Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51375 |
| ensemblid | ENSG00000162627.17 |
| hgncid | 14971 |
| symbol | SNX7 |
| name | sorting nexin 7 |
| refseq_nuc | NM_015976.5 |
| refseq_prot | NP_057060.2 |
| ensembl_nuc | ENST00000306121.8 |
| ensembl_prot | ENSP00000304429.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 98661721 |
| end | 98760500 |
| strand | + |
| ver | v1.2 |
| region | chr1:98661721-98760500 |
| region5000 | chr1:98656721-98765500 |
| regionname0 | SNX7_chr1_98661721_98760500 |
| regionname5000 | SNX7_chr1_98656721_98765500 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 451 | 324 | 83 | 59 | 131 | 10 | 39 | 101 | SNX7_chr1_98656721_98765500 | SNX7 | MEGER others(446): Show |
chr1 | 98656721 | 98765500 |
| a0002 | 0/0 | 451 | 54 | 1 | 3 | 49 | 0 | 1 | 45 | SNX7_chr1_98656721_98765500 | SNX7 | MEGER others(446): Show |
chr1 | 98656721 | 98765500 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1353 | 246 | 54 | 47 | 110 | 8 | 27 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0002 | 0/1 | 1353 | 56 | 17 | 11 | 13 | 2 | 12 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0004 | 0/0 | 1353 | 12 | 9 | 1 | 2 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0005 | 0/0 | 1353 | 4 | 0 | 0 | 4 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0006 | 1/0 | 1353 | 4 | 3 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0007 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0001c0008 | 0/0 | 1353 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 | ||
| a0002c0003 | 0/0 | 1353 | 54 | 1 | 3 | 49 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | ATGGA others(1348): Show |
chr1 | 98656721 | 98765500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1736 | 244 | 53 | 47 | 109 | 8 | 27 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0001t0002 | 0/0 | 1736 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0001t0003 | 0/0 | 1736 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0002t0001 | 0/1 | 1736 | 56 | 17 | 11 | 13 | 2 | 12 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0004t0001 | 0/0 | 1736 | 12 | 9 | 1 | 2 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0005t0001 | 0/0 | 1736 | 4 | 0 | 0 | 4 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0006t0001 | 1/0 | 1736 | 4 | 3 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0007t0001 | 0/0 | 1736 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0001c0008t0001 | 0/0 | 1736 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| a0002c0003t0001 | 0/0 | 1736 | 54 | 1 | 3 | 49 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | GCACT others(1731): Show |
chr1 | 98656721 | 98765500 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0362 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0004t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0005t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0006t0001g0096 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0007t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0001c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | GBR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | FIN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0337 | EUR | FIN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0268 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0353 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0345 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0339 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0188 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0359 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0186 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0340 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0354 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0146 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0344 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0187 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0153 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0130 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0361 | EAS | CDX | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0324 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0346 | AMR | PEL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0347 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0348 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0119 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0121 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0335 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0009 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0118 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0355 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0352 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0356 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0120 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0098 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0341 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0349 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0364 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0332 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0357 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0350 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0328 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0351 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0327 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0360 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0001 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0363 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0330 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | STU | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0158 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0138 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18945 | hp1 | a0001 | c0005 | t0001 | g0069 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0124 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0134 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18951 | hp1 | a0002 | c0003 | t0001 | g0151 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18956 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0162 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18959 | hp2 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0157 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18972 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18974 | hp1 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18977 | hp1 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0140 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18984 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18987 | hp2 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18989 | hp2 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0152 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0154 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18998 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19004 | hp2 | a0002 | c0003 | t0001 | g0139 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0145 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0155 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0298 | AFR | LWK | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0325 | AFR | LWK | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0160 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19056 | hp2 | a0001 | c0005 | t0001 | g0070 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19063 | hp1 | a0001 | c0008 | t0001 | g0036 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19067 | hp1 | a0001 | c0004 | t0001 | g0179 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0123 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19076 | hp2 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19080 | hp2 | a0001 | c0007 | t0001 | g0329 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0159 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19090 | hp1 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0326 | AFR | ASW | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0333 | AFR | ASW | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0336 | EUR | TSI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | GIH | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | GIH | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0365 | AMR | CLM | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0097 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0338 | AFR | ACB | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | USA | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | USA | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0362 | REF | REF | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0096 | REF | REF | SNX7_chr1_98656721_98765500 | SNX7 | chr1 | 98656721 | 98765500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:98691078 | T | A | 1 | a0002 | 54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
missense_variant | MODERATE | c.367T>A | p.Ser123Thr | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 3/9 | 378/1736 | 367/1356 | 123/451 | chr1 | 98691078 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:98661836 | T | C | 7 | a0001c0001 a0001c0002 a0001c0004 others(4): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
synonymous_variant | LOW | c.105T>C | p.Ser35Ser | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/9 | 116/1736 | 105/1356 | 35/451 | chr1 | 98661836 | |||
| chr1:98698800 | C | T | 1 | a0001c0008 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.933C>T | p.Ser311Ser | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/9 | 944/1736 | 933/1356 | 311/451 | chr1 | 98698800 | |||
| chr1:98698878 | G | A | 2 | a0001c0002 a0001c0007 |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
synonymous_variant | LOW | c.1011G>A | p.Glu337Glu | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/9 | 1022/1736 | 1011/1356 | 337/451 | chr1 | 98698878 | |||
| chr1:98738281 | T | C | 2 | a0001c0005 a0001c0007 |
5 | NA18945.hp1 NA18984.hp1 NA19056.hp2 others(2): Show |
synonymous_variant | LOW | c.1170T>C | p.Ala390Ala | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/9 | 1181/1736 | 1170/1356 | 390/451 | chr1 | 98738281 | |||
| chr1:98760071 | G | A | 5 | a0001c0001 a0001c0002 a0001c0005 others(2): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
synonymous_variant | LOW | c.1296G>A | p.Glu432Glu | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 9/9 | 1307/1736 | 1296/1356 | 432/451 | chr1 | 98760071 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:98760389 | A | G | 1 | a0001c0001t0003 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*258A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 9/9 | 258 | chr1 | 98760389 | ||||||
| chr1:98760462 | A | G | 1 | a0001c0001t0002 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*331A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 9/9 | 331 | chr1 | 98760462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:98662147 | C | A | 1 | a0001c0001t0001g0012 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+236C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98662147 | |||||||
| chr1:98662393 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.180+482G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98662393 | |||||||
| chr1:98662490 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01884.hp2 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.180+579G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98662490 | |||||||
| chr1:98662742 | G | C | 1 | a0001c0001t0001g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.180+831G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98662742 | |||||||
| chr1:98662994 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180+1083T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98662994 | |||||||
| chr1:98663003 | C | G | 42 | a0001c0001t0001g0323 a0001c0001t0001g0358 a0001c0001t0001g0363 others(39): Show |
42 | HG00323.hp2 HG01081.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.180+1092C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663003 | |||||||
| chr1:98663015 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.180+1104G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663015 | |||||||
| chr1:98663061 | C | T | 2 | a0001c0002t0001g0364 a0001c0002t0001g0365 |
2 | HG01123.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.180+1150C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663061 | |||||||
| chr1:98663220 | A | G | 1 | a0001c0001t0001g0322 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.180+1309A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663220 | |||||||
| chr1:98663230 | A | G | 127 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0199 others(124): Show |
128 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+1319A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663230 | |||||||
| chr1:98663251 | TG | T | 7 | a0001c0001t0001g0194 a0002c0003t0001g0188 a0002c0003t0001g0189 others(4): Show |
7 | HG01496.hp1 HG02129.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+1342delG | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98663251 | ||||||
| chr1:98663252 | GGT | G | 8 | a0001c0001t0001g0099 a0002c0003t0001g0122 a0002c0003t0001g0124 others(5): Show |
8 | HG02040.hp1 HG02965.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1342_180+1343d others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTT | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0002c0003t0001g0001 others(1): Show |
4 | HG02615.hp1 HG03834.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1342_180+1344d others(5): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTT | G | 13 | a0001c0001t0001g0103 a0001c0001t0001g0116 a0001c0001t0001g0126 others(10): Show |
13 | HG00642.hp2 HG02647.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+1342_180+1345d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTT | G | 23 | a0001c0001t0001g0169 a0001c0001t0001g0176 a0001c0001t0001g0177 others(20): Show |
23 | HG00673.hp1 HG01943.hp1 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.180+1342_180+1346d others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTT | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0166 a0001c0002t0001g0115 others(1): Show |
4 | HG02717.hp1 HG02723.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1342_180+1347d others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0107 others(13): Show |
18 | HG02040.hp2 HG02071.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.180+1342_180+1348d others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(1): Show |
G | 14 | a0001c0001t0001g0106 a0001c0001t0001g0185 a0001c0001t0001g0275 others(11): Show |
14 | HG00738.hp2 HG01243.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+1342_180+1349d others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(2): Show |
G | 47 | a0001c0001t0001g0017 a0001c0001t0001g0104 a0001c0001t0001g0199 others(44): Show |
47 | HG00544.hp1 HG00642.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.180+1342_180+1350d others(11): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(3): Show |
G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0220 others(102): Show |
107 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.180+1342_180+1351d others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(4): Show |
G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0264 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+1342_180+1352d others(13): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0314 a0002c0003t0001g0141 |
3 | HG02300.hp1 HG02615.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.180+1342_180+1353d others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(6): Show |
G | 2 | a0001c0001t0001g0282 a0002c0003t0001g0158 |
2 | HG01433.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.180+1342_180+1354d others(15): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(7): Show |
G | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0001g0359 |
3 | HG01928.hp2 HG03017.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.180+1342_180+1355d others(16): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(9): Show |
G | 5 | a0001c0002t0001g0331 a0001c0004t0001g0009 a0001c0004t0001g0118 others(2): Show |
6 | HG02258.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+1342_180+1357d others(18): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(10): Show |
G | 2 | a0001c0001t0001g0021 a0001c0004t0001g0119 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.180+1342_180+1358d others(19): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(13): Show |
G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0171 |
2 | HG00438.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.180+1342_180+1361d others(22): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(14): Show |
G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(17): Show |
20 | HG00597.hp2 HG01175.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.180+1342_180+1362d others(23): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(15): Show |
G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.180+1342_180+1363d others(24): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(16): Show |
G | 6 | a0001c0001t0001g0050 a0002c0003t0001g0132 a0002c0003t0001g0133 others(3): Show |
6 | NA18959.hp2 NA18989.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+1342_180+1364d others(25): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663252 | GGTTTTTT others(19): Show |
G | 2 | a0002c0003t0001g0129 a0002c0003t0001g0130 |
2 | HG02132.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.180+1342_180+1367d others(28): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663252 | |||||||
| chr1:98663253 | G | T | 4 | a0001c0001t0001g0195 a0002c0003t0001g0196 a0002c0003t0001g0197 others(1): Show |
4 | HG03239.hp2 NA18974.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1342G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663253 | |||||||
| chr1:98663266 | T | G | 21 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(18): Show |
21 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(18): Show |
intron_variant | MODIFIER | c.180+1355T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663266 | |||||||
| chr1:98663267 | T | G | 46 | a0001c0001t0001g0011 a0001c0001t0001g0220 a0001c0001t0001g0221 others(43): Show |
47 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.180+1356T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663267 | |||||||
| chr1:98663268 | T | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | HG03579.hp1 NA19054.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.180+1357T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663268 | |||||||
| chr1:98663270 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180+1359T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663270 | |||||||
| chr1:98663277 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.180+1366T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663277 | |||||||
| chr1:98663342 | C | G | 1 | a0002c0003t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.180+1431C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663342 | |||||||
| chr1:98663609 | C | CAGAAGCA others(1167): Show |
1 | a0002c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.180+1710_180+1711i others(1176): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98663609 | ||||||
| chr1:98663702 | G | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0171 others(14): Show |
20 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+1791G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663702 | |||||||
| chr1:98663947 | C | G | 127 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0199 others(124): Show |
128 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+2036C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98663947 | |||||||
| chr1:98664048 | C | G | 1 | a0001c0001t0001g0321 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.180+2137C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664048 | |||||||
| chr1:98664064 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0161 others(23): Show |
29 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.180+2153A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664064 | |||||||
| chr1:98664071 | A | G | 4 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG00558.hp2 NA18946.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+2160A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664071 | |||||||
| chr1:98664135 | C | T | 53 | a0001c0001t0001g0126 a0001c0001t0001g0194 a0001c0004t0001g0170 others(50): Show |
55 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(52): Show |
intron_variant | MODIFIER | c.180+2224C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664135 | |||||||
| chr1:98664384 | C | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2473C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664384 | |||||||
| chr1:98664452 | C | T | 126 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0199 others(123): Show |
127 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.180+2541C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664452 | |||||||
| chr1:98664569 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.180+2658C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664569 | |||||||
| chr1:98664572 | C | T | 1 | a0001c0001t0001g0320 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.180+2661C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664572 | |||||||
| chr1:98664709 | T | C | 42 | a0001c0001t0001g0323 a0001c0001t0001g0358 a0001c0001t0001g0363 others(39): Show |
42 | HG00323.hp2 HG01081.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.180+2798T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664709 | |||||||
| chr1:98664809 | T | C | 2 | a0001c0001t0001g0267 a0001c0004t0001g0268 |
2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.180+2898T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664809 | |||||||
| chr1:98664819 | C | A | 1 | a0002c0003t0001g0122 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.180+2908C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664819 | |||||||
| chr1:98664905 | A | G | 126 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0199 others(123): Show |
127 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.180+2994A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664905 | |||||||
| chr1:98664931 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.180+3020C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98664931 | |||||||
| chr1:98665057 | T | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+3146T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665057 | |||||||
| chr1:98665094 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.180+3183A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665094 | |||||||
| chr1:98665167 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01884.hp2 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.180+3256G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665167 | |||||||
| chr1:98665185 | C | T | 1 | a0002c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.180+3274C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665185 | |||||||
| chr1:98665237 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.180+3326G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665237 | |||||||
| chr1:98665388 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.180+3477A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665388 | |||||||
| chr1:98665457 | A | C | 1 | a0002c0003t0001g0160 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.180+3546A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665457 | |||||||
| chr1:98665459 | T | C | 1 | a0002c0003t0001g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.180+3548T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665459 | |||||||
| chr1:98665978 | T | A | 1 | a0002c0003t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.180+4067T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98665978 | |||||||
| chr1:98666010 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.180+4099C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666010 | |||||||
| chr1:98666025 | A | G | 1 | a0001c0001t0001g0314 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.180+4114A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666025 | |||||||
| chr1:98666033 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.180+4122A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666033 | |||||||
| chr1:98666245 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.180+4334G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666245 | |||||||
| chr1:98666404 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
6 | HG01934.hp1 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+4493C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666404 | |||||||
| chr1:98666514 | A | G | 127 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0199 others(124): Show |
128 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+4603A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666514 | |||||||
| chr1:98666517 | T | C | 1 | a0001c0006t0001g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.180+4606T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666517 | |||||||
| chr1:98666559 | G | A | 72 | a0001c0001t0001g0011 a0001c0001t0001g0199 a0001c0001t0001g0200 others(69): Show |
73 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.180+4648G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666559 | |||||||
| chr1:98666649 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(28): Show |
35 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+4738A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666649 | |||||||
| chr1:98666665 | C | A | 6 | a0001c0001t0001g0021 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+4754C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666665 | |||||||
| chr1:98666842 | T | C | 5 | a0001c0002t0001g0325 a0001c0002t0001g0364 a0001c0002t0001g0365 others(2): Show |
5 | HG01123.hp2 HG02258.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+4931T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666842 | |||||||
| chr1:98666953 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.180+5042A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666953 | |||||||
| chr1:98666954 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.180+5043G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666954 | |||||||
| chr1:98666955 | T | G | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.180+5044T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98666955 | |||||||
| chr1:98667272 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(28): Show |
