Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2806 |
| ensemblid | ENSG00000125166.13 |
| hgncid | 4433 |
| symbol | GOT2 |
| name | glutamic-oxaloacetic transaminase 2 |
| refseq_nuc | NM_002080.4 |
| refseq_prot | NP_002071.2 |
| ensembl_nuc | ENST00000245206.10 |
| ensembl_prot | ENSP00000245206.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 58707131 |
| end | 58734316 |
| strand | - |
| ver | v1.2 |
| region | chr16:58707131-58734316 |
| region5000 | chr16:58702131-58739316 |
| regionname0 | GOT2_chr16_58707131_58734316 |
| regionname5000 | GOT2_chr16_58702131_58739316 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 430 | 264 | 71 | 46 | 117 | 4 | 26 | 88 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0002 | 1/1 | 430 | 105 | 11 | 14 | 65 | 5 | 8 | 50 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0003 | 0/0 | 430 | 17 | 4 | 7 | 1 | 2 | 3 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0004 | 0/0 | 430 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0005 | 0/0 | 430 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | MSLLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0006 | 0/0 | 430 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | MSLLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0007 | 0/0 | 438 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(433): Show |
chr16 | 58702131 | 58739316 |
| a0008 | 0/0 | 430 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| a0009 | 0/0 | 430 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | MALLH others(425): Show |
chr16 | 58702131 | 58739316 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1290 | 227 | 55 | 43 | 104 | 4 | 21 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0001c0004 | 0/0 | 1290 | 12 | 0 | 0 | 11 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0001c0005 | 0/0 | 1290 | 12 | 12 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0001c0006 | 0/0 | 1290 | 7 | 3 | 3 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0001c0008 | 0/0 | 1290 | 5 | 0 | 0 | 1 | 0 | 4 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0001c0015 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0002c0002 | 1/1 | 1290 | 102 | 11 | 14 | 62 | 5 | 8 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0002c0010 | 0/0 | 1290 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0002c0016 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0003c0003 | 0/0 | 1290 | 17 | 4 | 7 | 1 | 2 | 3 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0004c0007 | 0/0 | 1290 | 6 | 6 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0005c0009 | 0/0 | 1290 | 3 | 0 | 1 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | ATGTC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0006c0011 | 0/0 | 1290 | 2 | 0 | 0 | 0 | 1 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | ATGTC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0007c0012 | 0/0 | 1314 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1309): Show |
chr16 | 58702131 | 58739316 | ||
| a0008c0014 | 0/0 | 1290 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 | ||
| a0009c0013 | 0/0 | 1290 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ATGGC others(1285): Show |
chr16 | 58702131 | 58739316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2421 | 89 | 2 | 18 | 62 | 0 | 7 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0002 | 0/0 | 2421 | 96 | 25 | 15 | 41 | 4 | 11 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0003 | 0/0 | 2421 | 19 | 17 | 2 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0004 | 0/0 | 2421 | 8 | 0 | 6 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0005 | 0/0 | 2421 | 8 | 8 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0008 | 0/0 | 2421 | 2 | 0 | 2 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0010 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0011 | 0/0 | 2421 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0014 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0015 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0001t0017 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0004t0001 | 0/0 | 2421 | 12 | 0 | 0 | 11 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0005t0001 | 0/0 | 2421 | 8 | 8 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0005t0002 | 0/0 | 2421 | 4 | 4 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0006t0001 | 0/0 | 2421 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0006t0002 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0006t0006 | 0/0 | 2421 | 4 | 0 | 3 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0008t0002 | 0/0 | 2421 | 5 | 0 | 0 | 1 | 0 | 4 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0001c0015t0001 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0002t0001 | 1/1 | 2421 | 96 | 11 | 12 | 59 | 4 | 8 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0002t0007 | 0/0 | 2421 | 2 | 0 | 1 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0002t0009 | 0/0 | 2421 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0002t0012 | 0/0 | 2421 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0002t0013 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0010t0001 | 0/0 | 2421 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0002c0016t0001 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0003c0003t0002 | 0/0 | 2421 | 17 | 4 | 7 | 1 | 2 | 3 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0004c0007t0003 | 0/0 | 2421 | 6 | 6 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0005c0009t0002 | 0/0 | 2421 | 3 | 0 | 1 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0006c0011t0002 | 0/0 | 2421 | 2 | 0 | 0 | 0 | 1 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0007c0012t0001 | 0/0 | 2445 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2440): Show |
chr16 | 58702131 | 58739316 |
| a0008c0014t0016 | 0/0 | 2421 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| a0009c0013t0001 | 0/0 | 2421 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | ACCTT others(2416): Show |
chr16 | 58702131 | 58739316 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 4 | 12 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 4 | 1 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0003 | 0/0 | 14 | 1 | 0 | 9 | 1 | 3 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0004g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0004g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0005g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0010g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0014g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0015g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0001t0017g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0004t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0004t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0005t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0006t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0006t0006g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0006t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0008t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0008t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0008t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0008t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0001c0015t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0001 | 1/1 | 22 | 1 | 4 | 12 | 0 | 3 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0004 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0014 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0007g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0012g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0002t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0010t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0010t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0002c0016t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0003c0003t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0004c0007t0003g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0004c0007t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0005c0009t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0005c0009t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0005c0009t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0006c0011t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0006c0011t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0007c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0008c0014t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| a0009c0013t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00099 | hp2 | a0003 | c0003 | t0002 | g0196 | EUR | GBR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0065 | EUR | GBR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00140 | hp2 | a0003 | c0003 | t0002 | g0016 | EUR | GBR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00323 | hp1 | a0006 | c0011 | t0002 | g0228 | EUR | FIN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00323 | hp2 | a0002 | c0002 | t0007 | g0025 | EUR | FIN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00597 | hp2 | a0001 | c0006 | t0006 | g0019 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00673 | hp2 | a0002 | c0002 | t0009 | g0062 | EAS | CHS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00735 | hp2 | a0003 | c0003 | t0002 | g0195 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00738 | hp1 | a0002 | c0002 | t0007 | g0025 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG00741 | hp2 | a0003 | c0003 | t0002 | g0194 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0175 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0200 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01071 | hp1 | a0001 | c0001 | t0008 | g0174 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01081 | hp1 | a0002 | c0002 | t0012 | g0057 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01099 | hp1 | a0003 | c0003 | t0002 | g0202 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0016 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01358 | hp1 | a0005 | c0009 | t0002 | g0226 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01433 | hp1 | a0003 | c0003 | t0002 | g0198 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | CLM | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0069 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0045 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01891 | hp1 | a0003 | c0003 | t0002 | g0040 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01975 | hp2 | a0001 | c0006 | t0006 | g0019 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG01981 | hp2 | a0001 | c0006 | t0006 | g0019 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02040 | hp2 | a0002 | c0010 | t0001 | g0162 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0191 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0230 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02145 | hp2 | a0003 | c0003 | t0002 | g0181 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02148 | hp1 | a0001 | c0006 | t0006 | g0082 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02148 | hp2 | a0003 | c0003 | t0002 | g0016 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | CDX | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0026 