Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11336 |
| ensemblid | ENSG00000180104.16 |
| hgncid | 30378 |
| symbol | EXOC3 |
| name | exocyst complex component 3 |
| refseq_nuc | NM_007277.5 |
| refseq_prot | NP_009208.2 |
| ensembl_nuc | ENST00000512944.6 |
| ensembl_prot | ENSP00000425587.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 443176 |
| end | 467290 |
| strand | + |
| ver | v1.2 |
| region | chr5:443176-467290 |
| region5000 | chr5:438176-472290 |
| regionname0 | EXOC3_chr5_443176_467290 |
| regionname5000 | EXOC3_chr5_438176_472290 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 745 | 406 | 89 | 76 | 172 | 18 | 49 | 133 | EXOC3_chr5_438176_472290 | EXOC3 | MKETD others(740): Show |
chr5 | 438176 | 472290 |
| a0002 | 0/0 | 745 | 9 | 0 | 4 | 5 | 0 | 0 | 5 | EXOC3_chr5_438176_472290 | EXOC3 | MKETD others(740): Show |
chr5 | 438176 | 472290 |
| a0003 | 0/0 | 745 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | MKETD others(740): Show |
chr5 | 438176 | 472290 |
| a0004 | 0/0 | 745 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | MKETD others(740): Show |
chr5 | 438176 | 472290 |
| a0005 | 0/0 | 745 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | MKETD others(740): Show |
chr5 | 438176 | 472290 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2235 | 217 | 65 | 37 | 87 | 8 | 20 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0002 | 1/1 | 2235 | 150 | 4 | 29 | 78 | 9 | 28 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0003 | 0/0 | 2235 | 23 | 7 | 10 | 5 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0004 | 0/0 | 2235 | 7 | 7 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0006 | 0/0 | 2235 | 4 | 4 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0007 | 0/0 | 2235 | 2 | 1 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0010 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0013 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0001c0014 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0002c0005 | 0/0 | 2235 | 7 | 0 | 4 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0002c0008 | 0/0 | 2235 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0003c0011 | 0/0 | 2235 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0004c0009 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 | ||
| a0005c0012 | 0/0 | 2235 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | ATGAA others(2230): Show |
chr5 | 438176 | 472290 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2801 | 196 | 57 | 36 | 75 | 8 | 20 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0002 | 0/0 | 2801 | 7 | 7 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0004 | 0/0 | 2801 | 5 | 0 | 0 | 5 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0005 | 0/0 | 2801 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0007 | 0/0 | 2765 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2760): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0009 | 0/0 | 2801 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0010 | 0/0 | 2801 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0014 | 0/0 | 2801 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0015 | 0/0 | 2801 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0001t0016 | 0/0 | 2801 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0001 | 1/0 | 2801 | 123 | 4 | 15 | 78 | 5 | 20 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0003 | 0/0 | 2801 | 21 | 0 | 11 | 0 | 3 | 7 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0006 | 0/0 | 2747 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2742): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0008 | 0/1 | 2762 | 1 | 0 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2757): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0011 | 0/0 | 2801 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0012 | 0/0 | 2801 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0002t0013 | 0/0 | 2801 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0003t0002 | 0/0 | 2801 | 23 | 7 | 10 | 5 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0004t0002 | 0/0 | 2801 | 7 | 7 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0006t0001 | 0/0 | 2801 | 4 | 4 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0007t0001 | 0/0 | 2801 | 2 | 1 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0010t0001 | 0/0 | 2801 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0013t0001 | 0/0 | 2801 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0001c0014t0002 | 0/0 | 2801 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0002c0005t0001 | 0/0 | 2801 | 7 | 0 | 4 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0002c0008t0001 | 0/0 | 2801 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0003c0011t0001 | 0/0 | 2801 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0004c0009t0001 | 0/0 | 2801 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| a0005c0012t0001 | 0/0 | 2801 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | ACTTC others(2796): Show |
chr5 | 438176 | 472290 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 27 | 1 | 5 | 17 | 1 | 3 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0003 | 0/0 | 16 | 16 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0004 | 0/0 | 14 | 1 | 7 | 6 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0031 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0005g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0010g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0014g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0002 | 1/0 | 29 | 0 | 2 | 25 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0006 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0009 | 0/0 | 7 | 0 | 1 | 0 | 2 | 4 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0005 | 0/0 | 10 | 0 | 4 | 0 | 3 | 3 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0006g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0008g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0011g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0012g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0002t0013g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0008 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0004t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0004t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0006t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0007t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0013t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0001c0014t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0002c0005t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0002c0005t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0002c0005t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0002c0008t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0003c0011t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0004c0009t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| a0005c0012t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0187 | EUR | GBR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00099 | hp2 | a0001 | c0002 | t0012 | g0065 | EUR | GBR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0005 | EUR | GBR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0086 | EUR | FIN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0005 | EUR | FIN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0099 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0193 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01074 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01081 | hp2 | a0001 | c0002 | t0006 | g0005 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0053 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01106 | hp1 | a0001 | c0001 | t0010 | g0177 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01167 | hp1 | a0002 | c0005 | t0001 | g0022 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01167 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01168 | hp2 | a0001 | c0002 | t0013 | g0102 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01175 | hp1 | a0001 | c0002 | t0006 | g0098 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0096 | AMR | PUR | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01258 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0008 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0186 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01433 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0005 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01928 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01981 | hp1 | a0001 | c0003 | t0002 | g0008 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0097 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0008 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01993 | hp2 | a0002 | c0005 | t0001 | g0073 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02055 | hp1 | a0001 | c0014 | t0002 | g0199 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02074 | hp1 | a0003 | c0011 | t0001 | g0007 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02083 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | CDX | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CDX | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02258 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0053 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02280 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02293 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02300 | hp2 | a0002 | c0005 | t0001 | g0022 | AMR | PEL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02630 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02630 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0095 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0043 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0025 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0089 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0041 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02976 | hp2 | a0004 | c0009 | t0001 | g0090 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0041 