Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64089 |
| ensemblid | ENSG00000104497.15 |
| hgncid | 14980 |
| symbol | SNX16 |
| name | sorting nexin 16 |
| refseq_nuc | NM_152836.3 |
| refseq_prot | NP_690049.1 |
| ensembl_nuc | ENST00000345957.9 |
| ensembl_prot | ENSP00000322652.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 81799583 |
| end | 81842185 |
| strand | - |
| ver | v1.2 |
| region | chr8:81799583-81842185 |
| region5000 | chr8:81794583-81847185 |
| regionname0 | SNX16_chr8_81799583_81842185 |
| regionname5000 | SNX16_chr8_81794583_81847185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 344 | 300 | 77 | 69 | 96 | 10 | 46 | 70 | SNX16_chr8_81794583_81847185 | SNX16 | MATPY others(339): Show |
chr8 | 81794583 | 81847185 |
| a0002 | 0/0 | 344 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | MATPY others(339): Show |
chr8 | 81794583 | 81847185 |
| a0003 | 0/0 | 344 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | MATPY others(339): Show |
chr8 | 81794583 | 81847185 |
| a0004 | 0/0 | 120 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | MATPY others(115): Show |
chr8 | 81794583 | 81847185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1032 | 231 | 75 | 51 | 62 | 7 | 34 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1027): Show |
chr8 | 81794583 | 81847185 | ||
| a0001c0002 | 0/0 | 1032 | 68 | 2 | 18 | 33 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1027): Show |
chr8 | 81794583 | 81847185 | ||
| a0001c0005 | 0/0 | 1032 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1027): Show |
chr8 | 81794583 | 81847185 | ||
| a0002c0003 | 0/0 | 1032 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1027): Show |
chr8 | 81794583 | 81847185 | ||
| a0003c0004 | 0/0 | 1032 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1027): Show |
chr8 | 81794583 | 81847185 | ||
| a0004c0006 | 0/0 | 1012 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | ATGGC others(1007): Show |
chr8 | 81794583 | 81847185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3111 | 77 | 41 | 18 | 3 | 4 | 11 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0002 | 0/1 | 3109 | 68 | 4 | 17 | 33 | 1 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0004 | 0/0 | 3111 | 42 | 3 | 10 | 22 | 1 | 6 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0005 | 0/0 | 3111 | 15 | 5 | 5 | 0 | 1 | 4 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0006 | 0/0 | 3111 | 13 | 13 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0007 | 0/0 | 3111 | 4 | 4 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0008 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0009 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0010 | 1/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0012 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0013 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0014 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0015 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0016 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0017 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0001t0018 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3104): Show |
chr8 | 81794583 | 81847185 |
| a0001c0002t0003 | 0/0 | 3111 | 67 | 2 | 18 | 32 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0002t0011 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0001c0005t0004 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0002c0003t0007 | 0/0 | 3111 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0003c0004t0004 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3106): Show |
chr8 | 81794583 | 81847185 |
| a0004c0006t0006 | 0/0 | 3091 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | AAGGA others(3086): Show |
chr8 | 81794583 | 81847185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 9 | 0 | 2 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0008 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0002 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0007 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0002g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0031 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0007g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0008g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0010g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0015g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0016g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0001t0018g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0002t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0001c0005t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0002c0003t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0002c0003t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0003c0004t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0003c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| a0004c0006t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0094 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0095 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0137 | EUR | FIN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00558 | hp1 | a0001 | c0001 | t0013 | g0204 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0106 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0102 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00673 | hp2 | a0001 | c0005 | t0004 | g0126 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00733 | hp2 | a0001 | c0001 | t0015 | g0196 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0101 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0085 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0192 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01109 | hp2 | a0001 | c0002 | t0003 | g0076 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0073 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01169 | hp2 | a0004 | c0006 | t0006 | g0212 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0098 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0153 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01256 | hp1 | a0001 | c0002 | t0003 | g0111 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0097 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0096 | EUR | IBS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0182 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0104 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0110 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0090 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02015 | hp2 | a0001 | c0002 | t0011 | g0084 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02080 | hp2 | a0001 | c0001 | t0017 | g0218 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0109 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0208 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0031 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02572 | hp2 | a0002 | c0003 | t0007 | g0029 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0181 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0078 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0103 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02683 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0089 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02723 | hp1 | a0001 | c0001 | t0012 | g0141 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0158 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02818 | hp2 | a0002 | c0003 | t0007 | g0029 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0185 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0161 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0151 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0128 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03486 | hp1 | a0003 | c0004 | t0004 | g0115 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0083 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0155 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0105 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0088 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0222 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0100 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0156 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0157 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0129 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0107 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0093 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | CHB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | CHB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18906 | hp1 | a0003 | c0004 | t0004 | g0116 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18947 | hp1 | a0001 | c0001 | t0014 | g0197 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18951 | hp1 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18957 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0216 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0215 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19063 | hp1 | a0001 | c0001 | t0016 | g0224 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0160 | EUR | TSI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | GIH | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0086 | SAS | GIH | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0033 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0226 | REF | REF | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0052 | REF | REF | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:81801499 | A | G | 1 | a0001 | 1 | HG00558.hp1 | stop_lost | HIGH | c.1033T>C | p.Ter345Glnext*? | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1193/3109 | 1033/1035 | 345/344 | chr8 | 81801499 | |||
| chr8:81839610 | ACAGTAAA others(14): Show |
A | 1 | a0004 | 1 | HG01169.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.356_375+1delAAGAAA others(15): Show |
p.Glu119fs | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 356/1035 | 119/344 | chr8 | 81839610 | ||||
| chr8:81839694 | G | A | 1 | a0002 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.293C>T | p.Pro98Leu | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 453/3109 | 293/1035 | 98/344 | chr8 | 81839694 | |||
| chr8:81839722 | T | C | 1 | a0003 | 2 | HG03486.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.265A>G | p.Arg89Gly | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 425/3109 | 265/1035 | 89/344 | chr8 | 81839722 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:81803109 | A | C | 1 | a0001c0005 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.801T>G | p.Thr267Thr | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/8 | 961/3109 | 801/1035 | 267/344 | chr8 | 81803109 | |||
| chr8:81815334 | T | C | 1 | a0001c0002 | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
synonymous_variant | LOW | c.672A>G | p.Glu224Glu | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/8 | 832/3109 | 672/1035 | 224/344 | chr8 | 81815334 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:81799615 | T | A | 1 | a0001c0001t0009 | 2 | HG02055.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1882A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1882 | chr8 | 81799615 | ||||||
| chr8:81799692 | A | C | 1 | a0001c0001t0015 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1805T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1805 | chr8 | 81799692 | ||||||
| chr8:81799768 | C | T | 1 | a0001c0001t0008 | 2 | HG03540.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1729G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1729 | chr8 | 81799768 | ||||||
| chr8:81799918 | A | G | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0007 others(8): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1579T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1579 | chr8 | 81799918 | ||||||
| chr8:81799962 | T | C | 1 | a0001c0001t0017 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1535 | chr8 | 81799962 | ||||||
| chr8:81799999 | C | T | 1 | a0001c0001t0016 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1498 | chr8 | 81799999 | ||||||
| chr8:81800007 | C | CAA | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(12): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1489_*1490insTT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1489 | chr8 | 81800007 | ||||||
| chr8:81800090 | A | G | 2 | a0001c0001t0005 a0001c0001t0015 |
16 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1407T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1407 | chr8 | 81800090 | ||||||
| chr8:81800190 | C | T | 1 | a0001c0001t0014 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1307 | chr8 | 81800190 | ||||||
| chr8:81800213 | C | T | 1 | a0001c0002t0011 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1284 | chr8 | 81800213 | ||||||
| chr8:81800694 | A | C | 3 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 803 | chr8 | 81800694 | ||||||
