Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59345 |
| ensemblid | ENSG00000114450.11 |
| hgncid | 20731 |
| symbol | GNB4 |
| name | G protein subunit beta 4 |
| refseq_nuc | NM_021629.4 |
| refseq_prot | NP_067642.1 |
| ensembl_nuc | ENST00000232564.8 |
| ensembl_prot | ENSP00000232564.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 179396088 |
| end | 179451470 |
| strand | - |
| ver | v1.2 |
| region | chr3:179396088-179451470 |
| region5000 | chr3:179391088-179456470 |
| regionname0 | GNB4_chr3_179396088_179451470 |
| regionname5000 | GNB4_chr3_179391088_179456470 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 340 | 397 | 92 | 78 | 169 | 10 | 46 | 130 | GNB4_chr3_179391088_179456470 | GNB4 | MSELE others(335): Show |
chr3 | 179391088 | 179456470 |
| a0002 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | MSELE others(335): Show |
chr3 | 179391088 | 179456470 |
| a0003 | 0/0 | 340 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | MSELE others(335): Show |
chr3 | 179391088 | 179456470 |
| a0004 | 0/0 | 58 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | MSELE others(53): Show |
chr3 | 179391088 | 179456470 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1020 | 199 | 42 | 36 | 98 | 1 | 20 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(1015): Show |
chr3 | 179391088 | 179456470 | ||
| a0001c0002 | 0/0 | 1020 | 190 | 48 | 38 | 71 | 9 | 24 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(1015): Show |
chr3 | 179391088 | 179456470 | ||
| a0001c0003 | 0/0 | 1020 | 8 | 2 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(1015): Show |
chr3 | 179391088 | 179456470 | ||
| a0002c0004 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(1015): Show |
chr3 | 179391088 | 179456470 | ||
| a0003c0006 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(1015): Show |
chr3 | 179391088 | 179456470 | ||
| a0004c0005 | 0/0 | 1003 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | ATGAG others(998): Show |
chr3 | 179391088 | 179456470 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0002 | 1/1 | 6315 | 68 | 7 | 18 | 31 | 0 | 10 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0003 | 0/0 | 6307 | 39 | 4 | 2 | 27 | 0 | 6 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0004 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0005 | 0/0 | 6307 | 16 | 6 | 3 | 7 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0008 | 0/0 | 6315 | 8 | 0 | 0 | 8 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0009 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0010 | 0/0 | 6310 | 8 | 5 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0011 | 0/0 | 6307 | 7 | 1 | 4 | 0 | 1 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0012 | 0/0 | 6315 | 6 | 0 | 0 | 6 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0014 | 0/0 | 6310 | 4 | 4 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0017 | 0/0 | 6308 | 4 | 1 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6303): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0019 | 0/0 | 6310 | 4 | 4 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0020 | 0/0 | 6307 | 4 | 0 | 0 | 4 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0024 | 0/0 | 6307 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0025 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0027 | 0/0 | 6315 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0028 | 0/0 | 6316 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6311): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0036 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0037 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0038 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0044 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0045 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0046 | 0/0 | 6314 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6309): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0048 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0053 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0054 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0055 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0056 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6303): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0057 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6303): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0058 | 0/0 | 6390 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6385): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0060 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0061 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0067 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0069 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0070 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0071 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0001t0072 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0001 | 0/0 | 6311 | 69 | 2 | 17 | 44 | 2 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0002 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0004 | 0/0 | 6311 | 36 | 5 | 9 | 12 | 5 | 5 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0005 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6302): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0006 | 0/0 | 6311 | 12 | 0 | 2 | 9 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0007 | 0/0 | 6311 | 9 | 9 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0013 | 0/0 | 6311 | 6 | 3 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0014 | 0/0 | 6310 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0015 | 0/0 | 6311 | 5 | 3 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0016 | 0/0 | 6310 | 5 | 5 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0018 | 0/0 | 6311 | 4 | 0 | 0 | 0 | 0 | 4 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0021 | 0/0 | 6311 | 4 | 0 | 0 | 1 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0022 | 0/0 | 6311 | 3 | 2 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0023 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0026 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0029 | 0/0 | 6311 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0030 | 0/0 | 6311 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0031 | 0/0 | 6311 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0032 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6307): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0033 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0034 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0035 | 0/0 | 6311 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0039 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0040 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6307): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0041 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0042 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0043 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0047 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0049 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0050 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0051 | 0/0 | 6311 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0052 | 0/0 | 6311 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0063 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0064 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0065 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6307): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0066 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0002t0068 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6305): Show |
chr3 | 179391088 | 179456470 |
| a0001c0003t0009 | 0/0 | 6315 | 7 | 1 | 4 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0001c0003t0062 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0002c0004t0001 | 0/0 | 6311 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6306): Show |
chr3 | 179391088 | 179456470 |
| a0003c0006t0059 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6310): Show |
chr3 | 179391088 | 179456470 |
| a0004c0005t0002 | 0/0 | 6298 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | GTGGC others(6293): Show |
chr3 | 179391088 | 179456470 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0016 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0008g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0008g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0008g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0010g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0010g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0010g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0011g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0011g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0011g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0011g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0011g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0012g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0012g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0012g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0014g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0014g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0017g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0019g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0019g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0019g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0020g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0020g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0020g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0024g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0024g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0025g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0025g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0027g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0027g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0028g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0036g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0037g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0038g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0044g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0045g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0046g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0048g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0053g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0054g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0055g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0056g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0057g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0058g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0060g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0061g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0067g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0069g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0070g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0071g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0001t0072g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0013g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0014g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0014g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0015g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0015g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0016g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0016g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0018g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0018g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0018g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0018g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0021g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0021g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0021g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0021g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0022g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0022g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0022g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0023g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0026g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0029g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0030g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0030g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0031g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0031g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0032g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0032g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0033g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0033g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0034g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0034g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0035g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0035g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0039g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0040g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0041g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0042g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0043g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0047g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0049g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0050g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0051g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0052g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0063g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0064g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0065g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0066g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0002t0068g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0009g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0001c0003t0062g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0002c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0003c0006t0059g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| a0004c0005t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0177 | EUR | GBR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00140 | hp2 | a0001 | c0002 | t0052 | g0092 | EUR | GBR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0249 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00280 | hp2 | a0001 | c0002 | t0006 | g0088 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00323 | hp1 | a0001 | c0002 | t0004 | g0250 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00323 | hp2 | a0001 | c0002 | t0004 | g0230 | EUR | FIN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00423 | hp2 | a0002 | c0004 | t0001 | g0090 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0240 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00544 | hp1 | a0001 | c0002 | t0006 | g0086 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00544 | hp2 | a0001 | c0001 | t0008 | g0185 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0239 