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02257 | hp2 | a0007 | c0012 | t0001 | g0049 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02280 | hp1 | a0004 | c0007 | t0003 | g0012 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | KHV | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02572 | hp1 | a0004 | c0007 | t0003 | g0012 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02602 | hp1 | a0001 | c0004 | t0001 | g0104 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0232 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02683 | hp1 | a0003 | c0003 | t0002 | g0197 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02809 | hp1 | a0001 | c0005 | t0002 | g0192 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0044 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02895 | hp1 | a0001 | c0001 | t0015 | g0212 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02896 | hp1 | a0001 | c0005 | t0002 | g0189 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02897 | hp2 | a0001 | c0005 | t0002 | g0190 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0173 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0043 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03098 | hp2 | a0008 | c0014 | t0016 | g0136 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0043 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03453 | hp2 | a0001 | c0006 | t0002 | g0089 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03516 | hp1 | a0001 | c0006 | t0001 | g0026 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03579 | hp2 | a0001 | c0005 | t0002 | g0188 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03654 | hp2 | a0001 | c0008 | t0002 | g0085 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0154 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03704 | hp1 | a0005 | c0009 | t0002 | g0225 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03710 | hp2 | a0006 | c0011 | t0002 | g0227 | SAS | PJL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03831 | hp2 | a0001 | c0008 | t0002 | g0028 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0199 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0135 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0074 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04115 | hp1 | a0001 | c0008 | t0002 | g0028 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04184 | hp2 | a0005 | c0009 | t0002 | g0229 | SAS | BEB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04199 | hp1 | a0003 | c0003 | t0002 | g0016 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04199 | hp2 | a0001 | c0008 | t0002 | g0084 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18522 | hp1 | a0001 | c0015 | t0001 | g0138 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18747 | hp1 | a0001 | c0004 | t0001 | g0031 | EAS | CHB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18940 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18946 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18951 | hp2 | a0003 | c0003 | t0002 | g0201 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18967 | hp1 | a0002 | c0002 | t0009 | g0102 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18981 | hp1 | a0002 | c0016 | t0001 | g0067 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18987 | hp2 | a0009 | c0013 | t0001 | g0110 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0103 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18993 | hp1 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18999 | hp1 | a0001 | c0004 | t0001 | g0031 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19000 | hp2 | a0002 | c0010 | t0001 | g0151 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19003 | hp2 | a0001 | c0008 | t0002 | g0101 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19009 | hp1 | a0001 | c0001 | t0010 | g0130 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19009 | hp2 | a0002 | c0002 | t0013 | g0059 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0045 | AFR | LWK | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | LWK | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19043 | hp1 | a0004 | c0007 | t0003 | g0210 | AFR | LWK | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19077 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19081 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0006 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ASW | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA20129 | hp2 | a0004 | c0007 | t0003 | g0012 | AFR | ASW | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02109 | hp2 | a0003 | c0003 | t0002 | g0040 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0193 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03471 | hp1 | a0004 | c0007 | t0003 | g0012 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0178 | AFR | MSL | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG06807 | hp1 | a0001 | c0001 | t0017 | g0234 | AFR | USA | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| HG06807 | hp2 | a0004 | c0007 | t0003 | g0012 | AFR | USA | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | USA | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | USA | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0001 | REF | REF | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0001 | REF | REF | GOT2_chr16_58702131_58739316 | GOT2 | chr16 | 58702131 | 58739316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:58709550 | A | C | 8 | a0001 a0003 a0004 others(5): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
missense_variant | MODERATE | c.1037T>G | p.Val346Gly | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/10 | 1125/2421 | 1037/1293 | 346/430 | chr16 | 58709550 | |||
| chr16:58718233 | C | T | 1 | a0006 | 2 | HG00323.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.665G>A | p.Arg222His | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/10 | 753/2421 | 665/1293 | 222/430 | chr16 | 58718233 | |||
| chr16:58718562 | C | T | 1 | a0003 | 17 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(14): Show |
missense_variant | MODERATE | c.562G>A | p.Gly188Ser | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 5/10 | 650/2421 | 562/1293 | 188/430 | chr16 | 58718562 | |||
| chr16:58718664 | C | T | 1 | a0004 | 6 | HG02280.hp1 HG02572.hp1 HG03471.hp1 others(3): Show |
missense_variant | MODERATE | c.460G>A | p.Asp154Asn | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 5/10 | 548/2421 | 460/1293 | 154/430 | chr16 | 58718664 | |||
| chr16:58722260 | C | A | 1 | a0008 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.265G>T | p.Ala89Ser | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/10 | 353/2421 | 265/1293 | 89/430 | chr16 | 58722260 | |||
| chr16:58723766 | C | T | 1 | a0009 | 1 | NA18987.hp2 | missense_variant | MODERATE | c.226G>A | p.Val76Ile | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/10 | 314/2421 | 226/1293 | 76/430 | chr16 | 58723766 | |||
| chr16:58734157 | C | CGCGGCGG others(17): Show |
1 | a0007 | 1 | HG02257.hp2 | disruptive_inframe_insertion | MODERATE | c.48_71dupCTTCCACCCG others(14): Show |
p.Ala24_Ala25insPheH others(20): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/10 | 159/2421 | 71/1293 | 24/430 | chr16 | 58734157 | |||
| chr16:58734225 | C | A | 2 | a0005 a0006 |
5 | HG00323.hp1 HG01358.hp1 HG03704.hp1 others(2): Show |
missense_variant | MODERATE | c.4G>T | p.Ala2Ser | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/10 | 92/2421 | 4/1293 | 2/430 | chr16 | 58734225 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:58708216 | G | A | 2 | a0001c0015 a0007c0012 |
2 | HG02257.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1248C>T | p.Ser416Ser | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 1336/2421 | 1248/1293 | 416/430 | chr16 | 58708216 | |||
| chr16:58716700 | G | A | 13 | a0001c0001 a0001c0004 a0001c0005 others(10): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
synonymous_variant | LOW | c.816C>T | p.Cys272Cys | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/10 | 904/2421 | 816/1293 | 272/430 | chr16 | 58716700 | |||
| chr16:58722171 | G | A | 1 | a0001c0005 | 12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.354C>T | p.Ser118Ser | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/10 | 442/2421 | 354/1293 | 118/430 | chr16 | 58722171 | |||
| chr16:58723764 | A | C | 12 | a0001c0001 a0001c0004 a0001c0005 others(9): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
synonymous_variant | LOW | c.228T>G | p.Val76Val | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/10 | 316/2421 | 228/1293 | 76/430 | chr16 | 58723764 | |||
| chr16:58723779 | A | G | 9 | a0001c0001 a0001c0005 a0002c0010 others(6): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
synonymous_variant | LOW | c.213T>C | p.Asn71Asn | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/10 | 301/2421 | 213/1293 | 71/430 | chr16 | 58723779 | |||
| chr16:58723791 | G | A | 1 | a0001c0005 | 12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.201C>T | p.Tyr67Tyr | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/10 | 289/2421 | 201/1293 | 67/430 | chr16 | 58723791 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:58707140 | C | G | 1 | a0001c0006t0006 | 4 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1031G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 1031 | chr16 | 58707140 | ||||||
| chr16:58707244 | C | T | 1 | a0002c0002t0009 | 2 | HG00673.hp2 NA18967.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 927 | chr16 | 58707244 | ||||||
| chr16:58707283 | C | T | 2 | a0001c0001t0015 a0002c0002t0012 |
2 | HG01081.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*888G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 888 | chr16 | 58707283 | ||||||
| chr16:58707311 | A | T | 3 | a0001c0001t0003 a0001c0001t0015 a0004c0007t0003 |
26 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*860T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 860 | chr16 | 58707311 | ||||||
| chr16:58707383 | G | C | 1 | a0001c0001t0011 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*788C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 788 | chr16 | 58707383 | ||||||
| chr16:58707463 | A | G | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(10): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*708T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 708 | chr16 | 58707463 | ||||||
| chr16:58707602 | C | T | 1 | a0001c0001t0010 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 569 | chr16 | 58707602 | ||||||
| chr16:58707645 | G | T | 1 | a0001c0001t0008 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*526C>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 526 | chr16 | 58707645 | ||||||
| chr16:58707883 | T | A | 1 | a0002c0002t0013 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 288 | chr16 | 58707883 | ||||||
| chr16:58707893 | G | A | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 278 | chr16 | 58707893 | ||||||
| chr16:58707936 | A | C | 1 | a0001c0001t0017 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 235 | chr16 | 58707936 | ||||||
| chr16:58707946 | C | A | 4 | a0001c0001t0003 a0001c0001t0015 a0004c0007t0003 others(1): Show |
