Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 29886 |
| ensemblid | ENSG00000106266.11 |
| hgncid | 14972 |
| symbol | SNX8 |
| name | sorting nexin 8 |
| refseq_nuc | NM_013321.4 |
| refseq_prot | NP_037453.1 |
| ensembl_nuc | ENST00000222990.8 |
| ensembl_prot | ENSP00000222990.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 2251770 |
| end | 2314441 |
| strand | - |
| ver | v1.2 |
| region | chr7:2251770-2314441 |
| region5000 | chr7:2246770-2319441 |
| regionname0 | SNX8_chr7_2251770_2314441 |
| regionname5000 | SNX8_chr7_2246770_2319441 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 465 | 342 | 75 | 65 | 143 | 14 | 43 | 105 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0002 | 0/0 | 465 | 13 | 11 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0003 | 0/0 | 465 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0004 | 0/0 | 465 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0005 | 0/0 | 465 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0006 | 0/0 | 460 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(455): Show |
chr7 | 2246770 | 2319441 |
| a0007 | 0/0 | 99 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(94): Show |
chr7 | 2246770 | 2319441 |
| a0008 | 0/0 | 465 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0009 | 0/0 | 465 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| a0010 | 0/0 | 465 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | MTGRA others(460): Show |
chr7 | 2246770 | 2319441 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1395 | 254 | 49 | 58 | 100 | 13 | 33 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0002 | 1/0 | 1395 | 47 | 4 | 4 | 32 | 1 | 5 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0003 | 0/0 | 1395 | 23 | 21 | 1 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0005 | 0/0 | 1395 | 9 | 0 | 0 | 8 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0006 | 0/0 | 1395 | 6 | 0 | 2 | 0 | 0 | 4 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0010 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0015 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0001c0016 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0002c0004 | 0/0 | 1395 | 12 | 10 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0002c0019 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0003c0007 | 0/0 | 1395 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0004c0012 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0004c0013 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0005c0009 | 0/0 | 1395 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0006c0008 | 0/0 | 1380 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1375): Show |
chr7 | 2246770 | 2319441 | ||
| a0007c0017 | 0/0 | 1424 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1419): Show |
chr7 | 2246770 | 2319441 | ||
| a0008c0011 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0009c0018 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 | ||
| a0010c0014 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ATGAC others(1390): Show |
chr7 | 2246770 | 2319441 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4704 | 79 | 1 | 17 | 49 | 5 | 7 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0002 | 0/0 | 4690 | 43 | 11 | 5 | 18 | 3 | 6 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0003 | 0/1 | 4706 | 36 | 3 | 13 | 8 | 2 | 9 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0005 | 0/0 | 4691 | 11 | 10 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0007 | 0/0 | 4692 | 11 | 0 | 1 | 8 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4687): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0008 | 0/0 | 4729 | 10 | 8 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4724): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0009 | 0/0 | 4687 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4682): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0011 | 0/0 | 4706 | 8 | 0 | 6 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0013 | 0/0 | 4706 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0014 | 0/0 | 4706 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0016 | 0/0 | 4704 | 4 | 0 | 3 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0017 | 0/0 | 4651 | 4 | 1 | 0 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4646): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0019 | 0/0 | 4690 | 3 | 0 | 1 | 0 | 0 | 2 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0020 | 0/0 | 4704 | 3 | 0 | 3 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0021 | 0/0 | 4691 | 3 | 3 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0022 | 0/0 | 4698 | 2 | 1 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0023 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0024 | 0/0 | 4704 | 2 | 0 | 1 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0025 | 0/0 | 4692 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4687): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0026 | 0/0 | 4690 | 2 | 0 | 1 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0030 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0031 | 0/0 | 4679 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4674): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0032 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0033 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4713): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0034 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0035 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0036 | 0/0 | 4693 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4688): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0037 | 0/0 | 4690 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0040 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0041 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0042 | 0/0 | 4706 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0043 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0044 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0045 | 0/0 | 4698 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0001c0001t0049 | 0/0 | 4704 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0004 | 1/0 | 4704 | 32 | 3 | 2 | 22 | 1 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0010 | 0/0 | 4710 | 9 | 0 | 0 | 9 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4705): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0027 | 0/0 | 4710 | 2 | 0 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4705): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0029 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0046 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0047 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4700): Show |
chr7 | 2246770 | 2319441 |
| a0001c0002t0048 | 0/0 | 4702 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4697): Show |
chr7 | 2246770 | 2319441 |
| a0001c0003t0002 | 0/0 | 4690 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4685): Show |
chr7 | 2246770 | 2319441 |
| a0001c0003t0005 | 0/0 | 4691 | 10 | 9 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0001c0003t0006 | 0/0 | 4704 | 11 | 11 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0003t0028 | 0/0 | 4691 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0001c0005t0001 | 0/0 | 4704 | 5 | 0 | 0 | 4 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0005t0015 | 0/0 | 4705 | 4 | 0 | 0 | 4 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4700): Show |
chr7 | 2246770 | 2319441 |
| a0001c0006t0013 | 0/0 | 4706 | 5 | 0 | 2 | 0 | 0 | 3 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0001c0006t0039 | 0/0 | 4707 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4702): Show |
chr7 | 2246770 | 2319441 |
| a0001c0010t0001 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0001c0015t0007 | 0/0 | 4692 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4687): Show |
chr7 | 2246770 | 2319441 |
| a0001c0016t0003 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0002c0004t0005 | 0/0 | 4691 | 4 | 3 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0002c0004t0008 | 0/0 | 4729 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4724): Show |
chr7 | 2246770 | 2319441 |
| a0002c0004t0018 | 0/0 | 4651 | 4 | 4 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4646): Show |
chr7 | 2246770 | 2319441 |
| a0002c0004t0023 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4693): Show |
chr7 | 2246770 | 2319441 |
| a0002c0004t0038 | 0/0 | 4691 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0002c0019t0006 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0003c0007t0012 | 0/0 | 4691 | 5 | 5 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0004c0012t0006 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0004c0013t0003 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4701): Show |
chr7 | 2246770 | 2319441 |
| a0005c0009t0012 | 0/0 | 4691 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4686): Show |
chr7 | 2246770 | 2319441 |
| a0006c0008t0001 | 0/0 | 4689 | 2 | 0 | 0 | 2 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4684): Show |
chr7 | 2246770 | 2319441 |
| a0007c0017t0002 | 0/0 | 4719 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4714): Show |
chr7 | 2246770 | 2319441 |
| a0008c0011t0001 | 0/0 | 4704 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0009c0018t0001 | 0/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| a0010c0014t0001 | 0/0 | 4704 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | ACGTG others(4699): Show |
chr7 | 2246770 | 2319441 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0007g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0009g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0011g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0013g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0016g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0017g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0019g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0020g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0020g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0021g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0022g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0022g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0023g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0024g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0025g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0025g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0026g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0026g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0030g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0031g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0032g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0033g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0034g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0035g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0036g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0037g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0040g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0041g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0042g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0043g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0044g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0045g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0001t0049g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0315 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0010g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0027g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0027g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0029g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0046g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0047g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0002t0048g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0005g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0003t0028g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0005t0015g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0013g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0006t0039g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0010t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0015t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0001c0016t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0008g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0008g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0018g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0023g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0004t0038g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0002c0019t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0003c0007t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0004c0012t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0004c0013t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0005c0009t0012g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0005c0009t0012g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0006c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0006c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0007c0017t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0008c0011t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0009c0018t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| a0010c0014t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | GBR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0073 | EUR | FIN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00423 | hp1 | a0001 | c0005 | t0001 | g0059 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00558 | hp1 | a0001 | c0002 | t0004 | g0306 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0149 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0165 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00639 | hp1 | a0001 | c0002 | t0027 | g0346 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0076 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00673 | hp1 | a0001 | c0005 | t0001 | g0218 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00673 | hp2 | a0001 | c0001 | t0009 | g0106 | EAS | CHS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00733 | hp1 | a0007 | c0017 | t0002 | g0325 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00735 | hp2 | a0001 | c0006 | t0013 | g0232 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0102 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00738 | hp2 | a0001 | c0001 | t0026 | g0214 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0241 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01069 | hp1 | a0001 | c0001 | t0011 | g0101 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01069 | hp2 | a0001 | c0006 | t0013 | g0231 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0350 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01099 | hp2 | a0001 | c0001 | t0011 | g0093 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0268 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01109 | hp2 | a0001 | c0001 | t0031 | g0324 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01175 | hp2 | a0001 | c0001 | t0016 | g0331 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01243 | hp1 | a0001 | c0003 | t0005 | g0313 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0156 | AMR | PUR | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01255 | hp1 | a0002 | c0004 | t0038 | g0356 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0209 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0284 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01257 | hp2 | a0001 | c0001 | t0024 | g0100 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0322 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01261 | hp2 | a0001 | c0001 | t0020 | g0003 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01361 | hp1 | a0001 | c0001 | t0042 | g0138 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01361 | hp2 | a0001 | c0001 | t0049 | g0323 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01433 | hp2 | a0001 | c0001 | t0020 | g0003 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01496 | hp2 | a0002 | c0004 | t0005 | g0364 | AMR | CLM | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0070 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01515 | hp2 | a0001 | c0002 | t0004 | g0282 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0233 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01884 | hp1 | a0002 | c0004 | t0018 | g0358 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01891 | hp1 | a0001 | c0001 | t0040 | g0009 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01934 | hp1 | a0001 | c0001 | t0019 | g0224 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01934 | hp2 | a0001 | c0001 | t0016 | g0234 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01943 | hp1 | a0001 | c0001 | t0020 | g0208 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0112 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01975 | hp2 | a0001 | c0002 | t0027 | g0187 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01978 | hp1 | a0001 | c0001 | t0016 | g0235 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02015 | hp2 | a0001 | c0010 | t0001 | g0005 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02040 | hp1 | a0001 | c0002 | t0010 | g0334 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02055 | hp1 | a0001 | c0003 | t0005 | g0290 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02055 | hp2 | a0001 | c0003 | t0006 | g0320 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02056 | hp1 | a0001 | c0001 | t0036 | g0025 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02080 | hp1 | a0001 | c0002 | t0010 | g0337 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02083 | hp1 | a0001 | c0005 | t0001 | g0217 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02132 | hp1 | a0001 | c0002 | t0010 | g0335 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02155 | hp1 | a0001 | c0001 | t0009 | g0111 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CDX | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02257 | hp1 | a0008 | c0011 | t0001 | g0006 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02257 | hp2 | a0001 | c0001 | t0041 | g0150 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02258 | hp1 | a0004 | c0013 | t0003 | g0007 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02258 | hp2 | a0001 | c0001 | t0023 | g0122 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02280 | hp1 | a0002 | c0019 | t0006 | g0354 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02293 | hp2 | a0001 | c0001 | t0011 | g0155 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0104 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0044 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0298 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02523 | hp1 | a0001 | c0001 | t0043 | g0249 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02523 | hp2 | a0001 | c0002 | t0010 | g0333 | EAS | KHV | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0293 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02602 | hp2 | a0001 | c0001 | t0017 | g0211 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02622 | hp2 | a0002 | c0004 | t0005 | g0004 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02630 | hp2 | a0001 | c0003 | t0005 | g0330 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02647 | hp1 | a0001 | c0003 | t0005 | g0151 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0017 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0305 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02717 | hp2 | a0001 | c0003 | t0006 | g0016 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02723 | hp1 | a0002 | c0004 | t0008 | g0359 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02735 | hp2 | a0001 | c0001 | t0017 | g0205 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0179 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0296 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0352 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02818 | hp1 | a0005 | c0009 | t0012 | g0366 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02818 | hp2 | a0002 | c0004 | t0005 | g0365 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02886 | hp1 | a0003 | c0007 | t0012 | g0133 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02886 | hp2 | a0002 | c0004 | t0023 | g0357 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02895 | hp1 | a0002 | c0004 | t0018 | g0360 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0311 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02897 | hp1 | a0002 | c0004 | t0018 | g0361 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02922 | hp2 | a0003 | c0007 | t0012 | g0131 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0164 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0301 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02970 | hp2 | a0003 | c0007 | t0012 | g0094 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02976 | hp1 | a0001 | c0003 | t0006 | g0012 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02976 | hp2 | a0001 | c0003 | t0006 | g0046 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0327 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0243 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03041 | hp2 | a0001 | c0003 | t0005 | g0345 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0082 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03139 | hp1 | a0001 | c0001 | t0037 | g0121 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03139 | hp2 | a0003 | c0007 | t0012 | g0011 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0045 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03209 | hp1 | a0001 | c0001 | t0035 | g0152 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03209 | hp2 | a0002 | c0004 | t0005 | g0004 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0160 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03225 | hp2 | a0005 | c0009 | t0012 | g0355 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03453 | hp1 | a0001 | c0003 | t0005 | g0314 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0312 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03486 | hp1 | a0001 | c0001 | t0014 | g0049 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03491 | hp1 | a0001 | c0001 | t0019 | g0223 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03516 | hp2 | a0001 | c0003 | t0006 | g0015 | AFR | ESN | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03540 | hp2 | a0002 | c0004 | t0008 | g0363 | AFR | GWD | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03579 | hp1 | a0001 | c0001 | t0034 | g0297 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03654 | hp2 | a0009 | c0018 | t0001 | g0353 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03669 | hp1 | a0001 | c0002 | t0029 | g0077 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0304 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03710 | hp2 | a0001 | c0001 | t0030 | g0157 | SAS | PJL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03831 | hp1 | a0001 | c0006 | t0013 | g0274 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03831 | hp2 | a0001 | c0001 | t0011 | g0136 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03834 | hp2 | a0001 | c0001 | t0019 | g0071 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03927 | hp1 | a0001 | c0006 | t0013 | g0174 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0292 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03942 | hp2 | a0001 | c0001 | t0026 | g0199 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0129 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04115 | hp2 | a0001 | c0006 | t0013 | g0192 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04184 | hp1 | a0001 | c0002 | t0046 | g0169 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0254 | SAS | BEB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04199 | hp1 | a0001 | c0006 | t0039 | g0144 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04204 | hp1 | a0001 | c0001 | t0017 | g0201 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04204 | hp2 | a0001 | c0005 | t0001 | g0252 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18522 | hp1 | a0003 | c0007 | t0012 | g0041 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18522 | hp2 | a0002 | c0004 | t0018 | g0362 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0276 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0228 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0038 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18940 | hp2 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18941 | hp1 | a0001 | c0002 | t0010 | g0242 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18941 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18942 | hp2 | a0001 | c0001 | t0045 | g0251 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18943 | hp1 | a0001 | c0005 | t0015 | g0035 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18943 | hp2 | a0001 | c0001 | t0025 | g0110 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18944 | hp1 | a0001 | c0005 | t0015 | g0032 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18947 | hp1 | a0001 | c0001 | t0009 | g0148 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18947 | hp2 | a0001 | c0001 | t0007 | g0034 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18952 | hp2 | a0001 | c0005 | t0015 | g0033 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18959 | hp1 | a0001 | c0005 | t0015 | g0022 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18960 | hp2 | a0001 | c0002 | t0004 | g0226 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18963 | hp1 | a0001 | c0015 | t0007 | g0024 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18963 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18970 | hp1 | a0001 | c0001 | t0032 | g0303 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18971 | hp1 | a0001 | c0002 | t0048 | g0220 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18977 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0326 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0177 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18981 | hp2 | a0001 | c0002 | t0010 | g0342 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0204 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18983 | hp2 | a0001 | c0001 | t0044 | g0096 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18985 | hp1 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0321 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18991 | hp1 | a0001 | c0003 | t0002 | g0065 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18991 | hp2 | a0001 | c0002 | t0004 | g0329 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18997 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19005 | hp2 | a0001 | c0002 | t0004 | g0289 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19009 | hp1 | a0006 | c0008 | t0001 | g0247 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19010 | hp1 | a0001 | c0002 | t0004 | g0307 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19012 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19030 | hp1 | a0001 | c0002 | t0047 | g0159 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19030 | hp2 | a0001 | c0003 | t0006 | g0048 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19043 | hp1 | a0001 | c0001 | t0021 | g0349 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19043 | hp2 | a0001 | c0003 | t0006 | g0308 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19054 | hp1 | a0001 | c0002 | t0004 | g0180 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19054 | hp2 | a0001 | c0001 | t0009 | g0309 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19055 | hp1 | a0001 | c0001 | t0025 | g0095 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19057 | hp1 | a0001 | c0001 | t0033 | g0126 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19057 | hp2 | a0001 | c0002 | t0010 | g0347 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0127 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0258 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19081 | hp1 | a0001 | c0002 | t0010 | g0336 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19081 | hp2 | a0006 | c0008 | t0001 | g0212 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19082 | hp1 | a0001 | c0002 | t0010 | g0319 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19088 | hp2 | a0010 | c0014 | t0001 | g0207 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19240 | hp1 | a0001 | c0003 | t0006 | g0084 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | YRI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | ASW | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20129 | hp2 | a0001 | c0003 | t0005 | g0332 | AFR | ASW | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20805 | hp1 | a0001 | c0001 | t0022 | g0163 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20805 | hp2 | a0001 | c0001 | t0024 | g0099 | EUR | TSI | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0318 | SAS | GIH | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | GIH | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02109 | hp1 | a0001 | c0003 | t0006 | g0047 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0351 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02486 | hp1 | a0001 | c0003 | t0005 | g0018 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03471 | hp1 | a0004 | c0012 | t0006 | g0008 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0166 | AFR | MSL | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0050 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18955 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0154 | EAS | JPT | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20300 | hp1 | a0001 | c0003 | t0028 | g0291 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0194 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| NA21309 | hp2 | a0001 | c0016 | t0003 | g0067 | AFR | LWK | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0072 | REF | REF | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0315 | REF | REF | SNX8_chr7_2246770_2319441 | SNX8 | chr7 | 2246770 | 2319441 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2263342 | G | A | 2 | a0003 a0005 |
7 | HG02818.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.803C>T | p.Thr268Ile | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/11 | 823/4704 | 803/1398 | 268/465 | chr7 | 2263342 | |||
| chr7:2278158 | A | C | 1 | a0010 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.242T>G | p.Leu81Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 262/4704 | 242/1398 | 81/465 | chr7 | 2278158 | |||
| chr7:2278266 | ACGATGGC others(8): Show |
A | 1 | a0006 | 2 | NA19009.hp1 NA19081.hp2 |
disruptive_inframe_deletion | MODERATE | c.119_133delAGCCCCAG others(7): Show |
p.Glu40_Ile44del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 153/4704 | 119/1398 | 40/465 | chr7 | 2278266 | |||
| chr7:2278294 | G | GTGTCGGC others(22): Show |
1 | a0007 | 1 | HG00733.hp1 | frameshift_variant | HIGH | c.95-18_105dupTCACCA others(23): Show |
p.Pro36fs | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/11 | 125/4704 | 105/1398 | 35/465 | chr7 | 2278294 | |||
| chr7:2314345 | G | A | 1 | a0009 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.77C>T | p.Ala26Val | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 97/4704 | 77/1398 | 26/465 | chr7 | 2314345 | |||
| chr7:2314365 | C | G | 1 | a0004 | 2 | HG02258.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.57G>C | p.Glu19Asp | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 77/4704 | 57/1398 | 19/465 | chr7 | 2314365 | |||
| chr7:2314381 | A | C | 1 | a0008 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.41T>G | p.Val14Gly | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 61/4704 | 41/1398 | 14/465 | chr7 | 2314381 | |||
| chr7:2314399 | G | C | 2 | a0002 a0005 |
15 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
missense_variant | MODERATE | c.23C>G | p.Pro8Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 43/4704 | 23/1398 | 8/465 | chr7 | 2314399 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2257371 | A | G | 18 | a0001c0001 a0001c0003 a0001c0005 others(15): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
synonymous_variant | LOW | c.1128T>C | p.Ile376Ile | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/11 | 1148/4704 | 1128/1398 | 376/465 | chr7 | 2257371 | |||
| chr7:2257407 | G | C | 1 | a0001c0015 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.1092C>G | p.Arg364Arg | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/11 | 1112/4704 | 1092/1398 | 364/465 | chr7 | 2257407 | |||
| chr7:2264351 | T | C | 15 | a0001c0001 a0001c0005 a0001c0006 others(12): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
synonymous_variant | LOW | c.729A>G | p.Ala243Ala | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/11 | 749/4704 | 729/1398 | 243/465 | chr7 | 2264351 | |||
| chr7:2269574 | C | T | 1 | a0001c0006 | 6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
synonymous_variant | LOW | c.606G>A | p.Leu202Leu | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/11 | 626/4704 | 606/1398 | 202/465 | chr7 | 2269574 | |||
| chr7:2275167 | C | A | 1 | a0001c0016 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.363G>T | p.Leu121Leu | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/11 | 383/4704 | 363/1398 | 121/465 | chr7 | 2275167 | |||
| chr7:2275209 | G | A | 2 | a0001c0005 a0001c0010 |
10 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(7): Show |
synonymous_variant | LOW | c.321C>T | p.Tyr107Tyr | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/11 | 341/4704 | 321/1398 | 107/465 | chr7 | 2275209 | |||
| chr7:2314389 | C | T | 1 | a0001c0010 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.33G>A | p.Ala11Ala | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/11 | 53/4704 | 33/1398 | 11/465 | chr7 | 2314389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2251923 | A | C | 1 | a0001c0001t0040 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3133T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 3133 | chr7 | 2251923 | ||||||
| chr7:2252043 | G | A | 1 | a0001c0001t0022 | 2 | HG02965.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3013C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 3013 | chr7 | 2252043 | ||||||
| chr7:2252143 | ACCCCCCT others(7): Show |
A | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(14): Show |
99 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2899_*2912delCCGT others(10): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2899 | chr7 | 2252143 | ||||||
| chr7:2252162 | G | A | 1 | a0001c0001t0043 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2894C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2894 | chr7 | 2252162 | ||||||
| chr7:2252169 | G | A | 1 | a0001c0001t0044 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2887C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2887 | chr7 | 2252169 | ||||||
| chr7:2252259 | A | AGCTTGG | 2 | a0001c0002t0010 a0001c0002t0027 |
11 | HG00639.hp1 HG01975.hp2 HG02040.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2791_*2796dupCCAA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2796 | chr7 | 2252259 | ||||||
| chr7:2252275 | G | A | 10 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0023 others(7): Show |