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00621 | hp2 | a0001 | c0001 | t0012 | g0024 | EAS | CHS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0040 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0302 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00735 | hp1 | a0001 | c0002 | t0015 | g0217 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00735 | hp2 | a0001 | c0003 | t0009 | g0323 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00738 | hp1 | a0001 | c0001 | t0024 | g0221 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00741 | hp1 | a0001 | c0002 | t0040 | g0178 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01069 | hp1 | a0001 | c0002 | t0029 | g0035 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0004 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0032 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0032 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01081 | hp1 | a0001 | c0001 | t0027 | g0253 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01106 | hp1 | a0001 | c0001 | t0027 | g0254 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01106 | hp2 | a0001 | c0001 | t0058 | g0271 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01167 | hp1 | a0001 | c0002 | t0063 | g0305 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01167 | hp2 | a0001 | c0002 | t0014 | g0259 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01168 | hp1 | a0001 | c0002 | t0041 | g0081 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01169 | hp1 | a0001 | c0002 | t0014 | g0261 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0004 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01192 | hp1 | a0001 | c0002 | t0013 | g0296 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01192 | hp2 | a0001 | c0001 | t0038 | g0175 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0245 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01256 | hp1 | a0001 | c0003 | t0009 | g0325 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01257 | hp2 | a0001 | c0002 | t0006 | g0160 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01258 | hp2 | a0001 | c0003 | t0009 | g0326 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01261 | hp1 | a0001 | c0002 | t0004 | g0036 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01358 | hp1 | a0001 | c0002 | t0004 | g0234 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0038 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01433 | hp1 | a0001 | c0002 | t0015 | g0196 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01433 | hp2 | a0001 | c0002 | t0022 | g0187 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01496 | hp1 | a0001 | c0003 | t0009 | g0320 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0202 | AMR | CLM | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01515 | hp1 | a0001 | c0002 | t0004 | g0220 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0110 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01517 | hp1 | a0001 | c0001 | t0011 | g0040 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0112 | EUR | IBS | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0257 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01884 | hp2 | a0001 | c0002 | t0029 | g0035 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01928 | hp2 | a0001 | c0002 | t0004 | g0010 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01952 | hp1 | a0001 | c0002 | t0006 | g0083 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0211 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0266 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01993 | hp1 | a0001 | c0002 | t0004 | g0010 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0143 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02040 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0263 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02055 | hp2 | a0001 | c0002 | t0026 | g0031 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02132 | hp1 | a0001 | c0001 | t0017 | g0007 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02132 | hp2 | a0001 | c0001 | t0072 | g0329 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02145 | hp1 | a0001 | c0002 | t0035 | g0262 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02148 | hp2 | a0001 | c0002 | t0004 | g0252 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0062 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02165 | hp2 | a0001 | c0002 | t0006 | g0084 | EAS | CDX | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02257 | hp1 | a0001 | c0002 | t0033 | g0290 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02257 | hp2 | a0001 | c0002 | t0007 | g0009 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02258 | hp2 | a0001 | c0001 | t0019 | g0225 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02273 | hp2 | a0001 | c0002 | t0004 | g0010 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02280 | hp2 | a0001 | c0002 | t0022 | g0186 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02300 | hp2 | a0001 | c0001 | t0060 | g0301 | AMR | PEL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02572 | hp1 | a0001 | c0001 | t0061 | g0335 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02572 | hp2 | a0001 | c0002 | t0007 | g0198 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02602 | hp2 | a0001 | c0002 | t0049 | g0244 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02615 | hp1 | a0001 | c0001 | t0019 | g0226 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0332 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0213 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02647 | hp1 | a0001 | c0002 | t0013 | g0288 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02647 | hp2 | a0001 | c0001 | t0028 | g0020 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02683 | hp1 | a0001 | c0002 | t0039 | g0162 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0037 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02717 | hp1 | a0001 | c0002 | t0015 | g0216 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02717 | hp2 | a0001 | c0002 | t0023 | g0044 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02735 | hp1 | a0001 | c0001 | t0024 | g0208 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0231 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02738 | hp2 | a0001 | c0002 | t0031 | g0235 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0336 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0199 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02818 | hp2 | a0001 | c0001 | t0019 | g0224 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0243 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02895 | hp1 | a0001 | c0002 | t0016 | g0034 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02895 | hp2 | a0001 | c0002 | t0068 | g0258 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02896 | hp1 | a0001 | c0001 | t0046 | g0189 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02896 | hp2 | a0001 | c0002 | t0013 | g0268 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02897 | hp1 | a0001 | c0001 | t0048 | g0188 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02897 | hp2 | a0001 | c0002 | t0016 | g0034 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02922 | hp1 | a0001 | c0002 | t0016 | g0241 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02922 | hp2 | a0001 | c0002 | t0026 | g0031 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02965 | hp1 | a0001 | c0002 | t0016 | g0219 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02965 | hp2 | a0001 | c0002 | t0064 | g0291 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02970 | hp2 | a0001 | c0003 | t0009 | g0328 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02976 | hp1 | a0001 | c0001 | t0069 | g0318 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02976 | hp2 | a0001 | c0002 | t0022 | g0191 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03017 | hp1 | a0001 | c0002 | t0043 | g0079 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03017 | hp2 | a0001 | c0001 | t0011 | g0038 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03041 | hp1 | a0001 | c0002 | t0035 | g0260 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0214 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03098 | hp2 | a0001 | c0002 | t0034 | g0294 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03130 | hp1 | a0001 | c0002 | t0015 | g0218 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0009 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03195 | hp1 | a0001 | c0002 | t0004 | g0248 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03195 | hp2 | a0001 | c0002 | t0007 | g0201 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03225 | hp2 | a0001 | c0001 | t0028 | g0020 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03239 | hp1 | a0001 | c0003 | t0009 | g0324 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03453 | hp2 | a0001 | c0002 | t0066 | g0310 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0242 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03490 | hp1 | a0001 | c0001 | t0053 | g0255 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03516 | hp1 | a0001 | c0002 | t0034 | g0272 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03516 | hp2 | a0001 | c0003 | t0062 | g0322 | AFR | ESN | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03540 | hp1 | a0001 | c0002 | t0065 | g0315 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03579 | hp1 | a0001 | c0002 | t0023 | g0045 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03669 | hp2 | a0001 | c0002 | t0021 | g0307 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03688 | hp2 | a0001 | c0002 | t0018 | g0151 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03704 | hp2 | a0001 | c0002 | t0018 | g0153 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03831 | hp2 | a0001 | c0002 | t0013 | g0297 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0228 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0251 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0037 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03942 | hp2 | a0001 | c0002 | t0018 | g0152 | SAS | BEB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04115 | hp2 | a0001 | c0002 | t0047 | g0107 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04199 | hp1 | a0001 | c0002 | t0021 | g0308 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04199 | hp2 | a0001 | c0002 | t0021 | g0327 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04204 | hp2 | a0001 | c0002 | t0042 | g0087 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04228 | hp1 | a0001 | c0002 | t0018 | g0154 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG04228 | hp2 | a0001 | c0003 | t0009 | g0321 | SAS | STU | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0331 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0229 | EAS | CHB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | CHB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0009 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18906 | hp2 | a0001 | c0001 | t0010 | g0319 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18940 | hp2 | a0001 | c0001 | t0044 | g0174 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18942 | hp2 | a0001 | c0002 | t0004 | g0061 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0028 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18943 | hp2 | a0001 | c0001 | t0037 | g0207 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18944 | hp2 | a0001 | c0002 | t0006 | g0158 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18946 | hp1 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0236 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18952 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18953 | hp2 | a0001 | c0002 | t0004 | g0246 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18956 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18961 | hp2 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18963 | hp2 | a0001 | c0002 | t0030 | g0157 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18967 | hp2 | a0001 | c0001 | t0057 | g0314 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18968 | hp1 | a0001 | c0002 | t0006 | g0093 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18970 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18980 | hp1 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18983 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18985 | hp1 | a0001 | c0001 | t0008 | g0030 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18986 | hp2 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18990 | hp1 | a0001 | c0002 | t0013 | g0295 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0193 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18994 | hp1 | a0001 | c0002 | t0006 | g0161 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18995 | hp2 | a0001 | c0002 | t0006 | g0029 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA18999 | hp2 | a0001 | c0001 | t0008 | g0131 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19001 | hp2 | a0003 | c0006 | t0059 | g0300 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19004 | hp2 | a0001 | c0001 | t0045 | g0120 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19005 | hp2 | a0001 | c0002 | t0004 | g0227 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19012 | hp1 | a0001 | c0002 | t0030 | g0176 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19012 | hp2 | a0001 | c0001 | t0020 | g0338 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19030 | hp2 | a0001 | c0002 | t0013 | g0309 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19043 | hp1 | a0001 | c0002 | t0032 | g0317 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19043 | hp2 | a0001 | c0002 | t0015 | g0215 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19058 | hp2 | a0001 | c0002 | t0021 | g0311 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19065 | hp1 | a0001 | c0001 | t0020 | g0339 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0222 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19070 | hp2 | a0001 | c0001 | t0020 | g0043 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19072 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19072 | hp2 | a0001 | c0001 | t0054 | g0277 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19075 | hp1 | a0001 | c0001 | t0055 | g0285 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19081 | hp1 | a0001 | c0001 | t0036 | g0206 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19081 | hp2 | a0001 | c0001 | t0012 | g0021 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19082 | hp2 | a0004 | c0005 | t0002 | g0125 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19083 | hp2 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19084 | hp1 | a0001 | c0002 | t0006 | g0076 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19084 | hp2 | a0001 | c0002 | t0004 | g0247 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19085 | hp1 | a0001 | c0001 | t0025 | g0119 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19088 | hp1 | a0001 | c0002 | t0005 | g0049 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19088 | hp2 | a0001 | c0001 | t0025 | g0058 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19090 | hp2 | a0001 | c0001 | t0017 | g0007 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19091 | hp2 | a0001 | c0001 | t0056 | g0284 | EAS | JPT | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19240 | hp1 | a0001 | c0002 | t0007 | g0200 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA19240 | hp2 | a0001 | c0001 | t0070 | g0337 | AFR | YRI | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20129 | hp1 | a0001 | c0002 | t0050 | g0197 | AFR | ASW | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | ASW | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20905 | hp1 | a0001 | c0002 | t0031 | g0232 | SAS | GIH | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | GIH | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02109 | hp1 | a0001 | c0001 | t0071 | g0256 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0013 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0150 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0330 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02559 | hp1 | a0001 | c0002 | t0016 | g0233 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG02559 | hp2 | a0001 | c0002 | t0032 | g0316 | AFR | ACB | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG03471 | hp2 | a0001 | c0002 | t0051 | g0210 | AFR | MSL | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG06807 | hp1 | a0001 | c0001 | t0067 | g0306 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20300 | hp1 | a0001 | c0002 | t0033 | g0289 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | USA | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | LWK | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0052 | REF | REF | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0016 | REF | REF | GNB4_chr3_179391088_179456470 | GNB4 | chr3 | 179391088 | 179456470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:179405303 | T | C | 1 | a0002 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.803A>G | p.Asn268Ser | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/10 | 970/6315 | 803/1023 | 268/340 | chr3 | 179405303 | |||