27 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*225G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 225 | chr16 | 58707946 | ||||||
| chr16:58708045 | T | C | 1 | a0001c0001t0004 | 8 | HG00733.hp1 HG01074.hp2 HG01192.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*126A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 10/10 | 126 | chr16 | 58708045 | ||||||
| chr16:58734252 | G | A | 2 | a0001c0001t0005 a0001c0001t0017 |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-24C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/10 | 24 | chr16 | 58734252 | ||||||
| chr16:58734269 | C | G | 1 | a0002c0002t0007 | 2 | HG00323.hp2 HG00738.hp1 |
5_prime_UTR_variant | MODIFIER | c.-41G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/10 | 41 | chr16 | 58734269 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:58708366 | G | A | 1 | a0003c0003t0002g0200 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1171-73C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708366 | |||||||
| chr16:58708374 | A | T | 1 | a0001c0005t0002g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1171-81T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708374 | |||||||
| chr16:58708393 | G | A | 6 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(3): Show |
16 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1171-100C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708393 | |||||||
| chr16:58708451 | T | C | 3 | a0001c0001t0008g0174 a0001c0001t0008g0175 a0001c0006t0002g0089 |
3 | HG01069.hp1 HG01071.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1171-158A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708451 | |||||||
| chr16:58708467 | C | T | 16 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(13): Show |
27 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1171-174G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708467 | |||||||
| chr16:58708477 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA19001.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1171-184G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708477 | |||||||
| chr16:58708520 | G | A | 5 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1171-227C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708520 | |||||||
| chr16:58708558 | G | A | 16 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(13): Show |
27 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1171-265C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708558 | |||||||
| chr16:58708576 | G | A | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(57): Show |
109 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1171-283C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708576 | |||||||
| chr16:58708626 | GA | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(143): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1171-334delT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708626 | |||||||
| chr16:58708704 | T | G | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1171-411A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708704 | |||||||
| chr16:58708849 | T | TA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(155): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.1171-557dupT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58708849 | |||||||
| chr16:58709089 | ATG | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0137 |
4 | HG02809.hp2 HG03195.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+326_1170+327d others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58709089 | |||||||
| chr16:58709278 | AAAAAC | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(170): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1170+134_1170+138d others(7): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58709278 | |||||||
| chr16:58709318 | G | A | 5 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+99C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58709318 | |||||||
| chr16:58709363 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1170+54C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58709363 | |||||||
| chr16:58709386 | G | A | 3 | a0001c0001t0008g0174 a0001c0001t0008g0175 a0001c0006t0002g0089 |
3 | HG01069.hp1 HG01071.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1170+31C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 9/9 | chr16 | 58709386 | |||||||
| chr16:58709686 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-119C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58709686 | |||||||
| chr16:58709816 | C | T | 4 | a0001c0001t0005g0017 a0001c0001t0005g0232 a0001c0001t0005g0233 others(1): Show |
7 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020-249G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58709816 | |||||||
| chr16:58709819 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(171): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1020-252G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58709819 | |||||||
| chr16:58709850 | A | G | 2 | a0001c0001t0005g0230 a0001c0001t0005g0231 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1020-283T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58709850 | |||||||
| chr16:58709947 | T | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0232 a0001c0001t0005g0233 others(1): Show |
7 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020-380A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58709947 | |||||||
| chr16:58710047 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1020-480C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710047 | |||||||
| chr16:58710105 | G | A | 1 | a0002c0002t0001g0097 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1020-538C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710105 | |||||||
| chr16:58710106 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1020-539G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710106 | |||||||
| chr16:58710116 | A | T | 1 | a0002c0002t0001g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1020-549T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710116 | |||||||
| chr16:58710165 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(171): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1020-598G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710165 | |||||||
| chr16:58710176 | G | A | 4 | a0001c0001t0005g0017 a0001c0001t0005g0232 a0001c0001t0005g0233 others(1): Show |
7 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020-609C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710176 | |||||||
| chr16:58710193 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1020-626A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710193 | |||||||
| chr16:58710198 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1020-631G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710198 | |||||||
| chr16:58710396 | C | CT | 12 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0126 others(9): Show |
22 | HG00597.hp2 HG01517.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.1020-830dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710396 | |||||||
| chr16:58710397 | T | C | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1020-830A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710397 | |||||||
| chr16:58710401 | T | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0232 a0001c0001t0005g0233 others(1): Show |
7 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020-834A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710401 | |||||||
| chr16:58710438 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0217 others(2): Show |
13 | HG00423.hp2 HG01981.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.1020-871G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710438 | |||||||
| chr16:58710465 | C | T | 6 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(3): Show |
16 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-898G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710465 | |||||||
| chr16:58710664 | G | A | 1 | a0001c0008t0002g0101 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1020-1097C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710664 | |||||||
| chr16:58710716 | CTAAAAAT others(79): Show |
C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(90): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1020-1235_1020-115 others(90): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710716 | |||||||
| chr16:58710738 | C | G | 5 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020-1171G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710738 | |||||||
| chr16:58710915 | C | T | 1 | a0001c0006t0001g0026 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1020-1348G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710915 | |||||||
| chr16:58710951 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1020-1384C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710951 | |||||||
| chr16:58710967 | C | CA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(61): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1020-1401dupT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710967 | |||||||
| chr16:58710967 | C | CAA | 19 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0047 others(16): Show |
26 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1020-1402_1020-140 others(6): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710967 | |||||||
| chr16:58710967 | CA | C | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(61): Show |
126 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.1020-1401delT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710967 | |||||||
| chr16:58710985 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1020-1418T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58710985 | |||||||
| chr16:58711052 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(31): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1020-1485T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711052 | |||||||
| chr16:58711163 | CTGAGACA others(4): Show |
C | 1 | a0002c0002t0001g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1020-1607_1020-159 others(15): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711163 | |||||||
| chr16:58711238 | G | A | 1 | a0001c0001t0014g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1020-1671C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711238 | |||||||
| chr16:58711421 | T | C | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1020-1854A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711421 | |||||||
| chr16:58711437 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(90): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1020-1870A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711437 | |||||||
| chr16:58711513 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(168): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1020-1946A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711513 | |||||||
| chr16:58711513 | T | G | 6 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(3): Show |
16 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-1946A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711513 | |||||||
| chr16:58711689 | T | C | 2 | a0002c0002t0009g0062 a0002c0002t0009g0102 |