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03490 | hp2 | a0005 | c0012 | t0001 | g0046 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0042 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0094 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0042 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0024 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0001 | AFR | GWD | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0005 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0059 | SAS | PJL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03834 | hp2 | a0001 | c0010 | t0001 | g0001 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03927 | hp1 | a0001 | c0002 | t0011 | g0071 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0005 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18522 | hp2 | a0001 | c0004 | t0002 | g0024 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0190 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18952 | hp1 | a0002 | c0008 | t0001 | g0012 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18962 | hp2 | a0001 | c0007 | t0001 | g0142 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18971 | hp2 | a0001 | c0013 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18983 | hp1 | a0001 | c0001 | t0014 | g0141 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18986 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19009 | hp2 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19011 | hp2 | a0002 | c0008 | t0001 | g0012 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19059 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19067 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19070 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19079 | hp1 | a0002 | c0005 | t0001 | g0012 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0008 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20129 | hp1 | a0001 | c0006 | t0001 | g0088 | AFR | ASW | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0043 | EUR | TSI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0100 | EUR | TSI | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | GIH | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | GIH | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0189 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | ACB | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0105 | AFR | MSL | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | USA | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0008 | g0101 | REF | REF | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0002 | REF | REF | EXOC3_chr5_438176_472290 | EXOC3 | chr5 | 438176 | 472290 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:446262 | G | A | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.57G>A | p.Met19Ile | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/13 | 228/2801 | 57/2238 | 19/745 | chr5 | 446262 | |||
| chr5:453433 | G | A | 1 | a0003 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.428G>A | p.Arg143Gln | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 599/2801 | 428/2238 | 143/745 | chr5 | 453433 | |||
| chr5:453913 | C | G | 1 | a0002 | 9 | HG01167.hp1 HG01433.hp2 HG01993.hp2 others(6): Show |
missense_variant | MODERATE | c.908C>G | p.Pro303Arg | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 1079/2801 | 908/2238 | 303/745 | chr5 | 453913 | |||
| chr5:456908 | G | C | 1 | a0005 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.1066G>C | p.Val356Leu | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/13 | 1237/2801 | 1066/2238 | 356/745 | chr5 | 456908 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:446331 | C | T | 1 | a0001c0006 | 4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.126C>T | p.Ser42Ser | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/13 | 297/2801 | 126/2238 | 42/745 | chr5 | 446331 | |||
| chr5:447664 | C | A | 1 | a0001c0010 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.276C>A | p.Thr92Thr | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/13 | 447/2801 | 276/2238 | 92/745 | chr5 | 447664 | |||
| chr5:453452 | G | A | 7 | a0001c0001 a0001c0004 a0001c0007 others(4): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
synonymous_variant | LOW | c.447G>A | p.Glu149Glu | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 618/2801 | 447/2238 | 149/745 | chr5 | 453452 | |||
| chr5:453464 | C | T | 1 | a0001c0007 | 2 | HG03540.hp2 NA18962.hp2 |
synonymous_variant | LOW | c.459C>T | p.Asp153Asp | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 630/2801 | 459/2238 | 153/745 | chr5 | 453464 | |||
| chr5:453468 | C | T | 2 | a0001c0003 a0001c0014 |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
synonymous_variant | LOW | c.463C>T | p.Leu155Leu | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 634/2801 | 463/2238 | 155/745 | chr5 | 453468 | |||
| chr5:453626 | C | T | 1 | a0002c0008 | 2 | NA18952.hp1 NA19011.hp2 |
synonymous_variant | LOW | c.621C>T | p.Thr207Thr | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 792/2801 | 621/2238 | 207/745 | chr5 | 453626 | |||
| chr5:453773 | G | A | 1 | a0001c0004 | 7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.768G>A | p.Val256Val | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/13 | 939/2801 | 768/2238 | 256/745 | chr5 | 453773 | |||
| chr5:462238 | C | T | 1 | a0001c0014 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1584C>T | p.Asp528Asp | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/13 | 1755/2801 | 1584/2238 | 528/745 | chr5 | 462238 | |||
| chr5:465816 | C | T | 1 | a0001c0013 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.2037C>T | p.Ser679Ser | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/13 | 2208/2801 | 2037/2238 | 679/745 | chr5 | 465816 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:443202 | AGGCAGCG others(29): Show |
A | 1 | a0001c0001t0007 | 2 | NA18971.hp1 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141_-106delAGCGAA others(30): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2965 | INFO_REALIGN_3_PRIME | chr5 | 443202 | |||||
| chr5:443202 | AGGCAGCG others(47): Show |
A | 1 | a0001c0002t0006 | 2 | HG01081.hp2 HG01175.hp1 |
5_prime_UTR_variant | MODIFIER | c.-141_-88delAGCGAAG others(47): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2947 | INFO_REALIGN_3_PRIME | chr5 | 443202 | |||||
| chr5:443220 | G | GGGCGGAG others(23): Show |
1 | a0001c0002t0001 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122_-121insAGGGGG others(24): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2980 | INFO_REALIGN_3_PRIME | chr5 | 443220 | |||||
| chr5:443220 | GGGCGGCG others(26): Show |
G | 1 | a0001c0001t0005 | 2 | NA18962.hp1 NA18998.hp2 |
5_prime_UTR_variant | MODIFIER | c.-118_-86delGGGCGGC others(26): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2945 | INFO_REALIGN_3_PRIME | chr5 | 443220 | |||||
| chr5:443220 | GGGCGGCG others(32): Show |
G | 3 | a0001c0002t0001 a0001c0002t0003 a0001c0002t0013 |
37 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-118_-80delGGGCGGC others(32): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2939 | INFO_REALIGN_3_PRIME | chr5 | 443220 | |||||
| chr5:443220 | GGGCGGCG others(38): Show |
G | 1 | a0001c0002t0001 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-118_-74delGGGCGGC others(38): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2933 | INFO_REALIGN_3_PRIME | chr5 | 443220 | |||||
| chr5:443223 | C | CGGAGGGG others(8): Show |
1 | a0001c0002t0001 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122_-121insAGGGGG others(9): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2980 | INFO_REALIGN_3_PRIME | chr5 | 443223 | |||||
| chr5:443226 | C | A | 4 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0015 others(1): Show |
7 | HG02083.hp1 NA18966.hp1 NA18983.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-121C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2980 | chr5 | 443226 | ||||||
| chr5:443229 | G | C | 1 | a0001c0002t0001 | 2 | HG00280.hp1 HG00639.hp1 |
5_prime_UTR_variant | MODIFIER | c.-118G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2977 | chr5 | 443229 | ||||||
| chr5:443229 | G | GGGC | 3 | a0001c0002t0001 a0002c0005t0001 a0002c0008t0001 |
19 | HG00423.hp2 HG01167.hp1 HG01433.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-71_-69dupGCG | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGC | 1 | a0001c0002t0001 | 9 | HG02155.hp1 NA18968.hp2 NA18982.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-74_-69dupGCGGCG | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(2): Show |
2 | a0001c0002t0001 a0002c0005t0001 |
6 | HG02165.hp2 HG03017.hp1 NA18947.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-77_-69dupGCGGCGGC others(1): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(5): Show |
1 | a0001c0002t0001 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80_-69dupGCGGCGGC others(4): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(8): Show |
1 | a0001c0002t0001 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83_-69dupGCGGCGGC others(7): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(14): Show |
1 | a0001c0002t0001 | 2 | NA18747.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-89_-69dupGCGGCGGC others(13): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(20): Show |
1 | a0001c0002t0001 | 1 | NA18983.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95_-69dupGCGGCGGC others(19): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(38): Show |
1 | a0001c0002t0001 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113_-69dupGCGGCGG others(38): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(47): Show |
1 | a0001c0002t0001 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69_-68insGCGGCGGC others(46): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | G | GGGCGGCG others(131): Show |
1 | a0001c0002t0001 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69_-68insGCGGCGGC others(130): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2927 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGC | G | 4 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0016 others(1): Show |