35 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.180+5361A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667272 | |||||||
| chr1:98667487 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180+5576C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667487 | |||||||
| chr1:98667541 | A | AT | 22 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0219 others(19): Show |
22 | HG00544.hp1 HG00558.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.180+5642dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98667541 | ||||||
| chr1:98667662 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.180+5751G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667662 | |||||||
| chr1:98667696 | C | G | 1 | a0001c0002t0001g0361 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.180+5785C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667696 | |||||||
| chr1:98667907 | AG | A | 6 | a0001c0001t0001g0021 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+5998delG | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98667907 | ||||||
| chr1:98667908 | G | GA | 3 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0291 |
3 | HG02615.hp1 HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.180+5997_180+5998i others(3): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667908 | |||||||
| chr1:98667909 | G | A | 348 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(345): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.180+5998G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667909 | |||||||
| chr1:98667925 | A | C | 1 | a0001c0002t0001g0360 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.180+6014A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98667925 | |||||||
| chr1:98667942 | C | CA | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | NA18939.hp2 NA18983.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+6039dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98667942 | ||||||
| chr1:98668214 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01081.hp1 HG01109.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+6303A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668214 | |||||||
| chr1:98668448 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0161 others(23): Show |
29 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(26): Show |
intron_variant | MODIFIER | c.180+6537G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668448 | |||||||
| chr1:98668461 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.180+6550T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668461 | |||||||
| chr1:98668516 | T | G | 1 | a0002c0003t0001g0125 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.180+6605T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668516 | |||||||
| chr1:98668567 | A | T | 361 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(358): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.180+6656A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668567 | |||||||
| chr1:98668573 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.180+6662G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98668573 | |||||||
| chr1:98669003 | A | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(2): Show |
6 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+7092A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669003 | |||||||
| chr1:98669043 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.180+7132T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669043 | |||||||
| chr1:98669091 | A | G | 43 | a0001c0001t0001g0270 a0001c0001t0001g0323 a0001c0001t0001g0358 others(40): Show |
43 | HG00323.hp2 HG01081.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.180+7180A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669091 | |||||||
| chr1:98669112 | A | G | 4 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0315 others(1): Show |
4 | HG00408.hp2 HG02056.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+7201A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669112 | |||||||
| chr1:98669272 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.180+7361C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669272 | |||||||
| chr1:98669316 | G | A | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.180+7405G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669316 | |||||||
| chr1:98669359 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.180+7448T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669359 | |||||||
| chr1:98669445 | T | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0126 a0001c0001t0001g0199 others(68): Show |
72 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.180+7534T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669445 | |||||||
| chr1:98669506 | C | A | 172 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(169): Show |
173 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.180+7595C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669506 | |||||||
| chr1:98669571 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.180+7660A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669571 | |||||||
| chr1:98669640 | C | CAATTTGA others(4): Show |
1 | a0001c0001t0001g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.180+7729_180+7730i others(13): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669640 | |||||||
| chr1:98669641 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.180+7730C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669641 | |||||||
| chr1:98669822 | C | T | 1 | a0002c0003t0001g0157 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.180+7911C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98669822 | |||||||
| chr1:98670103 | A | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.180+8192A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670103 | |||||||
| chr1:98670211 | T | C | 1 | a0002c0003t0001g0123 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.180+8300T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670211 | |||||||
| chr1:98670240 | A | C | 1 | a0002c0003t0001g0156 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.180+8329A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670240 | |||||||
| chr1:98670256 | C | T | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.180+8345C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670256 | |||||||
| chr1:98670291 | A | C | 1 | a0001c0002t0001g0359 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.180+8380A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670291 | |||||||
| chr1:98670455 | G | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.180+8544G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670455 | |||||||
| chr1:98670745 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(136): Show |
146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.180+8834C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670745 | |||||||
| chr1:98670761 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0263 a0001c0001t0001g0266 |
3 | HG02280.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.180+8850C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670761 | |||||||
| chr1:98670857 | T | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0104 |
3 | HG02451.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.180+8946T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670857 | |||||||
| chr1:98670870 | T | TTTTA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0161 others(24): Show |
30 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(27): Show |
intron_variant | MODIFIER | c.180+8990_180+8993d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670870 | T | TTTTATTT others(1): Show |
9 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0104 others(6): Show |
10 | HG00642.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.180+8986_180+8993d others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670870 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0106 a0001c0004t0001g0100 a0001c0004t0001g0324 |
3 | HG01891.hp1 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.180+8982_180+8993d others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670870 | T | TTTTATTT others(9): Show |
2 | a0001c0001t0001g0107 a0001c0004t0001g0326 |
2 | HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.180+8978_180+8993d others(18): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670870 | TTTTA | T | 6 | a0001c0001t0001g0021 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+8990_180+8993d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670870 | TTTTATTT others(1): Show |
T | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(308): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.180+8986_180+8993d others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98670870 | ||||||
| chr1:98670934 | A | G | 6 | a0001c0001t0001g0021 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+9023A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670934 | |||||||
| chr1:98670988 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0099 a0001c0004t0001g0324 others(1): Show |
4 | HG02258.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+9077A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98670988 | |||||||
| chr1:98671101 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180+9190C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671101 | |||||||
| chr1:98671478 | T | A | 1 | a0001c0002t0001g0327 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.180+9567T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671478 | |||||||
| chr1:98671581 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.180+9670T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671581 | |||||||
| chr1:98671746 | T | C | 11 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(8): Show |
11 | HG01496.hp1 HG02132.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+9835T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671746 | |||||||
| chr1:98671789 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.180+9878C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671789 | |||||||
| chr1:98671953 | G | A | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(310): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.180+10042G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671953 | |||||||
| chr1:98671960 | A | G | 55 | a0001c0001t0001g0017 a0001c0001t0001g0267 a0001c0001t0001g0271 others(52): Show |
55 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.180+10049A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671960 | |||||||
| chr1:98671988 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.180+10077A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98671988 | |||||||
| chr1:98672137 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.180+10226A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672137 | |||||||
| chr1:98672141 | C | T | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(310): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.180+10230C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672141 | |||||||
| chr1:98672150 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(27): Show |
34 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.180+10239A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672150 | |||||||
| chr1:98672180 | T | G | 11 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(8): Show |
11 | HG01496.hp1 HG02132.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+10269T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672180 | |||||||
| chr1:98672218 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.180+10307C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672218 | |||||||
| chr1:98672432 | A | C | 2 | a0002c0003t0001g0154 a0002c0003t0001g0155 |
2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.180+10521A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672432 | |||||||
| chr1:98672650 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.180+10739C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672650 | |||||||
| chr1:98672800 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.180+10889T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672800 | |||||||
| chr1:98672894 | G | A | 52 | a0001c0001t0001g0194 a0002c0003t0001g0001 a0002c0003t0001g0122 others(49): Show |
54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
intron_variant | MODIFIER | c.180+10983G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672894 | |||||||
| chr1:98672900 | C | T | 128 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0126 others(125): Show |
129 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.180+10989C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672900 | |||||||
| chr1:98672918 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(137): Show |
147 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.180+11007G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672918 | |||||||
| chr1:98672925 | C | T | 2 | a0002c0003t0001g0154 a0002c0003t0001g0155 |
2 | NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.180+11014C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98672925 | |||||||
| chr1:98672930 | C | CA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0117 others(3): Show |
7 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+11041dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | C | CAA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(65): Show |
71 | HG00323.hp2 HG00438.hp1 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.180+11040_180+1104 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | C | CAAA | 48 | a0001c0001t0001g0194 a0001c0001t0001g0260 a0001c0002t0001g0328 others(45): Show |
50 | HG01256.hp2 HG01993.hp1 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.180+11039_180+1104 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | C | CAAAA | 64 | a0001c0001t0001g0011 a0001c0001t0001g0126 a0001c0001t0001g0202 others(61): Show |
65 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.180+11038_180+1104 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | C | CAAAAA | 63 | a0001c0001t0001g0103 a0001c0001t0001g0199 a0001c0001t0001g0200 others(60): Show |
63 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.180+11037_180+1104 others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | C | CAAAAAA | 8 | a0001c0001t0001g0017 a0001c0001t0001g0272 a0001c0001t0001g0273 others(5): Show |
8 | HG01175.hp1 HG01255.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.180+11036_180+1104 others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98672930 | CAAAA | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
94 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.180+11038_180+1104 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98672930 | ||||||
| chr1:98673349 | T | C | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | NA18952.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.180+11438T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673349 | |||||||
| chr1:98673391 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0161 others(22): Show |
28 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.180+11480A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673391 | |||||||
| chr1:98673403 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.181-11482C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673403 | |||||||
| chr1:98673587 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-11298A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673587 | |||||||
| chr1:98673590 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.181-11295G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673590 | |||||||
| chr1:98673861 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.181-11024G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673861 | |||||||
| chr1:98673939 | G | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01884.hp2 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.181-10946G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673939 | |||||||
| chr1:98673940 | T | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01884.hp2 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.181-10945T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98673940 | |||||||
| chr1:98674018 | T | G | 1 | a0002c0003t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.181-10867T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674018 | |||||||
| chr1:98674021 | G | C | 313 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(310): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.181-10864G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674021 | |||||||
| chr1:98674132 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.181-10753G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674132 | |||||||
| chr1:98674144 | G | A | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-10741G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674144 | |||||||
| chr1:98674337 | A | G | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.181-10548A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674337 | |||||||
| chr1:98674364 | A | T | 42 | a0001c0001t0001g0017 a0001c0001t0001g0271 a0001c0001t0001g0272 others(39): Show |
42 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.181-10521A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674364 | |||||||
| chr1:98674369 | C | T | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-10516C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674369 | |||||||
| chr1:98674402 | A | C | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-10483A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674402 | |||||||
| chr1:98674442 | C | T | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.181-10443C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674442 | |||||||
| chr1:98674445 | A | C | 319 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(316): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.181-10440A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674445 | |||||||
| chr1:98674546 | T | C | 319 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(316): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.181-10339T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674546 | |||||||
| chr1:98674617 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.181-10268T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674617 | |||||||
| chr1:98674621 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.181-10264A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674621 | |||||||
| chr1:98674644 | A | G | 1 | a0002c0003t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.181-10241A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674644 | |||||||
| chr1:98674656 | T | A | 1 | a0001c0001t0001g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.181-10229T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674656 | |||||||
| chr1:98674669 | C | T | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-10216C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98674669 | |||||||
| chr1:98675126 | A | T | 1 | a0001c0001t0001g0363 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.181-9759A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675126 | |||||||
| chr1:98675188 | T | G | 1 | a0002c0003t0001g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.181-9697T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675188 | |||||||
| chr1:98675296 | A | T | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(355): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.181-9589A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675296 | |||||||
| chr1:98675330 | T | C | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.181-9555T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675330 | |||||||
| chr1:98675437 | T | A | 57 | a0001c0001t0001g0363 a0001c0002t0001g0030 a0001c0002t0001g0031 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.181-9448T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675437 | |||||||
| chr1:98675448 | G | A | 56 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(53): Show |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.181-9437G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675448 | |||||||
| chr1:98675526 | C | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-9359C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675526 | |||||||
| chr1:98675892 | A | G | 57 | a0001c0001t0001g0363 a0001c0002t0001g0030 a0001c0002t0001g0031 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.181-8993A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675892 | |||||||
| chr1:98675967 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-8918C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675967 | |||||||
| chr1:98675994 | T | C | 1 | a0001c0002t0001g0030 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.181-8891T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98675994 | |||||||
| chr1:98676097 | A | G | 9 | a0002c0003t0001g0136 a0002c0003t0001g0137 a0002c0003t0001g0149 others(6): Show |
9 | NA18951.hp1 NA18961.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-8788A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676097 | |||||||
| chr1:98676281 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.181-8604C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676281 | |||||||
| chr1:98676304 | A | C | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG00738.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.181-8581A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676304 | |||||||
| chr1:98676307 | C | T | 353 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(350): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.181-8578C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676307 | |||||||
| chr1:98676750 | A | T | 1 | a0002c0003t0001g0148 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.181-8135A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676750 | |||||||
| chr1:98676883 | G | A | 1 | a0001c0002t0001g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.181-8002G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98676883 | |||||||
| chr1:98677030 | G | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG02109.hp2 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-7855G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677030 | |||||||
| chr1:98677234 | G | A | 321 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(318): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.181-7651G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677234 | |||||||
| chr1:98677322 | G | A | 1 | a0001c0002t0001g0328 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.181-7563G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677322 | |||||||
| chr1:98677409 | C | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-7476C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677409 | |||||||
| chr1:98677606 | G | T | 3 | a0001c0002t0001g0355 a0001c0002t0001g0356 a0001c0002t0001g0357 |
3 | HG02965.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.181-7279G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677606 | |||||||
| chr1:98677771 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.181-7114G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677771 | |||||||
| chr1:98677803 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.181-7082G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677803 | |||||||
| chr1:98677877 | CA | C | 303 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(300): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.181-6991delA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677877 | ||||||
| chr1:98677878 | A | C | 1 | a0002c0003t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.181-7007A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677878 | |||||||
| chr1:98677898 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0008t0001g0036 |
3 | NA18961.hp2 NA18993.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.181-6987A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677898 | |||||||
| chr1:98677978 | TGTGTGTG others(5): Show |
T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-6895_181-6884d others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677978 | ||||||
| chr1:98677990 | C | CAT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0035 others(6): Show |
10 | HG00140.hp1 HG01069.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.181-6895_181-6894i others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677990 | |||||||
| chr1:98677990 | C | CATGT | 45 | a0001c0001t0001g0270 a0001c0004t0001g0170 a0002c0003t0001g0001 others(42): Show |
47 | HG01943.hp1 HG01993.hp1 HG02040.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-6895_181-6894i others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677990 | |||||||
| chr1:98677990 | C | CATGTGT | 8 | a0002c0003t0001g0122 a0002c0003t0001g0127 a0002c0003t0001g0128 others(5): Show |
8 | HG01496.hp1 NA18941.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.181-6895_181-6894i others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677990 | |||||||
| chr1:98677990 | CGT | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
73 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.181-6862_181-6861d others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677990 | ||||||
| chr1:98677990 | CGTGT | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0077 others(9): Show |
12 | HG00642.hp2 HG02155.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.181-6864_181-6861d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677990 | ||||||
| chr1:98677990 | CGTGTGT | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0161 a0001c0004t0001g0009 others(6): Show |
10 | HG02258.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.181-6866_181-6861d others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677990 | ||||||
| chr1:98677990 | CGTGTGTG others(1): Show |
C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0167 others(16): Show |
22 | HG00438.hp1 HG00673.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.181-6868_181-6861d others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98677990 | ||||||
| chr1:98677991 | G | A | 182 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
183 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.181-6894G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677991 | |||||||
| chr1:98677993 | G | A | 69 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(66): Show |
73 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.181-6892G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677993 | |||||||
| chr1:98677995 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02155.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.181-6890G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677995 | |||||||