2 | HG00673.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1020-2122A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711689 | |||||||
| chr16:58711818 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0203 others(11): Show |
24 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.1020-2251G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711818 | |||||||
| chr16:58711942 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(173): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1020-2375A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711942 | |||||||
| chr16:58711975 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1020-2408A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58711975 | |||||||
| chr16:58712038 | C | T | 1 | a0003c0003t0002g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1020-2471G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712038 | |||||||
| chr16:58712078 | T | G | 1 | a0002c0002t0001g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1020-2511A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712078 | |||||||
| chr16:58712082 | T | C | 5 | a0002c0002t0001g0020 a0002c0002t0001g0021 a0002c0002t0001g0087 others(2): Show |
9 | HG02451.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1020-2515A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712082 | |||||||
| chr16:58712086 | A | G | 6 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(3): Show |
16 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1020-2519T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712086 | |||||||
| chr16:58712114 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(148): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1020-2547A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712114 | |||||||
| chr16:58712144 | C | T | 1 | a0001c0006t0002g0089 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1020-2577G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712144 | |||||||
| chr16:58712237 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1020-2670G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712237 | |||||||
| chr16:58712290 | T | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0037 a0001c0001t0011g0154 |
10 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1020-2723A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712290 | |||||||
| chr16:58712317 | G | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(12): Show |
26 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1020-2750C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712317 | |||||||
| chr16:58712339 | C | G | 1 | a0002c0002t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1020-2772G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712339 | |||||||
| chr16:58712354 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(148): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1020-2787T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712354 | |||||||
| chr16:58712522 | G | GAAC | 125 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(122): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1020-2958_1020-295 others(7): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712522 | |||||||
| chr16:58712568 | G | A | 2 | a0001c0001t0003g0214 a0001c0001t0003g0215 |
2 | HG02451.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1020-3001C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712568 | |||||||
| chr16:58712699 | A | G | 5 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1020-3132T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712699 | |||||||
| chr16:58712700 | T | C | 2 | a0006c0011t0002g0227 a0006c0011t0002g0228 |
2 | HG00323.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1020-3133A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712700 | |||||||
| chr16:58712712 | T | A | 1 | a0002c0002t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1020-3145A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712712 | |||||||
| chr16:58712875 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1019+3139G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712875 | |||||||
| chr16:58712990 | T | C | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+3024A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58712990 | |||||||
| chr16:58713002 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(174): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1019+3012T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713002 | |||||||
| chr16:58713124 | A | G | 1 | a0001c0001t0014g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1019+2890T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713124 | |||||||
| chr16:58713346 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1019+2668C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713346 | |||||||
| chr16:58713498 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1019+2516T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713498 | |||||||
| chr16:58713638 | T | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(31): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1019+2376A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713638 | |||||||
| chr16:58713702 | T | C | 8 | a0001c0001t0002g0009 a0001c0001t0002g0147 a0001c0001t0002g0149 others(5): Show |
14 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1019+2312A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713702 | |||||||
| chr16:58713755 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(32): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.1019+2259T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713755 | |||||||
| chr16:58713922 | C | T | 16 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(13): Show |
27 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1019+2092G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713922 | |||||||
| chr16:58713939 | T | C | 2 | a0002c0002t0001g0064 a0002c0002t0001g0076 |
2 | NA18948.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1019+2075A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58713939 | |||||||
| chr16:58714067 | T | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0114 a0001c0001t0001g0125 others(1): Show |
6 | NA18949.hp2 NA18967.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1019+1947A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714067 | |||||||
| chr16:58714117 | G | C | 87 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(84): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1019+1897C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714117 | |||||||
| chr16:58714366 | C | G | 6 | a0001c0001t0005g0017 a0001c0001t0005g0230 a0001c0001t0005g0231 others(3): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019+1648G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714366 | |||||||
| chr16:58714439 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(173): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.1019+1575C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714439 | |||||||
| chr16:58714538 | C | T | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1019+1476G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714538 | |||||||
| chr16:58714551 | C | CA | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(52): Show |
97 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1019+1462dupT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714551 | |||||||
| chr16:58714680 | TAGCCTGG others(7): Show |
T | 1 | a0001c0001t0002g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1019+1320_1019+133 others(18): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714680 | |||||||
| chr16:58714702 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1019+1312G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714702 | |||||||
| chr16:58714712 | A | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(12): Show |
26 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1019+1302T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714712 | |||||||
| chr16:58714796 | T | A | 1 | a0001c0001t0002g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1019+1218A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714796 | |||||||
| chr16:58714844 | A | G | 2 | a0001c0001t0001g0113 a0001c0008t0002g0101 |
2 | NA19003.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1019+1170T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714844 | |||||||
| chr16:58714900 | C | T | 1 | a0001c0001t0002g0167 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1019+1114G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714900 | |||||||
| chr16:58714957 | C | T | 1 | a0002c0002t0001g0056 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1019+1057G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58714957 | |||||||
| chr16:58715011 | T | C | 6 | a0001c0001t0002g0009 a0001c0001t0002g0147 a0001c0001t0002g0157 others(3): Show |
12 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1019+1003A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715011 | |||||||
| chr16:58715314 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1019+700C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715314 | |||||||
| chr16:58715340 | C | T | 5 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1019+674G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715340 | |||||||
| chr16:58715394 | T | A | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1019+620A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715394 | |||||||
| chr16:58715394 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(171): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.1019+620A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715394 | |||||||
| chr16:58715459 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1019+555G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715459 | |||||||
| chr16:58715562 | T | C | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1019+452A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715562 | |||||||
| chr16:58715621 | C | A | 1 | a0001c0001t0002g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1019+393G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715621 | |||||||
| chr16:58715628 | C | T | 16 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0041 others(13): Show |
27 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1019+386G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715628 | |||||||
| chr16:58715693 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1019+321G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715693 | |||||||
| chr16:58715713 | C | T | 5 | a0001c0001t0003g0013 a0001c0001t0003g0203 a0001c0001t0003g0205 others(2): Show |
9 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1019+301G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715713 | |||||||
| chr16:58715753 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1019+261A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715753 | |||||||
| chr16:58715831 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1019+183G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715831 | |||||||
| chr16:58715861 | T | A | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1019+153A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715861 | |||||||