| chr3:179413452 | T | C | 1 | a0003 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.659A>G | p.Gln220Arg | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/10 | 826/6315 | 659/1023 | 220/340 | chr3 | 179413452 | |||
| chr3:179419408 | TATCCCCA others(10): Show |
T | 1 | a0004 | 1 | NA19082.hp2 | frameshift_variant | HIGH | c.177_193delTGCTATGC others(9): Show |
p.Tyr59fs | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/10 | 360/6315 | 177/1023 | 59/340 | chr3 | 179419408 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:179419485 | A | G | 2 | a0001c0002 a0002c0004 |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
synonymous_variant | LOW | c.117T>C | p.Ser39Ser | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/10 | 284/6315 | 117/1023 | 39/340 | chr3 | 179419485 | |||
| chr3:179426153 | A | G | 1 | a0001c0003 | 8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
synonymous_variant | LOW | c.48T>C | p.Asn16Asn | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/10 | 215/6315 | 48/1023 | 16/340 | chr3 | 179426153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:179396154 | T | C | 1 | a0001c0001t0027 | 2 | HG01081.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5059A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 5059 | chr3 | 179396154 | ||||||
| chr3:179396256 | C | T | 1 | a0001c0002t0033 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4957G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4957 | chr3 | 179396256 | ||||||
| chr3:179396492 | A | G | 2 | a0001c0002t0018 a0001c0002t0021 |
8 | HG03669.hp2 HG03688.hp2 HG03704.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4721T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4721 | chr3 | 179396492 | ||||||
| chr3:179396619 | C | T | 1 | a0001c0002t0050 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4594G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4594 | chr3 | 179396619 | ||||||
| chr3:179396683 | T | C | 21 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(18): Show |
59 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*4530A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4530 | chr3 | 179396683 | ||||||
| chr3:179396726 | G | T | 1 | a0001c0002t0063 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4487 | chr3 | 179396726 | ||||||
| chr3:179396741 | GATTA | G | 62 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(59): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*4468_*4471delTAAT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4468 | chr3 | 179396741 | ||||||
| chr3:179396759 | T | C | 2 | a0001c0001t0046 a0001c0001t0048 |
2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4454A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4454 | chr3 | 179396759 | ||||||
| chr3:179396766 | A | T | 3 | a0001c0002t0007 a0001c0002t0034 a0001c0002t0050 |
12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4447T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4447 | chr3 | 179396766 | ||||||
| chr3:179396887 | T | C | 1 | a0001c0002t0033 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4326A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4326 | chr3 | 179396887 | ||||||
| chr3:179396996 | T | G | 9 | a0001c0002t0007 a0001c0002t0015 a0001c0002t0023 others(6): Show |
25 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*4217A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4217 | chr3 | 179396996 | ||||||
| chr3:179397026 | T | C | 1 | a0001c0001t0061 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4187A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 4187 | chr3 | 179397026 | ||||||
| chr3:179397230 | G | A | 1 | a0001c0002t0049 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3983C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3983 | chr3 | 179397230 | ||||||
| chr3:179397425 | C | T | 1 | a0001c0002t0030 | 2 | NA18963.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3788G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3788 | chr3 | 179397425 | ||||||
| chr3:179397441 | T | C | 4 | a0001c0001t0011 a0001c0001t0024 a0001c0001t0038 others(1): Show |
11 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3772A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3772 | chr3 | 179397441 | ||||||
| chr3:179397471 | C | A | 1 | a0001c0002t0031 | 2 | HG02738.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3742G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3742 | chr3 | 179397471 | ||||||
| chr3:179397534 | T | C | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3679A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3679 | chr3 | 179397534 | ||||||
| chr3:179397592 | C | T | 14 | a0001c0001t0001 a0001c0001t0054 a0001c0001t0061 others(11): Show |
94 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*3621G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3621 | chr3 | 179397592 | ||||||
| chr3:179397608 | G | C | 2 | a0001c0001t0008 a0001c0001t0044 |
9 | HG00544.hp2 NA18940.hp2 NA18951.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3605C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3605 | chr3 | 179397608 | ||||||
| chr3:179397612 | G | A | 8 | a0001c0002t0007 a0001c0002t0015 a0001c0002t0023 others(5): Show |
24 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3601C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3601 | chr3 | 179397612 | ||||||
| chr3:179397648 | T | C | 3 | a0001c0002t0007 a0001c0002t0034 a0001c0002t0050 |
12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3565A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3565 | chr3 | 179397648 | ||||||
| chr3:179397713 | A | T | 9 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0013 others(6): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3500T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3500 | chr3 | 179397713 | ||||||
| chr3:179397759 | C | T | 1 | a0001c0003t0062 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3454G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3454 | chr3 | 179397759 | ||||||
| chr3:179397760 | G | A | 1 | a0001c0001t0067 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3453C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3453 | chr3 | 179397760 | ||||||
| chr3:179397780 | G | A | 4 | a0001c0002t0007 a0001c0002t0015 a0001c0002t0034 others(1): Show |
17 | HG00735.hp1 HG01433.hp1 HG02257.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3433C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3433 | chr3 | 179397780 | ||||||
| chr3:179397824 | C | A | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | NA19075.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3389G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3389 | chr3 | 179397824 | ||||||
| chr3:179397841 | AT | A | 10 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(7): Show |
28 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3371delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3371 | chr3 | 179397841 | ||||||
| chr3:179397861 | G | A | 12 | a0001c0001t0001 a0001c0001t0054 a0001c0002t0001 others(9): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*3352C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3352 | chr3 | 179397861 | ||||||
| chr3:179397892 | G | A | 1 | a0001c0001t0012 | 6 | HG00597.hp2 HG00621.hp2 HG02027.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3321C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3321 | chr3 | 179397892 | ||||||
| chr3:179398322 | C | T | 1 | a0001c0001t0060 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2891G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2891 | chr3 | 179398322 | ||||||
| chr3:179398472 | A | G | 63 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(60): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*2741T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2741 | chr3 | 179398472 | ||||||
| chr3:179398523 | T | A | 1 | a0001c0002t0041 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2690A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2690 | chr3 | 179398523 | ||||||
| chr3:179398523 | T | TA | 4 | a0001c0001t0028 a0001c0001t0057 a0001c0002t0032 others(1): Show |
6 | HG02559.hp2 HG02647.hp2 HG03225.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2689dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | ||||||
| chr3:179398523 | T | TAAAAAAA others(76): Show |
1 | a0001c0001t0058 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2689_*2690insTTTT others(79): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | ||||||
| chr3:179398523 | TA | T | 23 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(20): Show |
60 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2689delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2689 | chr3 | 179398523 | ||||||
| chr3:179398673 | A | G | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2540 | chr3 | 179398673 | ||||||
| chr3:179398772 | A | AG | 20 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(17): Show |
57 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2440dupC | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2440 | chr3 | 179398772 | ||||||
| chr3:179398835 | TTAAA | T | 17 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(14): Show |
83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2374_*2377delTTTA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2374 | chr3 | 179398835 | ||||||
| chr3:179398855 | G | A | 1 | a0001c0002t0042 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2358C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2358 | chr3 | 179398855 | ||||||
| chr3:179399050 | T | A | 1 | a0001c0002t0065 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2163A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2163 | chr3 | 179399050 | ||||||
| chr3:179399077 | A | C | 1 | a0001c0001t0045 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2136 | chr3 | 179399077 | ||||||
| chr3:179399116 | T | C | 4 | a0001c0002t0023 a0001c0002t0029 a0001c0002t0035 others(1): Show |
7 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2097A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2097 | chr3 | 179399116 | ||||||
| chr3:179399154 | T | C | 1 | a0001c0001t0038 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2059A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2059 | chr3 | 179399154 | ||||||
| chr3:179399181 | T | A | 1 | a0001c0002t0043 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2032 | chr3 | 179399181 | ||||||
| chr3:179399201 | A | AT | 4 | a0001c0001t0017 a0001c0001t0055 a0001c0001t0056 others(1): Show |
7 | HG00741.hp1 HG02040.hp1 HG02132.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2011dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 2011 | chr3 | 179399201 | ||||||
| chr3:179399364 | G | A | 2 | a0001c0001t0054 a0001c0002t0006 |
13 | HG00280.hp2 HG00544.hp1 HG01257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1849C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1849 | chr3 | 179399364 | ||||||
| chr3:179399736 | C | T | 1 | a0001c0002t0066 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1477 | chr3 | 179399736 | ||||||
| chr3:179399797 | C | G | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | NA19075.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1416G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1416 | chr3 | 179399797 | ||||||
| chr3:179399804 | T | A | 6 | a0001c0001t0010 a0001c0001t0019 a0001c0001t0053 others(3): Show |
20 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1409A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1409 | chr3 | 179399804 | ||||||
| chr3:179399858 | G | A | 12 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(9): Show |
33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1355C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1355 | chr3 | 179399858 | ||||||
| chr3:179399875 | G | C | 8 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0013 others(5): Show |
50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1338C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1338 | chr3 | 179399875 | ||||||
| chr3:179400115 | T | C | 12 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(9): Show |
33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1098A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 1098 | chr3 | 179400115 | ||||||
| chr3:179400239 | G | A | 12 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0019 others(9): Show |
33 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*974C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 974 | chr3 | 179400239 | ||||||
| chr3:179400364 | A | C | 2 | a0001c0001t0025 a0003c0006t0059 |
3 | NA19001.hp2 NA19085.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*849T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 849 | chr3 | 179400364 | ||||||
| chr3:179400384 | C | T | 1 | a0001c0002t0039 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 829 | chr3 | 179400384 | ||||||
| chr3:179400386 | C | T | 1 | a0001c0001t0044 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 827 | chr3 | 179400386 | ||||||