51 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2781C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2781 | chr7 | 2252275 | ||||||
| chr7:2252308 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0016 others(16): Show |
121 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*2748C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2748 | chr7 | 2252308 | ||||||
| chr7:2252389 | G | A | 1 | a0001c0002t0046 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2667 | chr7 | 2252389 | ||||||
| chr7:2252533 | GC | G | 1 | a0001c0005t0015 | 4 | NA18943.hp1 NA18944.hp1 NA18952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2522delG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2522 | chr7 | 2252533 | ||||||
| chr7:2252585 | C | T | 1 | a0001c0001t0016 | 4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2471G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2471 | chr7 | 2252585 | ||||||
| chr7:2252624 | C | T | 3 | a0001c0001t0013 a0001c0006t0013 a0001c0006t0039 |
7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2432G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2432 | chr7 | 2252624 | ||||||
| chr7:2252670 | G | GC | 11 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0036 others(8): Show |
40 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2385dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2385 | chr7 | 2252670 | ||||||
| chr7:2252681 | T | G | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*2375A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2375 | chr7 | 2252681 | ||||||
| chr7:2252695 | C | CCACCCCT others(16): Show |
2 | a0001c0001t0008 a0002c0004t0008 |
12 | HG01081.hp2 HG01109.hp1 HG02615.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2338_*2360dupAGGA others(19): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2360 | chr7 | 2252695 | ||||||
| chr7:2252711 | GCTCTCCT others(18): Show |
G | 3 | a0001c0001t0017 a0001c0001t0031 a0002c0004t0018 |
9 | HG01109.hp2 HG01884.hp1 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2320_*2344delAGCA others(21): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2320 | chr7 | 2252711 | ||||||
| chr7:2252848 | TCTC | T | 1 | a0001c0001t0009 | 9 | HG00558.hp2 HG00673.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2205_*2207delGAG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2205 | chr7 | 2252848 | ||||||
| chr7:2252867 | CTGCTCTC others(15): Show |
C | 2 | a0001c0001t0017 a0002c0004t0018 |
8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2167_*2188delAGGG others(18): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2167 | chr7 | 2252867 | ||||||
| chr7:2252891 | GCT | G | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(30): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2163_*2164delAG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2163 | chr7 | 2252891 | ||||||
| chr7:2252982 | CCCTGTTC others(1): Show |
C | 13 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0022 others(10): Show |
31 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2066_*2073delAGAA others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 2066 | chr7 | 2252982 | ||||||
| chr7:2253092 | G | A | 1 | a0001c0001t0032 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1964C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1964 | chr7 | 2253092 | ||||||
| chr7:2253126 | T | C | 1 | a0001c0001t0041 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1930A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1930 | chr7 | 2253126 | ||||||
| chr7:2253246 | C | CTG | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1808_*1809dupCA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1809 | chr7 | 2253246 | ||||||
| chr7:2253292 | A | G | 1 | a0001c0001t0017 | 4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1764T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1764 | chr7 | 2253292 | ||||||
| chr7:2253423 | G | C | 1 | a0001c0001t0042 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1633C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1633 | chr7 | 2253423 | ||||||
| chr7:2253486 | G | A | 1 | a0002c0004t0038 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1570 | chr7 | 2253486 | ||||||
| chr7:2253570 | G | GGCCAGAA others(7): Show |
1 | a0001c0001t0033 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1472_*1485dupTGCT others(10): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1485 | chr7 | 2253570 | ||||||
| chr7:2253590 | C | T | 1 | a0001c0002t0027 | 2 | HG00639.hp1 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1466G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1466 | chr7 | 2253590 | ||||||
| chr7:2253721 | C | T | 1 | a0001c0001t0034 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1335 | chr7 | 2253721 | ||||||
| chr7:2253858 | G | A | 1 | a0001c0001t0020 | 3 | HG01261.hp2 HG01433.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1198 | chr7 | 2253858 | ||||||
| chr7:2253874 | G | A | 20 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(17): Show |
104 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1182 | chr7 | 2253874 | ||||||
| chr7:2253916 | C | T | 7 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0037 others(4): Show |
31 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1140 | chr7 | 2253916 | ||||||
| chr7:2253919 | CCAGGGA | C | 4 | a0001c0001t0007 a0001c0001t0025 a0001c0001t0036 others(1): Show |
15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1131_*1136delTCCC others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1131 | chr7 | 2253919 | ||||||
| chr7:2253926 | G | A | 1 | a0001c0001t0025 | 2 | NA18943.hp2 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1130C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1130 | chr7 | 2253926 | ||||||
| chr7:2253971 | T | C | 1 | a0001c0001t0026 | 2 | HG00738.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1085 | chr7 | 2253971 | ||||||
| chr7:2253974 | A | G | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*1082T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 1082 | chr7 | 2253974 | ||||||
| chr7:2254249 | C | T | 1 | a0001c0001t0035 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*807G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 807 | chr7 | 2254249 | ||||||
| chr7:2254288 | C | T | 2 | a0001c0001t0014 a0001c0001t0034 |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*768G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 768 | chr7 | 2254288 | ||||||
| chr7:2254488 | C | T | 15 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0020 others(12): Show |
106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*568G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 568 | chr7 | 2254488 | ||||||
| chr7:2254618 | C | T | 1 | a0001c0002t0029 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 438 | chr7 | 2254618 | ||||||
| chr7:2254749 | T | C | 1 | a0001c0001t0049 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 307 | chr7 | 2254749 | ||||||
| chr7:2254766 | A | G | 1 | a0001c0001t0019 | 3 | HG01934.hp1 HG03491.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*290T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 290 | chr7 | 2254766 | ||||||
| chr7:2254864 | A | T | 1 | a0001c0001t0022 | 2 | HG02965.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 192 | chr7 | 2254864 | ||||||
| chr7:2254947 | G | A | 1 | a0001c0001t0021 | 3 | HG02809.hp2 HG02970.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*109C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 109 | chr7 | 2254947 | ||||||
| chr7:2254972 | C | T | 1 | a0001c0001t0011 | 8 | HG00738.hp1 HG01069.hp1 HG01099.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 84 | chr7 | 2254972 | ||||||
| chr7:2255024 | G | T | 1 | a0001c0003t0028 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 11/11 | 32 | chr7 | 2255024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:2255209 | C | T | 1 | a0001c0003t0005g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1285-40G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255209 | |||||||
| chr7:2255210 | C | T | 1 | a0001c0001t0009g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1285-41G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255210 | |||||||
| chr7:2255348 | G | A | 1 | a0002c0004t0023g0357 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1285-179C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255348 | |||||||
| chr7:2255359 | C | A | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1285-190G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255359 | |||||||
| chr7:2255582 | C | G | 1 | a0001c0001t0008g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1285-413G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255582 | |||||||
| chr7:2255595 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0256 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1285-426G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255595 | |||||||
| chr7:2255886 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1285-717C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2255886 | |||||||
| chr7:2256167 | TA | T | 181 | a0001c0001t0001g0198 a0001c0001t0002g0019 a0001c0001t0002g0020 others(178): Show |
184 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.1284+706delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256167 | |||||||
| chr7:2256278 | C | G | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+596G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256278 | |||||||
| chr7:2256283 | G | A | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+591C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256283 | |||||||
| chr7:2256418 | G | C | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1284+456C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256418 | |||||||
| chr7:2256449 | G | A | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1284+425C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256449 | |||||||
| chr7:2256495 | G | A | 1 | a0001c0001t0030g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1284+379C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256495 | |||||||
| chr7:2256732 | T | C | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1284+142A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256732 | |||||||
| chr7:2256787 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0074 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1284+87C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256787 | |||||||
| chr7:2256858 | A | G | 291 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(288): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1284+16T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256858 | |||||||
| chr7:2256865 | C | A | 5 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284+9G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 10/10 | chr7 | 2256865 | |||||||
| chr7:2257061 | C | A | 99 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(96): Show |
100 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1135-38G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257061 | |||||||
| chr7:2257087 | A | T | 70 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1135-64T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257087 | |||||||
| chr7:2257088 | C | T | 7 | a0001c0005t0001g0059 a0001c0005t0001g0154 a0001c0005t0001g0252 others(4): Show |
7 | HG00423.hp1 HG04204.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1135-65G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257088 | |||||||
| chr7:2257095 | G | A | 5 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-72C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257095 | |||||||
| chr7:2257104 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0001g0339 others(2): Show |
5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1135-81C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257104 | |||||||
| chr7:2257189 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1135-166C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 9/10 | chr7 | 2257189 | |||||||
| chr7:2257577 | C | T | 41 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(38): Show |
41 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.985-63G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257577 | |||||||
| chr7:2257596 | C | T | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.985-82G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257596 | |||||||
| chr7:2257651 | C | T | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.984+84G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257651 | |||||||
| chr7:2257663 | G | T | 1 | a0001c0001t0003g0262 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.984+72C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257663 | |||||||
| chr7:2257685 | A | C | 1 | a0001c0002t0004g0305 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.984+50T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 8/10 | chr7 | 2257685 | |||||||
| chr7:2258008 | C | CT | 39 | a0001c0001t0001g0195 a0001c0001t0001g0273 a0001c0001t0002g0073 others(36): Show |
39 | HG00280.hp2 HG00642.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.916-206dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | |||||||
| chr7:2258008 | C | CTT | 30 | a0001c0001t0001g0119 a0001c0001t0005g0013 a0001c0001t0005g0014 others(27): Show |
32 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.916-207_916-206dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | |||||||
| chr7:2258008 | CT | C | 12 | a0001c0001t0003g0040 a0001c0001t0003g0279 a0001c0001t0023g0122 others(9): Show |
12 | HG00639.hp2 HG01167.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.916-206delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258008 | |||||||
| chr7:2258031 | T | A | 5 | a0001c0003t0005g0312 a0001c0003t0006g0012 a0001c0003t0006g0015 others(2): Show |
5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-228A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258031 | |||||||
| chr7:2258032 | C | T | 37 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(34): Show |
37 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.916-229G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258032 | |||||||
| chr7:2258038 | CT | C | 5 | a0001c0003t0005g0312 a0001c0003t0006g0012 a0001c0003t0006g0015 others(2): Show |
5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-236delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258038 | |||||||
| chr7:2258062 | A | G | 40 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0005g0013 others(37): Show |
42 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.916-259T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258062 | |||||||
| chr7:2258072 | A | G | 37 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0221 others(34): Show |
39 | HG00639.hp2 HG01070.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.916-269T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258072 | |||||||
| chr7:2258160 | T | G | 5 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-357A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258160 | |||||||
| chr7:2258167 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.916-364A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258167 | |||||||
| chr7:2258184 | GTATTTC | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-387_916-382del others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258184 | |||||||
| chr7:2258192 | T | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-389A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258192 | |||||||
| chr7:2258206 | C | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.916-403G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258206 | |||||||
| chr7:2258284 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.916-481C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258284 | |||||||
| chr7:2258295 | G | T | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.916-492C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258295 | |||||||
| chr7:2258436 | A | G | 304 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.916-633T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258436 | |||||||
| chr7:2258468 | A | G | 10 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(7): Show |
10 | HG02056.hp1 NA18940.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-665T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258468 | |||||||
| chr7:2258568 | G | A | 2 | a0001c0002t0004g0263 a0001c0002t0004g0326 |
2 | NA18977.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.916-765C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258568 | |||||||
| chr7:2258591 | C | G | 7 | a0001c0001t0013g0076 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-788G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258591 | |||||||
| chr7:2258592 | C | T | 105 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(102): Show |
106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.916-789G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258592 | |||||||
| chr7:2258763 | G | A | 1 | a0001c0002t0010g0337 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.916-960C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258763 | |||||||
| chr7:2258892 | T | C | 10 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(7): Show |
10 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-1089A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2258892 | |||||||
| chr7:2259047 | C | T | 3 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0002g0143 |
3 | NA18995.hp1 NA19009.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.916-1244G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259047 | |||||||
| chr7:2259211 | C | T | 12 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.916-1408G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259211 | |||||||
| chr7:2259222 | C | G | 1 | a0001c0001t0014g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.916-1419G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259222 | |||||||
| chr7:2259250 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.916-1447C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259250 | |||||||
| chr7:2259363 | C | A | 7 | a0001c0001t0013g0076 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1560G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259363 | |||||||
| chr7:2259375 | C | G | 3 | a0001c0001t0013g0076 a0001c0006t0013g0231 a0001c0006t0013g0232 |
3 | HG00642.hp1 HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.916-1572G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259375 | |||||||
| chr7:2259427 | T | C | 7 | a0001c0001t0013g0076 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1624A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259427 | |||||||
| chr7:2259482 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.916-1679A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259482 | |||||||
| chr7:2259497 | G | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0001g0255 |
3 | HG00621.hp2 NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.916-1694C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259497 | |||||||
| chr7:2259497 | G | C | 7 | a0001c0001t0013g0076 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.916-1694C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259497 | |||||||
| chr7:2259666 | G | A | 8 | a0001c0001t0017g0194 a0001c0001t0017g0201 a0001c0001t0017g0205 others(5): Show |
8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-1863C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259666 | |||||||
| chr7:2259676 | G | A | 1 | a0001c0015t0007g0024 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.916-1873C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259676 | |||||||
| chr7:2259707 | G | A | 1 | a0001c0003t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-1904C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259707 | |||||||
| chr7:2259793 | C | G | 5 | a0001c0003t0005g0312 a0001c0003t0006g0012 a0001c0003t0006g0015 others(2): Show |
5 | HG02717.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-1990G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259793 | |||||||
| chr7:2259925 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2122T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259925 | |||||||
| chr7:2259926 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2123C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259926 | |||||||
| chr7:2259927 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2124T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259927 | |||||||
| chr7:2259929 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2126C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259929 | |||||||
| chr7:2259930 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2127T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259930 | |||||||
| chr7:2259932 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2129A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259932 | |||||||
| chr7:2259935 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2132A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259935 | |||||||
| chr7:2259948 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2145T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259948 | |||||||
| chr7:2259953 | A | G | 3 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 |
3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.916-2150T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259953 | |||||||
| chr7:2259955 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2152T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259955 | |||||||
| chr7:2259957 | G | A | 1 | a0001c0010t0001g0005 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.916-2154C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259957 | |||||||
| chr7:2259957 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2154C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259957 | |||||||
| chr7:2259958 | C | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2155G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259958 | |||||||
| chr7:2259962 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2159G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259962 | |||||||
| chr7:2259964 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2161G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259964 | |||||||
| chr7:2259966 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2163T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259966 | |||||||
| chr7:2259968 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2165C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259968 | |||||||
| chr7:2259969 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2166T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259969 | |||||||
| chr7:2259970 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2167A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259970 | |||||||
| chr7:2259983 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2180T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259983 | |||||||
| chr7:2259984 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2181T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259984 | |||||||
| chr7:2259986 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2183T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259986 | |||||||
| chr7:2259987 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2184T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259987 | |||||||
| chr7:2259989 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2186T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259989 | |||||||
| chr7:2259990 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2187T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259990 | |||||||
| chr7:2259999 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2196C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2259999 | |||||||
| chr7:2260007 | AAAGAGAG others(38): Show |
A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2249_916-2205d others(47): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260007 | |||||||
| chr7:2260053 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2250C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260053 | |||||||
| chr7:2260055 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2252T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260055 | |||||||
| chr7:2260056 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2253C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260056 | |||||||
| chr7:2260057 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2254C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260057 | |||||||
| chr7:2260059 | C | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2256G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260059 | |||||||
| chr7:2260063 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2260C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260063 | |||||||
| chr7:2260065 | G | C | 113 | a0001c0001t0001g0277 a0001c0001t0002g0019 a0001c0001t0002g0020 others(110): Show |
116 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.916-2262C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260065 | |||||||
| chr7:2260067 | A | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2264T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260067 | |||||||
| chr7:2260068 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2265T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260068 | |||||||
| chr7:2260073 | C | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2270G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260073 | |||||||
| chr7:2260077 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2274T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260077 | |||||||
| chr7:2260080 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2277A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260080 | |||||||
| chr7:2260083 | T | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2280A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260083 | |||||||
| chr7:2260084 | C | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2281G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260084 | |||||||
| chr7:2260085 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2282T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260085 | |||||||
| chr7:2260086 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2283C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260086 | |||||||
| chr7:2260088 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2285T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260088 | |||||||
| chr7:2260090 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2287C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260090 | |||||||
| chr7:2260091 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2288A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260091 | |||||||
| chr7:2260095 | C | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2292G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260095 | |||||||
| chr7:2260097 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2294C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260097 | |||||||
| chr7:2260098 | A | ATAAGACC others(32): Show |
1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2296_916-2295i others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260098 | |||||||
| chr7:2260102 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2299C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260102 | |||||||
| chr7:2260103 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2300C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260103 | |||||||
| chr7:2260104 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2301G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260104 | |||||||
| chr7:2260118 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2315G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260118 | |||||||
| chr7:2260135 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2332T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260135 | |||||||
| chr7:2260152 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2349C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260152 | |||||||
| chr7:2260156 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2353G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260156 | |||||||
| chr7:2260165 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2362T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260165 | |||||||
| chr7:2260169 | C | CTCAGCTC others(6): Show |
1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2367_916-2366i others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260169 | |||||||
| chr7:2260181 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2378G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260181 | |||||||
| chr7:2260182 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2379C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260182 | |||||||
| chr7:2260189 | A | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2386T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260189 | |||||||
| chr7:2260191 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2388C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260191 | |||||||
| chr7:2260199 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2396C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260199 | |||||||
| chr7:2260214 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2411G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260214 | |||||||
| chr7:2260223 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2420C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260223 | |||||||
| chr7:2260232 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2429T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260232 | |||||||
| chr7:2260242 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2439A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260242 | |||||||
| chr7:2260243 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2440C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260243 | |||||||
| chr7:2260244 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2441G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260244 | |||||||
| chr7:2260247 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2444C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260247 | |||||||
| chr7:2260255 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2452C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260255 | |||||||
| chr7:2260258 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2455A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260258 | |||||||
| chr7:2260259 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2456C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260259 | |||||||
| chr7:2260265 | T | A | 122 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.916-2462A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260265 | |||||||
| chr7:2260266 | G | T | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2463C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260266 | |||||||
| chr7:2260286 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2483A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260286 | |||||||
| chr7:2260287 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.916-2484C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260287 | |||||||
| chr7:2260289 | G | T | 1 | a0001c0001t0003g0262 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.916-2486C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260289 | |||||||
| chr7:2260395 | A | G | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.916-2592T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260395 | |||||||
| chr7:2260500 | C | T | 3 | a0001c0001t0013g0076 a0001c0006t0013g0231 a0001c0006t0013g0232 |
3 | HG00642.hp1 HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.916-2697G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260500 | |||||||
| chr7:2260562 | C | T | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.915+2668G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260562 | |||||||
| chr7:2260724 | T | A | 1 | a0001c0003t0005g0332 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.915+2506A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260724 | |||||||
| chr7:2260923 | G | T | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915+2307C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2260923 | |||||||
| chr7:2261169 | G | A | 1 | a0001c0003t0006g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.915+2061C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261169 | |||||||
| chr7:2261219 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.915+2011C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261219 | |||||||
| chr7:2261242 | G | A | 5 | a0001c0001t0014g0276 a0001c0001t0014g0293 a0001c0001t0014g0296 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+1988C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261242 | |||||||
| chr7:2261288 | C | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1942G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261288 | |||||||
| chr7:2261290 | G | A | 3 | a0001c0002t0004g0017 a0001c0002t0004g0166 a0001c0002t0047g0159 |
3 | HG02647.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.915+1940C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261290 | |||||||
| chr7:2261319 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.915+1911C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261319 | |||||||
| chr7:2261340 | G | A | 8 | a0001c0001t0017g0194 a0001c0001t0017g0201 a0001c0001t0017g0205 others(5): Show |
8 | HG01884.hp1 HG02602.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+1890C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261340 | |||||||
| chr7:2261352 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.915+1878C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261352 | |||||||
| chr7:2261428 | G | A | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+1802C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261428 | |||||||
| chr7:2261476 | C | A | 2 | a0001c0002t0027g0187 a0001c0002t0027g0346 |
2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.915+1754G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261476 | |||||||
| chr7:2261607 | C | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1623G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261607 | |||||||
| chr7:2261745 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.915+1485G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261745 | |||||||
| chr7:2261745 | CG | C | 4 | a0001c0001t0017g0194 a0001c0001t0017g0201 a0001c0001t0017g0205 others(1): Show |
4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1484delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261745 | |||||||
| chr7:2261849 | A | G | 122 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.915+1381T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261849 | |||||||
| chr7:2261918 | G | T | 4 | a0001c0001t0017g0194 a0001c0001t0017g0201 a0001c0001t0017g0205 others(1): Show |
4 | HG02602.hp2 HG02735.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1312C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261918 | |||||||
| chr7:2261943 | T | G | 122 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.915+1287A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2261943 | |||||||