| chr16:58715861 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1019+153A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 8/9 | chr16 | 58715861 | |||||||
| chr16:58716254 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(31): Show |
57 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.854-75A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716254 | |||||||
| chr16:58716256 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.854-77G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716256 | |||||||
| chr16:58716559 | G | GAC | 14 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0182 others(11): Show |
17 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.853+102_853+103dup others(2): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | G | GACAC | 4 | a0002c0002t0001g0087 a0002c0002t0001g0090 a0003c0003t0002g0198 others(1): Show |
4 | HG01433.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+100_853+103dup others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | GAC | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(63): Show |
111 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.853+102_853+103del others(2): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | GACAC | G | 68 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(65): Show |
118 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.853+100_853+103del others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | GACACACA others(3): Show |
G | 1 | a0001c0001t0002g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.853+94_853+103delG others(9): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | GACACACA others(5): Show |
G | 6 | a0001c0001t0005g0017 a0001c0001t0005g0230 a0001c0001t0005g0231 others(3): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+92_853+103delG others(11): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716559 | GACACACA others(7): Show |
G | 1 | a0002c0002t0001g0020 | 3 | HG02647.hp2 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.853+90_853+103delG others(13): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716559 | |||||||
| chr16:58716588 | A | ACC | 5 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(2): Show |
15 | HG00597.hp2 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.853+73_853+74dupGG | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716588 | |||||||
| chr16:58716588 | A | C | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853+75T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 7/9 | chr16 | 58716588 | |||||||
| chr16:58716939 | G | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(14): Show |
28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.703-126C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58716939 | |||||||
| chr16:58716943 | T | G | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703-130A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58716943 | |||||||
| chr16:58716965 | A | T | 18 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0179 others(15): Show |
22 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-152T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58716965 | |||||||
| chr16:58716983 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.703-170G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58716983 | |||||||
| chr16:58717324 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(25): Show |
50 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.703-511G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58717324 | |||||||
| chr16:58717734 | A | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
11 | HG02056.hp1 HG02155.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.702+462T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58717734 | |||||||
| chr16:58717952 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(40): Show |
71 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.702+244C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58717952 | |||||||
| chr16:58717977 | G | A | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.702+219C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58717977 | |||||||
| chr16:58718006 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+190A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718006 | |||||||
| chr16:58718012 | T | A | 1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.702+184A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718012 | |||||||
| chr16:58718015 | G | A | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.702+181C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718015 | |||||||
| chr16:58718021 | A | G | 1 | a0002c0002t0001g0083 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.702+175T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718021 | |||||||
| chr16:58718093 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.702+103G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718093 | |||||||
| chr16:58718159 | A | G | 8 | a0001c0001t0014g0173 a0001c0004t0001g0006 a0001c0004t0001g0031 others(5): Show |
17 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.702+37T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 6/9 | chr16 | 58718159 | |||||||
| chr16:58718446 | T | C | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.597+81A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 5/9 | chr16 | 58718446 | |||||||
| chr16:58718482 | G | A | 1 | a0002c0002t0001g0093 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.597+45C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 5/9 | chr16 | 58718482 | |||||||
| chr16:58718747 | G | C | 4 | a0001c0001t0005g0017 a0001c0001t0005g0232 a0001c0001t0005g0233 others(1): Show |
7 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-59C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58718747 | |||||||
| chr16:58718777 | T | C | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.436-89A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58718777 | |||||||
| chr16:58718845 | G | C | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.436-157C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58718845 | |||||||
| chr16:58718937 | T | A | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.436-249A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58718937 | |||||||
| chr16:58718938 | C | A | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.436-250G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58718938 | |||||||
| chr16:58719193 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01255.hp2 | splice_region_variant&intron_variant | LOW | c.435+3G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 4/9 | chr16 | 58719193 | |||||||
| chr16:58719356 | T | C | 1 | a0001c0006t0001g0026 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.376-101A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719356 | |||||||
| chr16:58719401 | C | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.376-146G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719401 | |||||||
| chr16:58719578 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.376-323G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719578 | |||||||
| chr16:58719729 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.376-474A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719729 | |||||||
| chr16:58719746 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.376-491G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719746 | |||||||
| chr16:58719857 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(12): Show |
31 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.376-602C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58719857 | |||||||
| chr16:58720069 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.376-814G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720069 | |||||||
| chr16:58720091 | C | T | 10 | a0003c0003t0002g0016 a0003c0003t0002g0194 a0003c0003t0002g0195 others(7): Show |
13 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-836G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720091 | |||||||
| chr16:58720101 | C | G | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-846G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720101 | |||||||
| chr16:58720127 | A | G | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-872T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720127 | |||||||
| chr16:58720134 | G | A | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-879C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720134 | |||||||
| chr16:58720189 | C | T | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-934G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720189 | |||||||
| chr16:58720190 | G | A | 74 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(71): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.376-935C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720190 | |||||||
| chr16:58720321 | T | C | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-1066A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720321 | |||||||
| chr16:58720355 | A | G | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-1100T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720355 | |||||||
| chr16:58720544 | G | T | 1 | a0001c0001t0003g0204 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.376-1289C>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720544 | |||||||
| chr16:58720570 | G | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.376-1315C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720570 | |||||||
| chr16:58720578 | A | AT | 28 | a0001c0001t0001g0046 a0001c0001t0001g0123 a0001c0001t0001g0208 others(25): Show |
36 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.376-1324dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720578 | |||||||
| chr16:58720578 | A | ATT | 40 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(37): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.376-1325_376-1324d others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720578 | |||||||
| chr16:58720578 | AT | A | 13 | a0001c0001t0002g0180 a0001c0004t0001g0006 a0001c0004t0001g0031 others(10): Show |
22 | HG01515.hp1 HG02080.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.376-1324delA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720578 | |||||||
| chr16:58720689 | C | T | 2 | a0003c0003t0002g0194 a0003c0003t0002g0200 |
2 | HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.376-1434G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720689 | |||||||
| chr16:58720767 | C | CG | 25 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0131 others(22): Show |
38 | HG01175.hp1 HG01934.hp1 HG01934.hp2 others(35): Show |
intron_variant | MODIFIER | c.375+1382dupC | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720767 | |||||||
| chr16:58720775 | C | T | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.375+1375G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720775 | |||||||
| chr16:58720837 | T | C | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.375+1313A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720837 | |||||||
| chr16:58720838 | G | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.375+1312C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720838 | |||||||