| chr3:179400553 | T | C | 1 | a0001c0001t0069 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*660A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 660 | chr3 | 179400553 | ||||||
| chr3:179400609 | A | C | 12 | a0001c0001t0001 a0001c0001t0054 a0001c0001t0071 others(9): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*604T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 604 | chr3 | 179400609 | ||||||
| chr3:179400650 | T | C | 4 | a0001c0002t0007 a0001c0002t0034 a0001c0002t0050 others(1): Show |
13 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*563A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 563 | chr3 | 179400650 | ||||||
| chr3:179400916 | T | G | 1 | a0001c0001t0020 | 4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 297 | chr3 | 179400916 | ||||||
| chr3:179400977 | T | C | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 236 | chr3 | 179400977 | ||||||
| chr3:179400978 | A | T | 1 | a0001c0001t0036 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 235 | chr3 | 179400978 | ||||||
| chr3:179401088 | T | C | 1 | a0001c0002t0035 | 2 | HG02145.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 125 | chr3 | 179401088 | ||||||
| chr3:179401106 | T | C | 1 | a0001c0002t0052 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 107 | chr3 | 179401106 | ||||||
| chr3:179401210 | C | T | 16 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(13): Show |
82 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 10/10 | 3 | chr3 | 179401210 | ||||||
| chr3:179426233 | G | A | 6 | a0001c0001t0010 a0001c0001t0019 a0001c0001t0053 others(3): Show |
16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/10 | 33 | chr3 | 179426233 | ||||||
| chr3:179451372 | C | T | 1 | a0001c0001t0053 | 1 | HG03490.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25172 | chr3 | 179451372 | ||||||
| chr3:179451442 | T | G | 35 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(32): Show |
112 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(109): Show |
5_prime_UTR_variant | MODIFIER | c.-139A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25242 | chr3 | 179451442 | ||||||
| chr3:179451464 | C | T | 1 | a0001c0002t0023 | 2 | HG02717.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-161G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/10 | 25264 | chr3 | 179451464 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:179401348 | C | T | 1 | a0001c0002t0004g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.917-29G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401348 | |||||||
| chr3:179401445 | AAAT | A | 81 | a0001c0001t0001g0212 a0001c0002t0001g0002 a0001c0002t0001g0005 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.917-129_917-127del others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401445 | |||||||
| chr3:179401445 | AAATAAT | A | 10 | a0001c0002t0021g0307 a0001c0002t0021g0308 a0001c0002t0021g0311 others(7): Show |
11 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-132_917-127del others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401445 | |||||||
| chr3:179401466 | AAAC | A | 19 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(16): Show |
22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.917-150_917-148del others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401466 | |||||||
| chr3:179401472 | C | G | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.917-153G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401472 | |||||||
| chr3:179401499 | T | A | 1 | a0001c0001t0002g0190 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.917-180A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401499 | |||||||
| chr3:179401512 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-193C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401512 | |||||||
| chr3:179401562 | G | C | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.917-243C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401562 | |||||||
| chr3:179401585 | C | T | 19 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(16): Show |
22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.917-266G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401585 | |||||||
| chr3:179401611 | A | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0067g0306 |
5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-292T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401611 | |||||||
| chr3:179401618 | G | A | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.917-299C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401618 | |||||||
| chr3:179401800 | A | G | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.917-481T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401800 | |||||||
| chr3:179401958 | A | C | 1 | a0001c0001t0002g0181 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.917-639T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401958 | |||||||
| chr3:179401994 | CAA | C | 22 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(19): Show |
27 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.917-677_917-676del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179401994 | |||||||
| chr3:179402245 | T | C | 25 | a0001c0001t0003g0039 a0001c0001t0003g0041 a0001c0001t0003g0267 others(22): Show |
27 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.917-926A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402245 | |||||||
| chr3:179402398 | T | C | 2 | a0001c0001t0002g0124 a0001c0001t0002g0171 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.917-1079A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402398 | |||||||
| chr3:179402772 | G | C | 3 | a0001c0002t0035g0260 a0001c0002t0035g0262 a0001c0002t0068g0258 |
3 | HG02145.hp1 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.917-1453C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402772 | |||||||
| chr3:179402832 | A | T | 1 | a0001c0001t0036g0206 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.917-1513T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402832 | |||||||
| chr3:179402848 | C | A | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.917-1529G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402848 | |||||||
| chr3:179402874 | A | G | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-1555T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402874 | |||||||
| chr3:179402881 | C | T | 2 | a0001c0002t0033g0289 a0001c0002t0033g0290 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.917-1562G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402881 | |||||||
| chr3:179402893 | C | T | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.917-1574G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402893 | |||||||
| chr3:179402899 | G | A | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.917-1580C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402899 | |||||||
| chr3:179402922 | G | A | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.917-1603C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179402922 | |||||||
| chr3:179403038 | T | C | 1 | a0001c0001t0019g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.917-1719A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403038 | |||||||
| chr3:179403194 | C | A | 8 | a0001c0001t0004g0126 a0001c0002t0004g0010 a0001c0002t0004g0037 others(5): Show |
11 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-1875G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403194 | |||||||
| chr3:179403195 | G | A | 72 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(69): Show |
85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.917-1876C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403195 | |||||||
| chr3:179403222 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.917-1903C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403222 | |||||||
| chr3:179403249 | T | G | 2 | a0001c0002t0033g0289 a0001c0002t0033g0290 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.917-1930A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403249 | |||||||
| chr3:179403303 | G | GA | 14 | a0001c0001t0002g0132 a0001c0001t0010g0004 a0001c0001t0010g0319 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.916+1886dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403303 | |||||||
| chr3:179403364 | C | A | 1 | a0001c0001t0060g0301 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.916+1826G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403364 | |||||||
| chr3:179403385 | A | C | 1 | a0001c0001t0008g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.916+1805T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403385 | |||||||
| chr3:179403435 | G | A | 1 | a0001c0001t0010g0331 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.916+1755C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403435 | |||||||
| chr3:179403555 | G | A | 2 | a0001c0002t0001g0102 a0001c0002t0001g0192 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.916+1635C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403555 | |||||||
| chr3:179403602 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1588C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403602 | |||||||
| chr3:179403631 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1559C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403631 | |||||||
| chr3:179403793 | G | A | 2 | a0001c0001t0011g0040 a0001c0001t0060g0301 |
3 | HG00639.hp1 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.916+1397C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403793 | |||||||
| chr3:179403797 | C | CAAAAA | 75 | a0001c0001t0001g0212 a0001c0001t0061g0335 a0001c0002t0001g0002 others(72): Show |
85 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.916+1388_916+1392d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403797 | |||||||
| chr3:179403800 | A | AAAAAT | 169 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(166): Show |
197 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.916+1385_916+1389d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403800 | |||||||
| chr3:179403805 | T | A | 69 | a0001c0001t0001g0212 a0001c0002t0001g0002 a0001c0002t0001g0005 others(66): Show |
78 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.916+1385A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403805 | |||||||
| chr3:179403806 | A | AAAAAT | 4 | a0001c0002t0001g0069 a0001c0002t0001g0091 a0001c0002t0001g0094 others(1): Show |
4 | HG01074.hp1 HG01081.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.916+1383_916+1384i others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403806 | |||||||
| chr3:179403810 | T | A | 2 | a0001c0002t0001g0073 a0001c0002t0040g0178 |
2 | HG00741.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.916+1380A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403810 | |||||||
| chr3:179403826 | T | G | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.916+1364A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403826 | |||||||
| chr3:179403850 | A | G | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.916+1340T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403850 | |||||||
| chr3:179403855 | A | G | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.916+1335T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403855 | |||||||
| chr3:179403885 | C | T | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.916+1305G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403885 | |||||||
| chr3:179403963 | C | T | 1 | a0001c0001t0008g0022 | 2 | NA18956.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.916+1227G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179403963 | |||||||
| chr3:179404220 | C | T | 40 | a0001c0002t0004g0032 a0001c0002t0004g0033 a0001c0002t0004g0061 others(37): Show |
43 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.916+970G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404220 | |||||||
| chr3:179404401 | G | A | 2 | a0001c0002t0006g0158 a0001c0002t0006g0161 |
2 | NA18944.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.916+789C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404401 | |||||||
| chr3:179404704 | C | T | 2 | a0001c0002t0014g0259 a0001c0002t0014g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.916+486G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404704 | |||||||
| chr3:179404806 | A | G | 1 | a0001c0002t0015g0218 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.916+384T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404806 | |||||||
| chr3:179404854 | G | A | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916+336C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404854 | |||||||
| chr3:179404919 | C | G | 82 | a0001c0001t0001g0212 a0001c0001t0061g0335 a0001c0002t0001g0002 others(79): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.916+271G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179404919 | |||||||
| chr3:179405130 | T | C | 51 | a0001c0001t0002g0155 a0001c0001t0004g0126 a0001c0002t0004g0010 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.916+60A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 9/9 | chr3 | 179405130 | |||||||
| chr3:179405421 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.700-15T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405421 | |||||||
| chr3:179405522 | G | A | 1 | a0001c0002t0015g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.700-116C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405522 | |||||||
| chr3:179405641 | A | G | 5 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-235T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405641 | |||||||
| chr3:179405716 | AAT | A | 55 | a0001c0001t0004g0126 a0001c0002t0004g0010 a0001c0002t0004g0032 others(52): Show |
62 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.700-312_700-311del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405716 | |||||||
| chr3:179405881 | A | C | 10 | a0001c0002t0021g0307 a0001c0002t0021g0308 a0001c0002t0021g0311 others(7): Show |
11 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.700-475T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405881 | |||||||
| chr3:179405916 | A | G | 43 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(40): Show |
52 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.700-510T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405916 | |||||||
| chr3:179405956 | C | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.700-550G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179405956 | |||||||
| chr3:179406069 | A | G | 8 | a0001c0001t0011g0038 a0001c0001t0011g0040 a0001c0001t0011g0266 others(5): Show |
10 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-663T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406069 | |||||||
| chr3:179406116 | T | C | 1 | a0001c0001t0002g0146 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.700-710A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406116 | |||||||
| chr3:179406140 | G | A | 24 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(21): Show |
28 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.700-734C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406140 | |||||||
| chr3:179406171 | A | C | 1 | a0001c0001t0002g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.700-765T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406171 | |||||||