| chr1:98677997 | G | A | 6 | a0001c0001t0001g0014 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02615.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-6888G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677997 | |||||||
| chr1:98677998 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-6887T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98677998 | |||||||
| chr1:98678193 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.181-6692C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678193 | |||||||
| chr1:98678239 | G | A | 56 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(53): Show |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.181-6646G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678239 | |||||||
| chr1:98678450 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.181-6435A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678450 | |||||||
| chr1:98678643 | G | A | 56 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(53): Show |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.181-6242G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678643 | |||||||
| chr1:98678753 | G | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-6132G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678753 | |||||||
| chr1:98678907 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-5978A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678907 | |||||||
| chr1:98678930 | A | T | 115 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0087 others(112): Show |
116 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.181-5955A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98678930 | |||||||
| chr1:98679054 | C | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-5831C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679054 | |||||||
| chr1:98679104 | G | C | 2 | a0002c0003t0001g0132 a0002c0003t0001g0133 |
2 | NA18989.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.181-5781G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679104 | |||||||
| chr1:98679124 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.181-5761C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679124 | |||||||
| chr1:98679336 | CAT | C | 4 | a0001c0002t0001g0351 a0001c0002t0001g0352 a0001c0002t0001g0353 others(1): Show |
4 | HG01081.hp2 HG01978.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-5548_181-5547d others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679336 | |||||||
| chr1:98679413 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.181-5472C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679413 | |||||||
| chr1:98679414 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | NA18522.hp2 NA18965.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-5471G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679414 | |||||||
| chr1:98679510 | G | A | 1 | a0001c0002t0001g0361 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.181-5375G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679510 | |||||||
| chr1:98679695 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0045 others(6): Show |
9 | HG02071.hp2 HG02155.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-5190G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98679695 | |||||||
| chr1:98680007 | C | A | 1 | a0002c0003t0001g0155 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.181-4878C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680007 | |||||||
| chr1:98680016 | C | T | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-4869C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680016 | |||||||
| chr1:98680067 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-4818G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680067 | |||||||
| chr1:98680153 | G | C | 52 | a0001c0001t0001g0103 a0002c0003t0001g0001 a0002c0003t0001g0122 others(49): Show |
54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
intron_variant | MODIFIER | c.181-4732G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680153 | |||||||
| chr1:98680290 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.181-4595C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680290 | |||||||
| chr1:98680314 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.181-4571G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680314 | |||||||
| chr1:98680713 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-4172A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680713 | |||||||
| chr1:98680755 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0075 |
2 | NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.181-4130C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680755 | |||||||
| chr1:98680782 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-4103C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680782 | |||||||
| chr1:98680895 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.181-3990T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680895 | |||||||
| chr1:98680949 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.181-3936A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98680949 | |||||||
| chr1:98681077 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181-3808G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681077 | |||||||
| chr1:98681297 | C | T | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.181-3588C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681297 | |||||||
| chr1:98681317 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(27): Show |
34 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.181-3568A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681317 | |||||||
| chr1:98681333 | G | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-3552G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681333 | |||||||
| chr1:98681432 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG01167.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.181-3453G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681432 | |||||||
| chr1:98681663 | G | A | 70 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(67): Show |
71 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.181-3222G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681663 | |||||||
| chr1:98681674 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.181-3211G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681674 | |||||||
| chr1:98681845 | T | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-3040T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681845 | |||||||
| chr1:98681865 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.181-3020T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681865 | |||||||
| chr1:98681982 | C | G | 1 | a0002c0003t0001g0122 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.181-2903C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98681982 | |||||||
| chr1:98682023 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.181-2862A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682023 | |||||||
| chr1:98682066 | GTTTTC | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(31): Show |
39 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.181-2811_181-2807d others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98682066 | ||||||
| chr1:98682075 | TCTTCCTT others(17): Show |
T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.181-2797_181-2774d others(26): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr1 | 98682075 | ||||||
| chr1:98682111 | T | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-2774T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682111 | |||||||
| chr1:98682151 | G | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.181-2734G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682151 | |||||||
| chr1:98682188 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0071 others(3): Show |
7 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-2697C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682188 | |||||||
| chr1:98682198 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.181-2687C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682198 | |||||||
| chr1:98682541 | A | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-2344A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682541 | |||||||
| chr1:98682796 | A | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2089A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682796 | |||||||
| chr1:98682982 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.181-1903A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98682982 | |||||||
| chr1:98683433 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(85): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.181-1452G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683433 | |||||||
| chr1:98683493 | T | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.181-1392T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683493 | |||||||
| chr1:98683647 | C | T | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.181-1238C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683647 | |||||||
| chr1:98683726 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.181-1159T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683726 | |||||||
| chr1:98683814 | C | T | 48 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0024 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.181-1071C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683814 | |||||||
| chr1:98683929 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | NA19070.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.181-956G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98683929 | |||||||
| chr1:98684004 | G | C | 1 | a0001c0001t0001g0052 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.181-881G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684004 | |||||||
| chr1:98684062 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.181-823T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684062 | |||||||
| chr1:98684097 | C | A | 51 | a0002c0003t0001g0001 a0002c0003t0001g0122 a0002c0003t0001g0123 others(48): Show |
53 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-788C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684097 | |||||||
| chr1:98684128 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.181-757G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684128 | |||||||
| chr1:98684283 | C | G | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.181-602C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684283 | |||||||
| chr1:98684404 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01884.hp2 HG02055.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.181-481G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684404 | |||||||
| chr1:98684585 | A | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.181-300A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 1/8 | chr1 | 98684585 | |||||||
| chr1:98685079 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.363+12G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685079 | |||||||
| chr1:98685241 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.363+174G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685241 | |||||||
| chr1:98685444 | G | T | 3 | a0001c0005t0001g0005 a0001c0005t0001g0069 a0001c0005t0001g0070 |
4 | NA18945.hp1 NA18984.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+377G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685444 | |||||||
| chr1:98685504 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.363+437G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685504 | |||||||
| chr1:98685528 | A | G | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+461A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685528 | |||||||
| chr1:98685579 | C | T | 174 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0015 others(171): Show |
175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.363+512C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685579 | |||||||
| chr1:98685668 | G | T | 321 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(318): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.363+601G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685668 | |||||||
| chr1:98685703 | G | A | 1 | a0001c0004t0001g0324 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+636G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685703 | |||||||
| chr1:98685806 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+739A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685806 | |||||||
| chr1:98685915 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.363+848C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98685915 | |||||||
| chr1:98686074 | C | T | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+1007C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686074 | |||||||
| chr1:98686103 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.363+1036C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686103 | |||||||
| chr1:98686137 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.363+1070T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686137 | |||||||
| chr1:98686445 | C | A | 1 | a0002c0003t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.363+1378C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686445 | |||||||
| chr1:98686464 | A | G | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+1397A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686464 | |||||||
| chr1:98686595 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.363+1528T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686595 | |||||||
| chr1:98686863 | T | C | 2 | a0001c0002t0001g0351 a0001c0002t0001g0352 |
2 | HG03041.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.363+1796T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686863 | |||||||
| chr1:98686985 | T | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.363+1918T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98686985 | |||||||
| chr1:98687058 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.363+1991A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687058 | |||||||
| chr1:98687273 | T | C | 54 | a0001c0001t0001g0103 a0001c0001t0003g0092 a0001c0004t0001g0170 others(51): Show |
56 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(53): Show |
intron_variant | MODIFIER | c.363+2206T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687273 | |||||||
| chr1:98687415 | C | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.363+2348C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687415 | |||||||
| chr1:98687426 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0054 others(1): Show |
4 | HG02074.hp2 NA18961.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+2359G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687426 | |||||||
| chr1:98687464 | T | G | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.363+2397T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687464 | |||||||
| chr1:98687647 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.363+2580G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687647 | |||||||
| chr1:98687680 | G | A | 353 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(350): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.363+2613G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687680 | |||||||
| chr1:98687712 | A | G | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.363+2645A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687712 | |||||||
| chr1:98687887 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.363+2820A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687887 | |||||||
| chr1:98687997 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.363+2930A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98687997 | |||||||
| chr1:98688199 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.364-2876G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688199 | |||||||
| chr1:98688378 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.364-2697G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688378 | |||||||
| chr1:98688628 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.364-2447G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688628 | |||||||
| chr1:98688655 | G | A | 43 | a0001c0001t0001g0017 a0001c0001t0001g0267 a0001c0001t0001g0270 others(40): Show |
43 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.364-2420G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688655 | |||||||
| chr1:98688703 | A | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.364-2372A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688703 | |||||||
| chr1:98688714 | T | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.364-2361T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688714 | |||||||
| chr1:98688763 | C | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.364-2312C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688763 | |||||||
| chr1:98688935 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-2140C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98688935 | |||||||
| chr1:98689005 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.364-2070A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689005 | |||||||
| chr1:98689183 | G | A | 1 | a0001c0002t0001g0332 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.364-1892G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689183 | |||||||
| chr1:98689450 | A | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(86): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.364-1625A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689450 | |||||||
| chr1:98689522 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(27): Show |
34 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.364-1553T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689522 | |||||||
| chr1:98689531 | T | G | 1 | a0002c0003t0001g0139 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.364-1544T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689531 | |||||||
| chr1:98689567 | G | A | 357 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(354): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.364-1508G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689567 | |||||||
| chr1:98689572 | G | A | 168 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0087 others(165): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.364-1503G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689572 | |||||||
| chr1:98689942 | C | T | 2 | a0001c0002t0001g0312 a0001c0002t0001g0313 |
2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.364-1133C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98689942 | |||||||
| chr1:98690210 | A | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG00280.hp2 HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.364-865A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98690210 | |||||||
| chr1:98690569 | T | C | 6 | a0001c0001t0003g0092 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-506T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98690569 | |||||||
| chr1:98691041 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0072 |
2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.364-34T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2/8 | chr1 | 98691041 | |||||||
| chr1:98691211 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.474+26A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 3/8 | chr1 | 98691211 | |||||||
| chr1:98691338 | AT | A | 68 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(65): Show |
69 | HG00280.hp2 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.474+163delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr1 | 98691338 | ||||||
| chr1:98691348 | T | A | 32 | a0001c0001t0001g0017 a0001c0001t0001g0113 a0001c0001t0001g0207 others(29): Show |
32 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.474+163T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 3/8 | chr1 | 98691348 | |||||||
| chr1:98691349 | A | T | 5 | a0001c0002t0001g0350 a0001c0002t0001g0351 a0001c0002t0001g0352 others(2): Show |
5 | HG01081.hp2 HG01978.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.474+164A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 3/8 | chr1 | 98691349 | |||||||
| chr1:98691779 | G | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+80G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691779 | |||||||
| chr1:98691876 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.639+177A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691876 | |||||||
| chr1:98691906 | C | CAT | 51 | a0001c0001t0001g0014 a0001c0001t0001g0208 a0002c0003t0001g0001 others(48): Show |
53 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(50): Show |
intron_variant | MODIFIER | c.639+215_639+216dup others(2): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691906 | ||||||
| chr1:98691906 | C | CATAT | 7 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0303 others(4): Show |
7 | HG00544.hp1 HG01884.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+213_639+216dup others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691906 | ||||||
| chr1:98691914 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.639+215T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691914 | |||||||
| chr1:98691914 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0013 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.639+230_639+239dup others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATACAC | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(47): Show |
53 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.639+216_639+217ins others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATACACA others(3): Show |
47 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0025 others(44): Show |
49 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.639+216_639+217ins others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATACACA others(5): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0054 others(3): Show |
6 | HG02074.hp2 HG03688.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.639+216_639+217ins others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATATAC | 51 | a0001c0001t0001g0256 a0001c0001t0001g0283 a0001c0001t0001g0297 others(48): Show |
51 | HG00323.hp2 HG00738.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.639+216_639+217ins others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATATACA others(1): Show |
5 | a0001c0002t0001g0333 a0001c0002t0001g0351 a0001c0002t0001g0352 others(2): Show |
5 | HG03041.hp1 HG03486.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.639+216_639+217ins others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691914 | T | TATATACA others(3): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0008t0001g0036 |
3 | NA18961.hp2 NA18993.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.639+216_639+217ins others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691914 | ||||||
| chr1:98691916 | C | T | 143 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(140): Show |
146 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.639+217C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691916 | |||||||
| chr1:98691935 | ACACTCTC others(3): Show |
A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.639+238_639+247del others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691935 | ||||||
| chr1:98691937 | A | ACACACAC others(5): Show |
3 | a0001c0001t0001g0274 a0001c0001t0001g0279 a0001c0001t0001g0299 |
3 | HG03669.hp1 HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.639+239_639+240ins others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACAC others(3): Show |
7 | a0001c0001t0001g0017 a0001c0001t0001g0103 a0001c0001t0001g0238 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+239_639+240ins others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACAC others(5): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0205 a0001c0001t0001g0243 others(3): Show |
7 | HG00408.hp2 HG02055.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.639+239_639+240ins others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACAC others(7): Show |
27 | a0001c0001t0001g0267 a0001c0001t0001g0270 a0001c0001t0001g0271 others(24): Show |
27 | HG00140.hp2 HG00558.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.639+239_639+240ins others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACAC others(11): Show |
3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0314 |
3 | HG02300.hp1 HG03017.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.639+239_639+240ins others(18): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACTC others(3): Show |
36 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0209 others(33): Show |
36 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.639+239_639+240ins others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACTC others(5): Show |
2 | a0001c0001t0001g0210 a0001c0001t0001g0247 |
2 | HG02056.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.639+239_639+240ins others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACACTC others(9): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.639+239_639+240ins others(16): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACTCT | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 |
3 | HG01884.hp2 HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.639+239_639+240ins others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACACTCTC others(3): Show |
5 | a0001c0001t0001g0090 a0001c0001t0001g0212 a0001c0001t0001g0219 others(2): Show |
5 | HG00280.hp2 HG02280.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+239_639+240ins others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACTCT | 48 | a0001c0001t0001g0297 a0001c0001t0001g0363 a0001c0002t0001g0030 others(45): Show |
48 | HG00323.hp2 HG00738.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.639+265_639+268dup others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACTCTCT | 6 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0303 others(3): Show |
6 | HG00544.hp1 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+263_639+268dup others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | ACTCTCTC others(3): Show |
1 | a0001c0007t0001g0329 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.639+259_639+268dup others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | A | T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0087 a0001c0001t0001g0088 others(18): Show |
21 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.639+238A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691937 | |||||||
| chr1:98691937 | ACT | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0175 a0001c0004t0001g0100 |
4 | HG02723.hp2 NA18974.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.639+267_639+268del others(2): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | ACTCT | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(25): Show |