| chr16:58720878 | G | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | NA19001.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.375+1272C>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720878 | |||||||
| chr16:58720882 | G | A | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.375+1268C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720882 | |||||||
| chr16:58720912 | G | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.375+1238C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720912 | |||||||
| chr16:58720943 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.375+1207A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720943 | |||||||
| chr16:58720984 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(72): Show |
131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.375+1166C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58720984 | |||||||
| chr16:58721055 | A | C | 7 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(4): Show |
16 | HG02080.hp2 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.375+1095T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721055 | |||||||
| chr16:58721073 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.375+1077G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721073 | |||||||
| chr16:58721272 | C | T | 118 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(115): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.375+878G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721272 | |||||||
| chr16:58721333 | C | T | 9 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.375+817G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721333 | |||||||
| chr16:58721454 | T | C | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.375+696A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721454 | |||||||
| chr16:58721535 | A | G | 1 | a0001c0001t0014g0173 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.375+615T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721535 | |||||||
| chr16:58721618 | C | T | 7 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0179 others(4): Show |
8 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+532G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721618 | |||||||
| chr16:58721658 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.375+492A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721658 | |||||||
| chr16:58721724 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.375+426A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721724 | |||||||
| chr16:58721781 | AT | A | 116 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(113): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.375+368delA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721781 | |||||||
| chr16:58721781 | ATT | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(46): Show |
77 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.375+367_375+368del others(2): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721781 | |||||||
| chr16:58721883 | T | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(12): Show |
31 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.375+267A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721883 | |||||||
| chr16:58721944 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.375+206G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58721944 | |||||||
| chr16:58722023 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.375+127T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 3/9 | chr16 | 58722023 | |||||||
| chr16:58722314 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.247-36A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722314 | |||||||
| chr16:58722316 | C | T | 2 | a0001c0001t0003g0024 a0001c0001t0015g0212 |
4 | HG02717.hp1 HG02818.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-38G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722316 | |||||||
| chr16:58722378 | C | CT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(13): Show |
32 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-101dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722378 | |||||||
| chr16:58722662 | G | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0230 a0001c0001t0005g0231 others(3): Show |
9 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-384C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722662 | |||||||
| chr16:58722664 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(12): Show |
31 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.247-386G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722664 | |||||||
| chr16:58722674 | C | CT | 8 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(5): Show |
11 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-397dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58722674 | |||||||
| chr16:58723249 | A | G | 1 | a0001c0001t0005g0232 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.246+497T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723249 | |||||||
| chr16:58723415 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.246+331T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723415 | |||||||
| chr16:58723427 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.246+319C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723427 | |||||||
| chr16:58723494 | G | A | 75 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(72): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.246+252C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723494 | |||||||
| chr16:58723664 | G | A | 2 | a0003c0003t0002g0194 a0003c0003t0002g0199 |
2 | HG00741.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.246+82C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723664 | |||||||
| chr16:58723714 | C | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.246+32G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 2/9 | chr16 | 58723714 | |||||||
| chr16:58724073 | C | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(41): Show |
72 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.90-171G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724073 | |||||||
| chr16:58724188 | A | G | 1 | a0001c0001t0010g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.90-286T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724188 | |||||||
| chr16:58724285 | C | CT | 10 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(7): Show |
13 | HG01884.hp2 HG02040.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.90-384dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724285 | |||||||
| chr16:58724285 | CT | C | 10 | a0001c0001t0002g0145 a0001c0001t0002g0163 a0001c0001t0002g0185 others(7): Show |
10 | HG01069.hp2 HG01070.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.90-384delA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724285 | |||||||
| chr16:58724319 | G | A | 1 | a0005c0009t0002g0226 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.90-417C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724319 | |||||||
| chr16:58724334 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.90-432C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724334 | |||||||
| chr16:58724403 | C | T | 9 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-501G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724403 | |||||||
| chr16:58724421 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0127 |
3 | NA18983.hp1 NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.90-519A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724421 | |||||||
| chr16:58724442 | G | A | 103 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0001g0209 others(100): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.90-540C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724442 | |||||||
| chr16:58724462 | C | G | 9 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-560G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724462 | |||||||
| chr16:58724468 | C | T | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.90-566G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724468 | |||||||
| chr16:58724902 | C | T | 7 | a0001c0001t0005g0017 a0001c0001t0005g0230 a0001c0001t0005g0231 others(4): Show |
10 | HG02040.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.90-1000G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58724902 | |||||||
| chr16:58725112 | C | CT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.90-1211dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725112 | |||||||
| chr16:58725112 | C | CTT | 86 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(83): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.90-1212_90-1211dup others(2): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725112 | |||||||
| chr16:58725112 | C | CTTT | 16 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(13): Show |
26 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.90-1213_90-1211dup others(3): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725112 | |||||||
| chr16:58725169 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.90-1267A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725169 | |||||||
| chr16:58725225 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.90-1323G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725225 | |||||||
| chr16:58725428 | C | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.90-1526G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725428 | |||||||
| chr16:58725580 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.90-1678A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725580 | |||||||
| chr16:58725654 | G | C | 2 | a0001c0001t0005g0230 a0001c0001t0005g0231 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.90-1752C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725654 | |||||||
| chr16:58725929 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.90-2027A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725929 | |||||||
| chr16:58725931 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.90-2029A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725931 | |||||||
| chr16:58725974 | T | C | 6 | a0001c0001t0002g0010 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
11 | HG02056.hp1 HG02155.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-2072A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725974 | |||||||
| chr16:58725982 | G | T | 1 | a0001c0001t0002g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.90-2080C>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58725982 | |||||||
| chr16:58726035 | T | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(165): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.90-2133A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726035 | |||||||
| chr16:58726052 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.90-2150A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726052 | |||||||
| chr16:58726288 | C | T | 19 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0185 others(16): Show |
30 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.90-2386G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726288 | |||||||
| chr16:58726371 | A | T | 4 | a0001c0006t0002g0089 a0002c0002t0001g0087 a0002c0002t0001g0088 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-2469T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726371 | |||||||