| chr7:2262008 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.915+1222C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262008 | |||||||
| chr7:2262195 | C | A | 4 | a0001c0002t0004g0127 a0001c0002t0004g0183 a0001c0002t0004g0226 others(1): Show |
4 | NA18960.hp2 NA18963.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1035G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262195 | |||||||
| chr7:2262204 | A | T | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+1026T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262204 | |||||||
| chr7:2262345 | A | T | 17 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0178 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+885T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262345 | |||||||
| chr7:2262354 | C | T | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.915+876G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262354 | |||||||
| chr7:2262443 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+787C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262443 | |||||||
| chr7:2262479 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.915+751C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262479 | |||||||
| chr7:2262496 | G | C | 46 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(43): Show |
46 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.915+734C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262496 | |||||||
| chr7:2262503 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0001g0339 others(2): Show |
5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+727C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262503 | |||||||
| chr7:2262726 | C | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.915+504G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262726 | |||||||
| chr7:2262730 | C | G | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.915+500G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262730 | |||||||
| chr7:2262746 | C | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+484G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262746 | |||||||
| chr7:2262779 | T | C | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.915+451A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262779 | |||||||
| chr7:2262836 | G | A | 31 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0178 others(28): Show |
31 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.915+394C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262836 | |||||||
| chr7:2262889 | G | A | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.915+341C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262889 | |||||||
| chr7:2262892 | C | T | 17 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0178 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.915+338G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262892 | |||||||
| chr7:2262930 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.915+300C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2262930 | |||||||
| chr7:2263057 | T | C | 14 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(11): Show |
14 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.915+173A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263057 | |||||||
| chr7:2263072 | T | C | 2 | a0001c0001t0003g0140 a0001c0001t0003g0241 |
2 | HG00741.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.915+158A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263072 | |||||||
| chr7:2263101 | G | A | 5 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+129C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263101 | |||||||
| chr7:2263137 | G | A | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+93C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263137 | |||||||
| chr7:2263192 | T | C | 3 | a0001c0001t0003g0221 a0001c0001t0040g0009 a0002c0004t0023g0357 |
3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.915+38A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 7/10 | chr7 | 2263192 | |||||||
| chr7:2263422 | G | A | 1 | a0001c0002t0004g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.783-60C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263422 | |||||||
| chr7:2263436 | C | T | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.783-74G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263436 | |||||||
| chr7:2263439 | C | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-77G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263439 | |||||||
| chr7:2263439 | C | T | 15 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(12): Show |
15 | HG01192.hp2 HG02056.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.783-77G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263439 | |||||||
| chr7:2263465 | C | T | 14 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(11): Show |
14 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.783-103G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263465 | |||||||
| chr7:2263474 | G | A | 136 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(133): Show |
139 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.783-112C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263474 | |||||||
| chr7:2263483 | C | T | 3 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 |
3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.783-121G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263483 | |||||||
| chr7:2263524 | C | A | 1 | a0001c0001t0019g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.783-162G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263524 | |||||||
| chr7:2263524 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.783-162G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263524 | |||||||
| chr7:2263616 | G | T | 1 | a0001c0002t0004g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.783-254C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263616 | |||||||
| chr7:2263643 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783-281C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263643 | |||||||
| chr7:2263676 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-314C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263676 | |||||||
| chr7:2263715 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-353C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263715 | |||||||
| chr7:2263719 | C | CT | 7 | a0001c0001t0003g0039 a0001c0001t0005g0013 a0001c0001t0005g0014 others(4): Show |
7 | HG01109.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.783-358dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263719 | |||||||
| chr7:2263725 | T | G | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-363A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263725 | |||||||
| chr7:2263783 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.783-421C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263783 | |||||||
| chr7:2263838 | G | A | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.782+460C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263838 | |||||||
| chr7:2263928 | C | A | 1 | a0001c0001t0002g0128 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.782+370G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263928 | |||||||
| chr7:2263946 | C | CCTCGTGA others(17): Show |
1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.782+328_782+351dup others(24): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2263946 | |||||||
| chr7:2264263 | G | A | 1 | a0001c0002t0010g0337 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.782+35C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 6/10 | chr7 | 2264263 | |||||||
| chr7:2264495 | C | T | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-37G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264495 | |||||||
| chr7:2264556 | A | C | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.622-98T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264556 | |||||||
| chr7:2264640 | C | T | 131 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.622-182G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264640 | |||||||
| chr7:2264670 | G | A | 1 | a0001c0001t0011g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.622-212C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264670 | |||||||
| chr7:2264805 | C | T | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-347G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2264805 | |||||||
| chr7:2265008 | T | C | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.622-550A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265008 | |||||||
| chr7:2265014 | G | A | 4 | a0001c0001t0016g0233 a0001c0001t0016g0234 a0001c0001t0016g0235 others(1): Show |
4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-556C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265014 | |||||||
| chr7:2265035 | AAAAC | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-581_622-578del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265035 | |||||||
| chr7:2265194 | T | G | 1 | a0001c0001t0037g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.622-736A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265194 | |||||||
| chr7:2265199 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.622-741C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265199 | |||||||
| chr7:2265396 | C | T | 5 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-938G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265396 | |||||||
| chr7:2265736 | C | T | 1 | a0001c0001t0019g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.622-1278G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265736 | |||||||
| chr7:2265737 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1279C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265737 | |||||||
| chr7:2265756 | T | G | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622-1298A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2265756 | |||||||
| chr7:2266172 | T | C | 1 | a0001c0003t0005g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.622-1714A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266172 | |||||||
| chr7:2266179 | T | TTTG | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-1724_622-1722d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266179 | |||||||
| chr7:2266247 | C | T | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1789G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266247 | |||||||
| chr7:2266289 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1831C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266289 | |||||||
| chr7:2266308 | C | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-1850G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266308 | |||||||
| chr7:2266351 | A | AT | 241 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.622-1894dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266351 | |||||||
| chr7:2266386 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-1928C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266386 | |||||||
| chr7:2266395 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.622-1937C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266395 | |||||||
| chr7:2266575 | G | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2117C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266575 | |||||||
| chr7:2266577 | C | T | 1 | a0001c0001t0020g0003 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.622-2119G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266577 | |||||||
| chr7:2266608 | G | C | 8 | a0001c0001t0002g0118 a0003c0007t0012g0011 a0003c0007t0012g0041 others(5): Show |
8 | HG01891.hp2 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.622-2150C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266608 | |||||||
| chr7:2266641 | G | A | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.622-2183C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266641 | |||||||
| chr7:2266643 | C | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2185G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266643 | |||||||
| chr7:2266675 | G | C | 15 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(12): Show |
15 | HG01192.hp2 HG02056.hp1 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.622-2217C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266675 | |||||||
| chr7:2266690 | T | A | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.622-2232A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266690 | |||||||
| chr7:2266763 | C | T | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.622-2305G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266763 | |||||||
| chr7:2266813 | G | A | 1 | a0001c0002t0004g0188 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.622-2355C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266813 | |||||||
| chr7:2266962 | C | G | 304 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.622-2504G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266962 | |||||||
| chr7:2266977 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.622-2519C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2266977 | |||||||
| chr7:2267020 | G | A | 131 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.621+2539C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267020 | |||||||
| chr7:2267046 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0117 |
2 | NA18966.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.621+2513C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267046 | |||||||
| chr7:2267073 | C | T | 56 | a0001c0001t0002g0028 a0001c0001t0002g0043 a0001c0001t0002g0056 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2486G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267073 | |||||||
| chr7:2267106 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+2453A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267106 | |||||||
| chr7:2267142 | T | C | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+2417A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267142 | |||||||
| chr7:2267159 | C | T | 40 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(37): Show |
40 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.621+2400G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267159 | |||||||
| chr7:2267178 | C | T | 1 | a0001c0001t0021g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.621+2381G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267178 | |||||||
| chr7:2267211 | G | A | 280 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.621+2348C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267211 | |||||||
| chr7:2267256 | G | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2303C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267256 | |||||||
| chr7:2267299 | GCCCTCTC others(5): Show |
G | 1 | a0002c0004t0005g0364 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.621+2248_621+2259d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267299 | |||||||
| chr7:2267305 | TCCCTCC | T | 34 | a0001c0001t0001g0119 a0001c0001t0002g0153 a0001c0001t0003g0040 others(31): Show |
34 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.621+2248_621+2253d others(8): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267305 | |||||||
| chr7:2267335 | T | C | 2 | a0001c0001t0021g0301 a0001c0001t0021g0352 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.621+2224A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267335 | |||||||
| chr7:2267339 | T | G | 10 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+2220A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267339 | |||||||
| chr7:2267349 | C | T | 148 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(145): Show |
151 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.621+2210G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267349 | |||||||
| chr7:2267375 | C | T | 16 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(13): Show |
16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.621+2184G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267375 | |||||||
| chr7:2267402 | C | G | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+2157G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267402 | |||||||
| chr7:2267411 | G | A | 132 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(129): Show |
133 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.621+2148C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267411 | |||||||
| chr7:2267442 | T | C | 56 | a0001c0001t0002g0028 a0001c0001t0002g0043 a0001c0001t0002g0056 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2117A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267442 | |||||||
| chr7:2267450 | A | G | 56 | a0001c0001t0002g0028 a0001c0001t0002g0043 a0001c0001t0002g0056 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.621+2109T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267450 | |||||||
| chr7:2267457 | C | T | 73 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(70): Show |
73 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.621+2102G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267457 | |||||||
| chr7:2267503 | G | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2056C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267503 | |||||||
| chr7:2267511 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2048C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267511 | |||||||
| chr7:2267536 | G | A | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2023C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267536 | |||||||
| chr7:2267565 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0001g0339 others(2): Show |
5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1994G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267565 | |||||||
| chr7:2267570 | T | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+1989A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267570 | |||||||
| chr7:2267601 | C | A | 10 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(7): Show |
10 | HG00735.hp2 HG01069.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+1958G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267601 | |||||||
| chr7:2267618 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1941T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267618 | |||||||
| chr7:2267635 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0001g0339 others(2): Show |
5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1924C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267635 | |||||||
| chr7:2267643 | A | G | 8 | a0001c0001t0003g0040 a0001c0001t0023g0122 a0001c0006t0013g0174 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.621+1916T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267643 | |||||||
| chr7:2267644 | C | A | 1 | a0001c0002t0004g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.621+1915G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267644 | |||||||
| chr7:2267644 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.621+1915G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267644 | |||||||
| chr7:2267729 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1830C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267729 | |||||||
| chr7:2267732 | A | AC | 12 | a0001c0001t0001g0029 a0001c0001t0001g0173 a0001c0001t0001g0222 others(9): Show |
12 | HG00438.hp1 HG00741.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+1826dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267732 | |||||||
| chr7:2267735 | CCGTCTGG others(32): Show |
C | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+1785_621+1823d others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267735 | |||||||
| chr7:2267754 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1805A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267754 | |||||||
| chr7:2267775 | C | A | 16 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(13): Show |
16 | HG00544.hp2 HG00597.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.621+1784G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267775 | |||||||
| chr7:2267784 | TGTGAGGA others(492): Show |
T | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+1276_621+1774d others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267784 | |||||||
| chr7:2267785 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.621+1774C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267785 | |||||||
| chr7:2267795 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.621+1764G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267795 | |||||||
| chr7:2267912 | T | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1647A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267912 | |||||||
| chr7:2267931 | A | C | 296 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(293): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.621+1628T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267931 | |||||||
| chr7:2267944 | GGGAGCGC others(30): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.621+1578_621+1614d others(39): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267944 | |||||||
| chr7:2267986 | C | T | 1 | a0002c0004t0038g0356 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.621+1573G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267986 | |||||||
| chr7:2267996 | C | G | 1 | a0001c0002t0046g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.621+1563G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2267996 | |||||||
| chr7:2268008 | C | T | 141 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(138): Show |
142 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.621+1551G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268008 | |||||||
| chr7:2268047 | C | T | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.621+1512G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268047 | |||||||
| chr7:2268054 | G | A | 7 | a0001c0001t0002g0042 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+1505C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268054 | |||||||
| chr7:2268071 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.621+1488C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268071 | |||||||
| chr7:2268080 | A | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1479T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268080 | |||||||
| chr7:2268081 | C | A | 10 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+1478G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268081 | |||||||
| chr7:2268086 | T | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1473A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268086 | |||||||
| chr7:2268105 | G | C | 1 | a0001c0002t0004g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.621+1454C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268105 | |||||||
| chr7:2268121 | GTCAGCCC others(42): Show |
G | 1 | a0001c0006t0013g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1389_621+1437d others(51): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268121 | |||||||
| chr7:2268135 | TGGCCAGC others(43): Show |
T | 5 | a0001c0006t0013g0192 a0001c0006t0013g0231 a0001c0006t0013g0232 others(2): Show |
5 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+1374_621+1423d others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268135 | |||||||
| chr7:2268179 | T | C | 1 | a0001c0006t0013g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1380A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268179 | |||||||
| chr7:2268185 | C | T | 1 | a0001c0006t0013g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.621+1374G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268185 | |||||||
| chr7:2268226 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1333G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268226 | |||||||
| chr7:2268229 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.621+1330G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268229 | |||||||
| chr7:2268230 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1329C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268230 | |||||||
| chr7:2268244 | G | C | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+1315C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268244 | |||||||
| chr7:2268256 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+1303C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268256 | |||||||
| chr7:2268317 | C | A | 4 | a0001c0002t0004g0127 a0001c0002t0004g0183 a0001c0002t0004g0226 others(1): Show |
4 | NA18960.hp2 NA18963.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1242G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268317 | |||||||
| chr7:2268336 | T | C | 4 | a0001c0003t0006g0012 a0001c0003t0006g0015 a0001c0003t0006g0016 others(1): Show |
4 | HG02717.hp2 HG02976.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+1223A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268336 | |||||||
| chr7:2268339 | G | A | 1 | a0001c0003t0005g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.621+1220C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268339 | |||||||
| chr7:2268354 | T | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1205A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268354 | |||||||
| chr7:2268385 | C | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1174G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268385 | |||||||
| chr7:2268394 | C | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+1165G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268394 | |||||||
| chr7:2268435 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1124T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268435 | |||||||
| chr7:2268443 | G | A | 105 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(102): Show |
108 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.621+1116C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268443 | |||||||
| chr7:2268449 | T | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+1110A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268449 | |||||||
| chr7:2268514 | C | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1045G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268514 | |||||||
| chr7:2268520 | C | T | 109 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(106): Show |
110 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.621+1039G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268520 | |||||||
| chr7:2268537 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+1022G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268537 | |||||||
| chr7:2268586 | C | T | 3 | a0001c0001t0003g0221 a0001c0001t0040g0009 a0002c0004t0023g0357 |
3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.621+973G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268586 | |||||||
| chr7:2268598 | G | T | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.621+961C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268598 | |||||||
| chr7:2268635 | T | TGGGAGGT others(122): Show |
3 | a0001c0002t0004g0017 a0001c0002t0004g0166 a0001c0002t0047g0159 |
3 | HG02647.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.621+795_621+923dup others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268635 | |||||||
| chr7:2268635 | T | TGGGAGGT others(121): Show |
20 | a0001c0001t0001g0119 a0001c0001t0005g0013 a0001c0001t0005g0014 others(17): Show |
20 | HG01109.hp1 HG01192.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.621+923_621+924ins others(128): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268635 | |||||||
| chr7:2268660 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.621+899C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268660 | |||||||
| chr7:2268686 | CCCCTCTG others(122): Show |
C | 1 | a0001c0001t0005g0351 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.621+744_621+872del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268686 | |||||||
| chr7:2268694 | C | CCCGGCCA others(43): Show |
1 | a0001c0001t0002g0141 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.621+864_621+865ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | |||||||
| chr7:2268694 | C | CCCGGCCA others(42): Show |
106 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.621+864_621+865ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | |||||||
| chr7:2268694 | C | CCCGGCCA others(41): Show |
1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.621+864_621+865ins others(48): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268694 | |||||||
| chr7:2268697 | A | AGCCAGCC others(43): Show |
4 | a0001c0001t0003g0088 a0001c0001t0003g0137 a0001c0001t0003g0181 others(1): Show |
4 | HG02056.hp2 HG02738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+861_621+862ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | |||||||
| chr7:2268697 | A | AGCCAGCC others(42): Show |
46 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(43): Show |
46 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.621+861_621+862ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | |||||||
| chr7:2268697 | A | G | 253 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.621+862T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268697 | |||||||
| chr7:2268714 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+845C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | |||||||
| chr7:2268714 | G | GGGAGGGA others(122): Show |
2 | a0001c0001t0001g0256 a0001c0001t0007g0185 |
2 | HG03239.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.621+844_621+845ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | |||||||
| chr7:2268714 | G | GGGAGGGA others(121): Show |
102 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0037 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.621+844_621+845ins others(128): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268714 | |||||||
| chr7:2268724 | T | TGGGGGTG others(122): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0173 others(2): Show |
5 | HG00544.hp2 HG00597.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+834_621+835ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | |||||||
| chr7:2268724 | T | TGGGGGTG others(122): Show |
1 | a0001c0001t0007g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.621+834_621+835ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | |||||||
| chr7:2268724 | T | TGGGGGTG others(43): Show |
3 | a0001c0001t0002g0225 a0001c0001t0002g0302 a0001c0003t0005g0290 |
3 | HG01346.hp2 HG02055.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.621+834_621+835ins others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268724 | |||||||
| chr7:2268727 | G | GGGTGTCA others(42): Show |
5 | a0001c0001t0009g0023 a0001c0001t0009g0083 a0001c0001t0009g0106 others(2): Show |
5 | HG00673.hp2 HG02155.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+831_621+832ins others(49): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268727 | |||||||
| chr7:2268731 | G | T | 8 | a0001c0001t0001g0277 a0001c0006t0013g0174 a0001c0006t0013g0192 others(5): Show |
8 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.621+828C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268731 | |||||||
| chr7:2268743 | A | C | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.621+816T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268743 | |||||||
| chr7:2268747 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.621+812G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268747 | |||||||
| chr7:2268762 | T | TCCGGGAG others(122): Show |
1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.621+796_621+797ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268762 | |||||||
| chr7:2268793 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+766C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268793 | |||||||
| chr7:2268815 | G | C | 303 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(300): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.621+744C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268815 | |||||||
| chr7:2268826 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+733C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268826 | |||||||
| chr7:2268834 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+725C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268834 | |||||||
| chr7:2268838 | C | CGCCCGGG others(39): Show |
1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.621+720_621+721ins others(46): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268838 | |||||||
| chr7:2268853 | TG | T | 124 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.621+705delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268853 | |||||||
| chr7:2268853 | TGGGGGGG others(43): Show |
T | 3 | a0001c0001t0002g0085 a0001c0001t0002g0132 a0001c0001t0008g0160 |
3 | HG03098.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.621+656_621+705del others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268853 | |||||||
| chr7:2268854 | G | GGGGGGGG others(122): Show |
1 | a0001c0015t0007g0024 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.621+704_621+705ins others(129): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268854 | |||||||
| chr7:2268859 | G | T | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+700C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268859 | |||||||
| chr7:2268870 | C | CTGCCCGG others(150): Show |
6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+688_621+689ins others(157): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268870 | |||||||
| chr7:2268871 | G | A | 5 | a0001c0001t0001g0200 a0001c0001t0016g0233 a0001c0001t0016g0234 others(2): Show |
5 | HG01175.hp2 HG01256.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+688C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268871 | |||||||
| chr7:2268871 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+688C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268871 | |||||||
| chr7:2268872 | C | G | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+687G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268872 | |||||||
| chr7:2268874 | CGGCCAGC others(45): Show |
C | 2 | a0001c0001t0011g0129 a0001c0001t0011g0136 |
2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.621+633_621+684del others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268874 | |||||||
| chr7:2268902 | TG | T | 343 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(340): Show |
347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.621+656delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268902 | |||||||
| chr7:2268904 | G | GGGGGGGT others(120): Show |
1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.621+654_621+655ins others(127): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268904 | |||||||
| chr7:2268906 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+653C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268906 | |||||||
| chr7:2268906 | G | C | 106 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.621+653C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268906 | |||||||
| chr7:2268907 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.621+652C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268907 | |||||||
| chr7:2268926 | T | C | 7 | a0001c0001t0003g0137 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+633A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268926 | |||||||
| chr7:2268944 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0041g0150 |
2 | HG02257.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.621+615C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268944 | |||||||
| chr7:2268972 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+587T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2268972 | |||||||