| chr8:81800891 | G | C | 3 | a0001c0001t0004 a0001c0005t0004 a0003c0004t0004 |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*606C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 606 | chr8 | 81800891 | ||||||
| chr8:81800988 | G | A | 2 | a0001c0002t0003 a0001c0002t0011 |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*509C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 509 | chr8 | 81800988 | ||||||
| chr8:81801169 | C | A | 1 | a0001c0001t0012 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 328 | chr8 | 81801169 | ||||||
| chr8:81801460 | T | C | 1 | a0001c0001t0018 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 37 | chr8 | 81801460 | ||||||
| chr8:81840056 | A | G | 6 | a0001c0001t0004 a0001c0001t0012 a0001c0002t0003 others(3): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-70T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 70 | chr8 | 81840056 | ||||||
| chr8:81842130 | C | A | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(15): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
5_prime_UTR_variant | MODIFIER | c.-105G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/8 | 2144 | chr8 | 81842130 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:81801597 | C | CA | 51 | a0001c0001t0012g0141 a0001c0002t0003g0003 a0001c0002t0003g0011 others(48): Show |
69 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(66): Show |
splice_region_variant&intron_variant | LOW | c.939-5dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801597 | |||||||
| chr8:81801597 | C | CAA | 35 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(32): Show |
44 | HG00280.hp1 HG00423.hp2 HG01099.hp2 others(41): Show |
splice_region_variant&intron_variant | LOW | c.939-6_939-5dupTT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801597 | |||||||
| chr8:81801647 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.939-54T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801647 | |||||||
| chr8:81801695 | A | AGAGT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.939-103_939-102ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801695 | |||||||
| chr8:81801783 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.939-190C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801783 | |||||||
| chr8:81801787 | G | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(33): Show |
63 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.939-194C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801787 | |||||||
| chr8:81801924 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0140 |
2 | NA18950.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.939-331A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801924 | |||||||
| chr8:81802089 | T | TA | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.938+290dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802089 | |||||||
| chr8:81802092 | A | G | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.938+288T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802092 | |||||||
| chr8:81802103 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.938+277T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802103 | |||||||
| chr8:81802186 | T | A | 2 | a0003c0004t0004g0115 a0003c0004t0004g0116 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.938+194A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802186 | |||||||
| chr8:81802246 | A | G | 1 | a0001c0001t0007g0216 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.938+134T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802246 | |||||||
| chr8:81802262 | C | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.938+118G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802262 | |||||||
| chr8:81802344 | C | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0114 |
3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.938+36G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802344 | |||||||
| chr8:81802685 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.819-186A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802685 | |||||||
| chr8:81802823 | T | A | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.818+269A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802823 | |||||||
| chr8:81802918 | T | C | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.818+174A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802918 | |||||||
| chr8:81802976 | GC | G | 34 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(31): Show |
42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.818+115delG | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802976 | |||||||
| chr8:81802990 | G | A | 6 | a0001c0001t0004g0006 a0001c0001t0004g0120 a0001c0001t0004g0121 others(3): Show |
10 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.818+102C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802990 | |||||||
| chr8:81803380 | C | A | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.682-152G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803380 | |||||||
| chr8:81803516 | T | C | 1 | a0001c0002t0003g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.682-288A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803516 | |||||||
| chr8:81803561 | A | G | 1 | a0001c0002t0003g0070 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682-333T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803561 | |||||||
| chr8:81803617 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-389G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803617 | |||||||
| chr8:81803900 | T | C | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-672A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803900 | |||||||
| chr8:81803931 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-703T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803931 | |||||||
| chr8:81803963 | A | AAT | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-737_682-736dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803963 | |||||||
| chr8:81804033 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-805C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804033 | |||||||
| chr8:81804194 | GAAAC | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0120 a0001c0001t0004g0121 others(3): Show |
10 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.682-970_682-967del others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804194 | |||||||
| chr8:81804334 | A | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1106T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804334 | |||||||
| chr8:81804578 | T | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(32): Show |
62 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.682-1350A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804578 | |||||||
| chr8:81804661 | A | G | 1 | a0001c0002t0003g0104 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682-1433T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804661 | |||||||
| chr8:81804671 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1443G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804671 | |||||||
| chr8:81804748 | A | G | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-1520T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804748 | |||||||
| chr8:81804802 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.682-1574G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804802 | |||||||
| chr8:81804965 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.682-1737C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804965 | |||||||
| chr8:81805023 | T | TA | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1796_682-1795i others(3): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805023 | |||||||
| chr8:81805087 | G | A | 1 | a0001c0001t0006g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.682-1859C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805087 | |||||||
| chr8:81805215 | A | T | 2 | a0001c0001t0004g0134 a0001c0001t0004g0135 |
2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.682-1987T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805215 | |||||||
| chr8:81805218 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.682-1990T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805218 | |||||||
| chr8:81805435 | A | C | 1 | a0001c0002t0003g0081 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.682-2207T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805435 | |||||||
| chr8:81805440 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.682-2212T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805440 | |||||||
| chr8:81805458 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2230G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805458 | |||||||
| chr8:81805541 | G | T | 1 | a0001c0001t0004g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682-2313C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805541 | |||||||
| chr8:81805790 | G | A | 1 | a0001c0002t0003g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.682-2562C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805790 | |||||||
| chr8:81805791 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2563T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805791 | |||||||
| chr8:81805793 | G | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2565C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805793 | |||||||
| chr8:81805808 | A | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2580T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805808 | |||||||
| chr8:81805853 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.682-2625C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805853 | |||||||
| chr8:81805872 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.682-2644T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805872 | |||||||
| chr8:81805904 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2676C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805904 | |||||||
| chr8:81805915 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.682-2687A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805915 | |||||||
| chr8:81805919 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2691G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805919 | |||||||
| chr8:81805921 | C | CA | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-2694dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805921 | |||||||
| chr8:81806102 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.682-2874A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806102 | |||||||
| chr8:81806429 | G | A | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-3201C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806429 | |||||||
| chr8:81806495 | T | C | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-3267A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806495 | |||||||
| chr8:81806619 | T | G | 1 | a0001c0002t0003g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.682-3391A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806619 | |||||||
| chr8:81806765 | T | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-3537A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806765 | |||||||
| chr8:81806771 | A | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0162 |
2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.682-3543T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806771 | |||||||
| chr8:81806787 | AAACT | A | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-3563_682-3560d others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806787 | |||||||
| chr8:81806903 | C | A | 2 | a0001c0002t0003g0079 a0001c0002t0003g0082 |
2 | NA18957.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.682-3675G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806903 | |||||||
| chr8:81806951 | TA | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(33): Show |
63 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.682-3724delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806951 | |||||||
| chr8:81807056 | T | C | 1 | a0001c0002t0011g0084 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682-3828A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807056 | |||||||
| chr8:81807066 | A | G | 1 | a0001c0002t0003g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.682-3838T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807066 | |||||||
| chr8:81807348 | G | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4120C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807348 | |||||||
| chr8:81807374 | C | A | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.682-4146G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807374 | |||||||
| chr8:81807378 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4150T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807378 | |||||||
| chr8:81807427 | G | A | 29 | a0001c0002t0003g0011 a0001c0002t0003g0012 a0001c0002t0003g0014 others(26): Show |