| chr16:58726385 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90-2483G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726385 | |||||||
| chr16:58726400 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90-2498C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726400 | |||||||
| chr16:58726436 | G | A | 1 | a0002c0002t0001g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.90-2534C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726436 | |||||||
| chr16:58726463 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.90-2561G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726463 | |||||||
| chr16:58726470 | C | T | 1 | a0001c0001t0003g0041 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.90-2568G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726470 | |||||||
| chr16:58726483 | C | CTTTA | 5 | a0002c0002t0001g0030 a0002c0002t0001g0076 a0002c0002t0001g0097 others(2): Show |
6 | HG02300.hp1 HG03098.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-2585_90-2582dup others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726483 | C | CTTTATTT others(1): Show |
76 | a0001c0001t0001g0107 a0001c0001t0001g0159 a0001c0001t0002g0003 others(73): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.90-2589_90-2582dup others(8): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726483 | C | CTTTATTT others(5): Show |
36 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(33): Show |
62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.90-2593_90-2582dup others(12): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726483 | C | CTTTATTT others(9): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(40): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.90-2597_90-2582dup others(16): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726483 | C | CTTTATTT others(13): Show |
3 | a0001c0001t0001g0129 a0001c0001t0002g0023 a0001c0001t0003g0215 |
5 | HG02809.hp2 HG02886.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.90-2601_90-2582dup others(20): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726483 | C | CTTTATTT others(17): Show |
2 | a0001c0001t0010g0130 a0001c0005t0002g0188 |
2 | HG03579.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.90-2605_90-2582dup others(24): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726483 | |||||||
| chr16:58726510 | T | TATTTATT others(5): Show |
1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.90-2609_90-2608ins others(12): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726510 | |||||||
| chr16:58726574 | A | C | 103 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0001g0209 others(100): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.90-2672T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726574 | |||||||
| chr16:58726690 | C | A | 1 | a0001c0001t0002g0170 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90-2788G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726690 | |||||||
| chr16:58726743 | C | T | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-2841G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726743 | |||||||
| chr16:58726754 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(15): Show |
29 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.90-2852G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726754 | |||||||
| chr16:58726765 | G | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
103 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.90-2863C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726765 | |||||||
| chr16:58726784 | G | A | 1 | a0002c0002t0001g0077 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.90-2882C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726784 | |||||||
| chr16:58726840 | CT | C | 17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(14): Show |
28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.90-2939delA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726840 | |||||||
| chr16:58726861 | A | G | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.90-2959T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726861 | |||||||
| chr16:58726876 | G | A | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.90-2974C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726876 | |||||||
| chr16:58726981 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.90-3079G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58726981 | |||||||
| chr16:58727007 | A | G | 1 | a0002c0002t0001g0079 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.90-3105T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727007 | |||||||
| chr16:58727026 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.90-3124G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727026 | |||||||
| chr16:58727085 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.90-3183G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727085 | |||||||
| chr16:58727086 | G | A | 1 | a0002c0002t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.90-3184C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727086 | |||||||
| chr16:58727279 | C | A | 1 | a0002c0002t0001g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.90-3377G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727279 | |||||||
| chr16:58727325 | T | C | 4 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(1): Show |
12 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-3423A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727325 | |||||||
| chr16:58727367 | G | GT | 68 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(65): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.90-3466dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727367 | |||||||
| chr16:58727380 | T | A | 17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(14): Show |
28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.90-3478A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727380 | |||||||
| chr16:58727380 | T | TA | 4 | a0001c0001t0002g0182 a0001c0001t0014g0173 a0002c0002t0001g0018 others(1): Show |
6 | HG00609.hp1 HG01934.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-3479dupT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727380 | |||||||
| chr16:58727381 | A | T | 18 | a0001c0001t0002g0005 a0001c0001t0002g0134 a0001c0001t0002g0142 others(15): Show |
39 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.90-3479T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727381 | |||||||
| chr16:58727444 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.90-3542A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727444 | |||||||
| chr16:58727546 | A | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-3644T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727546 | |||||||
| chr16:58727559 | C | T | 1 | a0001c0005t0001g0044 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.90-3657G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727559 | |||||||
| chr16:58727676 | G | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-3774C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727676 | |||||||
| chr16:58727780 | G | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(18): Show |
40 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.90-3878C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727780 | |||||||
| chr16:58727806 | T | C | 1 | a0001c0001t0017g0234 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.90-3904A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727806 | |||||||
| chr16:58727840 | T | C | 1 | a0001c0006t0001g0026 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.90-3938A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727840 | |||||||
| chr16:58727985 | AG | A | 124 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(121): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.90-4084delC | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727985 | |||||||
| chr16:58727997 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-4095A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58727997 | |||||||
| chr16:58728173 | G | A | 2 | a0001c0001t0008g0174 a0001c0001t0008g0175 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.90-4271C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728173 | |||||||
| chr16:58728199 | T | C | 4 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(1): Show |
12 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-4297A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728199 | |||||||
| chr16:58728255 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.90-4353A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728255 | |||||||
| chr16:58728259 | C | T | 1 | a0003c0003t0002g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90-4357G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728259 | |||||||
| chr16:58728407 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-4505T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728407 | |||||||
| chr16:58728549 | A | G | 3 | a0001c0005t0001g0043 a0001c0005t0002g0189 a0001c0005t0002g0190 |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-4647T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728549 | |||||||
| chr16:58728581 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.90-4679A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728581 | |||||||
| chr16:58728841 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.90-4939G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728841 | |||||||
| chr16:58728852 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.90-4950A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728852 | |||||||
| chr16:58728967 | G | A | 1 | a0002c0002t0001g0027 | 2 | NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.90-5065C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728967 | |||||||
| chr16:58728969 | G | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.90-5067C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58728969 | |||||||
| chr16:58729183 | C | A | 1 | a0002c0002t0001g0099 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.89+4957G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729183 | |||||||
| chr16:58729258 | CCTGT | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(121): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.89+4878_89+4881del others(4): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729258 | |||||||
| chr16:58729266 | T | G | 1 | a0001c0001t0002g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.89+4874A>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729266 | |||||||
| chr16:58729289 | C | T | 1 | a0008c0014t0016g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.89+4851G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729289 | |||||||
| chr16:58729368 | A | C | 1 | a0003c0003t0002g0194 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.89+4772T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729368 | |||||||
| chr16:58729370 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.89+4770T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729370 | |||||||
| chr16:58729484 | C | A | 1 | a0002c0002t0001g0081 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.89+4656G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729484 | |||||||