14 | HG01070.hp1 HG01071.hp1 HG02602.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-71_-69delGCG | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(2): Show |
G | 2 | a0001c0001t0001 a0001c0002t0001 |
8 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-77_-69delGCGGCGGC others(1): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(5): Show |
G | 2 | a0001c0001t0004 a0001c0006t0001 |
6 | HG02970.hp1 HG03098.hp1 NA18966.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-80_-69delGCGGCGGC others(4): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(8): Show |
G | 4 | a0001c0001t0001 a0001c0002t0001 a0001c0006t0001 others(1): Show |
23 | HG01109.hp2 HG01952.hp2 HG02056.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-83_-69delGCGGCGGC others(7): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(11): Show |
G | 2 | a0001c0001t0001 a0002c0005t0001 |
5 | HG01975.hp2 HG01993.hp2 HG02976.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-86_-69delGCGGCGGC others(10): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(14): Show |
G | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(10): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(192): Show |
5_prime_UTR_variant | MODIFIER | c.-89_-69delGCGGCGGC others(13): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(17): Show |
G | 2 | a0001c0002t0001 a0004c0009t0001 |
3 | HG02976.hp2 NA18950.hp2 NA19087.hp1 |
5_prime_UTR_variant | MODIFIER | c.-92_-69delGCGGCGGC others(16): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(20): Show |
G | 1 | a0001c0002t0001 | 2 | HG03453.hp2 NA18957.hp1 |
5_prime_UTR_variant | MODIFIER | c.-95_-69delGCGGCGGC others(19): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(23): Show |
G | 1 | a0001c0002t0001 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-98_-69delGCGGCGGC others(22): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(26): Show |
G | 2 | a0001c0001t0001 a0001c0001t0010 |
34 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-101_-69delGCGGCGG others(26): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443229 | GGGCGGCG others(29): Show |
G | 1 | a0001c0002t0001 | 2 | HG01257.hp1 NA18943.hp2 |
5_prime_UTR_variant | MODIFIER | c.-104_-69delGCGGCGG others(29): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2928 | INFO_REALIGN_3_PRIME | chr5 | 443229 | |||||
| chr5:443235 | C | A | 1 | a0001c0001t0015 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-112C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2971 | chr5 | 443235 | ||||||
| chr5:443238 | C | A | 1 | a0001c0001t0016 | 1 | NA18986.hp1 | 5_prime_UTR_variant | MODIFIER | c.-109C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2968 | chr5 | 443238 | ||||||
| chr5:443238 | C | G | 1 | a0001c0001t0015 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-109C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2968 | chr5 | 443238 | ||||||
| chr5:443241 | C | G | 2 | a0001c0001t0007 a0001c0001t0016 |
3 | NA18971.hp1 NA18986.hp1 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-106C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2965 | chr5 | 443241 | ||||||
| chr5:443247 | C | G | 1 | a0001c0001t0015 | 1 | HG02083.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2959 | chr5 | 443247 | ||||||
| chr5:443250 | C | G | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0016 |
8 | NA18945.hp1 NA18966.hp1 NA18971.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-97C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2956 | chr5 | 443250 | ||||||
| chr5:443259 | C | G | 2 | a0001c0001t0014 a0001c0002t0006 |
3 | HG01081.hp2 HG01175.hp1 NA18983.hp1 |
5_prime_UTR_variant | MODIFIER | c.-88C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2947 | chr5 | 443259 | ||||||
| chr5:443262 | C | A | 1 | a0001c0001t0005 | 2 | NA18962.hp1 NA18998.hp2 |
5_prime_UTR_variant | MODIFIER | c.-85C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2944 | chr5 | 443262 | ||||||
| chr5:443262 | C | T | 4 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 others(1): Show |
38 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-85C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/13 | 2944 | chr5 | 443262 | ||||||
| chr5:466931 | A | G | 1 | a0001c0002t0013 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*33A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 33 | chr5 | 466931 | ||||||
| chr5:466937 | G | A | 1 | a0001c0001t0009 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 39 | chr5 | 466937 | ||||||
| chr5:467028 | G | T | 2 | a0001c0002t0003 a0001c0002t0006 |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 130 | chr5 | 467028 | ||||||
| chr5:467029 | T | C | 2 | a0001c0002t0003 a0001c0002t0006 |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*131T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 131 | chr5 | 467029 | ||||||
| chr5:467040 | G | C | 1 | a0001c0001t0010 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 142 | chr5 | 467040 | ||||||
| chr5:467048 | C | T | 1 | a0001c0002t0012 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 150 | chr5 | 467048 | ||||||
| chr5:467275 | G | C | 1 | a0001c0002t0011 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 13/13 | 377 | chr5 | 467275 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:443326 | C | T | 2 | a0001c0003t0002g0198 a0001c0014t0002g0199 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-57+36C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443326 | |||||||
| chr5:443332 | A | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.-57+42A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443332 | |||||||
| chr5:443561 | G | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-57+271G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443561 | |||||||
| chr5:443578 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-57+288A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443578 | |||||||
| chr5:443686 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-57+396C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443686 | |||||||
| chr5:443734 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.-57+444A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443734 | |||||||
| chr5:443763 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0195 |
3 | HG02486.hp1 HG02809.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-57+473C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443763 | |||||||
| chr5:443791 | T | A | 1 | a0001c0002t0001g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-57+501T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 443791 | |||||||
| chr5:443925 | TCAAGGTG others(11): Show |
T | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-57+656_-57+673del others(18): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 443925 | ||||||
| chr5:444006 | C | A | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+716C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444006 | |||||||
| chr5:444125 | T | C | 1 | a0001c0001t0001g0044 | 2 | NA18963.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-57+835T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444125 | |||||||
| chr5:444126 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-57+836C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444126 | |||||||
| chr5:444154 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-57+864G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444154 | |||||||
| chr5:444387 | T | C | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-57+1097T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444387 | |||||||
| chr5:444504 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57+1214G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444504 | |||||||
| chr5:444506 | C | G | 1 | a0001c0003t0002g0193 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-57+1216C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444506 | |||||||
| chr5:444690 | G | T | 2 | a0001c0002t0001g0040 a0001c0002t0001g0087 |
3 | HG00423.hp2 NA18982.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-57+1400G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444690 | |||||||
| chr5:444694 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG01099.hp1 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-57+1404C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444694 | |||||||
| chr5:444695 | G | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-57+1405G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 444695 | |||||||
| chr5:444814 | T | TGAGATTT others(53): Show |
17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-56-1324_-56-1323i others(62): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 444814 | ||||||
| chr5:445141 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-56-1009A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445141 | |||||||
| chr5:445247 | C | T | 1 | a0001c0002t0001g0043 | 2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-56-903C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445247 | |||||||
| chr5:445352 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-798T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445352 | |||||||
| chr5:445353 | C | CT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.-56-783dupT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr5 | 445353 | ||||||
| chr5:445353 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-797C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445353 | |||||||
| chr5:445372 | C | T | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.-56-778C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445372 | |||||||
| chr5:445382 | C | G | 14 | a0001c0001t0001g0052 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
28 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-56-768C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445382 | |||||||
| chr5:445413 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-56-737G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445413 | |||||||