| chr3:179406247 | G | A | 4 | a0001c0002t0004g0061 a0001c0002t0004g0062 a0001c0002t0004g0240 others(1): Show |
4 | HG00438.hp2 HG02165.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-841C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406247 | |||||||
| chr3:179406311 | G | A | 1 | a0001c0001t0053g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.700-905C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406311 | |||||||
| chr3:179406569 | T | C | 1 | a0001c0003t0062g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-1163A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406569 | |||||||
| chr3:179406635 | CAG | C | 8 | a0001c0003t0009g0320 a0001c0003t0009g0321 a0001c0003t0009g0323 others(5): Show |
8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.700-1231_700-1230d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406635 | |||||||
| chr3:179406700 | C | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0067g0306 |
5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1294G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406700 | |||||||
| chr3:179406925 | T | C | 5 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1519A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406925 | |||||||
| chr3:179406972 | T | C | 1 | a0001c0002t0049g0244 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.700-1566A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179406972 | |||||||
| chr3:179407026 | G | T | 82 | a0001c0001t0001g0212 a0001c0001t0061g0335 a0001c0002t0001g0002 others(79): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-1620C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407026 | |||||||
| chr3:179407112 | T | C | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.700-1706A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407112 | |||||||
| chr3:179407150 | G | A | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.700-1744C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407150 | |||||||
| chr3:179407153 | C | T | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.700-1747G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407153 | |||||||
| chr3:179407328 | G | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0278 a0001c0001t0003g0280 others(2): Show |
9 | HG00558.hp2 HG00609.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-1922C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407328 | |||||||
| chr3:179407608 | A | C | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-2202T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407608 | |||||||
| chr3:179407655 | G | C | 5 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(2): Show |
5 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-2249C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407655 | |||||||
| chr3:179407740 | A | C | 1 | a0001c0001t0010g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700-2334T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407740 | |||||||
| chr3:179407749 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-2343C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407749 | |||||||
| chr3:179407777 | G | GAA | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-2372_700-2371i others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407777 | |||||||
| chr3:179407797 | G | A | 50 | a0001c0001t0004g0126 a0001c0002t0004g0010 a0001c0002t0004g0032 others(47): Show |
57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.700-2391C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407797 | |||||||
| chr3:179407849 | A | C | 128 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(125): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.700-2443T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407849 | |||||||
| chr3:179407883 | A | G | 1 | a0001c0001t0070g0337 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.700-2477T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407883 | |||||||
| chr3:179407917 | G | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0279 |
4 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-2511C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407917 | |||||||
| chr3:179407996 | A | G | 1 | a0001c0002t0021g0327 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.700-2590T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179407996 | |||||||
| chr3:179408168 | C | T | 2 | a0001c0001t0003g0264 a0001c0001t0003g0276 |
2 | HG02027.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.700-2762G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408168 | |||||||
| chr3:179408221 | A | C | 6 | a0001c0002t0015g0196 a0001c0002t0015g0215 a0001c0002t0015g0216 others(3): Show |
7 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-2815T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408221 | |||||||
| chr3:179408303 | C | T | 1 | a0001c0001t0005g0144 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.700-2897G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408303 | |||||||
| chr3:179408541 | A | G | 1 | a0001c0002t0032g0316 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700-3135T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408541 | |||||||
| chr3:179408816 | C | CA | 82 | a0001c0001t0001g0212 a0001c0001t0061g0335 a0001c0002t0001g0002 others(79): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-3411dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408816 | |||||||
| chr3:179408822 | A | G | 1 | a0001c0001t0004g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.700-3416T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408822 | |||||||
| chr3:179408943 | C | T | 1 | a0001c0002t0004g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.700-3537G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408943 | |||||||
| chr3:179408956 | G | C | 1 | a0001c0003t0009g0321 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.700-3550C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179408956 | |||||||
| chr3:179409062 | T | G | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-3656A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409062 | |||||||
| chr3:179409108 | G | A | 70 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(67): Show |
83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.700-3702C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409108 | |||||||
| chr3:179409125 | TA | T | 220 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(217): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.700-3720delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409125 | |||||||
| chr3:179409193 | T | C | 26 | a0001c0002t0004g0032 a0001c0002t0004g0061 a0001c0002t0004g0062 others(23): Show |
27 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.700-3787A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409193 | |||||||
| chr3:179409239 | A | G | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.700-3833T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409239 | |||||||
| chr3:179409252 | T | C | 128 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(125): Show |
148 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.700-3846A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409252 | |||||||
| chr3:179409308 | C | A | 1 | a0001c0002t0015g0216 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.700-3902G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409308 | |||||||
| chr3:179409369 | G | A | 82 | a0001c0001t0001g0212 a0001c0001t0061g0335 a0001c0002t0001g0002 others(79): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.700-3963C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409369 | |||||||
| chr3:179409404 | C | T | 2 | a0001c0002t0014g0259 a0001c0002t0014g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.700-3998G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409404 | |||||||
| chr3:179409431 | G | GA | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3980dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409431 | |||||||
| chr3:179409517 | A | C | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3895T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409517 | |||||||
| chr3:179409518 | C | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3894G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409518 | |||||||
| chr3:179409523 | A | AC | 75 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(72): Show |
88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.699+3888_699+3889i others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409523 | |||||||
| chr3:179409523 | A | C | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699+3889T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409523 | |||||||
| chr3:179409680 | T | C | 84 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(81): Show |
100 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.699+3732A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409680 | |||||||
| chr3:179409680 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.699+3732A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409680 | |||||||
| chr3:179409682 | C | T | 1 | a0001c0001t0009g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699+3730G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409682 | |||||||
| chr3:179409704 | G | A | 1 | a0001c0002t0043g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+3708C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409704 | |||||||
| chr3:179409808 | C | CA | 66 | a0001c0001t0002g0114 a0001c0001t0002g0146 a0001c0001t0002g0171 others(63): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.699+3603dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409808 | |||||||
| chr3:179409828 | C | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0067g0306 |
5 | HG02109.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3584G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409828 | |||||||
| chr3:179409828 | CA | C | 7 | a0001c0001t0003g0265 a0001c0002t0001g0060 a0001c0002t0001g0080 others(4): Show |
7 | HG01515.hp2 HG01517.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.699+3583delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409828 | |||||||
| chr3:179409831 | A | C | 6 | a0001c0002t0001g0017 a0001c0002t0001g0063 a0001c0002t0001g0113 others(3): Show |
7 | HG02698.hp1 HG03688.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.699+3581T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409831 | |||||||
| chr3:179409832 | A | C | 4 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(1): Show |
5 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3580T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409832 | |||||||
| chr3:179409832 | AC | A | 168 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(165): Show |
192 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.699+3579delG | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409832 | |||||||
| chr3:179409833 | C | A | 7 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0067g0306 others(4): Show |
10 | HG01069.hp1 HG01433.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.699+3579G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409833 | |||||||
| chr3:179409833 | CA | C | 18 | a0001c0001t0003g0281 a0001c0001t0005g0144 a0001c0001t0010g0004 others(15): Show |
23 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.699+3578delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409833 | |||||||
| chr3:179409835 | A | C | 4 | a0001c0002t0014g0259 a0001c0002t0014g0261 a0001c0002t0032g0316 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+3577T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409835 | |||||||
| chr3:179409862 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3550C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179409862 | |||||||
| chr3:179410058 | G | A | 1 | a0001c0002t0006g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.699+3354C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410058 | |||||||
| chr3:179410102 | A | G | 2 | a0001c0002t0014g0259 a0001c0002t0014g0261 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.699+3310T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410102 | |||||||
| chr3:179410118 | T | C | 81 | a0001c0001t0001g0212 a0001c0002t0001g0002 a0001c0002t0001g0005 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.699+3294A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410118 | |||||||
| chr3:179410124 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0071 |
3 | HG02071.hp1 HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.699+3288C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410124 | |||||||
| chr3:179410212 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+3200C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410212 | |||||||
| chr3:179410351 | G | T | 1 | a0001c0001t0003g0293 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.699+3061C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410351 | |||||||
| chr3:179410354 | T | A | 1 | a0001c0002t0004g0238 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.699+3058A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410354 | |||||||
| chr3:179410573 | T | C | 1 | a0001c0002t0004g0239 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.699+2839A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410573 | |||||||
| chr3:179410592 | T | C | 1 | a0001c0001t0003g0269 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.699+2820A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410592 | |||||||
| chr3:179410663 | A | T | 8 | a0001c0001t0011g0038 a0001c0001t0011g0040 a0001c0001t0011g0266 others(5): Show |
10 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+2749T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410663 | |||||||
| chr3:179410786 | A | G | 1 | a0001c0001t0005g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.699+2626T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179410786 | |||||||
| chr3:179411026 | T | C | 1 | a0001c0002t0043g0079 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.699+2386A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411026 | |||||||
| chr3:179411466 | C | CA | 21 | a0001c0001t0005g0149 a0001c0001t0057g0314 a0001c0002t0001g0005 others(18): Show |
25 | HG00609.hp1 HG01433.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.699+1945dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | |||||||
| chr3:179411466 | C | CAA | 48 | a0001c0001t0004g0126 a0001c0002t0004g0010 a0001c0002t0004g0032 others(45): Show |
55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.699+1944_699+1945d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | |||||||
| chr3:179411466 | CA | C | 8 | a0001c0001t0003g0333 a0001c0001t0010g0330 a0001c0001t0010g0331 others(5): Show |
9 | HG01069.hp1 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.699+1945delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411466 | |||||||
| chr3:179411494 | T | C | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1918A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411494 | |||||||
| chr3:179411534 | G | A | 1 | a0001c0001t0003g0333 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.699+1878C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411534 | |||||||
