22 | HG00642.hp2 HG00735.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.9+7325delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882548 | |||||||
| chr8:28882549 | A | G | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.9+7325T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882549 | |||||||
| chr8:28882605 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+7269C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882605 | |||||||
| chr8:28882610 | A | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+7264T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882610 | |||||||
| chr8:28882955 | C | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+6919G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28882955 | |||||||
| chr8:28883225 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+6649A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883225 | |||||||
| chr8:28883510 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+6364G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883510 | |||||||
| chr8:28883678 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9+6196A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883678 | |||||||
| chr8:28883688 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.9+6186G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883688 | |||||||
| chr8:28883710 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.9+6164C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883710 | |||||||
| chr8:28883732 | ATC | A | 7 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(4): Show |
7 | HG00423.hp2 HG02071.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+6140_9+6141delGA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28883732 | |||||||
| chr8:28884067 | T | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0163 a0001c0001t0001g0164 others(63): Show |
67 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.9+5807A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884067 | |||||||
| chr8:28884168 | CT | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0129 a0001c0001t0001g0130 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.9+5705delA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(104): Show |
109 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.9+5704_9+5705delAA | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTT | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(104): Show |
108 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.9+5703_9+5705delAA others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTT | C | 10 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG01070.hp2 HG01167.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+5702_9+5705delAA others(2): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.9+5696_9+5705delAA others(8): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0311 a0001c0001t0003g0309 a0001c0001t0003g0310 |
3 | HG00558.hp1 HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.9+5695_9+5705delAA others(9): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0312 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+5694_9+5705delAA others(10): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0313 a0001c0010t0003g0348 |
2 | HG02055.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.9+5693_9+5705delAA others(11): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884168 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.9+5690_9+5705delAA others(14): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884168 | |||||||
| chr8:28884217 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.9+5657C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884217 | |||||||
| chr8:28884627 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.9+5247G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884627 | |||||||
| chr8:28884768 | G | A | 12 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(9): Show |
12 | HG02056.hp1 HG02809.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.9+5106C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884768 | |||||||
| chr8:28884831 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+5043G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28884831 | |||||||
| chr8:28885057 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.9+4817G>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885057 | |||||||
| chr8:28885057 | C | T | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+4817G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885057 | |||||||
| chr8:28885109 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.9+4765A>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885109 | |||||||
| chr8:28885247 | C | T | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0004g0002 others(5): Show |
9 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.9+4627G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885247 | |||||||
| chr8:28885390 | C | T | 1 | a0001c0001t0002g0349 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.9+4484G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885390 | |||||||
| chr8:28885624 | A | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+4250T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885624 | |||||||
| chr8:28885645 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+4229A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885645 | |||||||
| chr8:28885726 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.9+4148T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885726 | |||||||
| chr8:28885910 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.9+3964T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885910 | |||||||
| chr8:28885964 | G | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG01975.hp2 HG02602.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.9+3910C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28885964 | |||||||
| chr8:28886009 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.9+3865G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886009 | |||||||
| chr8:28886091 | A | G | 4 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3783T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886091 | |||||||
| chr8:28886208 | TA | T | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG02896.hp2 NA18963.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3665delT | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886208 | |||||||
| chr8:28886216 | A | T | 9 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(6): Show |
9 | HG02056.hp1 NA18943.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.9+3658T>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886216 | |||||||
| chr8:28886217 | T | A | 1 | a0001c0003t0001g0316 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.9+3657A>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886217 | |||||||
| chr8:28886405 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0317 a0001c0001t0001g0318 others(22): Show |
26 | HG01109.hp2 HG03490.hp2 HG03927.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+3469C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28886405 | |||||||
| chr8:28887369 | G | A | 1 | a0001c0001t0001g0340 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.9+2505C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887369 | |||||||
| chr8:28887557 | T | C | 1 | a0001c0001t0001g0341 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.9+2317A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887557 | |||||||
| chr8:28887957 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0342 |
2 | HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.9+1917C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28887957 | |||||||
| chr8:28888031 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.9+1843T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888031 | |||||||
| chr8:28888228 | C | T | 1 | a0001c0003t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.9+1646G>A | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888228 | |||||||
| chr8:28888316 | T | C | 1 | a0001c0001t0001g0343 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9+1558A>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888316 | |||||||
| chr8:28888450 | CGCG | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(321): Show |
intron_variant | MODIFIER | c.9+1421_9+1423delCG others(1): Show |
INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888450 | |||||||
| chr8:28888456 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+1418C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888456 | |||||||
| chr8:28888507 | G | A | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+1367C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888507 | |||||||
| chr8:28888694 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+1180C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888694 | |||||||
| chr8:28888751 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+1123C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888751 | |||||||
| chr8:28888752 | A | C | 1 | a0001c0001t0001g0102 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+1122T>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888752 | |||||||
| chr8:28888761 | C | A | 1 | a0001c0001t0001g0347 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+1113G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888761 | |||||||
| chr8:28888776 | C | A | 1 | a0001c0010t0003g0348 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.9+1098G>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888776 | |||||||
| chr8:28888807 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
96 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.9+1067T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28888807 | |||||||
| chr8:28889093 | G | A | 5 | a0001c0001t0001g0352 a0001c0001t0002g0349 a0001c0001t0002g0350 others(2): Show |
5 | HG02280.hp2 HG02965.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+781C>T | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889093 | |||||||
| chr8:28889285 | A | G | 1 | a0003c0008t0001g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.9+589T>C | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889285 | |||||||
| chr8:28889391 | G | C | 1 | a0001c0001t0001g0353 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.9+483C>G | INTS9 | ENSG00000104299.15 | transcript | ENST00000521022.6 | protein_coding | 1/16 | chr8 | 28889391 |