| chr5:445507 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0182 a0001c0001t0001g0183 |
6 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-643G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445507 | |||||||
| chr5:445590 | G | A | 1 | a0001c0002t0001g0032 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-56-560G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445590 | |||||||
| chr5:445611 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-56-539G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445611 | |||||||
| chr5:445812 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
12 | HG00408.hp2 HG00423.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.-56-338G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445812 | |||||||
| chr5:445886 | A | C | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-56-264A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 445886 | |||||||
| chr5:446075 | G | C | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-56-75G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 446075 | |||||||
| chr5:446131 | G | A | 1 | a0001c0001t0001g0026 | 3 | HG00544.hp2 NA18944.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-56-19G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 446131 | |||||||
| chr5:446143 | C | A | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-56-7C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 1/12 | chr5 | 446143 | |||||||
| chr5:446462 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
182 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.144+113G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446462 | |||||||
| chr5:446579 | G | A | 14 | a0001c0001t0001g0052 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
28 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.144+230G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446579 | |||||||
| chr5:446615 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.144+266G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446615 | |||||||
| chr5:446808 | G | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.144+459G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446808 | |||||||
| chr5:446836 | AAC | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.144+489_144+490del others(2): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 446836 | ||||||
| chr5:446861 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.144+512A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446861 | |||||||
| chr5:446862 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.144+513G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 446862 | |||||||
| chr5:446932 | AAGG | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
8 | HG02486.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.144+586_144+588del others(3): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | 446932 | ||||||
| chr5:447111 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.145-422A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 447111 | |||||||
| chr5:447232 | G | C | 1 | a0001c0001t0009g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.145-301G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 447232 | |||||||
| chr5:447236 | A | G | 1 | a0001c0002t0001g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.145-297A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 447236 | |||||||
| chr5:447241 | C | T | 7 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(4): Show |
16 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.145-292C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 2/12 | chr5 | 447241 | |||||||
| chr5:448023 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364+271A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448023 | |||||||
| chr5:448083 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.364+331C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448083 | |||||||
| chr5:448087 | G | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+335G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448087 | |||||||
| chr5:448173 | G | A | 2 | a0001c0006t0001g0088 a0001c0006t0001g0089 |
2 | HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.364+421G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448173 | |||||||
| chr5:448176 | C | A | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+424C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448176 | |||||||
| chr5:448202 | C | T | 1 | a0001c0001t0001g0054 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.364+450C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448202 | |||||||
| chr5:448244 | G | T | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.364+492G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448244 | |||||||
| chr5:448465 | C | T | 1 | a0001c0002t0001g0084 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.364+713C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448465 | |||||||
| chr5:448548 | C | T | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+796C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448548 | |||||||
| chr5:448735 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0123 a0001c0001t0001g0182 others(5): Show |
11 | HG01099.hp1 HG01261.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.364+983G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448735 | |||||||
| chr5:448771 | C | T | 1 | a0001c0002t0003g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364+1019C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448771 | |||||||
| chr5:448772 | G | A | 12 | a0001c0001t0001g0027 a0001c0003t0002g0008 a0001c0003t0002g0016 others(9): Show |
27 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.364+1020G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448772 | |||||||
| chr5:448791 | A | G | 7 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(4): Show |
16 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.364+1039A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448791 | |||||||
| chr5:448829 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.364+1077G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448829 | |||||||
| chr5:448836 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(15): Show |
34 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.364+1084C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448836 | |||||||
| chr5:448849 | T | C | 7 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(4): Show |
16 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.364+1097T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448849 | |||||||
| chr5:448858 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0124 |
6 | NA18939.hp1 NA18990.hp1 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.364+1106G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 448858 | |||||||
| chr5:449367 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.364+1615T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449367 | |||||||
| chr5:449468 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.364+1716C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449468 | |||||||
| chr5:449577 | C | T | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+1825C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449577 | |||||||
| chr5:449586 | A | T | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+1834A>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449586 | |||||||
| chr5:449618 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364+1866G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449618 | |||||||
| chr5:449656 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364+1904A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449656 | |||||||
| chr5:449658 | T | G | 1 | a0001c0004t0002g0024 | 3 | HG02630.hp1 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.364+1906T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449658 | |||||||
| chr5:449923 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.364+2171C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449923 | |||||||
| chr5:449964 | G | T | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.364+2212G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449964 | |||||||
| chr5:449974 | G | A | 1 | a0001c0002t0012g0065 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.364+2222G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449974 | |||||||
| chr5:449987 | C | T | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.364+2235C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 449987 | |||||||
| chr5:450009 | G | C | 2 | a0001c0002t0001g0040 a0001c0002t0001g0087 |
3 | HG00423.hp2 NA18982.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.364+2257G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450009 | |||||||
| chr5:450011 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.364+2259T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450011 | |||||||
| chr5:450103 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(15): Show |
34 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.364+2351G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450103 | |||||||
| chr5:450106 | C | T | 2 | a0001c0006t0001g0088 a0001c0006t0001g0089 |
2 | HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.364+2354C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450106 | |||||||
| chr5:450205 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.364+2453C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450205 | |||||||
| chr5:450212 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.364+2460C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450212 | |||||||
| chr5:450220 | A | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.364+2468A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450220 | |||||||
| chr5:450353 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.364+2601T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450353 | |||||||
| chr5:450415 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364+2663A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450415 | |||||||