| chr7:2269005 | G | A | 3 | a0001c0001t0003g0221 a0001c0001t0040g0009 a0002c0004t0023g0357 |
3 | HG01070.hp2 HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.621+554C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269005 | |||||||
| chr7:2269012 | A | AC | 4 | a0001c0001t0001g0139 a0001c0001t0002g0141 a0001c0002t0004g0326 others(1): Show |
4 | NA18977.hp2 NA18991.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+546dupG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269012 | |||||||
| chr7:2269015 | C | T | 1 | a0002c0004t0038g0356 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.621+544G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269015 | |||||||
| chr7:2269070 | G | A | 1 | a0001c0002t0004g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.621+489C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269070 | |||||||
| chr7:2269108 | G | A | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.621+451C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269108 | |||||||
| chr7:2269156 | TG | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+402delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269156 | |||||||
| chr7:2269161 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+398C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269161 | |||||||
| chr7:2269161 | G | C | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+398C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269161 | |||||||
| chr7:2269222 | G | C | 2 | a0001c0001t0021g0301 a0001c0001t0021g0352 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.621+337C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269222 | |||||||
| chr7:2269238 | C | CTGTGCTC others(9): Show |
9 | a0001c0001t0002g0078 a0001c0001t0002g0178 a0001c0001t0002g0229 others(6): Show |
9 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.621+320_621+321ins others(16): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269238 | |||||||
| chr7:2269279 | G | A | 1 | a0001c0002t0004g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.621+280C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269279 | |||||||
| chr7:2269282 | G | A | 10 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(7): Show |
10 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+277C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269282 | |||||||
| chr7:2269299 | C | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+260G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269299 | |||||||
| chr7:2269323 | G | A | 8 | a0001c0001t0008g0001 a0001c0001t0008g0002 a0001c0001t0008g0050 others(5): Show |
10 | HG01081.hp2 HG02615.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+236C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269323 | |||||||
| chr7:2269384 | C | T | 51 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(48): Show |
51 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.621+175G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269384 | |||||||
| chr7:2269391 | T | A | 304 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(301): Show |
308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.621+168A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269391 | |||||||
| chr7:2269479 | C | T | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.621+80G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269479 | |||||||
| chr7:2269523 | T | TA | 7 | a0001c0001t0002g0079 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.621+35dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269523 | |||||||
| chr7:2269523 | TA | T | 19 | a0001c0001t0003g0241 a0001c0001t0003g0318 a0001c0001t0005g0013 others(16): Show |
19 | HG00741.hp2 HG01109.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.621+35delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269523 | |||||||
| chr7:2269524 | A | T | 12 | a0001c0001t0001g0175 a0001c0001t0005g0311 a0001c0003t0005g0010 others(9): Show |
12 | HG01243.hp1 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.621+35T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269524 | |||||||
| chr7:2269535 | A | G | 2 | a0001c0001t0002g0057 a0001c0003t0002g0065 |
2 | NA18971.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.621+24T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269535 | |||||||
| chr7:2269536 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.621+23T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269536 | |||||||
| chr7:2269540 | A | G | 1 | a0001c0005t0015g0022 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+19T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 5/10 | chr7 | 2269540 | |||||||
| chr7:2269720 | G | A | 103 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0028 others(100): Show |
106 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.541-81C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269720 | |||||||
| chr7:2269903 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-264C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269903 | |||||||
| chr7:2269903 | G | T | 2 | a0001c0001t0003g0262 a0001c0001t0013g0076 |
2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.541-264C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2269903 | |||||||
| chr7:2270014 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.541-375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270014 | |||||||
| chr7:2270134 | C | T | 1 | a0001c0001t0008g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.541-495G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270134 | |||||||
| chr7:2270167 | A | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-528T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270167 | |||||||
| chr7:2270255 | C | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-616G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270255 | |||||||
| chr7:2270314 | C | CA | 13 | a0001c0002t0004g0127 a0001c0002t0004g0147 a0001c0002t0004g0183 others(10): Show |
13 | HG01884.hp1 HG02080.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-676dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAA | 16 | a0001c0001t0001g0058 a0001c0001t0001g0120 a0001c0001t0001g0210 others(13): Show |
16 | HG00639.hp2 HG01070.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.541-677_541-676dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAAA | 89 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0037 others(86): Show |
90 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.541-678_541-676dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAAAA | 111 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0001c0001t0001g0086 others(108): Show |
113 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.541-679_541-676dup others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAAAAA | 28 | a0001c0001t0002g0042 a0001c0001t0002g0066 a0001c0001t0002g0085 others(25): Show |
28 | HG00741.hp2 HG01346.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.541-680_541-676dup others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAAAAAA | 21 | a0001c0001t0002g0134 a0001c0001t0002g0142 a0001c0001t0005g0082 others(18): Show |
22 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.541-681_541-676dup others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | C | CAAAAAAA | 10 | a0001c0001t0002g0080 a0001c0001t0005g0311 a0001c0001t0005g0351 others(7): Show |
10 | HG01496.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-682_541-676dup others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | CA | C | 14 | a0001c0002t0004g0017 a0001c0002t0004g0156 a0001c0002t0004g0166 others(11): Show |
14 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-676delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | CAAA | C | 15 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(12): Show |
15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-678_541-676del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270314 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0022g0163 a0001c0001t0022g0164 a0001c0002t0004g0228 |
3 | HG02965.hp1 NA18939.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.541-686_541-676del others(11): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270314 | |||||||
| chr7:2270397 | C | T | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-758G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270397 | |||||||
| chr7:2270398 | G | A | 9 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-759C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270398 | |||||||
| chr7:2270408 | C | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-769G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270408 | |||||||
| chr7:2270466 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-827T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270466 | |||||||
| chr7:2270520 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.541-881C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270520 | |||||||
| chr7:2270558 | A | G | 253 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.541-919T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270558 | |||||||
| chr7:2270707 | G | A | 16 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(13): Show |
16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.541-1068C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270707 | |||||||
| chr7:2270756 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.540+1094G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270756 | |||||||
| chr7:2270932 | C | T | 6 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+918G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270932 | |||||||
| chr7:2270988 | C | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+862G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2270988 | |||||||
| chr7:2271042 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.540+808C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271042 | |||||||
| chr7:2271082 | C | T | 2 | a0001c0002t0029g0077 a0001c0002t0046g0169 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.540+768G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271082 | |||||||
| chr7:2271339 | C | T | 129 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(126): Show |
130 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.540+511G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271339 | |||||||
| chr7:2271370 | T | G | 1 | a0001c0001t0001g0215 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.540+480A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271370 | |||||||
| chr7:2271438 | A | C | 1 | a0001c0003t0002g0065 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.540+412T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271438 | |||||||
| chr7:2271611 | G | A | 2 | a0001c0001t0002g0230 a0001c0001t0002g0302 |
2 | HG01346.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.540+239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271611 | |||||||
| chr7:2271617 | C | T | 1 | a0001c0003t0006g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.540+233G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271617 | |||||||
| chr7:2271628 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.540+222G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271628 | |||||||
| chr7:2271629 | G | A | 2 | a0001c0001t0003g0039 a0001c0002t0010g0347 |
2 | HG02572.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.540+221C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271629 | |||||||
| chr7:2271631 | G | A | 108 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(105): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.540+219C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271631 | |||||||
| chr7:2271754 | A | G | 1 | a0001c0001t0014g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.540+96T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271754 | |||||||
| chr7:2271806 | G | A | 2 | a0001c0002t0004g0147 a0001c0002t0004g0156 |
2 | HG01243.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.540+44C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 4/10 | chr7 | 2271806 | |||||||
| chr7:2272013 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.419-42G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272013 | |||||||
| chr7:2272075 | A | G | 11 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(8): Show |
11 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-104T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272075 | |||||||
| chr7:2272138 | C | T | 2 | a0001c0002t0027g0187 a0001c0002t0027g0346 |
2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.419-167G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272138 | |||||||
| chr7:2272139 | G | A | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.419-168C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272139 | |||||||
| chr7:2272201 | C | A | 11 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(8): Show |
11 | HG01255.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-230G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272201 | |||||||
| chr7:2272207 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-236T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272207 | |||||||
| chr7:2272255 | G | A | 1 | a0001c0002t0010g0337 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.419-284C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272255 | |||||||
| chr7:2272324 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-353T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272324 | |||||||
| chr7:2272377 | C | CT | 16 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(13): Show |
16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.419-407dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272377 | |||||||
| chr7:2272377 | CT | C | 7 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 others(4): Show |
7 | HG00639.hp2 HG01070.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-407delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272377 | |||||||
| chr7:2272529 | A | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-558T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272529 | |||||||
| chr7:2272628 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-657C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272628 | |||||||
| chr7:2272730 | A | T | 1 | a0001c0001t0030g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.419-759T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272730 | |||||||
| chr7:2272872 | C | T | 247 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.419-901G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272872 | |||||||
| chr7:2272929 | G | T | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-958C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272929 | |||||||
| chr7:2272933 | A | G | 108 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(105): Show |
109 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.419-962T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272933 | |||||||
| chr7:2272936 | C | T | 3 | a0001c0001t0008g0002 a0001c0001t0008g0050 a0001c0001t0008g0160 |
4 | HG01081.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.419-965G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2272936 | |||||||
| chr7:2273091 | C | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0295 |
2 | HG02015.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.419-1120G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273091 | |||||||
| chr7:2273370 | G | A | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-1399C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273370 | |||||||
| chr7:2273442 | C | A | 1 | a0001c0001t0003g0284 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.419-1471G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273442 | |||||||
| chr7:2273447 | G | A | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-1476C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273447 | |||||||
| chr7:2273543 | A | T | 1 | a0001c0001t0043g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.418+1569T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273543 | |||||||
| chr7:2273552 | C | G | 1 | a0001c0006t0013g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.418+1560G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273552 | |||||||
| chr7:2273630 | G | A | 16 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(13): Show |
16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+1482C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273630 | |||||||
| chr7:2273662 | G | C | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1450C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273662 | |||||||
| chr7:2273699 | T | C | 1 | a0001c0001t0014g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.418+1413A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273699 | |||||||
| chr7:2273794 | C | T | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+1318G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273794 | |||||||
| chr7:2273902 | T | TA | 34 | a0001c0001t0001g0064 a0001c0001t0001g0170 a0001c0001t0001g0216 others(31): Show |
34 | HG00438.hp1 HG01070.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.418+1209dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273902 | |||||||
| chr7:2273903 | A | T | 1 | a0001c0002t0004g0321 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.418+1209T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273903 | |||||||
| chr7:2273972 | T | C | 44 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(41): Show |
44 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.418+1140A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2273972 | |||||||
| chr7:2274014 | C | T | 44 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(41): Show |
44 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.418+1098G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274014 | |||||||
| chr7:2274029 | G | T | 1 | a0001c0001t0017g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+1083C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274029 | |||||||
| chr7:2274128 | T | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+984A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274128 | |||||||
| chr7:2274129 | C | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+983G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274129 | |||||||
| chr7:2274171 | G | A | 1 | a0001c0001t0021g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.418+941C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274171 | |||||||
| chr7:2274178 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+934C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274178 | |||||||
| chr7:2274209 | C | G | 7 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0181 others(4): Show |
7 | HG00741.hp1 HG01884.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+903G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274209 | |||||||
| chr7:2274290 | C | T | 1 | a0001c0002t0010g0334 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.418+822G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274290 | |||||||
| chr7:2274291 | G | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+821C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274291 | |||||||
| chr7:2274351 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.418+761G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274351 | |||||||
| chr7:2274356 | T | C | 1 | a0002c0019t0006g0354 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.418+756A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274356 | |||||||
| chr7:2274412 | T | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.418+700A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274412 | |||||||
| chr7:2274502 | G | A | 1 | a0001c0003t0006g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.418+610C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274502 | |||||||
| chr7:2274513 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.418+599C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274513 | |||||||
| chr7:2274519 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+593T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274519 | |||||||
| chr7:2274620 | C | T | 1 | a0001c0001t0019g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.418+492G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274620 | |||||||
| chr7:2274992 | TC | T | 318 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(315): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.418+119delG | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2274992 | |||||||
| chr7:2275017 | G | A | 124 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.418+95C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2275017 | |||||||
| chr7:2275087 | C | T | 1 | a0001c0001t0009g0130 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.418+25G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 3/10 | chr7 | 2275087 | |||||||
| chr7:2275259 | G | A | 1 | a0001c0001t0002g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.301-30C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275259 | |||||||
| chr7:2275372 | G | A | 1 | a0001c0003t0005g0314 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.301-143C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275372 | |||||||
| chr7:2275373 | G | C | 302 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(299): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.301-144C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275373 | |||||||
| chr7:2275421 | C | T | 115 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(112): Show |
118 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.301-192G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275421 | |||||||
| chr7:2275470 | C | T | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.301-241G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275470 | |||||||
| chr7:2275571 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0255 |
2 | NA18978.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.301-342C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275571 | |||||||
| chr7:2275575 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.301-346C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275575 | |||||||
| chr7:2275584 | C | G | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-355G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275584 | |||||||
| chr7:2275589 | C | G | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-360G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275589 | |||||||
| chr7:2275590 | T | G | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-361A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275590 | |||||||
| chr7:2275594 | T | G | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-365A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275594 | |||||||
| chr7:2275596 | G | A | 1 | a0001c0001t0009g0309 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301-367C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275596 | |||||||
| chr7:2275689 | G | A | 44 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(41): Show |
44 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.301-460C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275689 | |||||||
| chr7:2275765 | G | A | 9 | a0001c0001t0003g0039 a0001c0001t0021g0301 a0001c0001t0021g0352 others(6): Show |
9 | HG00735.hp2 HG01069.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-536C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275765 | |||||||
| chr7:2275942 | G | A | 1 | a0001c0002t0004g0285 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.301-713C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275942 | |||||||
| chr7:2275954 | C | T | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.301-725G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275954 | |||||||
| chr7:2275985 | G | A | 1 | a0001c0001t0005g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.301-756C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275985 | |||||||
| chr7:2275997 | C | CA | 12 | a0001c0001t0001g0031 a0001c0001t0001g0139 a0001c0001t0002g0302 others(9): Show |
12 | HG01069.hp2 HG01192.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-769dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2275997 | |||||||
| chr7:2276146 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.301-917C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276146 | |||||||
| chr7:2276163 | G | C | 22 | a0001c0001t0001g0119 a0001c0001t0005g0013 a0001c0001t0005g0014 others(19): Show |
22 | HG01109.hp1 HG01192.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.301-934C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276163 | |||||||
| chr7:2276204 | G | A | 8 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.301-975C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276204 | |||||||
| chr7:2276267 | G | A | 12 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(9): Show |
12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.301-1038C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276267 | |||||||
| chr7:2276315 | C | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.301-1086G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276315 | |||||||
| chr7:2276329 | G | A | 1 | a0001c0002t0004g0263 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.301-1100C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276329 | |||||||
| chr7:2276417 | G | A | 1 | a0001c0001t0002g0043 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.301-1188C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276417 | |||||||
| chr7:2276480 | A | G | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0186 others(5): Show |
8 | HG00621.hp2 NA18612.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-1251T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276480 | |||||||
| chr7:2276642 | T | TA | 16 | a0001c0001t0002g0328 a0001c0001t0009g0309 a0001c0001t0021g0349 others(13): Show |
16 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.301-1414dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276642 | |||||||
| chr7:2276642 | TA | T | 141 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(138): Show |
142 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.301-1414delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276642 | |||||||
| chr7:2276886 | AGT | A | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.300+1212_300+1213d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276886 | |||||||
| chr7:2276942 | C | G | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.300+1158G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2276942 | |||||||
| chr7:2277003 | C | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+1097G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277003 | |||||||
| chr7:2277199 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.300+901C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277199 | |||||||
| chr7:2277217 | C | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.300+883G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277217 | |||||||
| chr7:2277229 | C | G | 1 | a0001c0002t0004g0243 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.300+871G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277229 | |||||||
| chr7:2277263 | C | G | 1 | a0001c0001t0009g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.300+837G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277263 | |||||||
| chr7:2277425 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.300+675C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277425 | |||||||
| chr7:2277449 | G | A | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300+651C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277449 | |||||||
| chr7:2277523 | G | C | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.300+577C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277523 | |||||||
| chr7:2277564 | G | T | 1 | a0001c0001t0023g0122 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.300+536C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277564 | |||||||
| chr7:2277611 | T | C | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.300+489A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277611 | |||||||
| chr7:2277636 | TA | T | 300 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(297): Show |
304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.300+463delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277636 | |||||||
| chr7:2277794 | A | G | 255 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(252): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.300+306T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277794 | |||||||
| chr7:2277804 | A | G | 3 | a0001c0001t0011g0101 a0001c0001t0011g0129 a0001c0001t0011g0136 |
3 | HG01069.hp1 HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.300+296T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277804 | |||||||
| chr7:2277806 | C | T | 2 | a0001c0001t0003g0284 a0001c0001t0003g0322 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.300+294G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277806 | |||||||
| chr7:2277810 | GA | G | 132 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(129): Show |
133 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.300+289delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277810 | |||||||
| chr7:2277836 | A | G | 1 | a0006c0008t0001g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.300+264T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2277836 | |||||||
| chr7:2278055 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.300+45A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 2/10 | chr7 | 2278055 | |||||||
| chr7:2278589 | CACTCACT others(76): Show |
C | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-367_95-285delCC others(81): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278589 | |||||||
| chr7:2278599 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-294G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278599 | |||||||
| chr7:2278618 | GACTC | G | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-317_95-314delGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278618 | |||||||
| chr7:2278633 | C | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-328G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278633 | |||||||
| chr7:2278642 | AGCCGGAC others(47): Show |
A | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-391_95-338delGT others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278642 | |||||||
| chr7:2278645 | C | T | 106 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.95-340G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278645 | |||||||
| chr7:2278646 | G | A | 43 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(40): Show |
43 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.95-341C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278646 | |||||||
| chr7:2278661 | A | C | 1 | a0001c0001t0011g0101 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.95-356T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278661 | |||||||
| chr7:2278667 | C | A | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-362G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | |||||||
| chr7:2278667 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-362G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | |||||||
| chr7:2278667 | CGCCGGAC others(362): Show |
C | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-731_95-363del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278667 | |||||||
| chr7:2278700 | G | A | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.95-395C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278700 | |||||||
| chr7:2278709 | C | G | 5 | a0001c0003t0005g0010 a0001c0006t0013g0174 a0001c0006t0013g0192 others(2): Show |
5 | HG02145.hp2 HG03831.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-404G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278709 | |||||||
| chr7:2278722 | C | T | 69 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(66): Show |
71 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.95-417G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278722 | |||||||
| chr7:2278723 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.95-418C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278723 | |||||||
| chr7:2278725 | A | C | 6 | a0001c0001t0016g0233 a0001c0001t0016g0234 a0001c0001t0016g0235 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-420T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278725 | |||||||
| chr7:2278738 | C | CACACTAC others(109): Show |
1 | a0001c0001t0002g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-434_95-433insCA others(114): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278738 | |||||||
| chr7:2278738 | C | G | 106 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.95-433G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278738 | |||||||
| chr7:2278754 | A | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-449T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278754 | |||||||
| chr7:2278754 | AGCCGGAC others(22): Show |
A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-478_95-450delGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278754 | |||||||
| chr7:2278758 | G | A | 1 | a0001c0002t0004g0329 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.95-453C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278758 | |||||||
| chr7:2278788 | GACTC | G | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-487_95-484delGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278788 | |||||||
| chr7:2278792 | CACTCACA others(18): Show |
C | 133 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(130): Show |
134 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.95-512_95-488delCC others(23): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278792 | |||||||
| chr7:2278792 | CACTCACA others(246): Show |
C | 4 | a0001c0001t0016g0233 a0001c0001t0016g0234 a0001c0001t0016g0235 others(1): Show |
4 | HG01175.hp2 HG01516.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-740_95-488del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278792 | |||||||
| chr7:2278812 | CGCCGGAC others(217): Show |
C | 3 | a0001c0001t0001g0173 a0001c0001t0035g0152 a0001c0001t0041g0150 |
3 | HG02257.hp2 HG03209.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.95-731_95-508del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278812 | |||||||
| chr7:2278812 | CGCCGGAC others(275): Show |
C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0256 |
2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.95-789_95-508del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278812 | |||||||
| chr7:2278816 | G | A | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278816 | |||||||
| chr7:2278817 | G | GACTC | 13 | a0001c0001t0002g0080 a0001c0001t0002g0097 a0001c0001t0002g0134 others(10): Show |
13 | HG02280.hp1 HG03831.hp1 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-516_95-513dupGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278817 | |||||||
| chr7:2278817 | G | GACTCACA others(22): Show |
1 | a0001c0001t0002g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.95-541_95-513dupGA others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278817 | |||||||
| chr7:2278834 | C | T | 48 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0068 others(45): Show |
48 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-529G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278834 | |||||||