36 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.682-4199C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807427 | |||||||
| chr8:81807501 | A | G | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-4273T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807501 | |||||||
| chr8:81807518 | C | CA | 56 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0053 others(53): Show |
66 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.682-4291dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | C | CAA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0060 a0001c0001t0001g0065 others(14): Show |
26 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.682-4292_682-4291d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | C | CAAA | 8 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0067 others(5): Show |
8 | HG01255.hp1 HG01993.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-4293_682-4291d others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | C | CAAAA | 5 | a0001c0001t0005g0031 a0001c0001t0005g0145 a0001c0001t0005g0154 others(2): Show |
6 | HG00733.hp2 HG00738.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-4294_682-4291d others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | CA | C | 7 | a0001c0001t0002g0172 a0001c0001t0002g0220 a0001c0001t0006g0182 others(4): Show |
7 | HG01884.hp2 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-4291delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | CAAAAAA | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(30): Show |
59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.682-4296_682-4291d others(8): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807518 | CAAAAAAA others(8): Show |
C | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-4305_682-4291d others(17): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | |||||||
| chr8:81807573 | G | A | 1 | a0001c0001t0001g0005 | 5 | HG01952.hp2 HG01975.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-4345C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807573 | |||||||
| chr8:81807587 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.682-4359T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807587 | |||||||
| chr8:81807872 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.682-4644A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807872 | |||||||
| chr8:81807921 | C | T | 34 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(31): Show |
42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.682-4693G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807921 | |||||||
| chr8:81807930 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.682-4702G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807930 | |||||||
| chr8:81807962 | C | T | 1 | a0001c0002t0003g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.682-4734G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807962 | |||||||
| chr8:81808116 | C | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4888G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808116 | |||||||
| chr8:81808169 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4941A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808169 | |||||||
| chr8:81808362 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.682-5134C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808362 | |||||||
| chr8:81808373 | C | A | 1 | a0001c0001t0014g0197 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.682-5145G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808373 | |||||||
| chr8:81808465 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
78 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.682-5237C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808465 | |||||||
| chr8:81808490 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-5262A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808490 | |||||||
| chr8:81808525 | G | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5297C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808525 | |||||||
| chr8:81808636 | A | G | 34 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(31): Show |
42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.682-5408T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808636 | |||||||
| chr8:81808668 | C | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-5440G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808668 | |||||||
| chr8:81808689 | G | A | 2 | a0001c0001t0004g0026 a0001c0001t0004g0114 |
3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682-5461C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808689 | |||||||
| chr8:81808810 | G | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5582C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808810 | |||||||
| chr8:81809068 | T | A | 1 | a0001c0001t0005g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.682-5840A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809068 | |||||||
| chr8:81809125 | G | C | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-5897C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809125 | |||||||
| chr8:81809155 | C | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5927G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809155 | |||||||
| chr8:81809333 | T | C | 2 | a0001c0001t0004g0026 a0001c0001t0004g0114 |
3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+5992A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809333 | |||||||
| chr8:81809356 | T | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+5969A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809356 | |||||||
| chr8:81809433 | T | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+5892A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809433 | |||||||
| chr8:81809439 | T | TA | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+5885dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809439 | |||||||
| chr8:81809454 | C | A | 1 | a0001c0002t0003g0111 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.681+5871G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809454 | |||||||
| chr8:81809587 | C | T | 2 | a0001c0001t0005g0150 a0001c0001t0005g0161 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.681+5738G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809587 | |||||||
| chr8:81809615 | G | A | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+5710C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809615 | |||||||
| chr8:81809700 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.681+5625A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809700 | |||||||
| chr8:81809794 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0163 |
2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.681+5531C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809794 | |||||||
| chr8:81809851 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.681+5474A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809851 | |||||||
| chr8:81809899 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+5426T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809899 | |||||||
| chr8:81809926 | T | G | 1 | a0001c0001t0004g0136 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.681+5399A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809926 | |||||||
| chr8:81810148 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.681+5177C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810148 | |||||||
| chr8:81810309 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+5016G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810309 | |||||||
| chr8:81810401 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.681+4924A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810401 | |||||||
| chr8:81810475 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.681+4850A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810475 | |||||||
| chr8:81810486 | T | A | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.681+4839A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810486 | |||||||
| chr8:81810508 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.681+4817C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810508 | |||||||
| chr8:81810548 | T | G | 1 | a0001c0002t0003g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.681+4777A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810548 | |||||||
| chr8:81810582 | T | C | 5 | a0001c0001t0004g0026 a0001c0001t0006g0181 a0001c0001t0006g0189 others(2): Show |
6 | HG01261.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+4743A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810582 | |||||||
| chr8:81810634 | G | A | 1 | a0001c0001t0004g0026 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.681+4691C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810634 | |||||||
| chr8:81810727 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+4598G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810727 | |||||||
| chr8:81810759 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.681+4566A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810759 | |||||||
| chr8:81810817 | C | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.681+4508G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810817 | |||||||
| chr8:81810876 | A | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+4449T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810876 | |||||||
| chr8:81810949 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+4376G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810949 | |||||||
| chr8:81811045 | C | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0065 others(1): Show |
9 | HG02109.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+4280G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811045 | |||||||
| chr8:81811093 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.681+4232A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811093 | |||||||
| chr8:81811101 | T | G | 1 | a0001c0001t0001g0017 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.681+4224A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811101 | |||||||
| chr8:81811173 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.681+4152G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811173 | |||||||
| chr8:81811308 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.681+4017T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811308 | |||||||
| chr8:81811439 | T | C | 2 | a0001c0001t0002g0142 a0001c0001t0002g0162 |
2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.681+3886A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811439 | |||||||
| chr8:81811574 | TGAG | T | 3 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0208 |
3 | HG02145.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.681+3748_681+3750d others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811574 | |||||||
| chr8:81811620 | G | A | 1 | a0001c0001t0006g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.681+3705C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811620 | |||||||
| chr8:81811634 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+3691G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811634 | |||||||
| chr8:81811727 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.681+3598A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811727 | |||||||
| chr8:81811756 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.681+3569A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811756 | |||||||
| chr8:81811821 | T | C | 1 | a0001c0002t0003g0073 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.681+3504A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811821 | |||||||
| chr8:81811912 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+3413T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811912 | |||||||
| chr8:81812056 | G | C | 1 | a0001c0001t0009g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.681+3269C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812056 | |||||||
| chr8:81812091 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+3234A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812091 | |||||||
| chr8:81812194 | A | G | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.681+3131T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812194 | |||||||
| chr8:81812296 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+3029T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812296 | |||||||
| chr8:81812727 | C | T | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(84): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.681+2598G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812727 | |||||||
| chr8:81812806 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.681+2519T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812806 | |||||||
| chr8:81812899 | T | C | 1 | a0001c0001t0017g0218 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.681+2426A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812899 | |||||||