| chr3:179411568 | A | G | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.699+1844T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411568 | |||||||
| chr3:179411818 | A | C | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1594T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411818 | |||||||
| chr3:179411867 | A | T | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.699+1545T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411867 | |||||||
| chr3:179411913 | A | G | 2 | a0001c0001t0005g0204 a0001c0001t0005g0211 |
2 | HG01346.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.699+1499T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411913 | |||||||
| chr3:179411985 | C | T | 5 | a0001c0002t0007g0198 a0001c0002t0007g0199 a0001c0002t0007g0201 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+1427G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179411985 | |||||||
| chr3:179412094 | T | C | 13 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(10): Show |
16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.699+1318A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412094 | |||||||
| chr3:179412146 | G | GT | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1265dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412146 | |||||||
| chr3:179412316 | A | AAAAC | 248 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(245): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.699+1092_699+1095d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412316 | |||||||
| chr3:179412320 | C | A | 1 | a0001c0001t0009g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699+1092G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412320 | |||||||
| chr3:179412322 | A | AAC | 10 | a0001c0001t0011g0038 a0001c0001t0011g0040 a0001c0001t0011g0263 others(7): Show |
12 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.699+1088_699+1089d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412322 | |||||||
| chr3:179412396 | T | C | 2 | a0001c0003t0009g0325 a0001c0003t0009g0326 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.699+1016A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412396 | |||||||
| chr3:179412469 | C | A | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.699+943G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412469 | |||||||
| chr3:179412673 | G | A | 1 | a0001c0001t0024g0208 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.699+739C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412673 | |||||||
| chr3:179412852 | A | G | 14 | a0001c0001t0001g0212 a0001c0002t0001g0017 a0001c0002t0001g0063 others(11): Show |
15 | HG00408.hp1 HG01515.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.699+560T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179412852 | |||||||
| chr3:179413138 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.699+274C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413138 | |||||||
| chr3:179413157 | G | A | 2 | a0001c0003t0009g0325 a0001c0003t0009g0326 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.699+255C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413157 | |||||||
| chr3:179413190 | AT | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+221delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413190 | |||||||
| chr3:179413275 | T | C | 6 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(3): Show |
6 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+137A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413275 | |||||||
| chr3:179413314 | G | T | 1 | a0001c0001t0002g0059 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.699+98C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413314 | |||||||
| chr3:179413362 | C | T | 1 | a0001c0001t0020g0338 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.699+50G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 8/9 | chr3 | 179413362 | |||||||
| chr3:179413806 | T | G | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-25A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413806 | |||||||
| chr3:179413830 | T | C | 1 | a0001c0001t0002g0138 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431-49A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413830 | |||||||
| chr3:179413864 | A | T | 114 | a0001c0001t0001g0212 a0001c0001t0044g0174 a0001c0002t0001g0002 others(111): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.431-83T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413864 | |||||||
| chr3:179413869 | T | C | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.431-88A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413869 | |||||||
| chr3:179413884 | A | C | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-103T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413884 | |||||||
| chr3:179413887 | A | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-106T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413887 | |||||||
| chr3:179413898 | A | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-117T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413898 | |||||||
| chr3:179413899 | T | C | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.431-118A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179413899 | |||||||
| chr3:179414092 | C | T | 11 | a0001c0002t0014g0259 a0001c0002t0014g0261 a0001c0002t0021g0307 others(8): Show |
12 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-311G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414092 | |||||||
| chr3:179414134 | T | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-353A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414134 | |||||||
| chr3:179414157 | C | T | 5 | a0001c0002t0004g0032 a0001c0002t0004g0177 a0001c0002t0004g0230 others(2): Show |
6 | HG00140.hp1 HG00323.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-376G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414157 | |||||||
| chr3:179414596 | A | C | 1 | a0001c0001t0053g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.430+289T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414596 | |||||||
| chr3:179414664 | C | A | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.430+221G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414664 | |||||||
| chr3:179414727 | C | CTA | 84 | a0001c0001t0001g0212 a0001c0001t0055g0285 a0001c0001t0056g0284 others(81): Show |
94 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.430+156_430+157dup others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414727 | |||||||
| chr3:179414784 | C | T | 3 | a0001c0002t0001g0113 a0001c0002t0001g0164 a0001c0002t0047g0107 |
3 | HG02698.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.430+101G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 6/9 | chr3 | 179414784 | |||||||
| chr3:179415447 | G | C | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.268-400C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415447 | |||||||
| chr3:179415640 | A | AAAGT | 123 | a0001c0001t0001g0212 a0001c0001t0055g0285 a0001c0001t0056g0284 others(120): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.268-594_268-593ins others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415640 | |||||||
| chr3:179415728 | A | G | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268-681T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415728 | |||||||
| chr3:179415980 | CTA | C | 68 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(65): Show |
81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.267+511_267+512del others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179415980 | |||||||
| chr3:179416095 | A | C | 2 | a0001c0002t0006g0158 a0001c0002t0006g0161 |
2 | NA18944.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.267+398T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416095 | |||||||
| chr3:179416121 | G | C | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.267+372C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416121 | |||||||
| chr3:179416220 | A | T | 1 | a0003c0006t0059g0300 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.267+273T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 5/9 | chr3 | 179416220 | |||||||
| chr3:179416559 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp2 | splice_region_variant&intron_variant | LOW | c.204-3T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416559 | |||||||
| chr3:179416610 | A | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-54T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416610 | |||||||
| chr3:179416623 | T | C | 8 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(5): Show |
8 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-67A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416623 | |||||||
| chr3:179416745 | A | G | 1 | a0001c0001t0003g0269 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.204-189T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416745 | |||||||
| chr3:179416795 | T | A | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-239A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416795 | |||||||
| chr3:179416833 | G | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-277C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416833 | |||||||
| chr3:179416846 | G | C | 82 | a0001c0001t0001g0212 a0001c0002t0001g0002 a0001c0002t0001g0005 others(79): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.204-290C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416846 | |||||||
| chr3:179416887 | A | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-331T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416887 | |||||||
| chr3:179416966 | T | A | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-410A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179416966 | |||||||
| chr3:179417008 | T | A | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-452A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417008 | |||||||
| chr3:179417340 | A | C | 1 | a0001c0002t0023g0044 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204-784T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417340 | |||||||
| chr3:179417388 | T | A | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-832A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417388 | |||||||
| chr3:179417388 | T | G | 49 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(46): Show |
56 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.204-832A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417388 | |||||||
| chr3:179417409 | A | AT | 22 | a0001c0001t0005g0148 a0001c0001t0005g0149 a0001c0001t0010g0004 others(19): Show |
27 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.204-854dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417409 | |||||||
| chr3:179417409 | AT | A | 53 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(50): Show |
60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.204-854delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417409 | |||||||
| chr3:179417471 | G | A | 4 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.204-915C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417471 | |||||||
| chr3:179417471 | G | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0014 others(83): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.204-915C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417471 | |||||||
| chr3:179417493 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.204-937G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417493 | |||||||
| chr3:179417533 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.204-977C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417533 | |||||||
| chr3:179417537 | A | T | 1 | a0001c0001t0044g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.204-981T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417537 | |||||||
| chr3:179417564 | C | T | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-1008G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417564 | |||||||
| chr3:179417831 | C | G | 1 | a0001c0002t0004g0249 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.204-1275G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417831 | |||||||
| chr3:179417940 | A | G | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.204-1384T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417940 | |||||||
| chr3:179417971 | T | C | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204-1415A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179417971 | |||||||
| chr3:179418194 | G | A | 46 | a0001c0001t0069g0318 a0001c0002t0004g0010 a0001c0002t0004g0032 others(43): Show |
52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.203+1205C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418194 | |||||||
| chr3:179418195 | C | T | 1 | a0001c0001t0002g0117 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.203+1204G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418195 | |||||||
| chr3:179418205 | C | A | 1 | a0001c0002t0001g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.203+1194G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418205 | |||||||
| chr3:179418253 | T | C | 4 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+1146A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418253 | |||||||
| chr3:179418394 | TG | T | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.203+1004delC | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418394 | |||||||
| chr3:179418470 | C | CAA | 38 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(35): Show |
45 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.203+927_203+928dup others(2): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | |||||||
| chr3:179418470 | C | CAAA | 14 | a0001c0002t0004g0228 a0001c0002t0004g0230 a0001c0002t0004g0234 others(11): Show |
14 | HG00323.hp2 HG01243.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.203+926_203+928dup others(3): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | |||||||
| chr3:179418470 | CA | C | 156 | a0001c0001t0001g0212 a0001c0001t0002g0129 a0001c0001t0003g0011 others(153): Show |
181 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.203+928delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | |||||||
| chr3:179418470 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0011g0302 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.203+916_203+928del others(13): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418470 | |||||||
| chr3:179418489 | G | A | 53 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(50): Show |
60 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.203+910C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179418489 | |||||||
| chr3:179419010 | G | A | 3 | a0001c0001t0003g0041 a0001c0001t0003g0312 a0001c0001t0057g0314 |
4 | NA18951.hp2 NA18967.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+389C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419010 | |||||||
| chr3:179419047 | A | T | 1 | a0001c0001t0003g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.203+352T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419047 | |||||||
| chr3:179419311 | T | C | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.203+88A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419311 | |||||||