| chr7:2278837 | C | A | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-532G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278837 | |||||||
| chr7:2278864 | G | A | 1 | a0001c0003t0005g0312 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.95-559C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278864 | |||||||
| chr7:2278866 | C | A | 7 | a0001c0001t0002g0097 a0001c0001t0002g0134 a0001c0001t0002g0328 others(4): Show |
7 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-561G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278866 | |||||||
| chr7:2278866 | CGCCGGAC others(221): Show |
C | 99 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(96): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.95-789_95-562del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278866 | |||||||
| chr7:2278895 | A | C | 19 | a0001c0001t0001g0075 a0001c0001t0001g0193 a0001c0001t0002g0097 others(16): Show |
19 | HG00735.hp2 HG01069.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.95-590T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278895 | |||||||
| chr7:2278953 | C | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-648G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278953 | |||||||
| chr7:2278953 | CGCCGGAC others(192): Show |
C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0193 |
2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.95-847_95-649del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278953 | |||||||
| chr7:2278962 | CACTCACA others(18): Show |
C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-682_95-658delCC others(23): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278962 | |||||||
| chr7:2278982 | C | A | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-677G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | |||||||
| chr7:2278982 | CGCCGGAC others(47): Show |
C | 1 | a0001c0001t0007g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.95-731_95-678delTT others(52): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | |||||||
| chr7:2278982 | CGCCGGAC others(105): Show |
C | 25 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(22): Show |
25 | HG01192.hp2 HG01884.hp1 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.95-789_95-678del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | |||||||
| chr7:2278982 | CGCCGGAC others(163): Show |
C | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-847_95-678del | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278982 | |||||||
| chr7:2278987 | G | GACTC | 13 | a0001c0001t0002g0097 a0001c0001t0002g0103 a0001c0001t0002g0107 others(10): Show |
13 | HG00735.hp2 HG01069.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-686_95-683dupGA others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | |||||||
| chr7:2278987 | G | GACTCACT others(26): Show |
73 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(70): Show |
75 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.95-683_95-682insGA others(31): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | |||||||
| chr7:2278987 | G | GACTCACT others(55): Show |
23 | a0001c0001t0005g0082 a0001c0001t0005g0109 a0001c0001t0005g0161 others(20): Show |
24 | HG01099.hp1 HG01243.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-683_95-682insGA others(60): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | |||||||
| chr7:2278987 | G | GACTCACT others(84): Show |
1 | a0001c0001t0005g0278 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.95-683_95-682insGA others(89): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | |||||||
| chr7:2278987 | G | GACTCACT others(482): Show |
2 | a0001c0001t0021g0301 a0001c0001t0021g0352 |
2 | HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.95-683_95-682insGA others(487): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278987 | |||||||
| chr7:2278998 | C | T | 2 | a0001c0002t0027g0187 a0001c0002t0027g0346 |
2 | HG00639.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.95-693G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2278998 | |||||||
| chr7:2279007 | C | A | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-702G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279007 | |||||||
| chr7:2279036 | A | C | 114 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(111): Show |
117 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.95-731T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279036 | |||||||
| chr7:2279040 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.95-735C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279040 | |||||||
| chr7:2279065 | C | A | 8 | a0001c0001t0022g0163 a0001c0001t0022g0164 a0001c0001t0035g0152 others(5): Show |
8 | HG02257.hp2 HG02965.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-760G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279065 | |||||||
| chr7:2279094 | A | AGCCGGAC others(22): Show |
1 | a0001c0001t0003g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.95-790_95-789insGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | |||||||
| chr7:2279094 | A | AGCCGGAC others(22): Show |
41 | a0001c0001t0003g0068 a0001c0001t0003g0070 a0001c0001t0003g0074 others(38): Show |
41 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.95-818_95-790dupGT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | |||||||
| chr7:2279094 | A | AGCCGGAC others(80): Show |
1 | a0001c0003t0006g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-876_95-790dupGT others(85): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | |||||||
| chr7:2279094 | A | C | 120 | a0001c0001t0001g0146 a0001c0001t0001g0173 a0001c0001t0002g0019 others(117): Show |
123 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.95-789T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279094 | |||||||
| chr7:2279098 | GGACTCAC others(21): Show |
G | 1 | a0001c0001t0001g0173 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.95-821_95-794delGG others(26): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279098 | |||||||
| chr7:2279115 | G | GGAGTCGA others(22): Show |
1 | a0001c0001t0002g0153 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.95-811_95-810insGG others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279115 | |||||||
| chr7:2279120 | C | T | 6 | a0001c0003t0005g0312 a0001c0003t0006g0012 a0001c0003t0006g0015 others(3): Show |
6 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-815G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279120 | |||||||
| chr7:2279123 | CGCCGGAC others(22): Show |
C | 1 | a0001c0001t0007g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.95-847_95-819delTT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279123 | |||||||
| chr7:2279152 | A | C | 278 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(275): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.95-847T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279152 | |||||||
| chr7:2279184 | C | T | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-879G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279184 | |||||||
| chr7:2279239 | CGCCGGAC others(22): Show |
C | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-963_95-935delTT others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279239 | |||||||
| chr7:2279268 | A | C | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-963T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279268 | |||||||
| chr7:2279288 | C | T | 1 | a0007c0017t0002g0325 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.95-983G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279288 | |||||||
| chr7:2279297 | A | C | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-992T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279297 | |||||||
| chr7:2279300 | CGGACTCA others(22): Show |
C | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1024_95-996delA others(28): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279300 | |||||||
| chr7:2279355 | C | A | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1050G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279355 | |||||||
| chr7:2279358 | T | C | 1 | a0001c0001t0003g0069 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.95-1053A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279358 | |||||||
| chr7:2279444 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0248 |
2 | NA19003.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.95-1139C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279444 | |||||||
| chr7:2279494 | G | A | 47 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(44): Show |
47 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.95-1189C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279494 | |||||||
| chr7:2279544 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-1239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279544 | |||||||
| chr7:2279571 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1266C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279571 | |||||||
| chr7:2279612 | G | A | 5 | a0001c0001t0005g0082 a0001c0001t0005g0350 a0001c0001t0005g0351 others(2): Show |
6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-1307C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279612 | |||||||
| chr7:2279697 | G | A | 12 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(9): Show |
12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-1392C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279697 | |||||||
| chr7:2279762 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.95-1457C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | |||||||
| chr7:2279762 | G | GA | 19 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0248 others(16): Show |
19 | HG01934.hp2 HG02056.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-1458dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | |||||||
| chr7:2279762 | GA | G | 50 | a0001c0001t0001g0206 a0001c0001t0001g0269 a0001c0001t0002g0145 others(47): Show |
50 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.95-1458delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | |||||||
| chr7:2279762 | GAAAAAAA | G | 8 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-1464_95-1458del others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279762 | |||||||
| chr7:2279951 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1646G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279951 | |||||||
| chr7:2279981 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-1676A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2279981 | |||||||
| chr7:2280116 | A | G | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-1811T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280116 | |||||||
| chr7:2280220 | G | A | 3 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0023g0122 |
3 | HG00639.hp2 HG01070.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-1915C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280220 | |||||||
| chr7:2280234 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0215 |
2 | NA18960.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.95-1929C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280234 | |||||||
| chr7:2280304 | GA | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2000delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280304 | |||||||
| chr7:2280413 | C | T | 1 | a0001c0005t0001g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.95-2108G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280413 | |||||||
| chr7:2280477 | CA | C | 9 | a0001c0001t0002g0080 a0001c0001t0014g0049 a0001c0001t0014g0276 others(6): Show |
9 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-2173delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280477 | |||||||
| chr7:2280493 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-2188A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280493 | |||||||
| chr7:2280723 | C | T | 12 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(9): Show |
12 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-2418G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280723 | |||||||
| chr7:2280747 | T | C | 6 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2442A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280747 | |||||||
| chr7:2280765 | A | C | 1 | a0002c0004t0018g0358 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.95-2460T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280765 | |||||||
| chr7:2280792 | C | CT | 235 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.95-2488dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280792 | |||||||
| chr7:2280825 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-2520G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2280825 | |||||||
| chr7:2281225 | G | A | 3 | a0001c0001t0017g0201 a0001c0001t0017g0205 a0001c0001t0017g0211 |
3 | HG02602.hp2 HG02735.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.95-2920C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281225 | |||||||
| chr7:2281469 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0001g0339 others(2): Show |
5 | HG00423.hp2 HG00438.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-3164G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281469 | |||||||
| chr7:2281497 | G | A | 3 | a0001c0001t0008g0002 a0001c0001t0008g0050 a0001c0001t0008g0160 |
4 | HG01081.hp2 HG03225.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3192C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281497 | |||||||
| chr7:2281544 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.95-3239C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281544 | |||||||
| chr7:2281547 | A | G | 16 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(13): Show |
16 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-3242T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281547 | |||||||
| chr7:2281612 | A | G | 7 | a0001c0001t0003g0039 a0001c0006t0013g0174 a0001c0006t0013g0192 others(4): Show |
7 | HG00735.hp2 HG01069.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-3307T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281612 | |||||||
| chr7:2281647 | A | T | 1 | a0001c0002t0010g0333 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.95-3342T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281647 | |||||||
| chr7:2281797 | G | A | 1 | a0001c0002t0004g0156 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.95-3492C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281797 | |||||||
| chr7:2281838 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3533A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281838 | |||||||
| chr7:2281925 | C | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-3620G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2281925 | |||||||
| chr7:2282031 | T | C | 1 | a0009c0018t0001g0353 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.95-3726A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282031 | |||||||
| chr7:2282413 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4108G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282413 | |||||||
| chr7:2282469 | A | G | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.95-4164T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282469 | |||||||
| chr7:2282495 | T | G | 13 | a0001c0001t0003g0039 a0001c0001t0014g0049 a0001c0001t0014g0276 others(10): Show |
13 | HG01884.hp1 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-4190A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282495 | |||||||
| chr7:2282521 | A | G | 15 | a0001c0001t0001g0119 a0001c0001t0007g0021 a0001c0001t0007g0026 others(12): Show |
15 | HG01192.hp2 HG02056.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-4216T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282521 | |||||||
| chr7:2282703 | G | A | 41 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0070 others(38): Show |
41 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.95-4398C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282703 | |||||||
| chr7:2282768 | G | A | 45 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(42): Show |
45 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-4463C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282768 | |||||||
| chr7:2282859 | C | G | 3 | a0001c0001t0005g0082 a0001c0001t0005g0350 a0001c0001t0005g0351 |
3 | HG01099.hp1 HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-4554G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282859 | |||||||
| chr7:2282860 | G | A | 2 | a0001c0001t0009g0309 a0001c0002t0029g0077 |
2 | HG03669.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.95-4555C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282860 | |||||||
| chr7:2282949 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-4644C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282949 | |||||||
| chr7:2282978 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4673C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282978 | |||||||
| chr7:2282982 | G | A | 280 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.95-4677C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282982 | |||||||
| chr7:2282989 | C | A | 45 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(42): Show |
45 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-4684G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282989 | |||||||
| chr7:2282992 | A | G | 45 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(42): Show |
45 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-4687T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282992 | |||||||
| chr7:2282993 | A | C | 45 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(42): Show |
45 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-4688T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282993 | |||||||
| chr7:2282998 | G | A | 1 | a0002c0004t0005g0364 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.95-4693C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2282998 | |||||||
| chr7:2283014 | G | A | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-4709C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283014 | |||||||
| chr7:2283028 | G | A | 60 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0068 others(57): Show |
60 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.95-4723C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283028 | |||||||
| chr7:2283037 | T | C | 45 | a0001c0001t0003g0040 a0001c0001t0003g0068 a0001c0001t0003g0069 others(42): Show |
45 | HG00544.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-4732A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283037 | |||||||
| chr7:2283075 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0265 |
2 | NA18954.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.95-4770G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283075 | |||||||
| chr7:2283076 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0009g0023 |
2 | NA18977.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.95-4771C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283076 | |||||||
| chr7:2283088 | T | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4783A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283088 | |||||||
| chr7:2283104 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4799T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283104 | |||||||
| chr7:2283106 | A | G | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4801T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283106 | |||||||
| chr7:2283129 | A | T | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-4824T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283129 | |||||||
| chr7:2283130 | A | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4825T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283130 | |||||||
| chr7:2283157 | G | A | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4852C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283157 | |||||||
| chr7:2283176 | C | G | 8 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-4871G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283176 | |||||||
| chr7:2283177 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4872C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283177 | |||||||
| chr7:2283254 | G | A | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4949C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283254 | |||||||
| chr7:2283267 | G | C | 1 | a0001c0001t0014g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.95-4962C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283267 | |||||||
| chr7:2283308 | T | C | 236 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(233): Show |
240 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.95-5003A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283308 | |||||||
| chr7:2283339 | A | C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-5034T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283339 | |||||||
| chr7:2283363 | T | A | 2 | a0001c0001t0035g0152 a0001c0001t0041g0150 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.95-5058A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283363 | |||||||
| chr7:2283384 | C | G | 121 | a0001c0001t0001g0119 a0001c0001t0001g0146 a0001c0001t0002g0019 others(118): Show |
124 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.95-5079G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283384 | |||||||
| chr7:2283408 | C | T | 1 | a0006c0008t0001g0247 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.95-5103G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283408 | |||||||
| chr7:2283411 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.95-5106G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283411 | |||||||
| chr7:2283526 | T | C | 6 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0231 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5221A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283526 | |||||||
| chr7:2283532 | G | C | 244 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.95-5227C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283532 | |||||||
| chr7:2283602 | G | A | 9 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-5297C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283602 | |||||||
| chr7:2283638 | G | A | 4 | a0001c0001t0011g0093 a0001c0001t0011g0104 a0001c0001t0011g0112 others(1): Show |
4 | HG01099.hp2 HG01975.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-5333C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283638 | |||||||
| chr7:2283670 | G | A | 10 | a0001c0005t0001g0059 a0001c0005t0001g0154 a0001c0005t0001g0217 others(7): Show |
10 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-5365C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283670 | |||||||
| chr7:2283758 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG01884.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.95-5453C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283758 | |||||||
| chr7:2283814 | G | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5509C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283814 | |||||||
| chr7:2283853 | T | C | 106 | a0001c0001t0001g0146 a0001c0001t0002g0019 a0001c0001t0002g0020 others(103): Show |
106 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.95-5548A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283853 | |||||||
| chr7:2283951 | A | G | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5646T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2283951 | |||||||
| chr7:2284044 | C | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(1): Show |
4 | HG01109.hp1 HG02280.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-5739G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284044 | |||||||
| chr7:2284077 | C | T | 1 | a0001c0002t0004g0282 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.95-5772G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284077 | |||||||
| chr7:2284121 | G | T | 53 | a0001c0001t0001g0119 a0001c0001t0002g0085 a0001c0001t0002g0132 others(50): Show |
56 | HG01081.hp2 HG01099.hp1 HG01192.hp2 others(53): Show |
intron_variant | MODIFIER | c.95-5816C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284121 | |||||||
| chr7:2284209 | C | T | 2 | a0001c0002t0029g0077 a0001c0002t0046g0169 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.95-5904G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284209 | |||||||
| chr7:2284258 | G | A | 1 | a0001c0001t0019g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.95-5953C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284258 | |||||||
| chr7:2284276 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.95-5971C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284276 | |||||||
| chr7:2284326 | G | A | 5 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6021C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284326 | |||||||
| chr7:2284344 | C | T | 3 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 |
3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-6039G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284344 | |||||||
| chr7:2284345 | G | A | 5 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6040C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284345 | |||||||
| chr7:2284350 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-6045G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284350 | |||||||
| chr7:2284396 | C | CT | 136 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(133): Show |
137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.95-6092dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | |||||||
| chr7:2284396 | C | CTT | 88 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0175 others(85): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.95-6093_95-6092dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | |||||||
| chr7:2284396 | C | CTTT | 18 | a0001c0001t0002g0132 a0001c0001t0003g0087 a0001c0001t0003g0091 others(15): Show |
19 | HG00738.hp1 HG01070.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-6094_95-6092dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284396 | |||||||
| chr7:2284422 | G | A | 1 | a0001c0001t0009g0106 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.95-6117C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284422 | |||||||
| chr7:2284432 | C | T | 51 | a0001c0001t0001g0119 a0001c0001t0002g0085 a0001c0001t0002g0132 others(48): Show |
54 | HG01081.hp2 HG01099.hp1 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.95-6127G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284432 | |||||||
| chr7:2284458 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0044g0096 |
2 | NA18983.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.95-6153T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284458 | |||||||
| chr7:2284587 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.95-6282C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284587 | |||||||
| chr7:2284625 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.95-6320G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284625 | |||||||
| chr7:2284647 | G | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6342C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284647 | |||||||
| chr7:2284690 | C | T | 5 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0204 others(2): Show |
5 | HG00558.hp2 NA18947.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6385G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284690 | |||||||
| chr7:2284693 | T | C | 5 | a0001c0001t0009g0148 a0001c0001t0009g0149 a0001c0001t0009g0204 others(2): Show |
5 | HG00558.hp2 NA18947.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6388A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284693 | |||||||
| chr7:2284709 | C | T | 13 | a0001c0001t0002g0085 a0001c0001t0002g0132 a0001c0001t0008g0001 others(10): Show |
15 | HG01081.hp2 HG02451.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-6404G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284709 | |||||||
| chr7:2284746 | G | A | 44 | a0001c0001t0001g0119 a0001c0001t0003g0040 a0001c0001t0005g0082 others(41): Show |
45 | HG00639.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.95-6441C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284746 | |||||||
| chr7:2284953 | T | C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-6648A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284953 | |||||||
| chr7:2284954 | G | A | 1 | a0001c0001t0020g0003 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.95-6649C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284954 | |||||||
| chr7:2284983 | T | C | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6678A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284983 | |||||||
| chr7:2284995 | A | G | 2 | a0001c0001t0032g0303 a0001c0002t0004g0326 |
2 | NA18970.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.95-6690T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2284995 | |||||||
| chr7:2285008 | C | G | 1 | a0001c0001t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95-6703G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285008 | |||||||
| chr7:2285009 | G | A | 133 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(130): Show |
134 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.95-6704C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285009 | |||||||
| chr7:2285023 | T | C | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG02647.hp1 HG03139.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6718A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285023 | |||||||
| chr7:2285030 | A | G | 51 | a0001c0001t0002g0310 a0001c0001t0003g0040 a0001c0001t0003g0158 others(48): Show |
51 | HG00639.hp2 HG01070.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.95-6725T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285030 | |||||||
| chr7:2285078 | G | A | 6 | a0001c0001t0003g0158 a0001c0001t0003g0279 a0001c0001t0003g0294 others(3): Show |
6 | HG01167.hp1 HG02559.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6773C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285078 | |||||||
| chr7:2285113 | G | A | 104 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(101): Show |
105 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.95-6808C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285113 | |||||||
| chr7:2285144 | A | G | 5 | a0001c0001t0005g0082 a0001c0001t0005g0350 a0001c0001t0005g0351 others(2): Show |
6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6839T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285144 | |||||||
| chr7:2285147 | A | G | 5 | a0001c0001t0005g0082 a0001c0001t0005g0350 a0001c0001t0005g0351 others(2): Show |
6 | HG01099.hp1 HG02109.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-6842T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285147 | |||||||
| chr7:2285148 | G | C | 179 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(176): Show |
181 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.95-6843C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285148 | |||||||
| chr7:2285177 | A | C | 1 | a0001c0001t0003g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.95-6872T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285177 | |||||||
| chr7:2285207 | G | A | 3 | a0001c0001t0003g0158 a0001c0001t0003g0294 a0001c0001t0030g0157 |
3 | HG03239.hp1 HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.95-6902C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285207 | |||||||
| chr7:2285211 | C | CA | 131 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(128): Show |
132 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.95-6907dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | |||||||
| chr7:2285211 | C | CAA | 36 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(33): Show |
36 | HG00738.hp2 HG01192.hp2 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.95-6908_95-6907dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | |||||||
| chr7:2285211 | CA | C | 9 | a0001c0002t0004g0183 a0001c0002t0010g0242 a0001c0002t0010g0333 others(6): Show |
9 | HG00639.hp1 HG01975.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-6907delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285211 | |||||||
| chr7:2285341 | T | A | 173 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(170): Show |
174 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.95-7036A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285341 | |||||||
| chr7:2285415 | C | A | 6 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-7110G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285415 | |||||||
| chr7:2285514 | C | T | 30 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(27): Show |
30 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-7209G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285514 | |||||||
| chr7:2285597 | T | C | 11 | a0001c0001t0002g0085 a0001c0001t0002g0132 a0001c0001t0008g0001 others(8): Show |
13 | HG01081.hp2 HG02615.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-7292A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285597 | |||||||
| chr7:2285659 | ACTTT | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-7358_95-7355del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285659 | |||||||
| chr7:2285672 | A | AT | 27 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(24): Show |
27 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.95-7368dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285672 | |||||||
| chr7:2285748 | C | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0261 a0001c0001t0001g0269 |
3 | NA18747.hp1 NA18946.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.95-7443G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285748 | |||||||
| chr7:2285786 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.95-7481G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285786 | |||||||
| chr7:2285833 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.95-7528T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285833 | |||||||
| chr7:2285868 | C | CG | 11 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(8): Show |
11 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-7564dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285868 | |||||||
| chr7:2285902 | C | T | 1 | a0002c0004t0008g0363 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-7597G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2285902 | |||||||
| chr7:2286007 | CT | C | 9 | a0001c0001t0001g0054 a0001c0001t0001g0267 a0001c0001t0003g0279 others(6): Show |
9 | HG01109.hp1 HG01167.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-7703delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286007 | |||||||
| chr7:2286201 | G | A | 1 | a0001c0006t0039g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.95-7896C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286201 | |||||||
| chr7:2286201 | G | C | 1 | a0001c0001t0002g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-7896C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286201 | |||||||
| chr7:2286236 | T | C | 1 | a0001c0001t0002g0257 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.95-7931A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286236 | |||||||
| chr7:2286318 | G | A | 1 | a0001c0001t0032g0303 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.95-8013C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286318 | |||||||
| chr7:2286358 | T | C | 3 | a0001c0001t0002g0310 a0001c0001t0007g0271 a0001c0002t0047g0159 |