30 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.639+265_639+268del others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | ACTCTCT | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+263_639+268del others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691937 | ACTCTCTC others(3): Show |
A | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.639+259_639+268del others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98691937 | ||||||
| chr1:98691939 | T | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(81): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.639+240T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691939 | |||||||
| chr1:98691941 | T | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.639+242T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691941 | |||||||
| chr1:98691943 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.639+244T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691943 | |||||||
| chr1:98691945 | T | A | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.639+246T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691945 | |||||||
| chr1:98691949 | T | A | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.639+250T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98691949 | |||||||
| chr1:98692676 | G | T | 350 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(347): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.639+977G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98692676 | |||||||
| chr1:98692986 | G | T | 350 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(347): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.639+1287G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98692986 | |||||||
| chr1:98693031 | T | C | 1 | a0002c0003t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639+1332T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693031 | |||||||
| chr1:98693172 | A | AGATG | 6 | a0001c0001t0003g0092 a0001c0004t0001g0009 a0001c0004t0001g0118 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+1500_639+1503d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98693172 | ||||||
| chr1:98693172 | A | AGATGGAT others(1): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0106 a0001c0001t0001g0107 |
4 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+1496_639+1503d others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98693172 | ||||||
| chr1:98693172 | A | AGATGGAT others(5): Show |
1 | a0001c0001t0001g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.639+1492_639+1503d others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98693172 | ||||||
| chr1:98693172 | AGATG | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.639+1500_639+1503d others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98693172 | ||||||
| chr1:98693194 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.639+1495A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693194 | |||||||
| chr1:98693327 | A | G | 1 | a0001c0002t0001g0303 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.639+1628A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693327 | |||||||
| chr1:98693574 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.639+1875C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693574 | |||||||
| chr1:98693741 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.640-1777A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693741 | |||||||
| chr1:98693818 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.640-1700A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98693818 | |||||||
| chr1:98694066 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.640-1452C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694066 | |||||||
| chr1:98694092 | T | C | 1 | a0001c0005t0001g0069 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.640-1426T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694092 | |||||||
| chr1:98694108 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640-1410C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694108 | |||||||
| chr1:98694136 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.640-1382C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694136 | |||||||
| chr1:98694186 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.640-1332C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694186 | |||||||
| chr1:98694231 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-1287G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694231 | |||||||
| chr1:98694238 | T | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.640-1280T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694238 | |||||||
| chr1:98694243 | A | G | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.640-1275A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694243 | |||||||
| chr1:98694302 | G | A | 52 | a0002c0003t0001g0001 a0002c0003t0001g0122 a0002c0003t0001g0123 others(49): Show |
54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
intron_variant | MODIFIER | c.640-1216G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694302 | |||||||
| chr1:98694349 | G | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0173 others(11): Show |
17 | HG00673.hp1 HG02040.hp2 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.640-1169G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694349 | |||||||
| chr1:98694369 | C | CA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(52): Show |
59 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.640-1128dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694369 | ||||||
| chr1:98694464 | T | C | 4 | a0001c0002t0001g0351 a0001c0002t0001g0352 a0001c0002t0001g0353 others(1): Show |
4 | HG01081.hp2 HG01978.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.640-1054T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694464 | |||||||
| chr1:98694564 | C | T | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.640-954C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694564 | |||||||
| chr1:98694596 | A | AT | 75 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0200 others(72): Show |
78 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.640-893dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | A | ATT | 63 | a0001c0001t0001g0017 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.640-894_640-893dup others(2): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | A | ATTT | 7 | a0001c0001t0001g0215 a0001c0001t0001g0253 a0001c0001t0001g0263 others(4): Show |
8 | HG01891.hp2 HG02129.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.640-895_640-893dup others(3): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | A | ATTTT | 18 | a0001c0002t0001g0031 a0001c0002t0001g0302 a0001c0002t0001g0304 others(15): Show |
18 | HG00323.hp2 HG01081.hp2 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.640-896_640-893dup others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | A | ATTTTT | 28 | a0001c0002t0001g0030 a0001c0002t0001g0032 a0001c0002t0001g0105 others(25): Show |
28 | HG00544.hp1 HG01106.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.640-897_640-893dup others(5): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | A | ATTTTTT | 15 | a0001c0001t0001g0014 a0001c0001t0001g0363 a0001c0002t0001g0094 others(12): Show |
15 | HG01255.hp1 HG01358.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.640-898_640-893dup others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | AT | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0163 others(13): Show |
17 | HG02155.hp1 HG02258.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.640-893delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | ATTT | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0023 others(38): Show |
42 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.640-895_640-893del others(3): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694596 | ATTTT | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(45): Show |
52 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.640-896_640-893del others(4): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr1 | 98694596 | ||||||
| chr1:98694641 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.640-877T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694641 | |||||||
| chr1:98694685 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.640-833G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694685 | |||||||
| chr1:98694798 | G | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.640-720G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694798 | |||||||
| chr1:98694810 | G | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-708G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694810 | |||||||
| chr1:98694829 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-689C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98694829 | |||||||
| chr1:98695128 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.640-390T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695128 | |||||||
| chr1:98695231 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.640-287C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695231 | |||||||
| chr1:98695251 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.640-267C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695251 | |||||||
| chr1:98695263 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.640-255A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695263 | |||||||
| chr1:98695271 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0026 others(18): Show |
22 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.640-247C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695271 | |||||||
| chr1:98695376 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.640-142G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695376 | |||||||
| chr1:98695492 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640-26A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 4/8 | chr1 | 98695492 | |||||||
| chr1:98695763 | A | G | 1 | a0002c0003t0001g0136 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.838+47A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98695763 | |||||||
| chr1:98695848 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.838+132T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98695848 | |||||||
| chr1:98696246 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.838+530A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696246 | |||||||
| chr1:98696308 | A | G | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | NA18946.hp2 NA18969.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.838+592A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696308 | |||||||
| chr1:98696392 | T | C | 2 | a0001c0001t0001g0273 a0001c0001t0001g0289 |
2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.838+676T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696392 | |||||||
| chr1:98696415 | G | A | 56 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(53): Show |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.838+699G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696415 | |||||||
| chr1:98696511 | G | A | 3 | a0001c0002t0001g0355 a0001c0002t0001g0356 a0001c0002t0001g0357 |
3 | HG02965.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.838+795G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696511 | |||||||
| chr1:98696546 | G | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+830G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696546 | |||||||
| chr1:98696564 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.838+848A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696564 | |||||||
| chr1:98696710 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0174 others(5): Show |
11 | HG02071.hp1 NA18942.hp2 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.838+994C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696710 | |||||||
| chr1:98696730 | C | CT | 12 | a0001c0001t0001g0252 a0001c0001t0001g0267 a0001c0001t0001g0276 others(9): Show |
12 | HG01070.hp1 HG01074.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.838+1024dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr1 | 98696730 | ||||||
| chr1:98696772 | T | C | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.838+1056T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696772 | |||||||
| chr1:98696897 | A | G | 1 | a0001c0002t0001g0356 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.838+1181A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98696897 | |||||||
| chr1:98697057 | A | G | 57 | a0001c0001t0001g0363 a0001c0002t0001g0030 a0001c0002t0001g0031 others(54): Show |
57 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.838+1341A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697057 | |||||||
| chr1:98697228 | T | C | 1 | a0001c0002t0001g0332 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.839-1478T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697228 | |||||||
| chr1:98697342 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.839-1364A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697342 | |||||||
| chr1:98697430 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0316 |
2 | HG02129.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.839-1276G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697430 | |||||||
| chr1:98697449 | T | C | 1 | a0002c0003t0001g0196 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.839-1257T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697449 | |||||||
| chr1:98697669 | A | C | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.839-1037A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697669 | |||||||
| chr1:98697786 | A | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-920A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697786 | |||||||
| chr1:98697787 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.839-919G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98697787 | |||||||
| chr1:98698192 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.839-514G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98698192 | |||||||
| chr1:98698516 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.839-190T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98698516 | |||||||
| chr1:98698574 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.839-132C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98698574 | |||||||
| chr1:98698575 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.839-131G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 5/8 | chr1 | 98698575 | |||||||
| chr1:98698929 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+24T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98698929 | |||||||
| chr1:98698978 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1038+73C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98698978 | |||||||
| chr1:98699155 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1038+250C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699155 | |||||||
| chr1:98699180 | A | G | 1 | a0001c0007t0001g0329 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1038+275A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699180 | |||||||
| chr1:98699364 | C | A | 1 | a0001c0002t0001g0338 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1038+459C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699364 | |||||||
| chr1:98699380 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(314): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1038+475T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699380 | |||||||
| chr1:98699571 | T | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 |
3 | HG02735.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1038+666T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699571 | |||||||
| chr1:98699627 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1038+722G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699627 | |||||||
| chr1:98699670 | TGATTTCT others(3): Show |
T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1038+773_1038+782d others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 98699670 | ||||||
| chr1:98699999 | A | G | 2 | a0001c0002t0001g0105 a0001c0002t0001g0343 |
2 | HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1038+1094A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98699999 | |||||||
| chr1:98700330 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+1425T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98700330 | |||||||
| chr1:98700347 | A | G | 56 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(53): Show |
56 | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1038+1442A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98700347 | |||||||
| chr1:98700399 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1039-1418G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98700399 | |||||||
| chr1:98700998 | C | A | 7 | a0001c0002t0001g0334 a0001c0002t0001g0339 a0001c0002t0001g0340 others(4): Show |
7 | HG01255.hp1 HG01257.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-819C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98700998 | |||||||
| chr1:98701020 | C | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1039-797C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701020 | |||||||
| chr1:98701083 | G | A | 54 | a0001c0001t0001g0103 a0001c0001t0001g0266 a0002c0003t0001g0001 others(51): Show |
56 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(53): Show |
intron_variant | MODIFIER | c.1039-734G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701083 | |||||||
| chr1:98701122 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | HG00673.hp1 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1039-695G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701122 | |||||||
| chr1:98701125 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1039-692A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701125 | |||||||
| chr1:98701144 | G | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(313): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1039-673G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701144 | |||||||
| chr1:98701254 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1039-563C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701254 | |||||||
| chr1:98701315 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1039-502T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701315 | |||||||
| chr1:98701329 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1039-488A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701329 | |||||||
| chr1:98701436 | A | G | 351 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(348): Show |
364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.1039-381A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701436 | |||||||
| chr1:98701439 | A | G | 1 | a0001c0002t0001g0346 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1039-378A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701439 | |||||||
| chr1:98701659 | CA | C | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(311): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1039-145delA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr1 | 98701659 | ||||||
| chr1:98701709 | T | C | 1 | a0002c0003t0001g0142 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1039-108T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 6/8 | chr1 | 98701709 | |||||||
| chr1:98701934 | A | G | 1 | a0001c0002t0001g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1125+31A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98701934 | |||||||
| chr1:98702089 | G | A | 1 | a0001c0002t0001g0339 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1125+186G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702089 | |||||||
| chr1:98702101 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1125+198C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702101 | |||||||
| chr1:98702161 | G | A | 52 | a0002c0003t0001g0001 a0002c0003t0001g0122 a0002c0003t0001g0123 others(49): Show |
54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
intron_variant | MODIFIER | c.1125+258G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702161 | |||||||
| chr1:98702251 | G | A | 52 | a0002c0003t0001g0001 a0002c0003t0001g0122 a0002c0003t0001g0123 others(49): Show |
54 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(51): Show |
intron_variant | MODIFIER | c.1125+348G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702251 | |||||||
| chr1:98702264 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1125+361T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702264 | |||||||
| chr1:98702327 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1125+424G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702327 | |||||||
| chr1:98702696 | A | G | 1 | a0002c0003t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1125+793A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702696 | |||||||
| chr1:98702792 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1125+889C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702792 | |||||||
| chr1:98702821 | T | C | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1125+918T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98702821 | |||||||
| chr1:98703223 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+1320G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703223 | |||||||
| chr1:98703538 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | NA18983.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1125+1635A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703538 | |||||||
| chr1:98703631 | C | T | 5 | a0001c0001t0001g0228 a0001c0001t0001g0244 a0001c0001t0001g0254 others(2): Show |
5 | HG00597.hp1 HG00673.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1125+1728C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703631 | |||||||
| chr1:98703642 | T | C | 322 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(319): Show |
331 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.1125+1739T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703642 | |||||||
| chr1:98703725 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0209 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1125+1822T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703725 | |||||||
| chr1:98703733 | G | T | 312 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(309): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1125+1830G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703733 | |||||||
| chr1:98703742 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
10 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1125+1839G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98703742 | |||||||
| chr1:98704085 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+2182C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704085 | |||||||
| chr1:98704170 | G | A | 358 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(355): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1125+2267G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704170 | |||||||
| chr1:98704340 | A | G | 9 | a0002c0003t0001g0127 a0002c0003t0001g0128 a0002c0003t0001g0129 others(6): Show |
9 | HG01496.hp1 HG02132.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1125+2437A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704340 | |||||||
| chr1:98704450 | T | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+2547T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704450 | |||||||
| chr1:98704456 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+2553T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704456 | |||||||
| chr1:98704613 | G | A | 1 | a0001c0002t0001g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1125+2710G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704613 | |||||||
| chr1:98704667 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1125+2764C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704667 | |||||||
| chr1:98704704 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1125+2801T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704704 | |||||||
| chr1:98704975 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+3072G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98704975 | |||||||
| chr1:98705075 | A | G | 312 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(309): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1125+3172A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705075 | |||||||
| chr1:98705128 | A | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1125+3225A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705128 | |||||||
| chr1:98705417 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0243 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1125+3514A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705417 | |||||||
| chr1:98705463 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1125+3560G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705463 | |||||||
| chr1:98705572 | T | A | 12 | a0001c0002t0001g0302 a0001c0002t0001g0303 a0001c0002t0001g0304 others(9): Show |
12 | HG00544.hp1 NA18948.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.1125+3669T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705572 | |||||||
| chr1:98705635 | T | C | 1 | a0001c0002t0001g0351 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1125+3732T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705635 | |||||||
| chr1:98705803 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1125+3900C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705803 | |||||||
| chr1:98705830 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1125+3927A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705830 | |||||||
| chr1:98705851 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+3948T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98705851 | |||||||
| chr1:98706360 | G | A | 4 | a0001c0002t0001g0349 a0001c0002t0001g0355 a0001c0002t0001g0356 others(1): Show |
4 | HG02965.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+4457G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98706360 | |||||||
| chr1:98706483 | G | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1125+4580G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98706483 | |||||||
| chr1:98706741 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1125+4838C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98706741 | |||||||
| chr1:98706744 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1125+4841A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98706744 | |||||||
| chr1:98707077 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1125+5174A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98707077 | |||||||
| chr1:98707094 | G | A | 54 | a0001c0001t0001g0103 a0001c0001t0001g0266 a0002c0003t0001g0001 others(51): Show |
56 | HG01496.hp1 HG01943.hp1 HG01993.hp1 others(53): Show |