| chr5:450428 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.364+2676A>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450428 | |||||||
| chr5:450431 | C | T | 1 | a0001c0006t0001g0089 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.364+2679C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450431 | |||||||
| chr5:450517 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.364+2765G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450517 | |||||||
| chr5:450595 | C | T | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.365-2775C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450595 | |||||||
| chr5:450662 | T | C | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.365-2708T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450662 | |||||||
| chr5:450790 | G | GT | 18 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(15): Show |
34 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.365-2567dupT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 450790 | ||||||
| chr5:450821 | A | G | 4 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-2549A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450821 | |||||||
| chr5:450873 | A | G | 12 | a0001c0002t0001g0083 a0001c0003t0002g0008 a0001c0003t0002g0016 others(9): Show |
25 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.365-2497A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450873 | |||||||
| chr5:450900 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.365-2470A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 450900 | |||||||
| chr5:451105 | C | T | 1 | a0001c0006t0001g0041 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.365-2265C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451105 | |||||||
| chr5:451106 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.365-2264G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451106 | |||||||
| chr5:451135 | A | AT | 11 | a0001c0001t0001g0162 a0001c0002t0003g0005 a0001c0002t0003g0018 others(8): Show |
24 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-2227dupT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr5 | 451135 | ||||||
| chr5:451144 | G | A | 14 | a0001c0001t0001g0052 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
28 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.365-2226G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451144 | |||||||
| chr5:451310 | C | T | 17 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(14): Show |
39 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.365-2060C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451310 | |||||||
| chr5:451482 | A | C | 1 | a0001c0002t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.365-1888A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451482 | |||||||
| chr5:451510 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0169 a0001c0001t0002g0126 |
3 | HG02273.hp2 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.365-1860G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451510 | |||||||
| chr5:451568 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.365-1802C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451568 | |||||||
| chr5:451791 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.365-1579T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451791 | |||||||
| chr5:451799 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.365-1571A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451799 | |||||||
| chr5:451800 | C | T | 2 | a0001c0001t0002g0118 a0001c0001t0002g0119 |
2 | HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.365-1570C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 451800 | |||||||
| chr5:452080 | A | G | 1 | a0001c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.365-1290A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452080 | |||||||
| chr5:452132 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(118): Show |
226 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.365-1238C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452132 | |||||||
| chr5:452159 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.365-1211G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452159 | |||||||
| chr5:452169 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.365-1201G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452169 | |||||||
| chr5:452190 | A | G | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-1180A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452190 | |||||||
| chr5:452221 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | NA18940.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.365-1149A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452221 | |||||||
| chr5:452240 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
182 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.365-1130C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452240 | |||||||
| chr5:452241 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.365-1129G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452241 | |||||||
| chr5:452337 | A | G | 14 | a0001c0001t0001g0052 a0001c0001t0001g0184 a0001c0001t0001g0185 others(11): Show |
28 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.365-1033A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452337 | |||||||
| chr5:452454 | T | TAA | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.365-916_365-915ins others(2): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452454 | |||||||
| chr5:452455 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.365-915C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452455 | |||||||
| chr5:452473 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0168 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.365-897C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452473 | |||||||
| chr5:452781 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.365-589C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452781 | |||||||
| chr5:452789 | G | A | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.365-581G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452789 | |||||||
| chr5:452832 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365-538A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452832 | |||||||
| chr5:452954 | T | C | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-416T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452954 | |||||||
| chr5:452971 | G | A | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.365-399G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 452971 | |||||||
| chr5:453006 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.365-364G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453006 | |||||||
| chr5:453022 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.365-348T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453022 | |||||||
| chr5:453096 | A | G | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.365-274A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453096 | |||||||
| chr5:453111 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.365-259C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453111 | |||||||
| chr5:453252 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.365-118G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453252 | |||||||
| chr5:453282 | T | C | 1 | a0001c0002t0001g0068 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.365-88T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 3/12 | chr5 | 453282 | |||||||
| chr5:454067 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1046+16C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454067 | |||||||
| chr5:454198 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1046+147T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454198 | |||||||
| chr5:454333 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1046+282G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454333 | |||||||
| chr5:454363 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1046+312C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454363 | |||||||
| chr5:454392 | A | AC | 14 | a0001c0001t0001g0031 a0001c0001t0001g0048 a0001c0001t0001g0158 others(11): Show |
18 | HG01168.hp1 HG01175.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.1046+345dupC | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 454392 | ||||||
| chr5:454617 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1046+566T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454617 | |||||||
| chr5:454868 | A | AT | 6 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
7 | NA18951.hp1 NA18957.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046+837dupT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 454868 | ||||||
| chr5:454868 | A | ATT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1046+836_1046+837d others(4): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 454868 | ||||||
| chr5:454868 | A | ATTT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(21): Show |
44 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1046+835_1046+837d others(5): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 454868 | ||||||
| chr5:454868 | AT | A | 8 | a0001c0002t0001g0033 a0001c0002t0001g0057 a0001c0002t0001g0069 others(5): Show |
10 | HG01169.hp1 HG02976.hp2 HG03491.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046+837delT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 454868 | ||||||
| chr5:454869 | T | TG | 8 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(5): Show |
21 | HG00099.hp1 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1046+818_1046+819i others(3): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454869 | |||||||
| chr5:454870 | T | G | 1 | a0001c0003t0002g0193 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1046+819T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454870 | |||||||
| chr5:454956 | A | G | 1 | a0001c0002t0001g0084 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1046+905A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 454956 | |||||||