| chr8:81812944 | T | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0195 |
2 | NA18964.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.681+2381A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812944 | |||||||
| chr8:81812993 | G | T | 1 | a0001c0001t0004g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.681+2332C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812993 | |||||||
| chr8:81813238 | A | AAC | 2 | a0001c0001t0004g0026 a0001c0001t0004g0114 |
3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+2085_681+2086d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813238 | |||||||
| chr8:81813342 | C | T | 29 | a0001c0002t0003g0011 a0001c0002t0003g0012 a0001c0002t0003g0014 others(26): Show |
36 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.681+1983G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813342 | |||||||
| chr8:81813416 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0044 |
5 | HG01081.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+1909G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813416 | |||||||
| chr8:81813529 | AAG | A | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+1794_681+1795d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813529 | |||||||
| chr8:81813631 | G | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+1694C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813631 | |||||||
| chr8:81813648 | T | G | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+1677A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813648 | |||||||
| chr8:81813671 | C | T | 11 | a0001c0002t0003g0003 a0001c0002t0003g0024 a0001c0002t0003g0069 others(8): Show |
18 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.681+1654G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813671 | |||||||
| chr8:81813678 | T | C | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.681+1647A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813678 | |||||||
| chr8:81813895 | GGCTAT | G | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+1425_681+1429d others(7): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813895 | |||||||
| chr8:81813905 | C | T | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.681+1420G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813905 | |||||||
| chr8:81814140 | C | T | 3 | a0001c0001t0004g0117 a0001c0001t0004g0125 a0001c0001t0004g0139 |
3 | HG03927.hp2 NA18951.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.681+1185G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814140 | |||||||
| chr8:81814250 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.681+1075T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814250 | |||||||
| chr8:81814447 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.681+878C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814447 | |||||||
| chr8:81814497 | G | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+828C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814497 | |||||||
| chr8:81814913 | C | T | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+412G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814913 | |||||||
| chr8:81814966 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+359A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814966 | |||||||
| chr8:81815061 | T | C | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681+264A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815061 | |||||||
| chr8:81815074 | A | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.681+251T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815074 | |||||||
| chr8:81815094 | T | C | 32 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(29): Show |
40 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+231A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815094 | |||||||
| chr8:81815122 | T | G | 1 | a0001c0002t0003g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681+203A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815122 | |||||||
| chr8:81815142 | G | C | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681+183C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815142 | |||||||
| chr8:81815280 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+45G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815280 | |||||||
| chr8:81815285 | A | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+40T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815285 | |||||||
| chr8:81815405 | GA | G | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.612-12delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815405 | |||||||
| chr8:81815598 | A | G | 1 | a0001c0002t0003g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.612-204T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815598 | |||||||
| chr8:81815789 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.612-395A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815789 | |||||||
| chr8:81815879 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-485A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815879 | |||||||
| chr8:81816068 | T | A | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.612-674A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816068 | |||||||
| chr8:81816089 | C | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-695G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816089 | |||||||
| chr8:81816181 | C | CTTTTT | 50 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(47): Show |
67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.612-792_612-788dup others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | |||||||
| chr8:81816181 | C | CTTTTTT | 12 | a0001c0001t0004g0026 a0001c0001t0004g0028 a0001c0001t0004g0113 others(9): Show |
14 | HG00280.hp1 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.612-793_612-788dup others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | |||||||
| chr8:81816181 | C | CTTTTTTT | 22 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(19): Show |
29 | HG00423.hp2 HG00673.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.612-794_612-788dup others(7): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | |||||||
| chr8:81816181 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.612-787G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | |||||||
| chr8:81816186 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.612-792A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816186 | |||||||
| chr8:81816303 | C | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(34): Show |
64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.612-909G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816303 | |||||||
| chr8:81816731 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0035 |
3 | HG01081.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.612-1337G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816731 | |||||||
| chr8:81816848 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-1454G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816848 | |||||||
| chr8:81816975 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.612-1581T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816975 | |||||||
| chr8:81817139 | C | T | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-1745G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817139 | |||||||
| chr8:81817253 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.612-1859G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817253 | |||||||
| chr8:81817296 | A | G | 1 | a0001c0002t0003g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.612-1902T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817296 | |||||||
| chr8:81817355 | G | A | 1 | a0001c0001t0018g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612-1961C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817355 | |||||||
| chr8:81817439 | C | A | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.612-2045G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817439 | |||||||
| chr8:81817563 | C | A | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612-2169G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817563 | |||||||
| chr8:81817720 | C | T | 5 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0168 others(2): Show |
5 | HG00741.hp2 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2326G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817720 | |||||||
| chr8:81817721 | A | G | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612-2327T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817721 | |||||||
| chr8:81818042 | T | C | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.612-2648A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818042 | |||||||
| chr8:81818050 | C | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2656G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818050 | |||||||
| chr8:81818051 | C | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2657G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818051 | |||||||
| chr8:81818052 | T | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2658A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818052 | |||||||
| chr8:81818059 | T | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2665A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818059 | |||||||
| chr8:81818060 | T | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2666A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818060 | |||||||
| chr8:81818086 | G | T | 1 | a0001c0001t0002g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.612-2692C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818086 | |||||||
| chr8:81818657 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.612-3263A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818657 | |||||||
| chr8:81818680 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.612-3286A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818680 | |||||||
| chr8:81818704 | G | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-3310C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818704 | |||||||
| chr8:81818789 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.612-3395G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818789 | |||||||
| chr8:81818922 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(153): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.612-3528A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818922 | |||||||
| chr8:81819171 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-3777G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819171 | |||||||
| chr8:81819242 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.612-3848C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819242 | |||||||
| chr8:81819569 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG01346.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.612-4175C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819569 | |||||||
| chr8:81819714 | ATC | A | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.611+4076_611+4077d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819714 | |||||||
| chr8:81819764 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.611+4028G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819764 | |||||||
| chr8:81819778 | T | C | 1 | a0001c0001t0004g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.611+4014A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819778 | |||||||
| chr8:81820231 | AT | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+3560delA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820231 | |||||||
| chr8:81820233 | T | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.611+3559A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820233 | |||||||
| chr8:81820256 | T | TA | 18 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(15): Show |
21 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.611+3535dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820256 | |||||||
| chr8:81820280 | C | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.611+3512G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820280 | |||||||
| chr8:81820370 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+3422A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820370 | |||||||
| chr8:81820476 | A | G | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+3316T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820476 | |||||||
| chr8:81820487 | G | C | 1 | a0004c0006t0006g0212 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.611+3305C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820487 | |||||||
| chr8:81820505 | C | G | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.611+3287G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820505 | |||||||
| chr8:81820590 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3202A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820590 | |||||||