intron_variant | MODIFIER | c.1125+5191G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98707094 | |||||||
| chr1:98707343 | C | T | 3 | a0001c0002t0001g0355 a0001c0002t0001g0356 a0001c0002t0001g0357 |
3 | HG02965.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1125+5440C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98707343 | |||||||
| chr1:98707806 | T | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+5903T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98707806 | |||||||
| chr1:98707878 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(26): Show |
33 | HG00438.hp1 HG00673.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1125+5975T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98707878 | |||||||
| chr1:98708061 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1125+6158T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708061 | |||||||
| chr1:98708125 | A | G | 226 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0029 others(223): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.1125+6222A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708125 | |||||||
| chr1:98708355 | C | G | 1 | a0001c0002t0001g0348 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1125+6452C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708355 | |||||||
| chr1:98708439 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1125+6536T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708439 | |||||||
| chr1:98708479 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+6576C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708479 | |||||||
| chr1:98708666 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1125+6763G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708666 | |||||||
| chr1:98708680 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+6777G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708680 | |||||||
| chr1:98708761 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1125+6858A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98708761 | |||||||
| chr1:98709056 | C | A | 224 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0029 others(221): Show |
228 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1125+7153C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709056 | |||||||
| chr1:98709106 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+7203T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709106 | |||||||
| chr1:98709152 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1125+7249A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709152 | |||||||
| chr1:98709239 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1125+7336A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709239 | |||||||
| chr1:98709918 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1125+8015C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709918 | |||||||
| chr1:98709942 | A | G | 52 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(49): Show |
53 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1125+8039A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98709942 | |||||||
| chr1:98710079 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+8176A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710079 | |||||||
| chr1:98710119 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+8216C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710119 | |||||||
| chr1:98710139 | T | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+8236T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710139 | |||||||
| chr1:98710355 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+8452G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710355 | |||||||
| chr1:98710356 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+8453A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710356 | |||||||
| chr1:98710377 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1125+8474C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710377 | |||||||
| chr1:98710393 | A | G | 1 | a0001c0002t0001g0328 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1125+8490A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710393 | |||||||
| chr1:98710438 | AT | A | 60 | a0001c0001t0001g0103 a0001c0001t0001g0266 a0001c0004t0001g0009 others(57): Show |
63 | HG00733.hp2 HG01496.hp1 HG01943.hp1 others(60): Show |
intron_variant | MODIFIER | c.1125+8545delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98710438 | ||||||
| chr1:98710551 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1125+8648C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710551 | |||||||
| chr1:98710554 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+8651T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710554 | |||||||
| chr1:98710707 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1125+8804G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710707 | |||||||
| chr1:98710740 | T | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1125+8837T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710740 | |||||||
| chr1:98710948 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1125+9045G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98710948 | |||||||
| chr1:98711126 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+9223C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711126 | |||||||
| chr1:98711275 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1125+9372C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711275 | |||||||
| chr1:98711422 | AG | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+9521delG | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98711422 | ||||||
| chr1:98711425 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+9522C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711425 | |||||||
| chr1:98711537 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1125+9634A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711537 | |||||||
| chr1:98711697 | G | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(142): Show |
151 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1125+9794G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711697 | |||||||
| chr1:98711757 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1125+9854G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711757 | |||||||
| chr1:98711891 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+9988A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98711891 | |||||||
| chr1:98712008 | G | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1125+10105G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712008 | |||||||
| chr1:98712021 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1125+10118A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712021 | |||||||
| chr1:98712056 | T | C | 1 | a0001c0002t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1125+10153T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712056 | |||||||
| chr1:98712119 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1125+10216C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712119 | |||||||
| chr1:98712229 | A | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1125+10326A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712229 | |||||||
| chr1:98712322 | C | G | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1125+10419C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712322 | |||||||
| chr1:98712322 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1125+10419C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712322 | |||||||
| chr1:98712382 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1125+10479T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712382 | |||||||
| chr1:98712522 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1125+10619C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712522 | |||||||
| chr1:98712529 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+10626G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712529 | |||||||
| chr1:98712604 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+10701G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712604 | |||||||
| chr1:98712691 | A | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+10788A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712691 | |||||||
| chr1:98712827 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1125+10924C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98712827 | |||||||
| chr1:98713057 | G | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1125+11154G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713057 | |||||||
| chr1:98713094 | G | GA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(96): Show |
102 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1125+11209dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98713094 | ||||||
| chr1:98713094 | G | GAA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0018 others(9): Show |
14 | HG02056.hp1 HG02135.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1125+11208_1125+11 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98713094 | ||||||
| chr1:98713094 | G | GAAAAAA | 54 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(51): Show |
55 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1125+11204_1125+11 others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98713094 | ||||||
| chr1:98713107 | A | AC | 3 | a0001c0001t0001g0057 a0001c0001t0001g0085 a0001c0001t0001g0102 |
3 | HG01106.hp1 HG01167.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1125+11204_1125+11 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713107 | |||||||
| chr1:98713107 | A | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(79): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1125+11204A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713107 | |||||||
| chr1:98713175 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1125+11272A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713175 | |||||||
| chr1:98713408 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+11505A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713408 | |||||||
| chr1:98713424 | C | T | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1125+11521C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713424 | |||||||
| chr1:98713447 | C | CT | 91 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(88): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1125+11553dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98713447 | ||||||
| chr1:98713512 | T | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1125+11609T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713512 | |||||||
| chr1:98713699 | A | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0195 |
3 | HG00642.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1125+11796A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713699 | |||||||
| chr1:98713948 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1125+12045C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98713948 | |||||||
| chr1:98714016 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1125+12113T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714016 | |||||||
| chr1:98714052 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1125+12149C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714052 | |||||||
| chr1:98714125 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0082 |
2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1125+12222C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714125 | |||||||
| chr1:98714166 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1125+12263A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714166 | |||||||
| chr1:98714352 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1125+12449G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714352 | |||||||
| chr1:98714362 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+12459A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714362 | |||||||
| chr1:98714386 | CAAATAGT others(100): Show |
C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+12486_1125+12 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98714386 | ||||||
| chr1:98714551 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1125+12648A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714551 | |||||||
| chr1:98714601 | G | T | 1 | a0002c0003t0001g0135 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1125+12698G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714601 | |||||||
| chr1:98714662 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0229 a0001c0001t0001g0260 |
3 | HG01070.hp2 HG01256.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1125+12759C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714662 | |||||||
| chr1:98714733 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+12830G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714733 | |||||||
| chr1:98714779 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1125+12876A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714779 | |||||||
| chr1:98714797 | G | A | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG02622.hp1 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1125+12894G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98714797 | |||||||
| chr1:98715085 | A | T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+13182A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715085 | |||||||
| chr1:98715216 | G | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+13313G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715216 | |||||||
| chr1:98715217 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1125+13314G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715217 | |||||||
| chr1:98715220 | A | C | 1 | a0002c0003t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1125+13317A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715220 | |||||||
| chr1:98715247 | C | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1125+13344C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715247 | |||||||
| chr1:98715311 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0084 |
2 | HG02683.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1125+13408C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715311 | |||||||
| chr1:98715354 | T | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1125+13451T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715354 | |||||||
| chr1:98715403 | G | C | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1125+13500G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715403 | |||||||
| chr1:98715446 | A | G | 3 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0320 |
3 | NA18946.hp2 NA18969.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1125+13543A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715446 | |||||||
| chr1:98715610 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+13707A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715610 | |||||||
| chr1:98715612 | G | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0203 others(4): Show |
7 | NA18939.hp2 NA18983.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1125+13709G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715612 | |||||||
| chr1:98715658 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+13755A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715658 | |||||||
| chr1:98715948 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1125+14045A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98715948 | |||||||
| chr1:98716149 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+14246G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716149 | |||||||
| chr1:98716182 | C | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1125+14279C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716182 | |||||||
| chr1:98716416 | A | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1125+14513A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716416 | |||||||
| chr1:98716561 | C | T | 6 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1125+14658C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716561 | |||||||
| chr1:98716648 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1125+14745C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716648 | |||||||
| chr1:98716746 | T | G | 1 | a0001c0002t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1125+14843T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716746 | |||||||
| chr1:98716854 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+14951T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716854 | |||||||
| chr1:98716886 | C | T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1125+14983C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98716886 | |||||||
| chr1:98717010 | TA | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1125+15118delA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98717010 | ||||||
| chr1:98717186 | A | G | 2 | a0002c0003t0001g0146 a0002c0003t0001g0186 |
2 | HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1125+15283A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717186 | |||||||
| chr1:98717426 | T | C | 6 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(3): Show |
7 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1125+15523T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717426 | |||||||
| chr1:98717602 | A | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1125+15699A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717602 | |||||||
| chr1:98717657 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1125+15754G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717657 | |||||||
| chr1:98717672 | T | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1125+15769T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717672 | |||||||
| chr1:98717704 | A | G | 1 | a0002c0003t0001g0141 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1125+15801A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717704 | |||||||
| chr1:98717759 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1125+15856T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717759 | |||||||
| chr1:98717903 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+16000A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98717903 | |||||||
| chr1:98718042 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1125+16139G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718042 | |||||||
| chr1:98718052 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1125+16149T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718052 | |||||||
| chr1:98718090 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0102 |
2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1125+16187C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718090 | |||||||
| chr1:98718126 | G | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0220 |
3 | NA18939.hp2 NA18993.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1125+16223G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718126 | |||||||
| chr1:98718230 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1125+16327T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718230 | |||||||
| chr1:98718462 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1125+16559A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718462 | |||||||
| chr1:98718500 | A | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1125+16597A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718500 | |||||||
| chr1:98718509 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1125+16606G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718509 | |||||||
| chr1:98718539 | A | C | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1125+16636A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718539 | |||||||
| chr1:98718631 | A | G | 1 | a0002c0003t0001g0151 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1125+16728A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718631 | |||||||
| chr1:98718716 | T | C | 65 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
66 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.1125+16813T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718716 | |||||||
| chr1:98718829 | G | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1125+16926G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718829 | |||||||
| chr1:98718974 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1125+17071A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718974 | |||||||
| chr1:98718989 | A | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1125+17086A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98718989 | |||||||
| chr1:98719017 | A | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(98): Show |
106 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1125+17114A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719017 | |||||||
| chr1:98719064 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1125+17161C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719064 | |||||||
| chr1:98719242 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(148): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1125+17339G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719242 | |||||||
| chr1:98719301 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1125+17398A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719301 | |||||||
| chr1:98719516 | A | G | 1 | a0001c0002t0001g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1125+17613A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719516 | |||||||
| chr1:98719768 | G | T | 1 | a0001c0002t0001g0357 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1125+17865G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719768 | |||||||
| chr1:98719845 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1125+17942G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719845 | |||||||
| chr1:98719870 | TAA | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(208): Show |
218 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1125+17970_1125+17 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98719870 | ||||||
| chr1:98719921 | A | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1125+18018A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719921 | |||||||
| chr1:98719949 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1125+18046A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719949 | |||||||
| chr1:98719961 | A | G | 4 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | HG01433.hp1 HG02300.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+18058A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719961 | |||||||
| chr1:98719978 | C | T | 59 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(56): Show |
62 | HG00733.hp2 HG01496.hp1 HG01943.hp1 others(59): Show |
intron_variant | MODIFIER | c.1125+18075C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98719978 | |||||||
| chr1:98720059 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1125+18156C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720059 | |||||||
| chr1:98720076 | A | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-18161A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720076 | |||||||
| chr1:98720119 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-18118C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720119 | |||||||
| chr1:98720301 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-17936C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720301 | |||||||
| chr1:98720322 | G | A | 1 | a0002c0003t0001g0141 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1126-17915G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720322 | |||||||
| chr1:98720415 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1126-17822G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720415 | |||||||
| chr1:98720427 | A | T | 4 | a0002c0003t0001g0136 a0002c0003t0001g0149 a0002c0003t0001g0154 others(1): Show |
4 | NA18972.hp2 NA18995.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-17810A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720427 | |||||||
| chr1:98720433 | T | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0358 a0001c0002t0001g0030 others(30): Show |
33 | HG00544.hp1 HG01106.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1126-17804T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720433 | |||||||
| chr1:98720451 | T | G | 1 | a0001c0002t0001g0331 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1126-17786T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720451 | |||||||
| chr1:98720465 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1126-17772C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720465 | |||||||
| chr1:98720554 | G | T | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1126-17683G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720554 | |||||||
| chr1:98720562 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-17675A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720562 | |||||||
| chr1:98720707 | T | G | 1 | a0001c0004t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1126-17530T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720707 | |||||||
| chr1:98720713 | T | A | 1 | a0001c0004t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1126-17524T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720713 | |||||||
| chr1:98720751 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1126-17486A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720751 | |||||||
| chr1:98720779 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1126-17458A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720779 | |||||||
| chr1:98720868 | A | G | 2 | a0002c0003t0001g0191 a0002c0003t0001g0192 |
2 | NA18956.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1126-17369A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98720868 | |||||||
| chr1:98721017 | C | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1126-17220C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721017 | |||||||
| chr1:98721049 | C | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1126-17188C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721049 | |||||||
| chr1:98721083 | A | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1126-17154A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721083 | |||||||
| chr1:98721098 | T | TG | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1126-17139_1126-17 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721098 | |||||||
| chr1:98721099 | T | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1126-17138T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721099 | |||||||
| chr1:98721136 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1126-17101C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721136 | |||||||
| chr1:98721164 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1126-17073C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721164 | |||||||