| chr3:179419314 | T | C | 31 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(28): Show |
35 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.203+85A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 4/9 | chr3 | 179419314 | |||||||
| chr3:179419743 | G | T | 1 | a0001c0002t0021g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.97-238C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419743 | |||||||
| chr3:179419939 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.97-434A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419939 | |||||||
| chr3:179419965 | A | T | 51 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.97-460T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179419965 | |||||||
| chr3:179420064 | A | G | 1 | a0001c0002t0004g0230 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.97-559T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420064 | |||||||
| chr3:179420277 | C | T | 1 | a0001c0001t0053g0255 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.96+612G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420277 | |||||||
| chr3:179420303 | G | GT | 7 | a0001c0001t0002g0181 a0001c0001t0011g0263 a0001c0001t0044g0174 others(4): Show |
7 | HG02055.hp1 HG02976.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+585dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420303 | |||||||
| chr3:179420303 | GT | G | 8 | a0001c0002t0021g0307 a0001c0002t0021g0308 a0001c0002t0021g0311 others(5): Show |
8 | HG02257.hp1 HG02559.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+585delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420303 | |||||||
| chr3:179420304 | T | G | 50 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(47): Show |
57 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.96+585A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420304 | |||||||
| chr3:179420331 | G | A | 1 | a0001c0001t0009g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.96+558C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420331 | |||||||
| chr3:179420467 | TA | T | 118 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(115): Show |
140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.96+421delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420467 | |||||||
| chr3:179420469 | TA | T | 92 | a0001c0001t0005g0145 a0001c0001t0024g0221 a0001c0001t0067g0306 others(89): Show |
102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.96+419delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420469 | |||||||
| chr3:179420470 | A | AT | 13 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(10): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+418dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420470 | |||||||
| chr3:179420470 | A | T | 131 | a0001c0001t0001g0212 a0001c0001t0002g0003 a0001c0001t0002g0055 others(128): Show |
154 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.96+419T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420470 | |||||||
| chr3:179420472 | T | A | 3 | a0001c0001t0028g0020 a0001c0001t0046g0189 a0001c0001t0048g0188 |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+417A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420472 | |||||||
| chr3:179420526 | G | A | 81 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0014 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.96+363C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420526 | |||||||
| chr3:179420540 | G | C | 1 | a0001c0001t0011g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+349C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420540 | |||||||
| chr3:179420755 | G | A | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+134C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420755 | |||||||
| chr3:179420769 | CAG | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+118_96+119delCT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420769 | |||||||
| chr3:179420794 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.96+95T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420794 | |||||||
| chr3:179420814 | T | A | 1 | a0001c0002t0004g0062 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.96+75A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 3/9 | chr3 | 179420814 | |||||||
| chr3:179420934 | T | TA | 6 | a0001c0002t0001g0064 a0001c0002t0022g0186 a0001c0002t0022g0187 others(3): Show |
6 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.58-8dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179420934 | |||||||
| chr3:179421196 | A | G | 72 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(69): Show |
85 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.58-269T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421196 | |||||||
| chr3:179421200 | C | G | 1 | a0001c0001t0067g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-273G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421200 | |||||||
| chr3:179421444 | A | G | 8 | a0001c0003t0009g0320 a0001c0003t0009g0321 a0001c0003t0009g0323 others(5): Show |
8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-517T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421444 | |||||||
| chr3:179421462 | T | C | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.58-535A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421462 | |||||||
| chr3:179421491 | A | C | 30 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(27): Show |
34 | HG00735.hp1 HG01069.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.58-564T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421491 | |||||||
| chr3:179421523 | A | C | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | NA18959.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.58-596T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421523 | |||||||
| chr3:179421656 | A | C | 4 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(1): Show |
4 | HG02647.hp1 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-729T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421656 | |||||||
| chr3:179421672 | C | T | 4 | a0001c0001t0003g0011 a0001c0001t0003g0278 a0001c0001t0003g0303 others(1): Show |
8 | HG00558.hp2 HG00609.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-745G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421672 | |||||||
| chr3:179421831 | A | G | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-904T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421831 | |||||||
| chr3:179421916 | T | G | 1 | a0001c0001t0067g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-989A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179421916 | |||||||
| chr3:179422054 | A | C | 1 | a0001c0002t0004g0236 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.58-1127T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422054 | |||||||
| chr3:179422185 | C | G | 257 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(254): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.58-1258G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422185 | |||||||
| chr3:179422195 | G | GT | 7 | a0001c0002t0001g0017 a0001c0002t0001g0063 a0001c0002t0001g0068 others(4): Show |
8 | HG00408.hp1 HG01978.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-1269dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422195 | |||||||
| chr3:179422352 | C | T | 1 | a0001c0003t0009g0320 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.58-1425G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422352 | |||||||
| chr3:179422444 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.58-1517G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422444 | |||||||
| chr3:179422464 | A | G | 71 | a0001c0001t0001g0212 a0001c0001t0002g0169 a0001c0001t0003g0011 others(68): Show |
84 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-1537T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422464 | |||||||
| chr3:179422486 | C | CA | 82 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(79): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.58-1560dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422486 | |||||||
| chr3:179422583 | T | C | 2 | a0001c0001t0055g0285 a0001c0001t0056g0284 |
2 | NA19075.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.58-1656A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422583 | |||||||
| chr3:179422832 | G | A | 70 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(67): Show |
83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.58-1905C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422832 | |||||||
| chr3:179422853 | C | T | 5 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 others(2): Show |
5 | HG01433.hp2 HG02257.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-1926G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422853 | |||||||
| chr3:179422854 | G | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-1927C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422854 | |||||||
| chr3:179422918 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58-1991C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422918 | |||||||
| chr3:179422926 | G | A | 1 | a0001c0001t0014g0336 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-1999C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422926 | |||||||
| chr3:179422950 | G | A | 71 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(68): Show |
84 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-2023C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422950 | |||||||
| chr3:179422993 | A | G | 1 | a0001c0001t0067g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-2066T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179422993 | |||||||
| chr3:179423017 | T | C | 2 | a0001c0002t0033g0289 a0001c0002t0033g0290 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.58-2090A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423017 | |||||||
| chr3:179423038 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.58-2111C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423038 | |||||||
| chr3:179423051 | A | G | 7 | a0001c0002t0004g0010 a0001c0002t0004g0037 a0001c0002t0004g0248 others(4): Show |
10 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-2124T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423051 | |||||||
| chr3:179423081 | G | A | 1 | a0001c0001t0067g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-2154C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423081 | |||||||
| chr3:179423200 | C | T | 3 | a0001c0002t0001g0060 a0001c0002t0001g0080 a0001c0002t0001g0085 |
3 | HG02523.hp2 NA18962.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.58-2273G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423200 | |||||||
| chr3:179423210 | A | G | 1 | a0001c0002t0006g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.58-2283T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423210 | |||||||
| chr3:179423292 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-2365A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423292 | |||||||
| chr3:179423320 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-2393G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423320 | |||||||
| chr3:179423526 | G | A | 9 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(6): Show |
11 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.58-2599C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423526 | |||||||
| chr3:179423580 | A | C | 1 | a0001c0001t0003g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+2564T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423580 | |||||||
| chr3:179423642 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.57+2502C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423642 | |||||||
| chr3:179423653 | T | C | 1 | a0001c0001t0003g0267 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.57+2491A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423653 | |||||||
| chr3:179423709 | A | G | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.57+2435T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423709 | |||||||
| chr3:179423786 | T | TA | 158 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(155): Show |
184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.57+2357dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423786 | |||||||
| chr3:179423812 | G | C | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.57+2332C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423812 | |||||||
| chr3:179423823 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+2321A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423823 | |||||||
| chr3:179423880 | C | T | 2 | a0001c0002t0004g0033 a0001c0002t0004g0228 |
3 | HG03225.hp1 HG03486.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.57+2264G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423880 | |||||||
| chr3:179423928 | G | A | 1 | a0001c0002t0001g0078 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.57+2216C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423928 | |||||||
| chr3:179423971 | A | G | 2 | a0001c0002t0006g0083 a0001c0002t0006g0160 |
2 | HG01257.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.57+2173T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179423971 | |||||||
| chr3:179424049 | C | T | 81 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0014 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.57+2095G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424049 | |||||||
| chr3:179424248 | C | A | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+1896G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424248 | |||||||
| chr3:179424290 | G | A | 2 | a0001c0002t0033g0289 a0001c0002t0033g0290 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.57+1854C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424290 | |||||||
| chr3:179424565 | G | A | 1 | a0001c0002t0004g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.57+1579C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424565 | |||||||
| chr3:179424714 | C | T | 1 | a0001c0002t0021g0307 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57+1430G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424714 | |||||||
| chr3:179424769 | T | C | 1 | a0001c0001t0067g0306 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+1375A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424769 | |||||||
| chr3:179424861 | G | A | 4 | a0001c0002t0004g0036 a0001c0002t0004g0243 a0001c0002t0007g0242 others(1): Show |
5 | HG01261.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+1283C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179424861 | |||||||
| chr3:179425179 | A | G | 1 | a0001c0002t0021g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.57+965T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425179 | |||||||
| chr3:179425344 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57+800G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425344 | |||||||
| chr3:179425345 | G | A | 2 | a0001c0001t0003g0012 a0001c0001t0003g0279 |
4 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+799C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425345 | |||||||
| chr3:179425544 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.57+600G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425544 | |||||||