| chr5:455007 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1046+956G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455007 | |||||||
| chr5:455011 | C | T | 1 | a0001c0001t0001g0030 | 3 | NA18960.hp2 NA18978.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1046+960C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455011 | |||||||
| chr5:455012 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1046+961G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455012 | |||||||
| chr5:455022 | A | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(15): Show |
34 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.1046+971A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455022 | |||||||
| chr5:455022 | A | G | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1046+971A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455022 | |||||||
| chr5:455024 | G | GGTGGCTC others(9): Show |
1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1046+984_1046+985i others(18): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 455024 | ||||||
| chr5:455043 | G | C | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1046+992G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455043 | |||||||
| chr5:455043 | G | GTGGCTCT others(11): Show |
123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1046+996_1046+997i others(20): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 455043 | ||||||
| chr5:455132 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1046+1081A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455132 | |||||||
| chr5:455155 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1046+1104C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455155 | |||||||
| chr5:455158 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0130 |
5 | HG00140.hp2 HG01074.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1046+1107C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455158 | |||||||
| chr5:455357 | T | G | 1 | a0001c0002t0001g0070 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1046+1306T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455357 | |||||||
| chr5:455394 | G | T | 9 | a0001c0002t0001g0006 a0001c0002t0001g0056 a0001c0002t0001g0057 others(6): Show |
18 | HG00408.hp1 HG01109.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.1046+1343G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455394 | |||||||
| chr5:455405 | T | G | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1046+1354T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455405 | |||||||
| chr5:455435 | G | A | 2 | a0001c0002t0001g0072 a0001c0002t0011g0071 |
2 | HG02735.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1046+1384G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455435 | |||||||
| chr5:455522 | C | T | 2 | a0001c0002t0001g0103 a0001c0002t0013g0102 |
2 | HG01168.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1047-1367C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455522 | |||||||
| chr5:455579 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1047-1310G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455579 | |||||||
| chr5:455581 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1047-1308A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455581 | |||||||
| chr5:455612 | TGAAA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1047-1273_1047-127 others(8): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 455612 | ||||||
| chr5:455665 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0132 a0001c0001t0001g0162 others(2): Show |
10 | HG00597.hp2 HG01934.hp2 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.1047-1224T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455665 | |||||||
| chr5:455667 | AT | A | 8 | a0001c0002t0001g0021 a0001c0002t0001g0074 a0001c0002t0001g0075 others(5): Show |
15 | HG01167.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-1217delT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 455667 | ||||||
| chr5:455689 | TGTA | T | 8 | a0001c0002t0001g0021 a0001c0002t0001g0074 a0001c0002t0001g0075 others(5): Show |
15 | HG01167.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-1199_1047-119 others(7): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455689 | |||||||
| chr5:455693 | T | A | 8 | a0001c0002t0001g0021 a0001c0002t0001g0074 a0001c0002t0001g0075 others(5): Show |
15 | HG01167.hp1 HG01433.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047-1196T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455693 | |||||||
| chr5:455696 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1047-1193C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455696 | |||||||
| chr5:455741 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0197 |
3 | HG01099.hp1 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1047-1148C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455741 | |||||||
| chr5:455787 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1047-1102A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455787 | |||||||
| chr5:455899 | C | T | 1 | a0001c0002t0001g0037 | 2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1047-990C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455899 | |||||||
| chr5:455901 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(64): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1047-988G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455901 | |||||||
| chr5:455915 | T | C | 4 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(1): Show |
4 | HG02922.hp2 HG02976.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047-974T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 455915 | |||||||
| chr5:456012 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1047-877C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456012 | |||||||
| chr5:456047 | C | T | 1 | a0001c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1047-842C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456047 | |||||||
| chr5:456093 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(20): Show |
43 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1047-796G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456093 | |||||||
| chr5:456140 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1047-749C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456140 | |||||||
| chr5:456271 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1047-618A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456271 | |||||||
| chr5:456342 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1047-547A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456342 | |||||||
| chr5:456400 | G | GC | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.1047-488dupC | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr5 | 456400 | ||||||
| chr5:456414 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1047-475C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456414 | |||||||
| chr5:456456 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1047-433G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456456 | |||||||
| chr5:456525 | C | A | 1 | a0001c0002t0003g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1047-364C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456525 | |||||||
| chr5:456542 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1047-347C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456542 | |||||||
| chr5:456662 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1047-227C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456662 | |||||||
| chr5:456732 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1047-157C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456732 | |||||||
| chr5:456800 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1047-89A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 4/12 | chr5 | 456800 | |||||||
| chr5:457061 | T | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(17): Show |
36 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1164+55T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457061 | |||||||
| chr5:457092 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1164+86G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457092 | |||||||
| chr5:457105 | G | A | 10 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(7): Show |
23 | HG01069.hp1 HG01099.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1164+99G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457105 | |||||||
| chr5:457116 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1164+110A>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457116 | |||||||
| chr5:457134 | G | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
244 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1164+128G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457134 | |||||||
| chr5:457146 | C | A | 13 | a0001c0002t0001g0023 a0001c0002t0001g0043 a0001c0002t0001g0104 others(10): Show |
29 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1164+140C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457146 | |||||||
| chr5:457309 | T | A | 1 | a0001c0002t0011g0071 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1164+303T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457309 | |||||||
| chr5:457331 | T | TG | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1164+332dupG | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr5 | 457331 | ||||||
| chr5:457365 | A | G | 1 | a0001c0001t0010g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1164+359A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457365 | |||||||
| chr5:457472 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0176 |
3 | HG01261.hp2 HG02148.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1165-428A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457472 | |||||||
| chr5:457482 | G | A | 6 | a0001c0001t0001g0127 a0001c0001t0001g0169 a0001c0001t0002g0126 others(3): Show |
6 | HG02273.hp2 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165-418G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457482 | |||||||