| chr8:81820594 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3198G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820594 | |||||||
| chr8:81820596 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3196A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820596 | |||||||
| chr8:81820602 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3190A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820602 | |||||||
| chr8:81820603 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3189A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820603 | |||||||
| chr8:81820607 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3185A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820607 | |||||||
| chr8:81820608 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3184C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820608 | |||||||
| chr8:81820608 | G | T | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.611+3184C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820608 | |||||||
| chr8:81820610 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3182A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820610 | |||||||
| chr8:81820611 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3181A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820611 | |||||||
| chr8:81820613 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3179A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820613 | |||||||
| chr8:81820614 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3178C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820614 | |||||||
| chr8:81820616 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3176G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820616 | |||||||
| chr8:81820618 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3174A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820618 | |||||||
| chr8:81820619 | A | T | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3173T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820619 | |||||||
| chr8:81820622 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3170A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820622 | |||||||
| chr8:81820623 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3169G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820623 | |||||||
| chr8:81820814 | G | A | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.611+2978C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820814 | |||||||
| chr8:81820905 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+2887G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820905 | |||||||
| chr8:81821004 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+2788T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821004 | |||||||
| chr8:81821132 | C | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.611+2660G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821132 | |||||||
| chr8:81821134 | A | C | 2 | a0003c0004t0004g0115 a0003c0004t0004g0116 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.611+2658T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821134 | |||||||
| chr8:81821160 | A | T | 11 | a0001c0002t0003g0003 a0001c0002t0003g0024 a0001c0002t0003g0069 others(8): Show |
18 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.611+2632T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821160 | |||||||
| chr8:81821352 | T | C | 1 | a0001c0002t0003g0086 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.611+2440A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821352 | |||||||
| chr8:81821369 | G | T | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+2423C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821369 | |||||||
| chr8:81821428 | G | A | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.611+2364C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821428 | |||||||
| chr8:81821512 | A | T | 2 | a0001c0001t0002g0220 a0001c0001t0002g0223 |
2 | NA18957.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.611+2280T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821512 | |||||||
| chr8:81821866 | T | C | 1 | a0001c0001t0005g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.611+1926A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821866 | |||||||
| chr8:81821896 | T | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+1896A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821896 | |||||||
| chr8:81822007 | C | G | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+1785G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822007 | |||||||
| chr8:81822031 | T | C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0210 |
2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.611+1761A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822031 | |||||||
| chr8:81822080 | G | GAA | 23 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(20): Show |
30 | HG00423.hp2 HG00673.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.611+1710_611+1711d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822080 | |||||||
| chr8:81822083 | C | T | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+1709G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822083 | |||||||
| chr8:81822422 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.611+1370T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822422 | |||||||
| chr8:81822668 | G | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+1124C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822668 | |||||||
| chr8:81822755 | C | T | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+1037G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822755 | |||||||
| chr8:81822781 | C | T | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+1011G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822781 | |||||||
| chr8:81822789 | C | T | 2 | a0001c0001t0009g0041 a0001c0001t0009g0042 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.611+1003G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822789 | |||||||
| chr8:81822816 | A | T | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+976T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822816 | |||||||
| chr8:81822926 | G | GTA | 3 | a0001c0001t0006g0185 a0001c0001t0006g0186 a0001c0001t0006g0208 |
3 | HG02145.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.611+864_611+865dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822926 | |||||||
| chr8:81822926 | GTA | G | 5 | a0001c0002t0003g0071 a0001c0002t0003g0072 a0001c0002t0003g0080 others(2): Show |
5 | HG02132.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+864_611+865del others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822926 | |||||||
| chr8:81822935 | T | TATAC | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.611+856_611+857ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822935 | |||||||
| chr8:81822941 | C | T | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.611+851G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822941 | |||||||
| chr8:81822947 | C | CAT | 7 | a0001c0001t0002g0162 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
7 | HG00099.hp2 HG03654.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.611+843_611+844dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | |||||||
| chr8:81822947 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.611+845G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | |||||||
| chr8:81822947 | CAT | C | 7 | a0001c0001t0002g0148 a0001c0001t0002g0152 a0001c0001t0002g0209 others(4): Show |
7 | HG01175.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.611+843_611+844del others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | |||||||
| chr8:81822958 | A | ATATG | 7 | a0001c0002t0003g0011 a0001c0002t0003g0014 a0001c0002t0003g0088 others(4): Show |
11 | HG01192.hp2 HG01256.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.611+833_611+834ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | |||||||
| chr8:81822958 | A | ATG | 68 | a0001c0001t0004g0015 a0001c0001t0004g0026 a0001c0001t0004g0027 others(65): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.611+833_611+834ins others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | |||||||
| chr8:81822958 | A | G | 1 | a0002c0003t0007g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.611+834T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | |||||||
| chr8:81822960 | A | ATATATG | 2 | a0001c0001t0001g0037 a0002c0003t0007g0029 |
3 | HG02572.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.611+831_611+832ins others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | |||||||
| chr8:81822960 | A | ATATG | 3 | a0001c0001t0001g0034 a0001c0001t0001g0055 a0001c0001t0009g0041 |
3 | HG02055.hp1 HG03927.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.611+831_611+832ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | |||||||
| chr8:81822960 | A | ATG | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
75 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.611+831_611+832ins others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | |||||||
| chr8:81822960 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.611+832T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | |||||||
| chr8:81822962 | A | ATATATAT others(13): Show |
2 | a0001c0001t0005g0150 a0001c0001t0005g0161 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.611+829_611+830ins others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822962 | |||||||
| chr8:81822962 | A | G | 1 | a0001c0001t0002g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.611+830T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822962 | |||||||
| chr8:81822964 | A | ACACATAT others(15): Show |
5 | a0001c0002t0003g0071 a0001c0002t0003g0072 a0001c0002t0003g0080 others(2): Show |
5 | HG02132.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATAT others(15): Show |
1 | a0001c0001t0006g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.611+827_611+828ins others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATAT others(13): Show |
4 | a0001c0001t0005g0030 a0001c0001t0005g0145 a0001c0001t0005g0153 others(1): Show |
5 | HG00639.hp2 HG00738.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATAT others(11): Show |
11 | a0001c0001t0005g0031 a0001c0001t0005g0155 a0001c0001t0005g0156 others(8): Show |
12 | HG00733.hp2 HG01106.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(18): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATAT others(9): Show |
4 | a0001c0001t0005g0175 a0001c0001t0006g0158 a0001c0001t0006g0185 others(1): Show |
4 | HG01169.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(16): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATAT others(7): Show |
2 | a0001c0001t0006g0186 a0001c0001t0006g0208 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.611+827_611+828ins others(14): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATATGT others(5): Show |
3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(12): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATATGTAT others(3): Show |
1 | a0001c0002t0003g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.611+827_611+828ins others(10): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | ATGTATAT others(1): Show |
7 | a0001c0001t0004g0006 a0001c0001t0004g0119 a0001c0001t0004g0120 others(4): Show |
11 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(8): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822964 | A | G | 76 | a0001c0001t0004g0015 a0001c0001t0004g0026 a0001c0001t0004g0027 others(73): Show |
98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.611+828T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | |||||||
| chr8:81822966 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.611+825_611+826ins others(14): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822966 | |||||||
| chr8:81822966 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
82 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.611+826T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822966 | |||||||
| chr8:81822977 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+815G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822977 | |||||||
| chr8:81822981 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+811A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822981 | |||||||
| chr8:81822984 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+808C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822984 | |||||||
| chr8:81822990 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+802C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822990 | |||||||
| chr8:81823012 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.611+780G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823012 | |||||||
| chr8:81823224 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+568T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823224 | |||||||
| chr8:81823285 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+507A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823285 | |||||||