3 | HG01192.hp2 HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.95-8053A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286358 | |||||||
| chr7:2286444 | T | TGTACA | 6 | a0001c0001t0003g0158 a0001c0001t0003g0279 a0001c0001t0003g0294 others(3): Show |
6 | HG01167.hp1 HG02559.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-8144_95-8140dup others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286444 | |||||||
| chr7:2286478 | T | C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8173A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286478 | |||||||
| chr7:2286521 | A | AT | 122 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(119): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.95-8217_95-8216ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286521 | |||||||
| chr7:2286522 | A | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8217T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286522 | |||||||
| chr7:2286523 | T | A | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-8218A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286523 | |||||||
| chr7:2286523 | T | TA | 3 | a0001c0001t0002g0254 a0001c0006t0013g0192 a0001c0006t0013g0274 |
3 | HG03831.hp1 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.95-8219_95-8218ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286523 | |||||||
| chr7:2286524 | T | A | 123 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-8219A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286524 | |||||||
| chr7:2286525 | T | A | 8 | a0001c0001t0002g0254 a0001c0001t0003g0040 a0001c0001t0021g0349 others(5): Show |
8 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8220A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286525 | |||||||
| chr7:2286526 | T | A | 123 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-8221A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286526 | |||||||
| chr7:2286527 | T | A | 8 | a0001c0001t0002g0254 a0001c0001t0003g0040 a0001c0001t0021g0349 others(5): Show |
8 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-8222A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286527 | |||||||
| chr7:2286528 | T | A | 121 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(118): Show |
122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8223A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286528 | |||||||
| chr7:2286529 | T | A | 2 | a0001c0001t0002g0254 a0001c0001t0003g0040 |
2 | HG00639.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.95-8224A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286529 | |||||||
| chr7:2286567 | G | A | 7 | a0001c0001t0040g0009 a0001c0003t0005g0312 a0001c0003t0006g0012 others(4): Show |
7 | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8262C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286567 | |||||||
| chr7:2286580 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-8275G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286580 | |||||||
| chr7:2286614 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-8309C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286614 | |||||||
| chr7:2286624 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.95-8319A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286624 | |||||||
| chr7:2286626 | C | A | 7 | a0003c0007t0012g0011 a0003c0007t0012g0041 a0003c0007t0012g0094 others(4): Show |
7 | HG02818.hp1 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8321G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286626 | |||||||
| chr7:2286651 | C | T | 223 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(220): Show |
227 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.95-8346G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286651 | |||||||
| chr7:2286680 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-8375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286680 | |||||||
| chr7:2286706 | G | C | 7 | a0001c0001t0040g0009 a0001c0003t0005g0312 a0001c0003t0006g0012 others(4): Show |
7 | HG01891.hp1 HG02717.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-8401C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286706 | |||||||
| chr7:2286818 | A | C | 13 | a0001c0002t0004g0036 a0001c0002t0004g0081 a0001c0002t0004g0228 others(10): Show |
13 | HG00558.hp1 HG02698.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-8513T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286818 | |||||||
| chr7:2286927 | T | G | 1 | a0001c0001t0016g0235 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.95-8622A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2286927 | |||||||
| chr7:2287011 | C | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0116 a0001c0001t0003g0117 |
3 | HG02165.hp2 NA18966.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.95-8706G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287011 | |||||||
| chr7:2287181 | C | T | 121 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(118): Show |
122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8876G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287181 | |||||||
| chr7:2287246 | ACT | A | 121 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(118): Show |
122 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.95-8943_95-8942del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287246 | |||||||
| chr7:2287297 | T | C | 1 | a0001c0002t0004g0165 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.95-8992A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287297 | |||||||
| chr7:2287483 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-9178C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287483 | |||||||
| chr7:2287500 | A | G | 1 | a0001c0001t0037g0121 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.95-9195T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287500 | |||||||
| chr7:2287686 | G | A | 1 | a0006c0008t0001g0212 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.95-9381C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287686 | |||||||
| chr7:2287769 | A | AAAC | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-9467_95-9465dup others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287769 | |||||||
| chr7:2287784 | C | A | 8 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(5): Show |
8 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-9479G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287784 | |||||||
| chr7:2287784 | CAAA | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-9482_95-9480del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287784 | |||||||
| chr7:2287787 | A | C | 10 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(7): Show |
10 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-9482T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287787 | |||||||
| chr7:2287811 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-9506C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287811 | |||||||
| chr7:2287869 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-9564G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287869 | |||||||
| chr7:2287894 | GA | G | 8 | a0001c0001t0002g0079 a0001c0001t0002g0189 a0001c0001t0003g0068 others(5): Show |
8 | HG00741.hp1 HG01175.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-9590delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287894 | |||||||
| chr7:2287923 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.95-9618C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287923 | |||||||
| chr7:2287942 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-9637A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287942 | |||||||
| chr7:2287991 | T | C | 1 | a0001c0001t0021g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-9686A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2287991 | |||||||
| chr7:2288084 | C | T | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-9779G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288084 | |||||||
| chr7:2288287 | T | C | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-9982A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288287 | |||||||
| chr7:2288347 | T | TA | 30 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0236 others(27): Show |
31 | HG00738.hp2 HG01099.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-10043dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | |||||||
| chr7:2288347 | T | TAA | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-10044_95-10043d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | |||||||
| chr7:2288347 | TA | T | 45 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(42): Show |
45 | HG00639.hp1 HG01069.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.95-10043delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288347 | |||||||
| chr7:2288580 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.95-10275C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288580 | |||||||
| chr7:2288660 | A | G | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.95-10355T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288660 | |||||||
| chr7:2288951 | G | A | 1 | a0001c0001t0021g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.95-10646C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288951 | |||||||
| chr7:2288989 | A | G | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-10684T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2288989 | |||||||
| chr7:2289059 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.95-10754C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289059 | |||||||
| chr7:2289079 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-10774C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289079 | |||||||
| chr7:2289170 | C | A | 2 | a0001c0003t0005g0290 a0001c0003t0028g0291 |
2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.95-10865G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289170 | |||||||
| chr7:2289186 | C | T | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10881G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289186 | |||||||
| chr7:2289237 | T | C | 2 | a0001c0001t0022g0163 a0001c0001t0022g0164 |
2 | HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.95-10932A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289237 | |||||||
| chr7:2289251 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-10946C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289251 | |||||||
| chr7:2289254 | G | A | 2 | a0001c0001t0041g0150 a0001c0003t0005g0151 |
2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.95-10949C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289254 | |||||||
| chr7:2289276 | G | A | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10971C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289276 | |||||||
| chr7:2289308 | G | A | 2 | a0003c0007t0012g0094 a0003c0007t0012g0131 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.95-11003C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289308 | |||||||
| chr7:2289319 | A | G | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-11014T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289319 | |||||||
| chr7:2289452 | C | G | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-11147G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289452 | |||||||
| chr7:2289495 | G | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-11190C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289495 | |||||||
| chr7:2289560 | T | C | 1 | a0001c0001t0005g0082 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.95-11255A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289560 | |||||||
| chr7:2289647 | A | G | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-11342T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289647 | |||||||
| chr7:2289671 | T | C | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-11366A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289671 | |||||||
| chr7:2289699 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-11394G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289699 | |||||||
| chr7:2289753 | C | T | 1 | a0001c0001t0026g0214 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.95-11448G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289753 | |||||||
| chr7:2289754 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.95-11449C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289754 | |||||||
| chr7:2289809 | G | A | 1 | a0002c0019t0006g0354 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-11504C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289809 | |||||||
| chr7:2289829 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0193 |
2 | HG01496.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.95-11524C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289829 | |||||||
| chr7:2289856 | C | G | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.95-11551G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289856 | |||||||
| chr7:2289862 | G | A | 189 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(186): Show |
190 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.95-11557C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289862 | |||||||
| chr7:2289873 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.95-11568C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289873 | |||||||
| chr7:2289964 | G | A | 26 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-11659C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289964 | |||||||
| chr7:2289967 | T | C | 26 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(23): Show |
26 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.95-11662A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289967 | |||||||
| chr7:2289979 | G | T | 1 | a0001c0001t0025g0110 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.95-11674C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2289979 | |||||||
| chr7:2290428 | CAGGAGGT | C | 28 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-12130_95-12124d others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290428 | |||||||
| chr7:2290510 | TAAAGA | T | 7 | a0001c0001t0001g0175 a0001c0001t0005g0161 a0001c0001t0005g0162 others(4): Show |
7 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-12210_95-12206d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290510 | |||||||
| chr7:2290714 | A | C | 1 | a0001c0001t0002g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.95-12409T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290714 | |||||||
| chr7:2290752 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.95-12447C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290752 | |||||||
| chr7:2290834 | C | T | 8 | a0001c0001t0003g0158 a0001c0001t0003g0279 a0001c0001t0003g0294 others(5): Show |
8 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-12529G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290834 | |||||||
| chr7:2290861 | A | G | 137 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(134): Show |
138 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.95-12556T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290861 | |||||||
| chr7:2290942 | G | C | 1 | a0001c0001t0014g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-12637C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290942 | |||||||
| chr7:2290969 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-12664A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2290969 | |||||||
| chr7:2291151 | C | A | 2 | a0001c0001t0001g0281 a0001c0001t0026g0214 |
2 | HG00738.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.95-12846G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291151 | |||||||
| chr7:2291239 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.95-12934C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291239 | |||||||
| chr7:2291330 | G | A | 1 | a0001c0002t0004g0259 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.95-13025C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291330 | |||||||
| chr7:2291787 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.95-13482T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291787 | |||||||
| chr7:2291934 | C | T | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-13629G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2291934 | |||||||
| chr7:2292092 | T | C | 1 | a0001c0001t0014g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-13787A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292092 | |||||||
| chr7:2292106 | A | C | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-13801T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292106 | |||||||
| chr7:2292109 | C | T | 8 | a0001c0001t0003g0158 a0001c0001t0003g0279 a0001c0001t0003g0294 others(5): Show |
8 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-13804G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292109 | |||||||
| chr7:2292409 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.95-14104C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292409 | |||||||
| chr7:2292443 | G | C | 2 | a0001c0001t0040g0009 a0002c0004t0023g0357 |
2 | HG01891.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.95-14138C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292443 | |||||||
| chr7:2292474 | C | T | 1 | a0001c0001t0017g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.95-14169G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292474 | |||||||
| chr7:2292475 | G | A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-14170C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292475 | |||||||
| chr7:2292480 | C | T | 6 | a0001c0001t0005g0082 a0001c0001t0005g0350 a0001c0001t0005g0351 others(3): Show |
7 | HG01099.hp1 HG01496.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-14175G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292480 | |||||||
| chr7:2292539 | G | C | 2 | a0001c0001t0003g0284 a0001c0001t0003g0322 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.95-14234C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292539 | |||||||
| chr7:2292590 | T | C | 2 | a0001c0001t0003g0284 a0001c0001t0003g0322 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.95-14285A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292590 | |||||||
| chr7:2292704 | C | A | 28 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-14399G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292704 | |||||||
| chr7:2292706 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.95-14401G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292706 | |||||||
| chr7:2292839 | G | T | 1 | a0002c0004t0008g0363 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.95-14534C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292839 | |||||||
| chr7:2292878 | C | T | 1 | a0001c0001t0003g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.95-14573G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2292878 | |||||||
| chr7:2293139 | C | T | 2 | a0001c0001t0005g0161 a0001c0001t0005g0167 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.95-14834G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293139 | |||||||
| chr7:2293245 | G | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-14940C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293245 | |||||||
| chr7:2293333 | G | T | 130 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.95-15028C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293333 | |||||||
| chr7:2293371 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0074 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.95-15066G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293371 | |||||||
| chr7:2293384 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-15079C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293384 | |||||||
| chr7:2293393 | C | T | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-15088G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293393 | |||||||
| chr7:2293422 | A | G | 190 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(187): Show |
191 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.95-15117T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293422 | |||||||
| chr7:2293439 | A | T | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-15134T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293439 | |||||||
| chr7:2293441 | G | C | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-15136C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293441 | |||||||
| chr7:2293469 | C | A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-15164G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293469 | |||||||
| chr7:2293578 | C | A | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-15273G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293578 | |||||||
| chr7:2293604 | G | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-15299C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293604 | |||||||
| chr7:2293618 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.95-15313G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293618 | |||||||
| chr7:2293735 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0033g0126 |
2 | NA18964.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.95-15430G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293735 | |||||||
| chr7:2293907 | A | G | 152 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(149): Show |
153 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.95-15602T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293907 | |||||||
| chr7:2293911 | A | C | 1 | a0001c0001t0008g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-15606T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293911 | |||||||
| chr7:2293966 | C | CA | 30 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(27): Show |
30 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-15662dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293966 | |||||||
| chr7:2293998 | T | C | 2 | a0001c0002t0004g0017 a0001c0002t0004g0166 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.95-15693A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2293998 | |||||||
| chr7:2294026 | G | A | 1 | a0001c0002t0029g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.95-15721C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294026 | |||||||
| chr7:2294268 | T | C | 1 | a0001c0001t0041g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.95-15963A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294268 | |||||||
| chr7:2294309 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16004G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294309 | |||||||
| chr7:2294349 | T | C | 1 | a0001c0002t0010g0342 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.95-16044A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294349 | |||||||
| chr7:2294390 | G | C | 175 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(172): Show |
176 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.95-16085C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294390 | |||||||
| chr7:2294515 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16210A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294515 | |||||||
| chr7:2294518 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.95-16213C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294518 | |||||||
| chr7:2294600 | G | A | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16295C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294600 | |||||||
| chr7:2294693 | G | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16388C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294693 | |||||||
| chr7:2294729 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-16424C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294729 | |||||||
| chr7:2294751 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.95-16446C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294751 | |||||||
| chr7:2294766 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-16461C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294766 | |||||||
| chr7:2294851 | T | C | 1 | a0001c0001t0014g0298 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.95-16546A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2294851 | |||||||
| chr7:2295045 | T | C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-16740A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295045 | |||||||
| chr7:2295131 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16826C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295131 | |||||||
| chr7:2295353 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-17048C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295353 | |||||||
| chr7:2295359 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.95-17054C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295359 | |||||||
| chr7:2295378 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.95-17073C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295378 | |||||||
| chr7:2295402 | C | CA | 145 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(142): Show |
146 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.95-17098dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295402 | |||||||
| chr7:2295465 | G | A | 1 | a0001c0002t0010g0336 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.95-17160C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295465 | |||||||
| chr7:2295563 | G | A | 2 | a0001c0001t0008g0002 a0001c0001t0008g0050 |
3 | HG01081.hp2 HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-17258C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295563 | |||||||
| chr7:2295592 | C | CA | 23 | a0001c0001t0001g0075 a0001c0001t0003g0090 a0001c0001t0003g0115 others(20): Show |
23 | HG00544.hp1 HG00597.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.95-17288dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CA | C | 6 | a0001c0001t0002g0300 a0001c0001t0003g0322 a0001c0001t0019g0071 others(3): Show |
6 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-17288delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAA | C | 7 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(4): Show |
7 | HG00639.hp2 HG02258.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-17290_95-17288d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAA | C | 13 | a0001c0001t0001g0055 a0001c0001t0005g0161 a0001c0001t0005g0162 others(10): Show |
13 | HG01255.hp1 HG02257.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.95-17291_95-17288d others(6): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAAA | C | 28 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(25): Show |
28 | HG01256.hp2 HG01258.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.95-17292_95-17288d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0221 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.95-17298_95-17288d others(13): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-17299_95-17288d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0007g0038 a0001c0005t0015g0035 |
2 | NA18940.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.95-17300_95-17288d others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295592 | CAAAAAAA others(7): Show |
C | 123 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(120): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.95-17301_95-17288d others(16): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295592 | |||||||
| chr7:2295763 | G | A | 1 | a0001c0003t0005g0151 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-17458C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295763 | |||||||
| chr7:2295766 | G | A | 1 | a0001c0005t0001g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.95-17461C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2295766 | |||||||
| chr7:2296038 | G | A | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.95-17733C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296038 | |||||||
| chr7:2296180 | CACAATAT others(2498): Show |
C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15643_95-17876d others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296180 | |||||||
| chr7:2296241 | A | G | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.95-17936T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296241 | |||||||
| chr7:2296453 | T | C | 1 | a0001c0001t0025g0095 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.94+17875A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296453 | |||||||
| chr7:2296517 | T | C | 1 | a0001c0001t0009g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.94+17811A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296517 | |||||||
| chr7:2296559 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+17769T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296559 | |||||||
| chr7:2296671 | C | T | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+17657G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296671 | |||||||
| chr7:2296697 | G | A | 1 | a0001c0002t0029g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94+17631C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296697 | |||||||
| chr7:2296717 | G | C | 2 | a0001c0001t0001g0124 a0001c0005t0001g0154 |
2 | HG00621.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.94+17611C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296717 | |||||||
| chr7:2296759 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.94+17569G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296759 | |||||||
| chr7:2296788 | G | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+17540C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296788 | |||||||
| chr7:2296903 | C | A | 10 | a0001c0001t0007g0271 a0001c0001t0008g0001 a0001c0001t0008g0002 others(7): Show |
12 | HG01081.hp2 HG01192.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+17425G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2296903 | |||||||
| chr7:2297027 | G | A | 1 | a0001c0001t0013g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+17301C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297027 | |||||||
| chr7:2297196 | A | G | 1 | a0001c0001t0019g0224 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.94+17132T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297196 | |||||||
| chr7:2297364 | A | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+16964T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297364 | |||||||
| chr7:2297406 | C | T | 2 | a0001c0001t0003g0039 a0001c0001t0007g0327 |
2 | HG02572.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.94+16922G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297406 | |||||||
| chr7:2297437 | C | G | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+16891G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297437 | |||||||
| chr7:2297525 | G | A | 3 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 |
3 | HG01074.hp2 HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.94+16803C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297525 | |||||||
| chr7:2297550 | C | CA | 69 | a0001c0001t0001g0146 a0001c0001t0001g0193 a0001c0001t0002g0042 others(66): Show |
69 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.94+16777dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | C | CAA | 22 | a0001c0001t0001g0075 a0001c0001t0002g0079 a0001c0001t0002g0097 others(19): Show |
22 | HG00642.hp1 HG00741.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+16776_94+16777d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | C | CAAA | 6 | a0001c0001t0001g0086 a0001c0001t0003g0221 a0002c0004t0018g0358 others(3): Show |
6 | HG01070.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16775_94+16777d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | C | CAAAAA | 62 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0037 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.94+16773_94+16777d others(7): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | C | CAAAAAA | 57 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0124 others(54): Show |
58 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.94+16772_94+16777d others(8): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | C | CAAAAAAA | 6 | a0001c0001t0001g0195 a0001c0001t0001g0198 a0001c0001t0001g0277 others(3): Show |
6 | HG00738.hp2 HG01074.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+16771_94+16777d others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | CA | C | 16 | a0001c0001t0001g0119 a0001c0001t0002g0028 a0001c0001t0002g0043 others(13): Show |
16 | HG02040.hp1 HG02080.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.94+16777delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | CAA | C | 9 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(6): Show |
9 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+16776_94+16777d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297550 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0003g0284 a0001c0001t0024g0099 a0001c0001t0024g0100 |
3 | HG01257.hp1 HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.94+16766_94+16777d others(14): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297550 | |||||||
| chr7:2297647 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0272 |
3 | HG00733.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.94+16681C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297647 | |||||||
| chr7:2297796 | C | G | 4 | a0001c0001t0014g0276 a0001c0001t0014g0293 a0001c0001t0014g0296 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16532G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297796 | |||||||
| chr7:2297838 | C | G | 1 | a0001c0001t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+16490G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297838 | |||||||
| chr7:2297959 | A | G | 1 | a0001c0002t0029g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.94+16369T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297959 | |||||||
| chr7:2297968 | C | T | 3 | a0001c0001t0003g0039 a0001c0001t0007g0327 a0001c0001t0035g0152 |
3 | HG02572.hp1 HG03017.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+16360G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297968 | |||||||
| chr7:2297981 | C | T | 2 | a0001c0005t0001g0059 a0001c0005t0001g0252 |
2 | HG00423.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+16347G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2297981 | |||||||
| chr7:2298023 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+16305A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298023 | |||||||
| chr7:2298072 | T | C | 1 | a0001c0001t0021g0301 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.94+16256A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298072 | |||||||
| chr7:2298087 | C | G | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16241G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298087 | |||||||
| chr7:2298091 | G | A | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+16237C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298091 | |||||||
| chr7:2298130 | A | G | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+16198T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298130 | |||||||
| chr7:2298172 | G | A | 29 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(26): Show |
29 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+16156C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298172 | |||||||
| chr7:2298290 | T | A | 1 | a0001c0001t0008g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.94+16038A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298290 | |||||||
| chr7:2298319 | A | G | 27 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(24): Show |