| chr16:58729498 | G | GA | 21 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0185 others(18): Show |
32 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.89+4641dupT | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729498 | |||||||
| chr16:58729583 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.89+4557A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729583 | |||||||
| chr16:58729631 | G | A | 1 | a0002c0002t0001g0081 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.89+4509C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729631 | |||||||
| chr16:58729659 | A | C | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.89+4481T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729659 | |||||||
| chr16:58729705 | G | A | 1 | a0004c0007t0003g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.89+4435C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729705 | |||||||
| chr16:58729723 | C | CT | 57 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(54): Show |
104 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.89+4416dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729723 | |||||||
| chr16:58729746 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.89+4394G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729746 | |||||||
| chr16:58729770 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.89+4370G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729770 | |||||||
| chr16:58729798 | C | T | 76 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.89+4342G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729798 | |||||||
| chr16:58729925 | T | A | 18 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0185 others(15): Show |
29 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.89+4215A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729925 | |||||||
| chr16:58729926 | T | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(149): Show |
258 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.89+4214A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729926 | |||||||
| chr16:58729927 | T | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.89+4213A>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729927 | |||||||
| chr16:58729928 | A | T | 4 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(1): Show |
12 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.89+4212T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58729928 | |||||||
| chr16:58730020 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.89+4120A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730020 | |||||||
| chr16:58730242 | A | G | 19 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0185 others(16): Show |
30 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.89+3898T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730242 | |||||||
| chr16:58730389 | C | T | 1 | a0002c0002t0001g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.89+3751G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730389 | |||||||
| chr16:58730391 | A | AT | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.89+3748dupA | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730391 | |||||||
| chr16:58730498 | G | A | 16 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(13): Show |
26 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.89+3642C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730498 | |||||||
| chr16:58730527 | C | T | 1 | a0001c0001t0003g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.89+3613G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730527 | |||||||
| chr16:58730626 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.89+3514T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730626 | |||||||
| chr16:58730647 | G | A | 1 | a0001c0008t0002g0101 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.89+3493C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730647 | |||||||
| chr16:58730683 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(159): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.89+3457A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730683 | |||||||
| chr16:58730821 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.89+3319C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730821 | |||||||
| chr16:58730892 | A | T | 1 | a0001c0001t0002g0037 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.89+3248T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730892 | |||||||
| chr16:58730918 | A | G | 1 | a0001c0001t0005g0230 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.89+3222T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730918 | |||||||
| chr16:58730951 | C | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(67): Show |
122 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.89+3189G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58730951 | |||||||
| chr16:58731056 | CTTACT | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.89+3079_89+3083del others(5): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731056 | |||||||
| chr16:58731109 | AAAAATGG others(31): Show |
A | 1 | a0002c0002t0009g0102 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.89+2993_89+3030del others(38): Show |
GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731109 | |||||||
| chr16:58731305 | C | T | 1 | a0001c0006t0001g0026 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.89+2835G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731305 | |||||||
| chr16:58731331 | G | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.89+2809C>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731331 | |||||||
| chr16:58731382 | A | G | 1 | a0001c0005t0002g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.89+2758T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731382 | |||||||
| chr16:58731650 | C | T | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.89+2490G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731650 | |||||||
| chr16:58731819 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.89+2321A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58731819 | |||||||
| chr16:58732073 | A | G | 1 | a0001c0001t0002g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.89+2067T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732073 | |||||||
| chr16:58732283 | A | T | 75 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(72): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.89+1857T>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732283 | |||||||
| chr16:58732298 | T | C | 3 | a0001c0001t0002g0185 a0001c0015t0001g0138 a0007c0012t0001g0049 |
3 | HG01884.hp1 HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.89+1842A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732298 | |||||||
| chr16:58732383 | A | C | 75 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0005 others(72): Show |
126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.89+1757T>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732383 | |||||||
| chr16:58732449 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89+1691G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732449 | |||||||
| chr16:58732518 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89+1622C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732518 | |||||||
| chr16:58732787 | T | C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00621.hp2 HG02080.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.89+1353A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58732787 | |||||||
| chr16:58733025 | G | A | 16 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0003g0013 others(13): Show |
26 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.89+1115C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733025 | |||||||
| chr16:58733076 | C | G | 2 | a0001c0015t0001g0138 a0007c0012t0001g0049 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.89+1064G>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733076 | |||||||
| chr16:58733192 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89+948C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733192 | |||||||
| chr16:58733397 | T | C | 6 | a0001c0001t0003g0024 a0001c0001t0003g0211 a0001c0001t0003g0213 others(3): Show |
8 | HG02145.hp1 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.89+743A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733397 | |||||||
| chr16:58733435 | T | C | 21 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0042 others(18): Show |
40 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.89+705A>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733435 | |||||||
| chr16:58733534 | A | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(35): Show |
63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.89+606T>C | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733534 | |||||||
| chr16:58733568 | C | CG | 6 | a0001c0001t0001g0032 a0001c0001t0001g0105 a0001c0001t0002g0134 others(3): Show |
7 | HG00621.hp2 HG03098.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.89+571dupC | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733568 | |||||||
| chr16:58733587 | G | A | 8 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(5): Show |
11 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.89+553C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733587 | |||||||
| chr16:58733605 | G | C | 2 | a0001c0001t0002g0186 a0001c0001t0002g0187 |
2 | HG01361.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.89+535C>G | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733605 | |||||||
| chr16:58733678 | C | A | 9 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.89+462G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733678 | |||||||
| chr16:58733781 | G | A | 9 | a0001c0005t0001g0043 a0001c0005t0001g0044 a0001c0005t0001g0045 others(6): Show |
12 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.89+359C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733781 | |||||||
| chr16:58733826 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0032 others(33): Show |
59 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.89+314G>A | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733826 | |||||||
| chr16:58733899 | C | A | 4 | a0001c0004t0001g0006 a0001c0004t0001g0031 a0001c0004t0001g0103 others(1): Show |
12 | HG02080.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.89+241G>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733899 | |||||||
| chr16:58733944 | G | A | 10 | a0003c0003t0002g0016 a0003c0003t0002g0194 a0003c0003t0002g0195 others(7): Show |
13 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.89+196C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58733944 | |||||||
| chr16:58734012 | AGT | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(161): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(270): Show |
intron_variant | MODIFIER | c.89+126_89+127delAC | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58734012 | |||||||
| chr16:58734058 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0046 others(33): Show |
64 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.89+82C>T | GOT2 | ENSG00000125166.13 | transcript | ENST00000245206.10 | protein_coding | 1/9 | chr16 | 58734058 |