| chr1:98721165 | A | G | 61 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(58): Show |
62 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.1126-17072A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721165 | |||||||
| chr1:98721169 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1126-17068C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721169 | |||||||
| chr1:98721291 | A | G | 9 | a0002c0003t0001g0122 a0002c0003t0001g0124 a0002c0003t0001g0138 others(6): Show |
9 | HG02040.hp1 HG02129.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.1126-16946A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721291 | |||||||
| chr1:98721343 | G | GTGCATGT others(4): Show |
1 | a0001c0004t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1126-16890_1126-16 others(17): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98721343 | ||||||
| chr1:98721348 | C | T | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-16889C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721348 | |||||||
| chr1:98721404 | G | A | 147 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(144): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1126-16833G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721404 | |||||||
| chr1:98721444 | A | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1126-16793A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721444 | |||||||
| chr1:98721626 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-16611G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721626 | |||||||
| chr1:98721690 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1126-16547T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721690 | |||||||
| chr1:98721869 | A | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1126-16368A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721869 | |||||||
| chr1:98721884 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-16353C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721884 | |||||||
| chr1:98721941 | T | C | 1 | a0002c0003t0001g0129 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1126-16296T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98721941 | |||||||
| chr1:98722147 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1126-16090G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722147 | |||||||
| chr1:98722228 | C | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-16009C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722228 | |||||||
| chr1:98722476 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1126-15761A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722476 | |||||||
| chr1:98722680 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0194 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1126-15557A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722680 | |||||||
| chr1:98722681 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0194 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1126-15556A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722681 | |||||||
| chr1:98722788 | AATG | A | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-15443_1126-15 others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98722788 | ||||||
| chr1:98722817 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1126-15420A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722817 | |||||||
| chr1:98722817 | A | T | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-15420A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722817 | |||||||
| chr1:98722911 | A | T | 1 | a0001c0004t0001g0179 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1126-15326A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98722911 | |||||||
| chr1:98723043 | C | T | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-15194C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723043 | |||||||
| chr1:98723090 | A | C | 1 | a0001c0004t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1126-15147A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723090 | |||||||
| chr1:98723158 | A | C | 3 | a0002c0003t0001g0136 a0002c0003t0001g0154 a0002c0003t0001g0155 |
3 | NA18972.hp2 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1126-15079A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723158 | |||||||
| chr1:98723250 | A | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-14987A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723250 | |||||||
| chr1:98723336 | AAAGT | A | 58 | a0001c0001t0001g0067 a0001c0001t0001g0358 a0001c0001t0001g0363 others(55): Show |
59 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.1126-14900_1126-14 others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723336 | |||||||
| chr1:98723346 | A | G | 4 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0249 others(1): Show |
4 | HG00558.hp1 HG03927.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-14891A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723346 | |||||||
| chr1:98723347 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1126-14890C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723347 | |||||||
| chr1:98723348 | G | GT | 6 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0054 others(3): Show |
6 | HG02074.hp2 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126-14889_1126-14 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723348 | |||||||
| chr1:98723349 | G | GT | 10 | a0001c0001t0001g0171 a0001c0001t0001g0175 a0001c0001t0001g0204 others(7): Show |
10 | HG00438.hp1 HG00733.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-14880dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98723349 | ||||||
| chr1:98723349 | G | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-14888G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723349 | |||||||
| chr1:98723407 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1126-14830T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723407 | |||||||
| chr1:98723429 | C | T | 1 | a0001c0006t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1126-14808C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723429 | |||||||
| chr1:98723456 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-14781A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723456 | |||||||
| chr1:98723461 | CT | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-14768delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98723461 | ||||||
| chr1:98723483 | G | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-14754G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723483 | |||||||
| chr1:98723709 | C | T | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1126-14528C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723709 | |||||||
| chr1:98723782 | T | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-14455T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723782 | |||||||
| chr1:98723786 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-14451G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723786 | |||||||
| chr1:98723790 | G | GGC | 145 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(142): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1126-14446_1126-14 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98723790 | ||||||
| chr1:98723815 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1126-14422C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723815 | |||||||
| chr1:98723831 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-14406A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98723831 | |||||||
| chr1:98723962 | CA | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-14266delA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98723962 | ||||||
| chr1:98724151 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1126-14086G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724151 | |||||||
| chr1:98724193 | T | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1126-14044T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724193 | |||||||
| chr1:98724368 | G | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-13869G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724368 | |||||||
| chr1:98724379 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-13858C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724379 | |||||||
| chr1:98724404 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1126-13833G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724404 | |||||||
| chr1:98724558 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1126-13679T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724558 | |||||||
| chr1:98724570 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-13667C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724570 | |||||||
| chr1:98724712 | TAGAG | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-13519_1126-13 others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98724712 | ||||||
| chr1:98724767 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-13470G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98724767 | |||||||
| chr1:98725012 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1126-13225C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725012 | |||||||
| chr1:98725125 | T | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-13112T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725125 | |||||||
| chr1:98725201 | T | C | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-13036T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725201 | |||||||
| chr1:98725300 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-12937A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725300 | |||||||
| chr1:98725393 | T | G | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-12844T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725393 | |||||||
| chr1:98725441 | A | G | 3 | a0002c0003t0001g0134 a0002c0003t0001g0160 a0002c0003t0001g0162 |
3 | NA18947.hp1 NA18957.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1126-12796A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725441 | |||||||
| chr1:98725456 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1126-12781G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725456 | |||||||
| chr1:98725507 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-12730C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725507 | |||||||
| chr1:98725587 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-12650C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725587 | |||||||
| chr1:98725684 | G | GA | 9 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0039 others(6): Show |
9 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1126-12549dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98725684 | ||||||
| chr1:98725853 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-12384A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725853 | |||||||
| chr1:98725913 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-12324C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98725913 | |||||||
| chr1:98726244 | A | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-11993A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726244 | |||||||
| chr1:98726297 | T | A | 1 | a0001c0002t0001g0338 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1126-11940T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726297 | |||||||
| chr1:98726325 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-11912G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726325 | |||||||
| chr1:98726424 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-11813T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726424 | |||||||
| chr1:98726426 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-11811G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726426 | |||||||
| chr1:98726436 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-11801G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726436 | |||||||
| chr1:98726659 | AT | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-11570delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98726659 | ||||||
| chr1:98726696 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1126-11541T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726696 | |||||||
| chr1:98726756 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-11481A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726756 | |||||||
| chr1:98726765 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1126-11472G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726765 | |||||||
| chr1:98726783 | G | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0243 a0001c0001t0001g0257 |
3 | HG02055.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1126-11454G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726783 | |||||||
| chr1:98726813 | C | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1126-11424C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726813 | |||||||
| chr1:98726871 | G | C | 2 | a0001c0001t0001g0018 a0001c0002t0001g0349 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1126-11366G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726871 | |||||||
| chr1:98726906 | G | A | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-11331G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726906 | |||||||
| chr1:98726971 | G | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0243 a0001c0001t0001g0257 |
3 | HG02055.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1126-11266G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98726971 | |||||||
| chr1:98727038 | G | A | 4 | a0001c0001t0001g0358 a0001c0002t0001g0327 a0001c0002t0001g0341 others(1): Show |
4 | HG01346.hp1 HG02683.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1126-11199G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727038 | |||||||
| chr1:98727049 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-11188G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727049 | |||||||
| chr1:98727057 | A | T | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1126-11180A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727057 | |||||||
| chr1:98727093 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-11144T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727093 | |||||||
| chr1:98727134 | C | T | 3 | a0001c0001t0001g0274 a0001c0001t0001g0279 a0001c0001t0001g0299 |
3 | HG03669.hp1 HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1126-11103C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727134 | |||||||
| chr1:98727135 | G | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0022 others(25): Show |
30 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1126-11102G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727135 | |||||||
| chr1:98727146 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-11091T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727146 | |||||||
| chr1:98727209 | CAAAT | C | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1126-11024_1126-11 others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98727209 | ||||||
| chr1:98727293 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10944G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727293 | |||||||
| chr1:98727381 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1126-10856G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727381 | |||||||
| chr1:98727399 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1126-10838T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727399 | |||||||
| chr1:98727430 | T | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10807T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727430 | |||||||
| chr1:98727433 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10804A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727433 | |||||||
| chr1:98727449 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1126-10788A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727449 | |||||||
| chr1:98727450 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10787A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727450 | |||||||
| chr1:98727548 | C | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1126-10689C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727548 | |||||||
| chr1:98727590 | G | A | 12 | a0001c0002t0001g0302 a0001c0002t0001g0303 a0001c0002t0001g0304 others(9): Show |
12 | HG00544.hp1 NA18948.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.1126-10647G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727590 | |||||||
| chr1:98727748 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-10489A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727748 | |||||||
| chr1:98727771 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10466G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727771 | |||||||
| chr1:98727888 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10349A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727888 | |||||||
| chr1:98727923 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10314G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98727923 | |||||||
| chr1:98728054 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-10183A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728054 | |||||||
| chr1:98728066 | A | G | 2 | a0001c0001t0001g0018 a0001c0002t0001g0349 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1126-10171A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728066 | |||||||
| chr1:98728220 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-10017G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728220 | |||||||
| chr1:98728220 | G | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1126-10017G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728220 | |||||||
| chr1:98728259 | A | G | 1 | a0001c0002t0001g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1126-9978A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728259 | |||||||
| chr1:98728293 | A | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-9944A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728293 | |||||||
| chr1:98728352 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1126-9885C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728352 | |||||||
| chr1:98728496 | C | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-9741C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728496 | |||||||
| chr1:98728555 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1126-9682A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728555 | |||||||
| chr1:98728576 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0075 |
2 | NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1126-9661A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728576 | |||||||
| chr1:98728701 | G | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1126-9536G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728701 | |||||||
| chr1:98728720 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1126-9517G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728720 | |||||||
| chr1:98728767 | A | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-9470A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728767 | |||||||
| chr1:98728798 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-9439G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728798 | |||||||
| chr1:98728801 | C | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1126-9436C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728801 | |||||||
| chr1:98728814 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1126-9423A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728814 | |||||||
| chr1:98728858 | T | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-9379T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728858 | |||||||
| chr1:98728870 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-9367G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728870 | |||||||
| chr1:98728905 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0082 |
2 | HG02738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1126-9332A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728905 | |||||||
| chr1:98728965 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-9272T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728965 | |||||||
| chr1:98728979 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-9258T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98728979 | |||||||
| chr1:98729185 | T | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-9052T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729185 | |||||||
| chr1:98729353 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-8884G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729353 | |||||||
| chr1:98729382 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(144): Show |
153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1126-8855A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729382 | |||||||
| chr1:98729465 | C | A | 59 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(56): Show |
62 | HG00733.hp2 HG01496.hp1 HG01943.hp1 others(59): Show |
intron_variant | MODIFIER | c.1126-8772C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729465 | |||||||
| chr1:98729496 | A | ATT | 145 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(142): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.1126-8732_1126-873 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98729496 | ||||||
| chr1:98729544 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1126-8693A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729544 | |||||||
| chr1:98729585 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1126-8652A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729585 | |||||||
| chr1:98729657 | C | T | 10 | a0001c0001t0001g0358 a0001c0002t0001g0327 a0001c0002t0001g0334 others(7): Show |
10 | HG01255.hp1 HG01346.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1126-8580C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729657 | |||||||
| chr1:98729713 | A | G | 1 | a0001c0002t0001g0325 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1126-8524A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729713 | |||||||
| chr1:98729788 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG00609.hp1 HG02135.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1126-8449G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729788 | |||||||
| chr1:98729824 | AG | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-8409delG | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98729824 | ||||||
| chr1:98729889 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-8348C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98729889 | |||||||
| chr1:98730015 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1126-8222A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730015 | |||||||
| chr1:98730109 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-8128G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730109 | |||||||
| chr1:98730233 | TA | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-8001delA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98730233 | ||||||
| chr1:98730276 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1126-7961G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730276 | |||||||
| chr1:98730308 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1126-7929A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730308 | |||||||
| chr1:98730485 | G | A | 3 | a0001c0002t0001g0355 a0001c0002t0001g0356 a0001c0002t0001g0357 |
3 | HG02965.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1126-7752G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730485 | |||||||
| chr1:98730494 | T | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0022 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1126-7743T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730494 | |||||||
| chr1:98730707 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-7530A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730707 | |||||||
| chr1:98730725 | C | A | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1126-7512C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730725 | |||||||
| chr1:98730765 | G | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(1): Show |
4 | HG02723.hp1 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-7472G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730765 | |||||||
| chr1:98730783 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1126-7454T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98730783 | |||||||
| chr1:98731124 | T | TA | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-7108dupA | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98731124 | ||||||
| chr1:98731151 | C | CT | 7 | a0001c0001t0001g0071 a0001c0001t0001g0180 a0001c0001t0001g0199 others(4): Show |
7 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126-7073dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98731151 | ||||||
| chr1:98731151 | C | CTT | 142 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(139): Show |
146 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1126-7074_1126-707 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98731151 | ||||||
| chr1:98731187 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-7050A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731187 | |||||||
| chr1:98731192 | A | G | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-7045A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731192 | |||||||
| chr1:98731281 | G | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02155.hp1 NA18954.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1126-6956G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731281 | |||||||
| chr1:98731442 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1126-6795T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731442 | |||||||
| chr1:98731485 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-6752T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731485 | |||||||
| chr1:98731567 | T | A | 1 | a0001c0002t0001g0357 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1126-6670T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731567 | |||||||
| chr1:98731637 | C | T | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-6600C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731637 | |||||||
| chr1:98731786 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1126-6451C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731786 | |||||||
| chr1:98731940 | G | A | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-6297G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98731940 | |||||||
| chr1:98732044 | G | A | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-6193G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732044 | |||||||
| chr1:98732061 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-6176T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732061 | |||||||