27 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+16009T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298319 | |||||||
| chr7:2298452 | C | A | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.94+15876G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298452 | |||||||
| chr7:2298662 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+15666T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298662 | |||||||
| chr7:2298690 | G | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15638C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298690 | |||||||
| chr7:2298697 | G | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15631C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298697 | |||||||
| chr7:2298704 | G | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15624C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298704 | |||||||
| chr7:2298714 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15614A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298714 | |||||||
| chr7:2298722 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15606A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298722 | |||||||
| chr7:2298731 | C | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15597G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298731 | |||||||
| chr7:2298737 | C | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15591G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298737 | |||||||
| chr7:2298738 | C | CCGGACTG | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15589_94+15590i others(9): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298738 | |||||||
| chr7:2298739 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15589A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298739 | |||||||
| chr7:2298743 | G | A | 1 | a0001c0001t0009g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.94+15585C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298743 | |||||||
| chr7:2298743 | G | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15585C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298743 | |||||||
| chr7:2298753 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15575T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298753 | |||||||
| chr7:2298755 | G | A | 6 | a0001c0001t0003g0040 a0001c0001t0003g0221 a0001c0001t0021g0349 others(3): Show |
6 | HG00639.hp2 HG01070.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+15573C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298755 | |||||||
| chr7:2298761 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15567T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298761 | |||||||
| chr7:2298773 | C | A | 1 | a0001c0001t0003g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.94+15555G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298773 | |||||||
| chr7:2298773 | C | G | 4 | a0001c0001t0021g0349 a0001c0001t0023g0122 a0001c0001t0041g0150 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+15555G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298773 | |||||||
| chr7:2298778 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15550T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298778 | |||||||
| chr7:2298780 | C | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15548G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298780 | |||||||
| chr7:2298785 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15543T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298785 | |||||||
| chr7:2298792 | A | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15536T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298792 | |||||||
| chr7:2298794 | A | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15534T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298794 | |||||||
| chr7:2298795 | G | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15533C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298795 | |||||||
| chr7:2298802 | A | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15526T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298802 | |||||||
| chr7:2298804 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15524T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298804 | |||||||
| chr7:2298817 | G | A | 2 | a0001c0001t0003g0262 a0001c0001t0013g0076 |
2 | HG00642.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.94+15511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298817 | |||||||
| chr7:2298817 | G | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15511C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298817 | |||||||
| chr7:2298820 | C | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15508G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298820 | |||||||
| chr7:2298829 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15499A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298829 | |||||||
| chr7:2298837 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15491T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298837 | |||||||
| chr7:2298839 | A | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15489T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298839 | |||||||
| chr7:2298840 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15488A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298840 | |||||||
| chr7:2298843 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15485A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298843 | |||||||
| chr7:2298847 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15481T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298847 | |||||||
| chr7:2298852 | T | C | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15476A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298852 | |||||||
| chr7:2298853 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15475T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298853 | |||||||
| chr7:2298866 | G | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15462C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298866 | |||||||
| chr7:2298873 | G | A | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15455C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298873 | |||||||
| chr7:2298882 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15446T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2298882 | |||||||
| chr7:2299079 | A | T | 1 | a0001c0001t0009g0083 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.94+15249T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299079 | |||||||
| chr7:2299300 | T | G | 1 | a0001c0001t0008g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94+15028A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299300 | |||||||
| chr7:2299309 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+15019C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299309 | |||||||
| chr7:2299373 | CAG | C | 9 | a0001c0001t0003g0158 a0001c0001t0003g0221 a0001c0001t0003g0279 others(6): Show |
9 | HG01070.hp2 HG01167.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+14953_94+14954d others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299373 | |||||||
| chr7:2299391 | G | A | 10 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(7): Show |
10 | HG01255.hp1 HG01884.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+14937C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299391 | |||||||
| chr7:2299468 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.94+14860G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299468 | |||||||
| chr7:2299634 | C | G | 1 | a0001c0001t0026g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.94+14694G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299634 | |||||||
| chr7:2299651 | A | G | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+14677T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299651 | |||||||
| chr7:2299770 | G | T | 177 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(174): Show |
178 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.94+14558C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299770 | |||||||
| chr7:2299872 | T | C | 22 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+14456A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299872 | |||||||
| chr7:2299973 | A | C | 6 | a0003c0007t0012g0011 a0003c0007t0012g0041 a0003c0007t0012g0094 others(3): Show |
6 | HG02818.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+14355T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2299973 | |||||||
| chr7:2300247 | C | T | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+14081G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300247 | |||||||
| chr7:2300313 | A | C | 1 | a0001c0002t0004g0156 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94+14015T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300313 | |||||||
| chr7:2300424 | T | C | 7 | a0001c0001t0003g0158 a0001c0001t0003g0294 a0001c0001t0003g0316 others(4): Show |
7 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+13904A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300424 | |||||||
| chr7:2300482 | A | G | 146 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(143): Show |
147 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.94+13846T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300482 | |||||||
| chr7:2300652 | A | T | 48 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(45): Show |
49 | HG01099.hp1 HG01243.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+13676T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300652 | |||||||
| chr7:2300663 | A | C | 13 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0193 others(10): Show |
13 | HG00544.hp1 HG00642.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+13665T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300663 | |||||||
| chr7:2300813 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+13515A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300813 | |||||||
| chr7:2300974 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+13354C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2300974 | |||||||
| chr7:2301007 | C | T | 6 | a0001c0001t0003g0158 a0001c0001t0003g0294 a0001c0001t0003g0316 others(3): Show |
6 | HG02559.hp1 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+13321G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301007 | |||||||
| chr7:2301306 | GCAC | G | 31 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0193 others(28): Show |
31 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+13019_94+13021d others(5): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301306 | |||||||
| chr7:2301325 | G | A | 22 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+13003C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301325 | |||||||
| chr7:2301420 | C | T | 125 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(122): Show |
126 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.94+12908G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301420 | |||||||
| chr7:2301427 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.94+12901C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301427 | |||||||
| chr7:2301462 | G | A | 1 | a0001c0005t0001g0252 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.94+12866C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301462 | |||||||
| chr7:2301516 | G | A | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12812C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301516 | |||||||
| chr7:2301644 | A | C | 3 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 |
3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+12684T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301644 | |||||||
| chr7:2301903 | C | T | 1 | a0002c0004t0005g0364 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.94+12425G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301903 | |||||||
| chr7:2301904 | A | C | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+12424T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301904 | |||||||
| chr7:2301970 | C | T | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12358G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2301970 | |||||||
| chr7:2302028 | G | A | 2 | a0001c0001t0002g0085 a0001c0001t0002g0132 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94+12300C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302028 | |||||||
| chr7:2302089 | A | ACCCTCTC others(17): Show |
1 | a0001c0001t0003g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94+12215_94+12238d others(26): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302089 | |||||||
| chr7:2302106 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0215 a0001c0006t0039g0144 |
3 | HG04199.hp1 NA18960.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.94+12222C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302106 | |||||||
| chr7:2302106 | GACGGTCT others(18): Show |
G | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+12197_94+12221d others(27): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302106 | |||||||
| chr7:2302147 | T | G | 32 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(29): Show |
32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+12181A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302147 | |||||||
| chr7:2302156 | G | A | 2 | a0001c0002t0010g0319 a0001c0002t0010g0347 |
2 | NA19057.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.94+12172C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302156 | |||||||
| chr7:2302240 | T | C | 22 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(19): Show |
22 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(19): Show |
intron_variant | MODIFIER | c.94+12088A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302240 | |||||||
| chr7:2302347 | A | G | 354 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.94+11981T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302347 | |||||||
| chr7:2302356 | G | A | 26 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(23): Show |
26 | HG00544.hp2 HG02056.hp1 NA18747.hp1 others(23): Show |
intron_variant | MODIFIER | c.94+11972C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302356 | |||||||
| chr7:2302391 | A | C | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+11937T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302391 | |||||||
| chr7:2302391 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.94+11937T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302391 | |||||||
| chr7:2302431 | T | C | 119 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(116): Show |
120 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+11897A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302431 | |||||||
| chr7:2302434 | T | C | 120 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(117): Show |
121 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.94+11894A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302434 | |||||||
| chr7:2302461 | C | G | 32 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(29): Show |
32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+11867G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302461 | |||||||
| chr7:2302462 | C | T | 32 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(29): Show |
32 | HG01256.hp2 HG01258.hp2 HG01943.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+11866G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302462 | |||||||
| chr7:2302470 | C | T | 1 | a0001c0002t0004g0288 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.94+11858G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302470 | |||||||
| chr7:2302500 | T | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11828A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302500 | |||||||
| chr7:2302515 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.94+11813C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302515 | |||||||
| chr7:2302541 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+11787C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302541 | |||||||
| chr7:2302547 | CTCTGCCT others(32): Show |
C | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+11742_94+11780d others(41): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302547 | |||||||
| chr7:2302579 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.94+11749C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302579 | |||||||
| chr7:2302586 | T | C | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11742A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302586 | |||||||
| chr7:2302675 | G | A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11653C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302675 | |||||||
| chr7:2302689 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+11639C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302689 | |||||||
| chr7:2302739 | C | T | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11589G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302739 | |||||||
| chr7:2302751 | A | G | 192 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(189): Show |
193 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.94+11577T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302751 | |||||||
| chr7:2302758 | C | T | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11570G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302758 | |||||||
| chr7:2302772 | G | A | 4 | a0001c0006t0013g0174 a0001c0006t0013g0192 a0001c0006t0013g0274 others(1): Show |
4 | HG03831.hp1 HG03927.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+11556C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302772 | |||||||
| chr7:2302817 | G | A | 8 | a0001c0001t0007g0271 a0001c0001t0008g0001 a0001c0001t0008g0002 others(5): Show |
10 | HG01081.hp2 HG01192.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+11511C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302817 | |||||||
| chr7:2302870 | C | T | 1 | a0001c0001t0007g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.94+11458G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302870 | |||||||
| chr7:2302876 | G | A | 1 | a0001c0001t0008g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.94+11452C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302876 | |||||||
| chr7:2302895 | C | CCTCCGCC others(33): Show |
1 | a0001c0001t0002g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.94+11393_94+11432d others(42): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302895 | |||||||
| chr7:2302910 | C | T | 9 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+11418G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302910 | |||||||
| chr7:2302927 | G | A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11401C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2302927 | |||||||
| chr7:2303000 | G | A | 1 | a0001c0001t0003g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.94+11328C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303000 | |||||||
| chr7:2303010 | TGGGGGTC others(41): Show |
T | 1 | a0001c0002t0010g0347 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.94+11270_94+11317d others(50): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303010 | |||||||
| chr7:2303011 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.94+11317C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303011 | |||||||
| chr7:2303023 | C | G | 6 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+11305G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303023 | |||||||
| chr7:2303061 | A | AGGTCAGC others(218): Show |
1 | a0001c0001t0001g0198 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.94+11266_94+11267i others(227): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303061 | |||||||
| chr7:2303074 | A | G | 181 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(178): Show |
182 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.94+11254T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303074 | |||||||
| chr7:2303087 | C | T | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+11241G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303087 | |||||||
| chr7:2303090 | C | T | 1 | a0001c0002t0004g0180 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.94+11238G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303090 | |||||||
| chr7:2303117 | C | A | 1 | a0001c0001t0011g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.94+11211G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303117 | |||||||
| chr7:2303144 | G | A | 2 | a0001c0002t0046g0169 a0001c0005t0001g0218 |
2 | HG00673.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.94+11184C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303144 | |||||||
| chr7:2303168 | A | G | 3 | a0001c0001t0021g0349 a0001c0001t0041g0150 a0001c0003t0005g0151 |
3 | HG02257.hp2 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.94+11160T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303168 | |||||||
| chr7:2303218 | G | A | 166 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(163): Show |
167 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.94+11110C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303218 | |||||||
| chr7:2303234 | AGGGGGTC others(42): Show |
A | 6 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 others(3): Show |
6 | HG01255.hp1 HG03041.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11045_94+11093d others(51): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303234 | |||||||
| chr7:2303287 | G | T | 27 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0304 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.94+11041C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303287 | |||||||
| chr7:2303299 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.94+11029C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303299 | |||||||
| chr7:2303307 | A | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11021T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303307 | |||||||
| chr7:2303309 | C | T | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+11019G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303309 | |||||||
| chr7:2303315 | C | T | 2 | a0001c0006t0013g0231 a0001c0006t0013g0232 |
2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.94+11013G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303315 | |||||||
| chr7:2303347 | C | T | 3 | a0001c0001t0005g0161 a0001c0001t0005g0162 a0001c0001t0005g0167 |
3 | HG03579.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.94+10981G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303347 | |||||||
| chr7:2303360 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+10968C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303360 | |||||||
| chr7:2303382 | C | T | 18 | a0001c0001t0002g0328 a0001c0002t0004g0036 a0001c0002t0004g0081 others(15): Show |
18 | HG00558.hp1 HG00597.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+10946G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303382 | |||||||
| chr7:2303396 | C | A | 1 | a0001c0001t0020g0003 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.94+10932G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303396 | |||||||
| chr7:2303397 | G | A | 7 | a0001c0001t0003g0221 a0001c0001t0005g0161 a0001c0001t0005g0162 others(4): Show |
7 | HG01070.hp2 HG01255.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+10931C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303397 | |||||||
| chr7:2303423 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10905A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303423 | |||||||
| chr7:2303426 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10902C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303426 | |||||||
| chr7:2303441 | C | T | 1 | a0001c0001t0003g0304 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.94+10887G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303441 | |||||||
| chr7:2303453 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.94+10875C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303453 | |||||||
| chr7:2303512 | G | A | 13 | a0001c0002t0004g0036 a0001c0002t0004g0081 a0001c0002t0004g0228 others(10): Show |
13 | HG00558.hp1 HG02698.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+10816C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303512 | |||||||
| chr7:2303521 | A | G | 5 | a0001c0005t0001g0059 a0001c0005t0001g0217 a0001c0005t0001g0218 others(2): Show |
5 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10807T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303521 | |||||||
| chr7:2303544 | C | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10784G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303544 | |||||||
| chr7:2303557 | T | G | 5 | a0001c0005t0001g0059 a0001c0005t0001g0217 a0001c0005t0001g0218 others(2): Show |
5 | HG00423.hp1 HG00673.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10771A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303557 | |||||||
| chr7:2303577 | G | A | 4 | a0001c0001t0002g0189 a0001c0001t0003g0181 a0001c0001t0003g0190 others(1): Show |
4 | HG00741.hp1 HG01981.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+10751C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303577 | |||||||
| chr7:2303656 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0256 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+10672T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303656 | |||||||
| chr7:2303657 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.94+10671G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303657 | |||||||
| chr7:2303664 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0256 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+10664A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303664 | |||||||
| chr7:2303702 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.94+10626T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303702 | |||||||
| chr7:2303727 | A | G | 7 | a0001c0001t0001g0197 a0001c0001t0001g0256 a0001c0001t0002g0028 others(4): Show |
7 | HG00735.hp1 HG01884.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+10601T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303727 | |||||||
| chr7:2303762 | C | G | 5 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0001t0008g0268 others(2): Show |
5 | HG01109.hp1 HG02258.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10566G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303762 | |||||||
| chr7:2303763 | G | A | 1 | a0001c0001t0003g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.94+10565C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303763 | |||||||
| chr7:2303816 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+10512A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303816 | |||||||
| chr7:2303822 | G | T | 7 | a0001c0001t0003g0158 a0001c0001t0003g0279 a0001c0001t0003g0316 others(4): Show |
7 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+10506C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303822 | |||||||
| chr7:2303878 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.94+10450G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303878 | |||||||
| chr7:2303978 | A | T | 124 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(121): Show |
125 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.94+10350T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303978 | |||||||
| chr7:2303979 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.94+10349T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303979 | |||||||
| chr7:2303986 | A | T | 186 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(183): Show |
187 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.94+10342T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303986 | |||||||
| chr7:2303995 | TA | T | 33 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(30): Show |
33 | HG01256.hp2 HG01258.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.94+10332delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2303995 | |||||||
| chr7:2304060 | G | A | 2 | a0001c0005t0001g0059 a0001c0005t0001g0252 |
2 | HG00423.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+10268C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304060 | |||||||
| chr7:2304110 | T | A | 1 | a0001c0003t0005g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+10218A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304110 | |||||||
| chr7:2304129 | T | C | 31 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0193 others(28): Show |
31 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+10199A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304129 | |||||||
| chr7:2304166 | CA | C | 11 | a0001c0001t0001g0196 a0001c0001t0001g0267 a0001c0001t0003g0158 others(8): Show |
11 | HG01167.hp1 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+10161delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304166 | |||||||
| chr7:2304181 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.94+10147T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304181 | |||||||
| chr7:2304271 | A | G | 1 | a0001c0001t0003g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.94+10057T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304271 | |||||||
| chr7:2304272 | C | T | 28 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0294 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10056G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304272 | |||||||
| chr7:2304275 | C | T | 28 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0294 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10053G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304275 | |||||||
| chr7:2304276 | A | G | 28 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0294 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10052T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304276 | |||||||
| chr7:2304282 | C | T | 28 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0294 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10046G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304282 | |||||||
| chr7:2304288 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+10040C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304288 | |||||||
| chr7:2304288 | G | T | 28 | a0001c0001t0001g0227 a0001c0001t0002g0328 a0001c0001t0003g0294 others(25): Show |
28 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.94+10040C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304288 | |||||||
| chr7:2304310 | C | G | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10018G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304310 | |||||||
| chr7:2304311 | A | G | 51 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0182 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.94+10017T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304311 | |||||||
| chr7:2304315 | T | C | 31 | a0001c0001t0001g0182 a0001c0001t0001g0227 a0001c0001t0002g0328 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.94+10013A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304315 | |||||||
| chr7:2304319 | C | A | 19 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0193 others(16): Show |
19 | HG00544.hp1 HG00642.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+10009G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304319 | |||||||
| chr7:2304320 | A | G | 51 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0182 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.94+10008T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304320 | |||||||
| chr7:2304327 | G | A | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+10001C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304327 | |||||||
| chr7:2304333 | A | G | 4 | a0001c0001t0002g0225 a0001c0001t0019g0071 a0001c0001t0019g0223 others(1): Show |
4 | HG01934.hp1 HG03491.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+9995T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304333 | |||||||
| chr7:2304338 | A | T | 1 | a0001c0001t0002g0043 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.94+9990T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304338 | |||||||
| chr7:2304339 | T | C | 13 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0193 others(10): Show |
13 | HG00544.hp1 HG00642.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+9989A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304339 | |||||||
| chr7:2304340 | A | C | 174 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(171): Show |
174 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.94+9988T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304340 | |||||||
| chr7:2304340 | A | G | 1 | a0001c0001t0007g0327 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.94+9988T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304340 | |||||||
| chr7:2304341 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0253 a0001c0003t0005g0010 |
3 | HG02145.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.94+9987C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304341 | |||||||
| chr7:2304344 | A | G | 4 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 others(1): Show |
4 | HG02451.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+9984T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304344 | |||||||
| chr7:2304345 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94+9983G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304345 | |||||||
| chr7:2304360 | G | C | 6 | a0001c0001t0007g0327 a0001c0001t0014g0293 a0001c0001t0014g0296 others(3): Show |
6 | HG00423.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+9968C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304360 | |||||||
| chr7:2304360 | G | T | 2 | a0001c0001t0007g0026 a0001c0001t0007g0027 |
2 | NA18946.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.94+9968C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304360 | |||||||
| chr7:2304361 | G | A | 3 | a0001c0001t0014g0293 a0001c0001t0014g0296 a0001c0001t0034g0297 |
3 | HG02572.hp2 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+9967C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304361 | |||||||
| chr7:2304372 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0269 |
2 | HG01978.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.94+9956T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304372 | |||||||
| chr7:2304401 | A | G | 1 | a0001c0002t0027g0187 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.94+9927T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304401 | |||||||
| chr7:2304405 | G | A | 5 | a0001c0001t0003g0158 a0001c0001t0007g0271 a0001c0002t0004g0017 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+9923C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304405 | |||||||
| chr7:2304406 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+9922A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304406 | |||||||
| chr7:2304416 | C | T | 5 | a0001c0001t0014g0049 a0001c0001t0014g0276 a0001c0001t0014g0293 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9912G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304416 | |||||||
| chr7:2304421 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+9907C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304421 | |||||||
| chr7:2304424 | G | T | 1 | a0001c0001t0001g0269 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.94+9904C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304424 | |||||||
| chr7:2304488 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9840C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304488 | |||||||
| chr7:2304539 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.94+9789T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304539 | |||||||