| chr5:457526 | G | A | 1 | a0001c0002t0001g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1165-374G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457526 | |||||||
| chr5:457555 | A | G | 2 | a0001c0001t0001g0046 a0005c0012t0001g0046 |
2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1165-345A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457555 | |||||||
| chr5:457614 | G | A | 1 | a0001c0003t0002g0187 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1165-286G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457614 | |||||||
| chr5:457840 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1165-60A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 5/12 | chr5 | 457840 | |||||||
| chr5:458069 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0157 |
4 | HG02257.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+44A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458069 | |||||||
| chr5:458303 | T | C | 1 | a0001c0002t0001g0091 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1290+278T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458303 | |||||||
| chr5:458385 | A | G | 7 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(4): Show |
16 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1290+360A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458385 | |||||||
| chr5:458468 | A | G | 1 | a0001c0002t0001g0036 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1290+443A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458468 | |||||||
| chr5:458573 | A | G | 1 | a0001c0002t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1290+548A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458573 | |||||||
| chr5:458600 | G | A | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+575G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458600 | |||||||
| chr5:458662 | C | T | 3 | a0001c0002t0001g0057 a0001c0002t0001g0060 a0001c0002t0001g0061 |
3 | NA18942.hp2 NA18961.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1290+637C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458662 | |||||||
| chr5:458678 | C | T | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+653C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458678 | |||||||
| chr5:458721 | A | T | 1 | a0001c0002t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1291-638A>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458721 | |||||||
| chr5:458726 | G | A | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291-633G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458726 | |||||||
| chr5:458742 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1291-617G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458742 | |||||||
| chr5:458858 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1291-501A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458858 | |||||||
| chr5:458884 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1291-475T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458884 | |||||||
| chr5:458888 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1291-471G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458888 | |||||||
| chr5:458953 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1291-406G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 458953 | |||||||
| chr5:459180 | G | GT | 8 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(5): Show |
21 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1291-165dupT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 459180 | ||||||
| chr5:459180 | GT | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1291-165delT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 459180 | ||||||
| chr5:459202 | CTT | C | 3 | a0001c0002t0001g0021 a0001c0002t0001g0074 a0001c0002t0001g0075 |
5 | NA18968.hp2 NA18983.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291-155_1291-154d others(4): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 459202 | ||||||
| chr5:459217 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1291-142C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 459217 | |||||||
| chr5:459226 | AT | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.1291-123delT | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr5 | 459226 | ||||||
| chr5:459300 | G | C | 2 | a0001c0002t0003g0018 a0001c0002t0003g0042 |
6 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291-59G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 6/12 | chr5 | 459300 | |||||||
| chr5:459566 | G | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0051 others(18): Show |
37 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.1391+107G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459566 | |||||||
| chr5:459619 | G | A | 4 | a0001c0002t0001g0034 a0001c0002t0001g0086 a0001c0002t0012g0065 others(1): Show |
5 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.1391+160G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459619 | |||||||
| chr5:459656 | C | T | 10 | a0001c0002t0001g0009 a0001c0002t0001g0023 a0001c0002t0001g0043 others(7): Show |
20 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1391+197C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459656 | |||||||
| chr5:459657 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1391+198A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459657 | |||||||
| chr5:459678 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1391+219T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459678 | |||||||
| chr5:459819 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1391+360G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459819 | |||||||
| chr5:459828 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1391+369T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459828 | |||||||
| chr5:459887 | A | G | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1391+428A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459887 | |||||||
| chr5:459964 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0010 others(69): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1391+505C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 459964 | |||||||
| chr5:460004 | C | T | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1391+545C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460004 | |||||||
| chr5:460020 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1391+561A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460020 | |||||||
| chr5:460161 | G | A | 2 | a0001c0002t0001g0092 a0004c0009t0001g0090 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1391+702G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460161 | |||||||
| chr5:460171 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1391+712T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460171 | |||||||
| chr5:460213 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0158 |
2 | NA18965.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1391+754T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460213 | |||||||
| chr5:460255 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1391+796C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460255 | |||||||
| chr5:460270 | C | T | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1391+811C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460270 | |||||||
| chr5:460469 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1391+1010C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460469 | |||||||
| chr5:460488 | C | A | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1391+1029C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460488 | |||||||
| chr5:460555 | G | A | 1 | a0001c0001t0009g0110 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1391+1096G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460555 | |||||||
| chr5:460595 | G | A | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1391+1136G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 460595 | |||||||
| chr5:460649 | GGTCTTAG others(19): Show |
G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0123 a0001c0001t0001g0183 |
6 | HG01261.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1391+1209_1391+123 others(30): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 460649 | ||||||
| chr5:461097 | G | A | 1 | a0001c0002t0001g0079 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1392-863G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 461097 | |||||||
| chr5:461169 | TAAATA | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
180 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1392-784_1392-780d others(7): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 461169 | ||||||
| chr5:461446 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1392-514C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 461446 | |||||||
| chr5:461612 | C | CA | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1392-335dupA | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 461612 | ||||||
| chr5:461612 | CA | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1392-335delA | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr5 | 461612 | ||||||
| chr5:461672 | G | A | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1392-288G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 461672 | |||||||
| chr5:461816 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1392-144T>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 7/12 | chr5 | 461816 | |||||||
| chr5:462344 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1653+37C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462344 | |||||||
| chr5:462350 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1653+43C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462350 | |||||||
| chr5:462408 | G | A | 6 | a0001c0003t0002g0008 a0001c0003t0002g0053 a0001c0003t0002g0187 others(3): Show |
15 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1653+101G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462408 | |||||||
| chr5:462441 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1653+134G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462441 | |||||||