| chr8:81823404 | A | G | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+388T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823404 | |||||||
| chr8:81823442 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0017 others(4): Show |
14 | HG01168.hp2 HG01169.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.611+350G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823442 | |||||||
| chr8:81823457 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+335T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823457 | |||||||
| chr8:81823459 | C | A | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+333G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823459 | |||||||
| chr8:81823554 | C | T | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+238G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823554 | |||||||
| chr8:81824140 | T | A | 1 | a0001c0001t0006g0187 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463-200A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824140 | |||||||
| chr8:81824160 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0055 |
3 | HG01346.hp1 HG02451.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.463-220A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824160 | |||||||
| chr8:81824196 | T | G | 1 | a0001c0001t0002g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.463-256A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824196 | |||||||
| chr8:81824255 | T | A | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-315A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824255 | |||||||
| chr8:81824470 | T | A | 1 | a0001c0001t0006g0188 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.463-530A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824470 | |||||||
| chr8:81824471 | T | A | 59 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(56): Show |
76 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.463-531A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824471 | |||||||
| chr8:81824519 | C | CT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0065 others(1): Show |
9 | HG02109.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-580dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824519 | |||||||
| chr8:81824534 | TA | T | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-595delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824534 | |||||||
| chr8:81824662 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-722T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824662 | |||||||
| chr8:81824691 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.463-751T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824691 | |||||||
| chr8:81825098 | T | G | 1 | a0001c0002t0003g0024 | 2 | NA18965.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.463-1158A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825098 | |||||||
| chr8:81825128 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-1188G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825128 | |||||||
| chr8:81825141 | T | C | 1 | a0002c0003t0007g0029 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.463-1201A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825141 | |||||||
| chr8:81825432 | T | C | 1 | a0001c0002t0003g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.463-1492A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825432 | |||||||
| chr8:81825453 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0050 |
4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-1513A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825453 | |||||||
| chr8:81825510 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.463-1570A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825510 | |||||||
| chr8:81825536 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(37): Show |
69 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.463-1596T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825536 | |||||||
| chr8:81825551 | C | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.463-1611G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825551 | |||||||
| chr8:81825624 | G | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-1684C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825624 | |||||||
| chr8:81825669 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.463-1729G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825669 | |||||||
| chr8:81825804 | T | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.463-1864A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825804 | |||||||
| chr8:81825808 | T | C | 1 | a0001c0002t0003g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.463-1868A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825808 | |||||||
| chr8:81825816 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463-1876T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825816 | |||||||
| chr8:81826031 | TC | T | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.463-2092delG | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826031 | |||||||
| chr8:81826032 | C | T | 1 | a0001c0001t0004g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.463-2092G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826032 | |||||||
| chr8:81826327 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-2387T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826327 | |||||||
| chr8:81826572 | C | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.463-2632G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826572 | |||||||
| chr8:81826602 | C | T | 1 | a0001c0001t0007g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463-2662G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826602 | |||||||
| chr8:81826894 | C | T | 6 | a0001c0001t0002g0178 a0001c0001t0002g0199 a0001c0001t0002g0200 others(3): Show |
6 | HG00733.hp1 HG01175.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+2536G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826894 | |||||||
| chr8:81827079 | G | A | 1 | a0001c0002t0003g0076 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.462+2351C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827079 | |||||||
| chr8:81827222 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.462+2208G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827222 | |||||||
| chr8:81827278 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+2152G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827278 | |||||||
| chr8:81827316 | A | AT | 20 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(17): Show |
27 | HG00423.hp2 HG00673.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+2113dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827316 | |||||||
| chr8:81827424 | A | G | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.462+2006T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827424 | |||||||
| chr8:81827555 | T | G | 2 | a0001c0002t0003g0090 a0001c0002t0003g0091 |
2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.462+1875A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827555 | |||||||
| chr8:81827813 | C | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+1617G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827813 | |||||||
| chr8:81827950 | A | C | 1 | a0001c0001t0004g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.462+1480T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827950 | |||||||
| chr8:81828091 | T | C | 1 | a0001c0002t0003g0104 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.462+1339A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828091 | |||||||
| chr8:81828267 | A | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.462+1163T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828267 | |||||||
| chr8:81828391 | A | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.462+1039T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828391 | |||||||
| chr8:81828502 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0068 |
8 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.462+928C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828502 | |||||||
| chr8:81828707 | T | C | 1 | a0001c0001t0005g0175 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462+723A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828707 | |||||||
| chr8:81828713 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0055 others(1): Show |
5 | HG00735.hp1 HG01346.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+717A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828713 | |||||||
| chr8:81828765 | T | C | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+665A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828765 | |||||||
| chr8:81828785 | C | T | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.462+645G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828785 | |||||||
| chr8:81828811 | G | A | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.462+619C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828811 | |||||||
| chr8:81828970 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.462+460C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828970 | |||||||
| chr8:81829273 | C | CTAAAAAT others(21): Show |
88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+156_462+157ins others(28): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81829273 | |||||||
| chr8:81829341 | C | CA | 178 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(175): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.462+88dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81829341 | |||||||
| chr8:81829716 | A | G | 1 | a0001c0002t0003g0080 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.376-200T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829716 | |||||||
| chr8:81829720 | A | G | 1 | a0001c0001t0002g0176 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.376-204T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829720 | |||||||
| chr8:81829758 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.376-242A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829758 | |||||||
| chr8:81830008 | G | C | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.376-492C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830008 | |||||||
| chr8:81830053 | G | C | 178 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(175): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-537C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830053 | |||||||
| chr8:81830094 | C | CAGGATAT others(8): Show |
1 | a0004c0006t0006g0212 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376-593_376-579dup others(15): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830094 | |||||||
| chr8:81830334 | C | T | 1 | a0001c0002t0003g0079 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.376-818G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830334 | |||||||
| chr8:81830336 | G | A | 1 | a0001c0001t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.376-820C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830336 | |||||||
| chr8:81830370 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-854T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830370 | |||||||
| chr8:81830428 | G | A | 34 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(31): Show |
42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.376-912C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830428 | |||||||
| chr8:81830438 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.376-922C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830438 | |||||||
| chr8:81830443 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0002g0163 |
2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-927G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830443 | |||||||
| chr8:81830465 | G | A | 16 | a0001c0001t0005g0030 a0001c0001t0005g0031 a0001c0001t0005g0145 others(13): Show |
18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-949C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830465 | |||||||
| chr8:81830549 | T | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | HG01070.hp1 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1033A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830549 | |||||||
| chr8:81830578 | G | GT | 2 | a0001c0001t0001g0038 a0001c0001t0007g0033 |
3 | HG03540.hp2 HG04228.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.376-1063dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830578 | |||||||
| chr8:81830579 | TA | T | 110 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0007 others(107): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.376-1064delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830579 | |||||||
| chr8:81830579 | TAA | T | 12 | a0001c0001t0002g0198 a0001c0001t0002g0217 a0001c0001t0006g0182 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-1065_376-1064d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830579 | |||||||