| chr7:2304568 | C | T | 150 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(147): Show |
151 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.94+9760G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304568 | |||||||
| chr7:2304668 | C | T | 5 | a0001c0001t0003g0040 a0001c0001t0021g0349 a0001c0001t0023g0122 others(2): Show |
5 | HG00639.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+9660G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304668 | |||||||
| chr7:2304738 | G | A | 1 | a0001c0001t0009g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.94+9590C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304738 | |||||||
| chr7:2304830 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+9498C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304830 | |||||||
| chr7:2304860 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.94+9468C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304860 | |||||||
| chr7:2304966 | G | C | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+9362C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2304966 | |||||||
| chr7:2305048 | G | A | 18 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(15): Show |
18 | HG00639.hp2 HG01256.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+9280C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305048 | |||||||
| chr7:2305086 | G | A | 9 | a0001c0001t0001g0173 a0001c0001t0001g0186 a0001c0001t0001g0255 others(6): Show |
9 | HG00621.hp2 NA18612.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+9242C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305086 | |||||||
| chr7:2305093 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+9235C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305093 | |||||||
| chr7:2305110 | C | CA | 5 | a0001c0001t0003g0279 a0001c0001t0003g0316 a0001c0001t0005g0278 others(2): Show |
5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9217dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305110 | |||||||
| chr7:2305213 | C | T | 5 | a0001c0001t0003g0279 a0001c0001t0003g0316 a0001c0001t0005g0278 others(2): Show |
5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9115G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305213 | |||||||
| chr7:2305360 | TTTTG | T | 5 | a0001c0001t0003g0279 a0001c0001t0003g0316 a0001c0001t0005g0278 others(2): Show |
5 | HG01167.hp1 HG01192.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+8964_94+8967del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305360 | |||||||
| chr7:2305456 | T | C | 183 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(180): Show |
186 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.94+8872A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305456 | |||||||
| chr7:2305520 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.94+8808G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305520 | |||||||
| chr7:2305565 | T | C | 3 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 |
3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+8763A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305565 | |||||||
| chr7:2305953 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.94+8375C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2305953 | |||||||
| chr7:2306077 | G | C | 1 | a0003c0007t0012g0133 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+8251C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306077 | |||||||
| chr7:2306139 | T | G | 3 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 |
3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+8189A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306139 | |||||||
| chr7:2306161 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94+8167A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306161 | |||||||
| chr7:2306205 | G | A | 1 | a0001c0001t0035g0152 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.94+8123C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306205 | |||||||
| chr7:2306273 | G | A | 2 | a0001c0001t0002g0042 a0002c0019t0006g0354 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.94+8055C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306273 | |||||||
| chr7:2306300 | G | C | 6 | a0001c0001t0002g0042 a0001c0001t0008g0268 a0001c0001t0035g0152 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+8028C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306300 | |||||||
| chr7:2306400 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.94+7928C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306400 | |||||||
| chr7:2306480 | C | T | 165 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.94+7848G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306480 | |||||||
| chr7:2306493 | T | C | 3 | a0001c0001t0014g0298 a0001c0001t0022g0163 a0001c0001t0022g0164 |
3 | HG02451.hp2 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.94+7835A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306493 | |||||||
| chr7:2306584 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.94+7744G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306584 | |||||||
| chr7:2306638 | C | T | 2 | a0001c0001t0003g0040 a0001c0001t0023g0122 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.94+7690G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306638 | |||||||
| chr7:2306639 | A | T | 8 | a0001c0001t0002g0080 a0001c0001t0002g0097 a0001c0001t0002g0134 others(5): Show |
8 | NA18978.hp1 NA18983.hp2 NA18988.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+7689T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306639 | |||||||
| chr7:2306646 | C | G | 1 | a0001c0001t0036g0025 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.94+7682G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306646 | |||||||
| chr7:2306708 | G | A | 4 | a0002c0004t0018g0358 a0002c0004t0018g0360 a0002c0004t0018g0361 others(1): Show |
4 | HG01884.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+7620C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306708 | |||||||
| chr7:2306739 | T | G | 2 | a0001c0001t0014g0298 a0001c0001t0035g0152 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.94+7589A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306739 | |||||||
| chr7:2306745 | A | G | 4 | a0001c0001t0003g0040 a0001c0001t0003g0140 a0001c0001t0021g0349 others(1): Show |
4 | HG00639.hp2 HG01192.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+7583T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306745 | |||||||
| chr7:2306765 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+7563C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306765 | |||||||
| chr7:2306929 | A | G | 2 | a0001c0001t0021g0301 a0001c0003t0006g0320 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.94+7399T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306929 | |||||||
| chr7:2306977 | T | A | 134 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(131): Show |
135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.94+7351A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306977 | |||||||
| chr7:2306983 | A | AATT | 134 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(131): Show |
135 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.94+7344_94+7345ins others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2306983 | |||||||
| chr7:2307173 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.94+7155A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307173 | |||||||
| chr7:2307273 | AT | A | 186 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.94+7054delA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307273 | |||||||
| chr7:2307359 | G | A | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+6969C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307359 | |||||||
| chr7:2307384 | G | A | 3 | a0001c0001t0035g0152 a0001c0001t0041g0150 a0001c0003t0005g0151 |
3 | HG02257.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+6944C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307384 | |||||||
| chr7:2307403 | C | CG | 13 | a0001c0001t0008g0050 a0001c0001t0014g0049 a0001c0001t0014g0276 others(10): Show |
13 | HG02109.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+6924dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307403 | |||||||
| chr7:2307544 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+6784G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307544 | |||||||
| chr7:2307581 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0256 |
3 | HG01516.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.94+6747C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307581 | |||||||
| chr7:2307606 | TG | T | 3 | a0001c0001t0003g0158 a0001c0001t0030g0157 a0001c0002t0004g0156 |
3 | HG01243.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.94+6721delC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307606 | |||||||
| chr7:2307634 | C | CA | 71 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(68): Show |
72 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.94+6693dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307634 | C | CAA | 21 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0139 others(18): Show |
21 | HG00621.hp1 HG01106.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+6692_94+6693dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307634 | CA | C | 129 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.94+6693delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307634 | CAA | C | 7 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0008g0002 others(4): Show |
8 | HG01081.hp2 HG02145.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+6692_94+6693del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307634 | CAAA | C | 7 | a0001c0001t0002g0042 a0001c0001t0005g0014 a0001c0002t0004g0017 others(4): Show |
7 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6691_94+6693del others(3): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307634 | CAAAA | C | 18 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0092 others(15): Show |
19 | HG01074.hp2 HG01106.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+6690_94+6693del others(4): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307634 | |||||||
| chr7:2307644 | A | T | 3 | a0001c0001t0035g0152 a0001c0001t0041g0150 a0001c0003t0005g0151 |
3 | HG02257.hp2 HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.94+6684T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307644 | |||||||
| chr7:2307657 | AAG | A | 24 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+6669_94+6670del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307657 | |||||||
| chr7:2307798 | G | A | 45 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(42): Show |
46 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.94+6530C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307798 | |||||||
| chr7:2307870 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+6458A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307870 | |||||||
| chr7:2307978 | A | AT | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+6349dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2307978 | |||||||
| chr7:2308118 | C | T | 83 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(80): Show |
84 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.94+6210G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308118 | |||||||
| chr7:2308219 | G | C | 90 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(87): Show |
91 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.94+6109C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308219 | |||||||
| chr7:2308229 | T | C | 16 | a0001c0001t0002g0042 a0002c0004t0005g0004 a0002c0004t0005g0364 others(13): Show |
17 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+6099A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308229 | |||||||
| chr7:2308230 | A | G | 3 | a0001c0001t0003g0040 a0001c0016t0003g0067 a0004c0013t0003g0007 |
3 | HG00639.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.94+6098T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308230 | |||||||
| chr7:2308352 | C | G | 2 | a0001c0001t0003g0040 a0001c0016t0003g0067 |
2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.94+5976G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308352 | |||||||
| chr7:2308447 | C | T | 5 | a0001c0001t0003g0140 a0001c0001t0005g0350 a0001c0001t0005g0351 others(2): Show |
5 | HG01099.hp1 HG01192.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5881G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308447 | |||||||
| chr7:2308496 | C | T | 4 | a0001c0001t0002g0134 a0001c0001t0003g0087 a0001c0001t0003g0088 others(1): Show |
4 | HG02056.hp2 NA18973.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+5832G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308496 | |||||||
| chr7:2308604 | T | G | 1 | a0001c0001t0001g0265 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.94+5724A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308604 | |||||||
| chr7:2308665 | C | CA | 51 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(48): Show |
51 | HG00544.hp2 HG00733.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.94+5662dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308665 | |||||||
| chr7:2308665 | CA | C | 83 | a0001c0001t0001g0075 a0001c0001t0001g0119 a0001c0001t0001g0120 others(80): Show |
84 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.94+5662delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308665 | |||||||
| chr7:2308681 | A | AG | 7 | a0001c0001t0035g0152 a0001c0001t0040g0009 a0001c0001t0041g0150 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5646_94+5647ins others(1): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308681 | |||||||
| chr7:2308687 | A | G | 87 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(84): Show |
88 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+5641T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308687 | |||||||
| chr7:2308704 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.94+5624G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308704 | |||||||
| chr7:2308774 | G | C | 1 | a0001c0001t0002g0266 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94+5554C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308774 | |||||||
| chr7:2308780 | A | AT | 53 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(50): Show |
54 | HG00597.hp1 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.94+5547dupA | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308780 | |||||||
| chr7:2308912 | C | T | 132 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.94+5416G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308912 | |||||||
| chr7:2308915 | G | A | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5413C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308915 | |||||||
| chr7:2308978 | G | A | 7 | a0001c0001t0035g0152 a0001c0001t0040g0009 a0001c0001t0041g0150 others(4): Show |
7 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+5350C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308978 | |||||||
| chr7:2308981 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | NA18952.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.94+5347C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2308981 | |||||||
| chr7:2309017 | G | T | 1 | a0001c0002t0004g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.94+5311C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309017 | |||||||
| chr7:2309052 | G | A | 6 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(3): Show |
6 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+5276C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309052 | |||||||
| chr7:2309131 | C | T | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5197G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309131 | |||||||
| chr7:2309255 | A | C | 151 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(148): Show |
154 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.94+5073T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309255 | |||||||
| chr7:2309280 | G | C | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+5048C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309280 | |||||||
| chr7:2309305 | T | C | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+5023A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309305 | |||||||
| chr7:2309454 | G | A | 1 | a0005c0009t0012g0366 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.94+4874C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309454 | |||||||
| chr7:2309496 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+4832G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309496 | |||||||
| chr7:2309510 | T | C | 48 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(45): Show |
50 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.94+4818A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309510 | |||||||
| chr7:2309624 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.94+4704T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309624 | |||||||
| chr7:2309697 | C | G | 1 | a0001c0001t0008g0002 | 2 | HG01081.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.94+4631G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309697 | |||||||
| chr7:2309717 | G | C | 1 | a0001c0003t0005g0332 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+4611C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309717 | |||||||
| chr7:2309765 | G | A | 1 | a0001c0002t0046g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.94+4563C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309765 | |||||||
| chr7:2309788 | T | C | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+4540A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309788 | |||||||
| chr7:2309835 | T | C | 150 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(147): Show |
153 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.94+4493A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309835 | |||||||
| chr7:2309864 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.94+4464C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309864 | |||||||
| chr7:2309865 | C | T | 2 | a0001c0001t0003g0158 a0001c0001t0030g0157 |
2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.94+4463G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309865 | |||||||
| chr7:2309973 | G | A | 148 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(145): Show |
150 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.94+4355C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2309973 | |||||||
| chr7:2310111 | G | A | 12 | a0001c0001t0001g0338 a0001c0001t0001g0339 a0001c0001t0001g0340 others(9): Show |
12 | HG02040.hp1 HG02080.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+4217C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310111 | |||||||
| chr7:2310151 | G | A | 3 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 |
3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+4177C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310151 | |||||||
| chr7:2310230 | G | A | 1 | a0001c0005t0001g0154 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.94+4098C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310230 | |||||||
| chr7:2310484 | G | A | 1 | a0001c0003t0005g0345 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.94+3844C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310484 | |||||||
| chr7:2310513 | A | G | 11 | a0001c0001t0001g0075 a0001c0001t0002g0073 a0001c0001t0002g0078 others(8): Show |
11 | HG00280.hp2 HG00642.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+3815T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310513 | |||||||
| chr7:2310549 | T | C | 149 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(146): Show |
152 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+3779A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310549 | |||||||
| chr7:2310593 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG01884.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.94+3735G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310593 | |||||||
| chr7:2310681 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.94+3647C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310681 | |||||||
| chr7:2310688 | G | A | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(23): Show |
26 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+3640C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310688 | |||||||
| chr7:2310733 | T | C | 95 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(92): Show |
96 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.94+3595A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310733 | |||||||
| chr7:2310757 | T | TG | 95 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(92): Show |
96 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.94+3570dupC | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310757 | |||||||
| chr7:2310777 | A | G | 1 | a0001c0001t0007g0271 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+3551T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310777 | |||||||
| chr7:2310798 | G | A | 148 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(145): Show |
151 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.94+3530C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310798 | |||||||
| chr7:2310816 | G | A | 101 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(98): Show |
102 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.94+3512C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310816 | |||||||
| chr7:2310845 | C | T | 4 | a0001c0002t0004g0286 a0001c0002t0004g0287 a0001c0002t0004g0288 others(1): Show |
4 | NA18985.hp1 NA19003.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+3483G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310845 | |||||||
| chr7:2310860 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0002g0145 a0001c0006t0039g0144 |
3 | HG03490.hp2 HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.94+3468C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310860 | |||||||
| chr7:2310880 | T | C | 135 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.94+3448A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2310880 | |||||||
| chr7:2311068 | T | A | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+3260A>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311068 | |||||||
| chr7:2311115 | T | G | 14 | a0002c0004t0005g0004 a0002c0004t0005g0364 a0002c0004t0005g0365 others(11): Show |
15 | HG01255.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.94+3213A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311115 | |||||||
| chr7:2311306 | C | G | 1 | a0001c0001t0014g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+3022G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311306 | |||||||
| chr7:2311312 | G | A | 1 | a0001c0003t0005g0010 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+3016C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311312 | |||||||
| chr7:2311324 | C | T | 47 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(44): Show |
49 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+3004G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311324 | |||||||
| chr7:2311373 | C | T | 4 | a0001c0001t0040g0009 a0001c0003t0005g0010 a0001c0003t0006g0012 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+2955G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311373 | |||||||
| chr7:2311447 | G | C | 23 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(20): Show |
23 | HG00423.hp1 HG00597.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+2881C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311447 | |||||||
| chr7:2311554 | C | T | 1 | a0001c0002t0004g0156 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94+2774G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311554 | |||||||
| chr7:2311613 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+2715A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311613 | |||||||
| chr7:2311794 | G | A | 1 | a0001c0001t0007g0271 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+2534C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311794 | |||||||
| chr7:2311810 | G | C | 2 | a0001c0003t0006g0012 a0003c0007t0012g0011 |
2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.94+2518C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311810 | |||||||
| chr7:2311854 | A | G | 149 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(146): Show |
152 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+2474T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311854 | |||||||
| chr7:2311860 | C | T | 1 | a0003c0007t0012g0041 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.94+2468G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311860 | |||||||
| chr7:2311884 | C | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+2444G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2311884 | |||||||
| chr7:2312020 | G | A | 1 | a0001c0002t0004g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.94+2308C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312020 | |||||||
| chr7:2312039 | C | T | 1 | a0001c0002t0004g0285 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.94+2289G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312039 | |||||||
| chr7:2312125 | C | T | 1 | a0001c0001t0020g0003 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.94+2203G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312125 | |||||||
| chr7:2312174 | G | GATCCAGC others(10): Show |
1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2153_94+2154ins others(17): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312174 | |||||||
| chr7:2312176 | A | T | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2152T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312176 | |||||||
| chr7:2312177 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2151T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312177 | |||||||
| chr7:2312179 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2149A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312179 | |||||||
| chr7:2312198 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2130T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312198 | |||||||
| chr7:2312200 | G | C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2128C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312200 | |||||||
| chr7:2312201 | G | C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2127C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312201 | |||||||
| chr7:2312203 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2125C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312203 | |||||||
| chr7:2312209 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2119G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312209 | |||||||
| chr7:2312217 | A | C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2111T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312217 | |||||||
| chr7:2312220 | G | T | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2108C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312220 | |||||||
| chr7:2312224 | CCTCAGGT others(8): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2089_94+2103del others(15): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312224 | |||||||
| chr7:2312268 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.94+2060A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312268 | |||||||
| chr7:2312346 | T | C | 148 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(145): Show |
151 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.94+1982A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312346 | |||||||
| chr7:2312418 | C | A | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1910G>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312418 | |||||||
| chr7:2312581 | GAC | G | 5 | a0001c0003t0006g0044 a0001c0003t0006g0045 a0001c0003t0006g0046 others(2): Show |
5 | HG02109.hp1 HG02451.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1745_94+1746del others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312581 | |||||||
| chr7:2312590 | T | G | 1 | a0001c0001t0014g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.94+1738A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312590 | |||||||
| chr7:2312609 | C | T | 3 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 |
3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+1719G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312609 | |||||||
| chr7:2312727 | C | G | 4 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 others(1): Show |
4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1601G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312727 | |||||||
| chr7:2312741 | A | T | 4 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 others(1): Show |
4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1587T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312741 | |||||||
| chr7:2312747 | CA | C | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1580delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312747 | |||||||
| chr7:2312755 | T | TCC | 24 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(21): Show |
24 | HG00423.hp1 HG00597.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.94+1571_94+1572dup others(2): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312755 | |||||||
| chr7:2312763 | C | G | 2 | a0001c0001t0003g0040 a0001c0016t0003g0067 |
2 | HG00639.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.94+1565G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312763 | |||||||
| chr7:2312912 | T | G | 6 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0009g0148 others(3): Show |
6 | HG00558.hp2 HG01099.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+1416A>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312912 | |||||||
| chr7:2312959 | G | C | 91 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(88): Show |
92 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.94+1369C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312959 | |||||||
| chr7:2312960 | C | G | 4 | a0001c0001t0040g0009 a0001c0003t0005g0010 a0001c0003t0006g0012 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+1368G>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312960 | |||||||
| chr7:2312992 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.94+1336C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2312992 | |||||||
| chr7:2313023 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+1305C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313023 | |||||||
| chr7:2313055 | G | A | 2 | a0001c0002t0010g0347 a0001c0002t0027g0346 |
2 | HG00639.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.94+1273C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313055 | |||||||
| chr7:2313058 | T | C | 91 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(88): Show |
92 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.94+1270A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313058 | |||||||
| chr7:2313090 | A | C | 1 | a0001c0001t0001g0348 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.94+1238T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313090 | |||||||
| chr7:2313090 | A | G | 3 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 |
3 | HG01099.hp1 HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+1238T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313090 | |||||||
| chr7:2313176 | A | C | 103 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(100): Show |
105 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.94+1152T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313176 | |||||||
| chr7:2313189 | G | A | 1 | a0001c0016t0003g0067 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.94+1139C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313189 | |||||||
| chr7:2313195 | A | G | 1 | a0001c0001t0011g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.94+1133T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313195 | |||||||
| chr7:2313317 | G | A | 1 | a0004c0012t0006g0008 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.94+1011C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313317 | |||||||
| chr7:2313391 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94+937A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313391 | |||||||
| chr7:2313523 | C | CA | 7 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0277 others(4): Show |
7 | HG01981.hp2 HG03831.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+804dupT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313523 | |||||||
| chr7:2313523 | CA | C | 107 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(104): Show |
108 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.94+804delT | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313523 | |||||||
| chr7:2313530 | A | G | 84 | a0001c0001t0001g0075 a0001c0001t0001g0086 a0001c0001t0001g0119 others(81): Show |
85 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.94+798T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313530 | |||||||
| chr7:2313535 | A | G | 44 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(41): Show |
45 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.94+793T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313535 | |||||||
| chr7:2313545 | G | C | 2 | a0001c0001t0003g0279 a0001c0001t0005g0278 |
2 | HG01167.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.94+783C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313545 | |||||||
| chr7:2313602 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+726G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313602 | |||||||
| chr7:2313706 | A | T | 18 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(15): Show |
18 | HG00544.hp2 HG02056.hp1 NA18940.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+622T>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313706 | |||||||
| chr7:2313714 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.94+614A>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313714 | |||||||
| chr7:2313732 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.94+596G>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313732 | |||||||
| chr7:2313772 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.94+556C>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313772 | |||||||
| chr7:2313857 | TACTGGCC others(7): Show |
T | 1 | a0001c0002t0004g0282 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.94+457_94+470delGG others(12): Show |
SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313857 | |||||||
| chr7:2313965 | A | G | 298 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(295): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.94+363T>C | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313965 | |||||||
| chr7:2313975 | G | T | 6 | a0001c0001t0005g0013 a0001c0001t0005g0014 a0001c0002t0004g0017 others(3): Show |
6 | HG02280.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+353C>A | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2313975 | |||||||
| chr7:2314008 | A | C | 4 | a0001c0001t0040g0009 a0001c0003t0005g0010 a0001c0003t0006g0012 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+320T>G | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2314008 | |||||||
| chr7:2314220 | G | A | 4 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0021g0349 others(1): Show |
4 | HG01099.hp1 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+108C>T | SNX8 | ENSG00000106266.11 | transcript | ENST00000222990.8 | protein_coding | 1/10 | chr7 | 2314220 |