| chr1:98732073 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1126-6164C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732073 | |||||||
| chr1:98732185 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
64 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126-6052C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732185 | |||||||
| chr1:98732224 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-6013T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732224 | |||||||
| chr1:98732316 | A | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-5921A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732316 | |||||||
| chr1:98732348 | T | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-5889T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732348 | |||||||
| chr1:98732457 | C | T | 2 | a0001c0002t0001g0334 a0001c0002t0001g0345 |
2 | HG01255.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1126-5780C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732457 | |||||||
| chr1:98732505 | C | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-5732C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732505 | |||||||
| chr1:98732598 | A | G | 1 | a0002c0003t0001g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1126-5639A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732598 | |||||||
| chr1:98732683 | T | C | 1 | a0001c0004t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1126-5554T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732683 | |||||||
| chr1:98732749 | C | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-5488C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732749 | |||||||
| chr1:98732986 | G | A | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1126-5251G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732986 | |||||||
| chr1:98732995 | A | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-5242A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98732995 | |||||||
| chr1:98733059 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-5178A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733059 | |||||||
| chr1:98733070 | T | A | 59 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(56): Show |
62 | HG00733.hp2 HG01496.hp1 HG01943.hp1 others(59): Show |
intron_variant | MODIFIER | c.1126-5167T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733070 | |||||||
| chr1:98733199 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1126-5038A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733199 | |||||||
| chr1:98733214 | TCTC | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-5020_1126-501 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98733214 | ||||||
| chr1:98733289 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
64 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126-4948C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733289 | |||||||
| chr1:98733361 | G | A | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
64 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126-4876G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733361 | |||||||
| chr1:98733433 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
64 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126-4804C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733433 | |||||||
| chr1:98733446 | C | T | 2 | a0001c0002t0001g0304 a0001c0002t0001g0310 |
2 | NA18995.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1126-4791C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733446 | |||||||
| chr1:98733651 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-4586A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733651 | |||||||
| chr1:98733656 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-4581T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733656 | |||||||
| chr1:98733746 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1126-4491G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733746 | |||||||
| chr1:98733890 | T | C | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(60): Show |
64 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126-4347T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733890 | |||||||
| chr1:98733901 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-4336G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98733901 | |||||||
| chr1:98734098 | A | G | 1 | a0001c0002t0001g0313 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1126-4139A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734098 | |||||||
| chr1:98734178 | G | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-4059G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734178 | |||||||
| chr1:98734186 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-4051G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734186 | |||||||
| chr1:98734398 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(147): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1126-3839A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734398 | |||||||
| chr1:98734551 | C | A | 1 | a0001c0001t0001g0322 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1126-3686C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734551 | |||||||
| chr1:98734642 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(149): Show |
158 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1126-3595G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734642 | |||||||
| chr1:98734860 | A | G | 57 | a0001c0001t0001g0067 a0001c0001t0001g0358 a0001c0002t0001g0030 others(54): Show |
58 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.1126-3377A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734860 | |||||||
| chr1:98734914 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(52): Show |
56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1126-3323G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734914 | |||||||
| chr1:98734988 | A | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-3249A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98734988 | |||||||
| chr1:98735027 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1126-3210C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735027 | |||||||
| chr1:98735055 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1126-3182A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735055 | |||||||
| chr1:98735112 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126-3125G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735112 | |||||||
| chr1:98735185 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-3052G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735185 | |||||||
| chr1:98735745 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-2492T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735745 | |||||||
| chr1:98735815 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(145): Show |
154 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1126-2422C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98735815 | |||||||
| chr1:98736117 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1126-2120C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736117 | |||||||
| chr1:98736209 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1126-2028A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736209 | |||||||
| chr1:98736216 | T | C | 64 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(61): Show |
65 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1126-2021T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736216 | |||||||
| chr1:98736232 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1126-2005C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736232 | |||||||
| chr1:98736347 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1126-1890G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736347 | |||||||
| chr1:98736524 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1126-1713T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736524 | |||||||
| chr1:98736550 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1126-1687C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736550 | |||||||
| chr1:98736624 | A | C | 1 | a0001c0001t0001g0242 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1126-1613A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736624 | |||||||
| chr1:98736707 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1126-1530C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736707 | |||||||
| chr1:98736936 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1126-1301A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736936 | |||||||
| chr1:98736966 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1126-1271T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98736966 | |||||||
| chr1:98737078 | G | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1126-1159G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737078 | |||||||
| chr1:98737079 | C | CT | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1126-1148dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr1 | 98737079 | ||||||
| chr1:98737188 | T | A | 5 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0287 others(2): Show |
5 | HG00140.hp2 HG00642.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126-1049T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737188 | |||||||
| chr1:98737193 | T | C | 1 | a0002c0003t0001g0187 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1126-1044T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737193 | |||||||
| chr1:98737407 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1126-830C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737407 | |||||||
| chr1:98737477 | G | T | 1 | a0002c0003t0001g0138 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1126-760G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737477 | |||||||
| chr1:98737550 | T | C | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1126-687T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737550 | |||||||
| chr1:98737616 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1126-621G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737616 | |||||||
| chr1:98737618 | G | A | 1 | a0001c0004t0001g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1126-619G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98737618 | |||||||
| chr1:98738039 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1126-198A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98738039 | |||||||
| chr1:98738128 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1126-109A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 7/8 | chr1 | 98738128 | |||||||
| chr1:98738828 | AT | A | 3 | a0001c0005t0001g0005 a0001c0005t0001g0069 a0001c0005t0001g0070 |
4 | NA18945.hp1 NA18984.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+443delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98738828 | ||||||
| chr1:98738886 | GT | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(164): Show |
173 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1278+507delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98738886 | ||||||
| chr1:98739040 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+651G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739040 | |||||||
| chr1:98739105 | T | A | 4 | a0001c0005t0001g0005 a0001c0005t0001g0069 a0001c0005t0001g0070 others(1): Show |
5 | NA18945.hp1 NA18984.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+716T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739105 | |||||||
| chr1:98739128 | A | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+739A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739128 | |||||||
| chr1:98739151 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1278+762G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739151 | |||||||
| chr1:98739198 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(164): Show |
173 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.1278+809T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739198 | |||||||
| chr1:98739244 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+855A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739244 | |||||||
| chr1:98739249 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278+860G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739249 | |||||||
| chr1:98739282 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1278+893C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739282 | |||||||
| chr1:98739296 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1278+907A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739296 | |||||||
| chr1:98739321 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1278+932A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739321 | |||||||
| chr1:98739459 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1278+1070C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739459 | |||||||
| chr1:98739576 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1278+1187T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739576 | |||||||
| chr1:98739616 | T | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+1227T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739616 | |||||||
| chr1:98739686 | CAGATA | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+1301_1278+130 others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98739686 | ||||||
| chr1:98739851 | T | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1278+1462T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739851 | |||||||
| chr1:98739956 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1278+1567A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739956 | |||||||
| chr1:98739972 | G | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+1583G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98739972 | |||||||
| chr1:98740436 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+2047G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740436 | |||||||
| chr1:98740447 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0209 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1278+2058T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740447 | |||||||
| chr1:98740450 | A | G | 1 | a0001c0002t0001g0337 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1278+2061A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740450 | |||||||
| chr1:98740467 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0035 a0001c0001t0001g0039 |
3 | HG00140.hp1 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1278+2078C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740467 | |||||||
| chr1:98740622 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1278+2233G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740622 | |||||||
| chr1:98740672 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1278+2283A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740672 | |||||||
| chr1:98740682 | A | C | 55 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(52): Show |
56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1278+2293A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740682 | |||||||
| chr1:98740717 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+2328C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740717 | |||||||
| chr1:98740909 | T | C | 1 | a0001c0001t0001g0291 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1278+2520T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740909 | |||||||
| chr1:98740986 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+2597G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98740986 | |||||||
| chr1:98741017 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1278+2628G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741017 | |||||||
| chr1:98741066 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278+2677A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741066 | |||||||
| chr1:98741217 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+2828C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741217 | |||||||
| chr1:98741232 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+2843G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741232 | |||||||
| chr1:98741323 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1278+2934T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741323 | |||||||
| chr1:98741501 | A | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 |
3 | HG01169.hp1 HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1278+3112A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741501 | |||||||
| chr1:98741570 | G | A | 1 | a0001c0004t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1278+3181G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741570 | |||||||
| chr1:98741591 | G | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278+3202G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741591 | |||||||
| chr1:98741637 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0076 a0001c0001t0001g0077 others(1): Show |
4 | HG02155.hp2 NA18944.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+3248G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741637 | |||||||
| chr1:98741787 | T | G | 1 | a0001c0001t0001g0236 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1278+3398T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741787 | |||||||
| chr1:98741921 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(191): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1278+3532A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98741921 | |||||||
| chr1:98742022 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(163): Show |
172 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.1278+3633G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742022 | |||||||
| chr1:98742042 | C | A | 1 | a0002c0003t0001g0149 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1278+3653C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742042 | |||||||
| chr1:98742089 | C | G | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1278+3700C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742089 | |||||||
| chr1:98742374 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1278+3985T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742374 | |||||||
| chr1:98742415 | G | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+4026G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742415 | |||||||
| chr1:98742656 | C | T | 9 | a0001c0001t0001g0202 a0001c0001t0001g0210 a0001c0001t0001g0213 others(6): Show |
9 | HG00544.hp2 HG00609.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1278+4267C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742656 | |||||||
| chr1:98742719 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1278+4330C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98742719 | |||||||
| chr1:98743091 | GTCTA | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+4708_1278+471 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98743091 | ||||||
| chr1:98743366 | TTTAAA | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+4981_1278+498 others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98743366 | ||||||
| chr1:98743562 | A | G | 4 | a0001c0001t0001g0071 a0001c0001t0001g0199 a0001c0001t0001g0217 others(1): Show |
4 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+5173A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98743562 | |||||||
| chr1:98743736 | G | A | 1 | a0001c0001t0001g0320 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1278+5347G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98743736 | |||||||
| chr1:98743972 | A | C | 3 | a0001c0001t0001g0214 a0001c0001t0001g0249 a0001c0001t0001g0250 |
3 | HG00558.hp1 NA19011.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1278+5583A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98743972 | |||||||
| chr1:98744047 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1278+5658A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744047 | |||||||
| chr1:98744056 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1278+5667A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744056 | |||||||
| chr1:98744075 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1278+5686T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744075 | |||||||
| chr1:98744163 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18971.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1278+5774A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744163 | |||||||
| chr1:98744171 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(165): Show |
174 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.1278+5782T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744171 | |||||||
| chr1:98744329 | G | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278+5940G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744329 | |||||||
| chr1:98744399 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+6010G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744399 | |||||||
| chr1:98744440 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1278+6051A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744440 | |||||||
| chr1:98744538 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1278+6149A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744538 | |||||||
| chr1:98744711 | C | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+6322C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744711 | |||||||
| chr1:98744911 | C | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0194 |
2 | NA18970.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1278+6522C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744911 | |||||||
| chr1:98744999 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1278+6610A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98744999 | |||||||
| chr1:98745202 | T | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1278+6813T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745202 | |||||||
| chr1:98745493 | G | A | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1278+7104G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745493 | |||||||
| chr1:98745720 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1278+7331T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745720 | |||||||
| chr1:98745762 | T | A | 1 | a0001c0008t0001g0036 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1278+7373T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745762 | |||||||
| chr1:98745805 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1278+7416A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745805 | |||||||
| chr1:98745865 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1278+7476A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745865 | |||||||
| chr1:98745942 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0034 others(15): Show |
19 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.1278+7553A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745942 | |||||||
| chr1:98745993 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1278+7604C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98745993 | |||||||
| chr1:98746381 | A | G | 1 | a0002c0003t0001g0151 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1278+7992A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98746381 | |||||||
| chr1:98746442 | T | C | 3 | a0002c0003t0001g0137 a0002c0003t0001g0150 a0002c0003t0001g0152 |
3 | NA18967.hp2 NA18994.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1278+8053T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98746442 | |||||||
| chr1:98746734 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1278+8345T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98746734 | |||||||
| chr1:98746755 | T | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(57): Show |
61 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(58): Show |
intron_variant | MODIFIER | c.1278+8366T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98746755 | |||||||
| chr1:98746946 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1278+8557T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98746946 | |||||||
| chr1:98747011 | T | G | 1 | a0001c0008t0001g0036 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1278+8622T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747011 | |||||||
| chr1:98747012 | G | A | 1 | a0001c0008t0001g0036 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1278+8623G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747012 | |||||||
| chr1:98747072 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1278+8683G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747072 | |||||||
| chr1:98747252 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1278+8863C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747252 | |||||||
| chr1:98747279 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0209 |
3 | HG02647.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1278+8890T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747279 | |||||||
| chr1:98747284 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1278+8895A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747284 | |||||||
| chr1:98747427 | C | G | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1278+9038C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747427 | |||||||
| chr1:98747448 | C | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1278+9059C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747448 | |||||||
| chr1:98747515 | A | G | 29 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0022 others(26): Show |
31 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1278+9126A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747515 | |||||||
| chr1:98747723 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1278+9334C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747723 | |||||||
| chr1:98747781 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1278+9392A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747781 | |||||||
| chr1:98747867 | T | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1278+9478T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747867 | |||||||
| chr1:98747941 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1278+9552G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747941 | |||||||
| chr1:98747968 | C | T | 9 | a0001c0001t0001g0202 a0001c0001t0001g0210 a0001c0001t0001g0213 others(6): Show |
9 | HG00544.hp2 HG00609.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1278+9579C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98747968 | |||||||
| chr1:98747978 | C | CT | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1278+9605dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98747978 | ||||||
| chr1:98748110 | A | G | 2 | a0001c0004t0001g0324 a0001c0004t0001g0326 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1278+9721A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748110 | |||||||