| chr8:81830591 | A | G | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-1075T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830591 | |||||||
| chr8:81830687 | G | A | 1 | a0001c0002t0003g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-1171C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830687 | |||||||
| chr8:81830724 | G | A | 178 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(175): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-1208C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830724 | |||||||
| chr8:81830785 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
5 | HG01070.hp1 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1269G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830785 | |||||||
| chr8:81830980 | T | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-1464A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830980 | |||||||
| chr8:81831122 | G | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-1606C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831122 | |||||||
| chr8:81831195 | A | G | 1 | a0002c0003t0007g0029 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.376-1679T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831195 | |||||||
| chr8:81831213 | T | G | 1 | a0001c0001t0004g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376-1697A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831213 | |||||||
| chr8:81831377 | A | G | 1 | a0001c0001t0014g0197 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.376-1861T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831377 | |||||||
| chr8:81831457 | CTGAGGTG others(11): Show |
C | 1 | a0001c0001t0002g0152 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.376-1959_376-1942d others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831457 | |||||||
| chr8:81831523 | C | T | 1 | a0001c0001t0004g0136 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.376-2007G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831523 | |||||||
| chr8:81831693 | C | CA | 9 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG00140.hp1 HG00140.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.376-2178dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831693 | |||||||
| chr8:81831693 | CA | C | 56 | a0001c0001t0002g0007 a0001c0001t0002g0142 a0001c0001t0002g0143 others(53): Show |
62 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.376-2178delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831693 | |||||||
| chr8:81831734 | A | C | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2218T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831734 | |||||||
| chr8:81831750 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-2234A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831750 | |||||||
| chr8:81831782 | A | C | 1 | a0001c0001t0006g0182 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.376-2266T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831782 | |||||||
| chr8:81831944 | G | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-2428C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831944 | |||||||
| chr8:81832107 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-2591T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832107 | |||||||
| chr8:81832234 | T | C | 1 | a0001c0001t0007g0215 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.376-2718A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832234 | |||||||
| chr8:81832602 | C | A | 1 | a0001c0002t0003g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.376-3086G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832602 | |||||||
| chr8:81832687 | T | C | 1 | a0001c0001t0005g0030 | 2 | HG00639.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.376-3171A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832687 | |||||||
| chr8:81832794 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.376-3278A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832794 | |||||||
| chr8:81832863 | T | G | 2 | a0003c0004t0004g0115 a0003c0004t0004g0116 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.376-3347A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832863 | |||||||
| chr8:81832939 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.376-3423G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832939 | |||||||
| chr8:81833011 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0002g0163 |
2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-3495G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833011 | |||||||
| chr8:81833153 | A | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0114 |
3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.376-3637T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833153 | |||||||
| chr8:81833157 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376-3641A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833157 | |||||||
| chr8:81833171 | T | C | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-3655A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833171 | |||||||
| chr8:81833172 | C | CT | 85 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(82): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.376-3657dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833172 | |||||||
| chr8:81833172 | C | T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-3656G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833172 | |||||||
| chr8:81833229 | T | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-3713A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833229 | |||||||
| chr8:81833330 | A | G | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-3814T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833330 | |||||||
| chr8:81833399 | T | TA | 89 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(86): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.376-3884dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833399 | |||||||
| chr8:81833407 | T | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-3891A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833407 | |||||||
| chr8:81833412 | C | T | 1 | a0001c0001t0005g0030 | 2 | HG00639.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.376-3896G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833412 | |||||||
| chr8:81833481 | G | T | 1 | a0001c0002t0003g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.376-3965C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833481 | |||||||
| chr8:81833593 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-4077G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833593 | |||||||
| chr8:81833636 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376-4120T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833636 | |||||||
| chr8:81833726 | T | C | 1 | a0001c0001t0004g0112 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.376-4210A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833726 | |||||||
| chr8:81833866 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.376-4350A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833866 | |||||||
| chr8:81833888 | G | C | 89 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(86): Show |
108 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.376-4372C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833888 | |||||||
| chr8:81833889 | T | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.376-4373A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833889 | |||||||
| chr8:81833909 | A | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.376-4393T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833909 | |||||||
| chr8:81833977 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.376-4461G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833977 | |||||||
| chr8:81834020 | C | T | 2 | a0002c0003t0007g0029 a0002c0003t0007g0151 |
3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.376-4504G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834020 | |||||||
| chr8:81834132 | A | C | 35 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(32): Show |
43 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-4616T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834132 | |||||||
| chr8:81834139 | TGGTGGAA others(21): Show |
T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-4651_376-4624d others(30): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834139 | |||||||
| chr8:81834201 | C | G | 178 | a0001c0001t0001g0036 a0001c0001t0002g0002 a0001c0001t0002g0007 others(175): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.376-4685G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834201 | |||||||
| chr8:81834317 | T | C | 1 | a0001c0002t0003g0096 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-4801A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834317 | |||||||
| chr8:81834370 | C | T | 2 | a0001c0002t0003g0100 a0001c0002t0003g0101 |
2 | HG00738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.376-4854G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834370 | |||||||
| chr8:81834462 | T | G | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-4946A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834462 | |||||||
| chr8:81834495 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-4979G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834495 | |||||||
| chr8:81834514 | C | T | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-4998G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834514 | |||||||
| chr8:81834516 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-5000A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834516 | |||||||
| chr8:81834524 | C | G | 1 | a0004c0006t0006g0212 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376-5008G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834524 | |||||||
| chr8:81834529 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0163 |
2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-5013T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834529 | |||||||
| chr8:81834576 | G | A | 4 | a0001c0002t0003g0014 a0001c0002t0003g0097 a0001c0002t0003g0098 others(1): Show |
6 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+5036C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834576 | |||||||
| chr8:81834582 | G | A | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+5030C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834582 | |||||||
| chr8:81834641 | A | T | 1 | a0001c0002t0003g0076 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.375+4971T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834641 | |||||||
| chr8:81834953 | A | C | 1 | a0001c0002t0003g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.375+4659T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834953 | |||||||
| chr8:81835220 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.375+4392T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835220 | |||||||
| chr8:81835282 | G | A | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+4330C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835282 | |||||||
| chr8:81835314 | G | A | 1 | a0001c0001t0004g0026 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.375+4298C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835314 | |||||||
| chr8:81835495 | T | C | 4 | a0001c0001t0006g0181 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+4117A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835495 | |||||||
| chr8:81835863 | G | A | 2 | a0001c0002t0003g0025 a0001c0002t0003g0099 |
3 | NA18980.hp2 NA19007.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.375+3749C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835863 | |||||||
| chr8:81835948 | T | C | 178 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0032 others(175): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.375+3664A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835948 | |||||||
| chr8:81836066 | A | G | 8 | a0001c0001t0006g0182 a0001c0001t0006g0183 a0001c0001t0006g0184 others(5): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+3546T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836066 | |||||||
| chr8:81836114 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3498A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836114 | |||||||
| chr8:81836172 | C | A | 1 | a0001c0002t0003g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.375+3440G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836172 | |||||||
| chr8:81836202 | A | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3410T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836202 | |||||||
| chr8:81836439 | T | A | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3173A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836439 | |||||||
| chr8:81836457 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.375+3155A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836457 | |||||||