| chr5:462516 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1653+209A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462516 | |||||||
| chr5:462542 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1653+235G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462542 | |||||||
| chr5:462619 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1653+312C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462619 | |||||||
| chr5:462651 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1653+344G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462651 | |||||||
| chr5:462672 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1653+365C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462672 | |||||||
| chr5:462880 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1653+573C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 462880 | |||||||
| chr5:463030 | G | A | 3 | a0001c0006t0001g0041 a0001c0006t0001g0088 a0001c0006t0001g0089 |
4 | HG02895.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+723G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463030 | |||||||
| chr5:463216 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1653+909G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463216 | |||||||
| chr5:463303 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1654-987T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463303 | |||||||
| chr5:463419 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1654-871C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463419 | |||||||
| chr5:463424 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1654-866G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463424 | |||||||
| chr5:463501 | T | C | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1654-789T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463501 | |||||||
| chr5:463563 | G | C | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-727G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463563 | |||||||
| chr5:463662 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1654-628A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463662 | |||||||
| chr5:463783 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.1654-507A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463783 | |||||||
| chr5:463822 | T | C | 1 | a0001c0001t0004g0140 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1654-468T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463822 | |||||||
| chr5:463910 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1654-380T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 463910 | |||||||
| chr5:464038 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1654-252C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464038 | |||||||
| chr5:464062 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.1654-228C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464062 | |||||||
| chr5:464078 | C | T | 1 | a0001c0002t0001g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1654-212C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464078 | |||||||
| chr5:464124 | GCTGCACG others(45): Show |
G | 1 | a0001c0007t0001g0142 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1654-113_1654-62de others(53): Show |
EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr5 | 464124 | ||||||
| chr5:464147 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1654-143G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464147 | |||||||
| chr5:464183 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA18963.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1654-107G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464183 | |||||||
| chr5:464224 | C | A | 10 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(7): Show |
23 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1654-66C>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464224 | |||||||
| chr5:464231 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0169 a0001c0001t0002g0126 others(3): Show |
6 | HG02273.hp2 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654-59C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 9/12 | chr5 | 464231 | |||||||
| chr5:464443 | C | T | 1 | a0001c0001t0010g0177 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1776+31C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464443 | |||||||
| chr5:464618 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1776+206C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464618 | |||||||
| chr5:464652 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1776+240C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464652 | |||||||
| chr5:464691 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1776+279C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464691 | |||||||
| chr5:464699 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1776+287C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464699 | |||||||
| chr5:464708 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1776+296T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464708 | |||||||
| chr5:464792 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
28 | HG00099.hp1 HG00408.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1777-319G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464792 | |||||||
| chr5:464820 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1777-291C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464820 | |||||||
| chr5:464889 | G | A | 1 | a0001c0002t0001g0035 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1777-222G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 464889 | |||||||
| chr5:465049 | A | G | 11 | a0001c0002t0003g0005 a0001c0002t0003g0018 a0001c0002t0003g0042 others(8): Show |
25 | HG00140.hp1 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1777-62A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 10/12 | chr5 | 465049 | |||||||
| chr5:465395 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1938+123T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 11/12 | chr5 | 465395 | |||||||
| chr5:465518 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(117): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1939-200C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 11/12 | chr5 | 465518 | |||||||
| chr5:465572 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0191 a0001c0001t0001g0192 others(2): Show |
6 | HG01099.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1939-146C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 11/12 | chr5 | 465572 | |||||||
| chr5:465593 | G | C | 1 | a0001c0001t0014g0141 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1939-125G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 11/12 | chr5 | 465593 | |||||||
| chr5:465909 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2066+64T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 465909 | |||||||
| chr5:465920 | C | T | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2066+75C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 465920 | |||||||
| chr5:465960 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2066+115G>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 465960 | |||||||
| chr5:465998 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2066+153A>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 465998 | |||||||
| chr5:466010 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2066+165T>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466010 | |||||||
| chr5:466026 | T | C | 3 | a0001c0004t0002g0024 a0001c0004t0002g0025 a0001c0004t0002g0105 |
7 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2066+181T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466026 | |||||||
| chr5:466071 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2066+226C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466071 | |||||||
| chr5:466075 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2066+230T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466075 | |||||||
| chr5:466101 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2066+256G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466101 | |||||||
| chr5:466103 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2066+258G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466103 | |||||||
| chr5:466143 | G | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(99): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.2066+298G>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466143 | |||||||
| chr5:466343 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
250 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.2067-384T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466343 | |||||||
| chr5:466403 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | NA18940.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2067-324C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466403 | |||||||
| chr5:466574 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2067-153G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466574 | |||||||
| chr5:466591 | G | A | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2067-136G>A | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466591 | |||||||
| chr5:466613 | C | T | 1 | a0001c0001t0005g0050 | 2 | NA18962.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2067-114C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466613 | |||||||
| chr5:466617 | C | T | 2 | a0001c0002t0001g0011 a0001c0002t0001g0070 |
7 | NA18942.hp1 NA18970.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.2067-110C>T | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466617 | |||||||
| chr5:466664 | C | G | 11 | a0001c0003t0002g0008 a0001c0003t0002g0016 a0001c0003t0002g0053 others(8): Show |
24 | HG00099.hp1 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.2067-63C>G | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466664 | |||||||
| chr5:466696 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.2067-31T>C | EXOC3 | ENSG00000180104.16 | transcript | ENST00000512944.6 | protein_coding | 12/12 | chr5 | 466696 |