| chr1:98748136 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0072 |
2 | HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1278+9747C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748136 | |||||||
| chr1:98748170 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1278+9781G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748170 | |||||||
| chr1:98748262 | A | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
105 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1278+9873A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748262 | |||||||
| chr1:98748328 | A | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(52): Show |
56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1278+9939A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748328 | |||||||
| chr1:98748478 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
100 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1278+10089G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748478 | |||||||
| chr1:98748498 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1278+10109A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748498 | |||||||
| chr1:98748504 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1278+10115A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748504 | |||||||
| chr1:98748600 | A | G | 1 | a0001c0002t0001g0360 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1278+10211A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748600 | |||||||
| chr1:98748637 | A | AAC | 85 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
89 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1278+10283_1278+10 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACAC | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0015 others(45): Show |
50 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1278+10281_1278+10 others(10): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACACAC | 28 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(25): Show |
28 | HG00544.hp1 HG00642.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.1278+10279_1278+10 others(12): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACACACA others(1): Show |
48 | a0001c0001t0001g0103 a0001c0001t0001g0266 a0001c0001t0001g0287 others(45): Show |
50 | HG01081.hp2 HG01123.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.1278+10277_1278+10 others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACACACA others(3): Show |
31 | a0001c0002t0001g0115 a0001c0002t0001g0364 a0001c0004t0001g0170 others(28): Show |
33 | HG00733.hp2 HG01943.hp1 HG01993.hp1 others(30): Show |
intron_variant | MODIFIER | c.1278+10275_1278+10 others(16): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACACACA others(5): Show |
16 | a0001c0001t0001g0288 a0001c0001t0003g0092 a0001c0002t0001g0360 others(13): Show |
16 | HG02040.hp1 HG02602.hp1 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.1278+10273_1278+10 others(18): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | AACACACA others(7): Show |
5 | a0001c0002t0001g0355 a0001c0002t0001g0356 a0002c0003t0001g0159 others(2): Show |
5 | HG02965.hp2 HG03195.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278+10271_1278+10 others(20): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98748637 | A | ACACACAC others(4): Show |
2 | a0002c0003t0001g0128 a0002c0003t0001g0188 |
2 | HG01496.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1278+10248_1278+10 others(17): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748637 | |||||||
| chr1:98748637 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1278+10248A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98748637 | |||||||
| chr1:98748637 | AAC | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(76): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1278+10283_1278+10 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98748637 | ||||||
| chr1:98749025 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1278+10636T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749025 | |||||||
| chr1:98749035 | G | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0267 a0001c0001t0001g0280 others(3): Show |
6 | HG00733.hp1 HG01070.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278+10646G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749035 | |||||||
| chr1:98749050 | C | T | 5 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278+10661C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749050 | |||||||
| chr1:98749062 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1278+10673T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749062 | |||||||
| chr1:98749446 | A | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-10608A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749446 | |||||||
| chr1:98749654 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(95): Show |
102 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1279-10400T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749654 | |||||||
| chr1:98749822 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0102 |
2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1279-10232G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749822 | |||||||
| chr1:98749985 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1279-10069C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98749985 | |||||||
| chr1:98750138 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-9916G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750138 | |||||||
| chr1:98750270 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-9784A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750270 | |||||||
| chr1:98750274 | C | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1279-9780C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750274 | |||||||
| chr1:98750274 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1279-9780C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750274 | |||||||
| chr1:98750297 | A | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(103): Show |
111 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1279-9757A>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750297 | |||||||
| chr1:98750333 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1279-9721C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750333 | |||||||
| chr1:98750404 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1279-9650G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750404 | |||||||
| chr1:98750712 | T | A | 1 | a0001c0001t0001g0316 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1279-9342T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98750712 | |||||||
| chr1:98751181 | G | A | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1279-8873G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751181 | |||||||
| chr1:98751202 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02451.hp1 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-8852T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751202 | |||||||
| chr1:98751227 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(93): Show |
100 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1279-8827C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751227 | |||||||
| chr1:98751274 | A | C | 1 | a0001c0002t0001g0343 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1279-8780A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751274 | |||||||
| chr1:98751311 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279-8743C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751311 | |||||||
| chr1:98751512 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-8542T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751512 | |||||||
| chr1:98751661 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-8393A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751661 | |||||||
| chr1:98751862 | G | C | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1279-8192G>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751862 | |||||||
| chr1:98751960 | A | G | 5 | a0002c0003t0001g0136 a0002c0003t0001g0149 a0002c0003t0001g0151 others(2): Show |
5 | NA18951.hp1 NA18972.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-8094A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98751960 | |||||||
| chr1:98752168 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1279-7886A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752168 | |||||||
| chr1:98752206 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-7848A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752206 | |||||||
| chr1:98752215 | C | G | 1 | a0001c0002t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1279-7839C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752215 | |||||||
| chr1:98752282 | T | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1279-7772T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752282 | |||||||
| chr1:98752344 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-7710A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752344 | |||||||
| chr1:98752348 | G | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1279-7706G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752348 | |||||||
| chr1:98752506 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-7548A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752506 | |||||||
| chr1:98752571 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-7483T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752571 | |||||||
| chr1:98752697 | A | G | 1 | a0001c0002t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1279-7357A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752697 | |||||||
| chr1:98752738 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1279-7316A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752738 | |||||||
| chr1:98752741 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1279-7313C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752741 | |||||||
| chr1:98752778 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1279-7276C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752778 | |||||||
| chr1:98752981 | G | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1279-7073G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98752981 | |||||||
| chr1:98753320 | C | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-6734C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753320 | |||||||
| chr1:98753362 | G | A | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1279-6692G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753362 | |||||||
| chr1:98753363 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1279-6691A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753363 | |||||||
| chr1:98753439 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG01884.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-6615C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753439 | |||||||
| chr1:98753458 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1279-6596G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753458 | |||||||
| chr1:98753533 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1279-6521G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753533 | |||||||
| chr1:98753656 | T | A | 1 | a0002c0003t0001g0142 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1279-6398T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753656 | |||||||
| chr1:98753777 | G | A | 1 | a0001c0002t0001g0328 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1279-6277G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753777 | |||||||
| chr1:98753810 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1279-6244T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753810 | |||||||
| chr1:98753825 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1279-6229C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753825 | |||||||
| chr1:98753917 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1279-6137G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98753917 | |||||||
| chr1:98754104 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1279-5950G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754104 | |||||||
| chr1:98754160 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-5894A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754160 | |||||||
| chr1:98754178 | G | A | 1 | a0001c0002t0001g0347 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1279-5876G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754178 | |||||||
| chr1:98754310 | A | C | 1 | a0002c0003t0001g0298 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1279-5744A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754310 | |||||||
| chr1:98754367 | C | G | 9 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(6): Show |
9 | HG00639.hp1 HG00738.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1279-5687C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754367 | |||||||
| chr1:98754650 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-5404C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98754650 | |||||||
| chr1:98755198 | C | G | 1 | a0001c0002t0001g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1279-4856C>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755198 | |||||||
| chr1:98755275 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0099 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1279-4779T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755275 | |||||||
| chr1:98755320 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1279-4734G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755320 | |||||||
| chr1:98755320 | G | T | 59 | a0001c0004t0001g0009 a0001c0004t0001g0118 a0001c0004t0001g0119 others(56): Show |
62 | HG00733.hp2 HG01496.hp1 HG01943.hp1 others(59): Show |
intron_variant | MODIFIER | c.1279-4734G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755320 | |||||||
| chr1:98755385 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(129): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1279-4669G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755385 | |||||||
| chr1:98755494 | A | AT | 360 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(357): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1279-4559dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98755494 | ||||||
| chr1:98755641 | A | C | 4 | a0001c0002t0001g0351 a0001c0002t0001g0352 a0001c0002t0001g0353 others(1): Show |
4 | HG01081.hp2 HG01978.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-4413A>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755641 | |||||||
| chr1:98755701 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-4353T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755701 | |||||||
| chr1:98755932 | A | G | 1 | a0001c0002t0001g0349 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1279-4122A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98755932 | |||||||
| chr1:98756019 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-4035A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756019 | |||||||
| chr1:98756026 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-4028A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756026 | |||||||
| chr1:98756041 | AT | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-4009delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756041 | ||||||
| chr1:98756133 | T | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-3921T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756133 | |||||||
| chr1:98756286 | G | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(99): Show |
107 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1279-3768G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756286 | |||||||
| chr1:98756358 | G | A | 1 | a0002c0003t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1279-3696G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756358 | |||||||
| chr1:98756372 | T | G | 1 | a0002c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1279-3682T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756372 | |||||||
| chr1:98756375 | T | TTATAGAT others(6109): Show |
1 | a0002c0003t0001g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6120): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6128): Show |
2 | a0002c0003t0001g0150 a0002c0003t0001g0152 |
2 | NA18994.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1279-3662_1279-366 others(6139): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6130): Show |
1 | a0002c0003t0001g0157 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6141): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6129): Show |
1 | a0002c0003t0001g0137 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6140): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6132): Show |
1 | a0002c0003t0001g0127 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6143): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6131): Show |
2 | a0002c0003t0001g0131 a0002c0003t0001g0188 |
2 | HG01496.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1279-3662_1279-366 others(6142): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6131): Show |
1 | a0002c0003t0001g0189 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6142): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6133): Show |
1 | a0001c0004t0001g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6144): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6136): Show |
1 | a0002c0003t0001g0190 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6147): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6132): Show |
1 | a0002c0003t0001g0129 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6143): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6134): Show |
1 | a0002c0003t0001g0128 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6145): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6128): Show |
1 | a0002c0003t0001g0192 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6139): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756375 | T | TTATAGAT others(6131): Show |
1 | a0002c0003t0001g0191 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1279-3662_1279-366 others(6142): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756375 | ||||||
| chr1:98756386 | T | A | 1 | a0002c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1279-3668T>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756386 | |||||||
| chr1:98756408 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1279-3646T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756408 | |||||||
| chr1:98756422 | G | GT | 139 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(136): Show |
146 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.1279-3608dupT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | G | GTT | 15 | a0001c0001t0001g0110 a0001c0001t0001g0167 a0001c0001t0001g0175 others(12): Show |
15 | HG00597.hp1 HG01069.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1279-3609_1279-360 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | G | GTTT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0041 others(15): Show |
19 | HG00597.hp2 HG00642.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279-3610_1279-360 others(7): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | G | GTTTT | 90 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(87): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1279-3611_1279-360 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | G | GTTTTT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0046 others(18): Show |
22 | HG00639.hp2 HG01109.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279-3612_1279-360 others(9): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0241 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1279-3617_1279-360 others(14): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756422 | GT | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0104 others(9): Show |
12 | HG01123.hp2 HG01346.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-3608delT | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98756422 | ||||||
| chr1:98756482 | T | C | 1 | a0002c0003t0001g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1279-3572T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756482 | |||||||
| chr1:98756499 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1279-3555A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756499 | |||||||
| chr1:98756628 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1279-3426G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756628 | |||||||
| chr1:98756842 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-3212A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756842 | |||||||
| chr1:98756896 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1279-3158C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756896 | |||||||
| chr1:98756932 | G | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1279-3122G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756932 | |||||||
| chr1:98756982 | T | C | 7 | a0001c0002t0001g0334 a0001c0002t0001g0340 a0001c0002t0001g0344 others(4): Show |
7 | HG01255.hp1 HG01358.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279-3072T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98756982 | |||||||
| chr1:98757062 | G | A | 4 | a0001c0005t0001g0005 a0001c0005t0001g0069 a0001c0005t0001g0070 others(1): Show |
5 | NA18945.hp1 NA18984.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-2992G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757062 | |||||||
| chr1:98757348 | G | A | 55 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0024 others(52): Show |
56 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.1279-2706G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757348 | |||||||
| chr1:98757361 | G | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1279-2693G>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757361 | |||||||
| chr1:98757566 | AAATATAG others(7): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1279-2487_1279-247 others(18): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757566 | |||||||
| chr1:98757652 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1279-2402C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757652 | |||||||
| chr1:98757686 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0063 |
3 | HG00408.hp1 NA18951.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.1279-2368C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757686 | |||||||
| chr1:98757707 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0106 others(1): Show |
5 | HG01891.hp1 HG02451.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-2347T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757707 | |||||||
| chr1:98757727 | C | CTGAT | 6 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0002c0003t0001g0136 others(3): Show |
6 | HG01884.hp1 HG03471.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-2299_1279-229 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98757727 | ||||||
| chr1:98757727 | CTGAT | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(150): Show |
159 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1279-2299_1279-229 others(8): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98757727 | ||||||
| chr1:98757811 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279-2243T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757811 | |||||||
| chr1:98757841 | A | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-2213A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757841 | |||||||
| chr1:98757872 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1279-2182G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757872 | |||||||
| chr1:98757908 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01891.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1279-2146T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757908 | |||||||
| chr1:98757952 | C | T | 58 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(55): Show |
59 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.1279-2102C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757952 | |||||||
| chr1:98757988 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-2066A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98757988 | |||||||
| chr1:98758028 | T | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-2026T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98758028 | |||||||
| chr1:98758172 | C | T | 1 | a0001c0002t0001g0360 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1279-1882C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98758172 | |||||||
| chr1:98758460 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1279-1594G>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98758460 | |||||||
| chr1:98758694 | T | G | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1279-1360T>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98758694 | |||||||
| chr1:98758785 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1279-1269C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98758785 | |||||||
| chr1:98758932 | T | TAC | 5 | a0001c0001t0001g0103 a0001c0001t0001g0266 a0002c0003t0001g0134 others(2): Show |
5 | HG02647.hp1 HG03579.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-1104_1279-110 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98758932 | ||||||
| chr1:98758932 | TAC | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0099 others(56): Show |
60 | HG00544.hp1 HG01081.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.1279-1104_1279-110 others(6): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr1 | 98758932 | ||||||
| chr1:98759285 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1279-769T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759285 | |||||||
| chr1:98759324 | T | C | 1 | a0001c0001t0003g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1279-730T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759324 | |||||||
| chr1:98759412 | T | C | 15 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0228 others(12): Show |
15 | HG00558.hp1 HG00597.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1279-642T>C | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759412 | |||||||
| chr1:98759489 | C | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1279-565C>A | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759489 | |||||||
| chr1:98759512 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0048 others(42): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1279-542C>T | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759512 | |||||||
| chr1:98759559 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1279-495A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759559 | |||||||
| chr1:98759767 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0266 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1279-287A>G | SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 8/8 | chr1 | 98759767 |