| chr8:81836614 | C | T | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+2998G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836614 | |||||||
| chr8:81836615 | G | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2997C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836615 | |||||||
| chr8:81836635 | T | G | 2 | a0001c0001t0005g0150 a0001c0001t0005g0161 |
2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.375+2977A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836635 | |||||||
| chr8:81836661 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+2951A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836661 | |||||||
| chr8:81836693 | T | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.375+2919A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836693 | |||||||
| chr8:81836836 | T | C | 1 | a0004c0006t0006g0212 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.375+2776A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836836 | |||||||
| chr8:81836898 | A | G | 2 | a0001c0001t0002g0142 a0001c0001t0002g0162 |
2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.375+2714T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836898 | |||||||
| chr8:81837396 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375+2216A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837396 | |||||||
| chr8:81837528 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.375+2084G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837528 | |||||||
| chr8:81837554 | T | G | 1 | a0001c0002t0003g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.375+2058A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837554 | |||||||
| chr8:81837739 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+1873G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837739 | |||||||
| chr8:81837822 | A | G | 1 | a0002c0003t0007g0029 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1790T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837822 | |||||||
| chr8:81837977 | A | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0119 a0001c0001t0004g0120 others(4): Show |
11 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.375+1635T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837977 | |||||||
| chr8:81837993 | T | C | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+1619A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837993 | |||||||
| chr8:81838332 | G | A | 2 | a0001c0001t0004g0134 a0001c0001t0004g0135 |
2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.375+1280C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838332 | |||||||
| chr8:81838414 | T | A | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1198A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838414 | |||||||
| chr8:81838414 | T | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.375+1198A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838414 | |||||||
| chr8:81838415 | T | C | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1197A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838415 | |||||||
| chr8:81838416 | A | T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1196T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838416 | |||||||
| chr8:81838561 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375+1051A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838561 | |||||||
| chr8:81838574 | G | GA | 18 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0211 others(15): Show |
18 | HG00280.hp1 HG00642.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.375+1037dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838574 | |||||||
| chr8:81838574 | GA | G | 18 | a0001c0001t0001g0035 a0001c0001t0002g0159 a0001c0001t0004g0119 others(15): Show |
20 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.375+1037delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838574 | |||||||
| chr8:81838663 | C | A | 1 | a0001c0001t0002g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+949G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838663 | |||||||
| chr8:81838731 | A | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+881T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838731 | |||||||
| chr8:81838970 | A | ATCCAAAC others(15): Show |
1 | a0001c0001t0006g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.375+620_375+641dup others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838970 | |||||||
| chr8:81838982 | CA | C | 4 | a0001c0001t0016g0224 a0001c0001t0017g0218 a0001c0002t0003g0070 others(1): Show |
4 | HG02080.hp2 NA18998.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+629delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838982 | |||||||
| chr8:81839223 | C | T | 1 | a0001c0001t0012g0141 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+389G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839223 | |||||||
| chr8:81839225 | A | T | 1 | a0001c0001t0002g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+387T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839225 | |||||||
| chr8:81839355 | T | C | 2 | a0001c0001t0006g0189 a0001c0001t0006g0190 |
2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.375+257A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839355 | |||||||
| chr8:81839400 | A | T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+212T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839400 | |||||||
| chr8:81839435 | A | T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+177T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839435 | |||||||
| chr8:81839587 | T | G | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+25A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839587 | |||||||
| chr8:81840100 | A | G | 4 | a0001c0001t0004g0015 a0001c0001t0004g0112 a0001c0001t0004g0117 others(1): Show |
6 | HG00423.hp2 NA18946.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96-18T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840100 | |||||||
| chr8:81840195 | T | C | 1 | a0001c0001t0004g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-96-113A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840195 | |||||||
| chr8:81840197 | C | A | 1 | a0001c0001t0004g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-96-115G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840197 | |||||||
| chr8:81840542 | T | A | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-460A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840542 | |||||||
| chr8:81840544 | A | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-462T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840544 | |||||||
| chr8:81840545 | A | T | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-463T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840545 | |||||||
| chr8:81840548 | T | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-466A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840548 | |||||||
| chr8:81840592 | A | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-510T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840592 | |||||||
| chr8:81840604 | G | A | 32 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0027 others(29): Show |
40 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-96-522C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840604 | |||||||
| chr8:81840647 | C | T | 2 | a0001c0001t0007g0033 a0001c0001t0007g0216 |
3 | HG03540.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-96-565G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840647 | |||||||
| chr8:81840666 | CAAAT | C | 36 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(33): Show |
45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-96-588_-96-585del others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840666 | |||||||
| chr8:81840870 | G | T | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96-788C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840870 | |||||||
| chr8:81840953 | CACA | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-96-874_-96-872del others(3): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840953 | |||||||
| chr8:81841115 | T | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-97+1007A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841115 | |||||||
| chr8:81841165 | A | C | 1 | a0001c0001t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97+957T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841165 | |||||||
| chr8:81841166 | C | A | 1 | a0001c0001t0006g0191 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97+956G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841166 | |||||||
| chr8:81841197 | CG | C | 3 | a0001c0001t0002g0152 a0001c0001t0002g0213 a0001c0001t0002g0223 |
3 | NA18747.hp1 NA18946.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-97+924delC | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841197 | |||||||
| chr8:81841341 | C | CA | 55 | a0001c0001t0001g0066 a0001c0001t0002g0007 a0001c0001t0002g0144 others(52): Show |
61 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-97+780dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | |||||||
| chr8:81841341 | C | CAA | 31 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0193 others(28): Show |
42 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-97+779_-97+780dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | |||||||
| chr8:81841341 | CA | C | 8 | a0001c0001t0001g0034 a0001c0001t0004g0112 a0001c0001t0004g0113 others(5): Show |
8 | HG01168.hp1 NA18939.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-97+780delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | |||||||
| chr8:81841360 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-97+762C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841360 | |||||||
| chr8:81841403 | A | G | 2 | a0001c0001t0004g0027 a0001c0001t0012g0141 |
2 | HG02723.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-97+719T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841403 | |||||||
| chr8:81841459 | C | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-97+663G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841459 | |||||||
| chr8:81841481 | G | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0215 a0001c0001t0007g0216 |
4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97+641C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841481 | |||||||
| chr8:81841630 | A | T | 1 | a0001c0002t0003g0069 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-97+492T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841630 | |||||||
| chr8:81841654 | A | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+468T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841654 | |||||||
| chr8:81841655 | C | A | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+467G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841655 | |||||||
| chr8:81841655 | C | CA | 15 | a0001c0001t0002g0217 a0001c0001t0002g0219 a0001c0001t0002g0220 others(12): Show |
15 | HG01978.hp2 HG02080.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.-97+466dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841655 | |||||||
| chr8:81841739 | C | A | 1 | a0001c0002t0003g0111 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-97+383G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841739 | |||||||
| chr8:81841788 | C | T | 51 | a0001c0002t0003g0003 a0001c0002t0003g0011 a0001c0002t0003g0012 others(48): Show |
68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-97+334G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841788 | |||||||
| chr8:81841791 | GAGGAAAG others(18): Show |
G | 1 | a0001c0001t0002g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-97+306_-97+330del others(25): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841791 | |||||||
| chr8:81841851 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-97+271G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841851 | |||||||
| chr8:81841883 | A | C | 87 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(84): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-97+239T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841883 | |||||||
| chr8:81841905 | A | C | 88 | a0001c0001t0004g0006 a0001c0001t0004g0015 a0001c0001t0004g0026 others(85): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-97+217T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841905 | |||||||
| chr8:81841917 | G | C | 1 | a0001c0001t0016g0224 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+205C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841917 | |||||||
| chr8:81841985 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-97+137C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841985 | |||||||
| chr8:81841990 | G | A | 1 | a0001c0001t0004g0225 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-97+132C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841990 | |||||||
| chr8:81842033 | C | A | 1 | a0001c0001t0004g0227 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-97+89G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81842033 |