| chr3:179425617 | T | C | 247 | a0001c0001t0001g0212 a0001c0001t0002g0053 a0001c0001t0003g0011 others(244): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+527A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425617 | |||||||
| chr3:179425618 | G | A | 247 | a0001c0001t0001g0212 a0001c0001t0002g0053 a0001c0001t0003g0011 others(244): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+526C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425618 | |||||||
| chr3:179425620 | A | G | 247 | a0001c0001t0001g0212 a0001c0001t0002g0053 a0001c0001t0003g0011 others(244): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.57+524T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425620 | |||||||
| chr3:179425639 | TTTTCTAT others(24): Show |
T | 1 | a0004c0005t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.57+474_57+504delGG others(29): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425639 | |||||||
| chr3:179425642 | T | C | 12 | a0001c0002t0015g0196 a0001c0002t0015g0215 a0001c0002t0015g0216 others(9): Show |
13 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+502A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425642 | |||||||
| chr3:179425715 | C | A | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.57+429G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425715 | |||||||
| chr3:179425751 | A | G | 1 | a0001c0002t0006g0093 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.57+393T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425751 | |||||||
| chr3:179425762 | T | C | 1 | a0001c0002t0007g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+382A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425762 | |||||||
| chr3:179425767 | A | G | 1 | a0001c0002t0007g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+377T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425767 | |||||||
| chr3:179425881 | G | A | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.57+263C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 2/9 | chr3 | 179425881 | |||||||
| chr3:179426407 | AT | A | 6 | a0001c0002t0015g0196 a0001c0002t0015g0215 a0001c0002t0015g0216 others(3): Show |
7 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-166delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426407 | |||||||
| chr3:179426640 | G | C | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-398C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426640 | |||||||
| chr3:179426646 | G | A | 18 | a0001c0001t0009g0257 a0001c0001t0014g0013 a0001c0001t0014g0336 others(15): Show |
21 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42-404C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426646 | |||||||
| chr3:179426652 | A | T | 173 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(170): Show |
201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.-42-410T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426652 | |||||||
| chr3:179426847 | G | A | 157 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(154): Show |
182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-42-605C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426847 | |||||||
| chr3:179426951 | C | T | 132 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(129): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-42-709G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426951 | |||||||
| chr3:179426987 | C | T | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-745G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426987 | |||||||
| chr3:179426988 | C | A | 174 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(171): Show |
202 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.-42-746G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179426988 | |||||||
| chr3:179427004 | G | A | 13 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(10): Show |
16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-762C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427004 | |||||||
| chr3:179427146 | C | T | 184 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(181): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-42-904G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427146 | |||||||
| chr3:179427269 | C | G | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-1027G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427269 | |||||||
| chr3:179427327 | T | G | 42 | a0001c0001t0009g0257 a0001c0001t0010g0004 a0001c0001t0010g0319 others(39): Show |
50 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42-1085A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427327 | |||||||
| chr3:179427425 | C | T | 11 | a0001c0002t0015g0196 a0001c0002t0015g0215 a0001c0002t0015g0216 others(8): Show |
12 | HG00735.hp1 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-42-1183G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427425 | |||||||
| chr3:179427469 | G | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-1227C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427469 | |||||||
| chr3:179427477 | T | C | 15 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(12): Show |
18 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-42-1235A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427477 | |||||||
| chr3:179427541 | G | T | 1 | a0004c0005t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1299C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427541 | |||||||
| chr3:179427562 | A | T | 1 | a0004c0005t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1320T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427562 | |||||||
| chr3:179427605 | T | TA | 16 | a0001c0001t0002g0006 a0001c0001t0002g0121 a0001c0001t0002g0136 others(13): Show |
21 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-42-1364dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | |||||||
| chr3:179427605 | TA | T | 138 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(135): Show |
166 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.-42-1364delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | |||||||
| chr3:179427605 | TAA | T | 108 | a0001c0001t0001g0212 a0001c0001t0002g0127 a0001c0001t0002g0134 others(105): Show |
125 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-42-1365_-42-1364d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | |||||||
| chr3:179427605 | TAAA | T | 51 | a0001c0001t0003g0278 a0001c0001t0003g0279 a0001c0001t0005g0145 others(48): Show |
58 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.-42-1366_-42-1364d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427605 | |||||||
| chr3:179427719 | C | A | 1 | a0001c0002t0013g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-42-1477G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427719 | |||||||
| chr3:179427734 | T | A | 1 | a0001c0002t0004g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-42-1492A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427734 | |||||||
| chr3:179427848 | T | C | 2 | a0001c0001t0003g0292 a0001c0001t0003g0293 |
2 | NA18982.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-42-1606A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427848 | |||||||
| chr3:179427863 | C | T | 14 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-1621G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427863 | |||||||
| chr3:179427983 | G | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-1741C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179427983 | |||||||
| chr3:179428011 | T | TGATTCCC others(6): Show |
1 | a0004c0005t0002g0125 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-42-1782_-42-1770d others(15): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428011 | |||||||
| chr3:179428045 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-42-1803C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428045 | |||||||
| chr3:179428051 | G | C | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-42-1809C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428051 | |||||||
| chr3:179428305 | C | CT | 258 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(255): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-42-2064dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428305 | |||||||
| chr3:179428401 | G | A | 14 | a0001c0001t0009g0257 a0001c0001t0014g0013 a0001c0001t0014g0336 others(11): Show |
17 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-2159C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428401 | |||||||
| chr3:179428515 | A | G | 47 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(44): Show |
54 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.-42-2273T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428515 | |||||||
| chr3:179428568 | G | C | 1 | a0001c0001t0010g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-42-2326C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428568 | |||||||
| chr3:179428699 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-42-2457A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179428699 | |||||||
| chr3:179429024 | G | A | 8 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(5): Show |
9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-2782C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429024 | |||||||
| chr3:179429031 | G | A | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-2789C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429031 | |||||||
| chr3:179429056 | A | G | 85 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(82): Show |
98 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-42-2814T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429056 | |||||||
| chr3:179429064 | C | A | 129 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(126): Show |
148 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-42-2822G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429064 | |||||||
| chr3:179429071 | C | T | 1 | a0001c0003t0062g0322 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-42-2829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429071 | |||||||
| chr3:179429079 | T | C | 69 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(66): Show |
81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-42-2837A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429079 | |||||||
| chr3:179429087 | A | G | 24 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(21): Show |
29 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.-42-2845T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429087 | |||||||
| chr3:179429188 | G | C | 9 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(6): Show |
11 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-42-2946C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429188 | |||||||
| chr3:179429322 | T | A | 6 | a0001c0002t0004g0222 a0001c0002t0004g0227 a0001c0002t0004g0236 others(3): Show |
6 | HG00621.hp1 NA18946.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-3080A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429322 | |||||||
| chr3:179429342 | G | A | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-3100C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429342 | |||||||
| chr3:179429383 | T | C | 257 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(254): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-42-3141A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429383 | |||||||
| chr3:179429562 | T | C | 3 | a0001c0001t0067g0306 a0001c0002t0063g0305 a0001c0002t0066g0310 |
3 | HG01167.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-3320A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429562 | |||||||
| chr3:179429691 | G | T | 253 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(250): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-42-3449C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429691 | |||||||
| chr3:179429961 | A | G | 2 | a0001c0001t0025g0058 a0001c0001t0025g0119 |
2 | NA19085.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-42-3719T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429961 | |||||||
| chr3:179429977 | C | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-3735G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179429977 | |||||||
| chr3:179430071 | G | C | 1 | a0001c0002t0021g0327 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-42-3829C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430071 | G | GAGAC | 38 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(35): Show |
50 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.-42-3833_-42-3830d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430071 | G | GAGACAGA others(1): Show |
3 | a0001c0001t0002g0077 a0001c0001t0002g0134 a0001c0002t0015g0218 |
3 | HG00733.hp1 HG03130.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-42-3837_-42-3830d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430071 | GAGAC | G | 55 | a0001c0001t0002g0122 a0001c0001t0002g0171 a0001c0001t0004g0126 others(52): Show |
63 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.-42-3833_-42-3830d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430071 | GAGACAGA others(1): Show |
G | 116 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(113): Show |
134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-42-3837_-42-3830d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430071 | GAGACAGA others(5): Show |
G | 4 | a0001c0001t0069g0318 a0001c0002t0001g0067 a0001c0002t0032g0316 others(1): Show |
4 | HG00639.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-3841_-42-3830d others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430071 | |||||||
| chr3:179430073 | GACAGAC | G | 69 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(66): Show |
81 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.-42-3837_-42-3832d others(8): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430073 | |||||||
| chr3:179430105 | GACAGACA others(5): Show |
G | 1 | a0001c0002t0022g0186 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-42-3875_-42-3864d others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430105 | |||||||
| chr3:179430109 | GACAGACA others(1): Show |
G | 4 | a0001c0002t0022g0187 a0001c0002t0022g0191 a0001c0002t0033g0289 others(1): Show |
4 | HG01433.hp2 HG02257.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-3875_-42-3868d others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430109 | |||||||
| chr3:179430117 | A | G | 5 | a0001c0002t0015g0196 a0001c0002t0015g0216 a0001c0002t0015g0217 others(2): Show |
6 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42-3875T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430117 | |||||||
| chr3:179430245 | C | A | 1 | a0001c0002t0004g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-42-4003G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430245 | |||||||
| chr3:179430252 | ATTTTCTT | A | 8 | a0001c0002t0015g0196 a0001c0002t0015g0215 a0001c0002t0015g0216 others(5): Show |
9 | HG00735.hp1 HG01433.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-42-4017_-42-4011d others(9): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430252 | |||||||
| chr3:179430326 | C | T | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-42-4084G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430326 | |||||||
| chr3:179430336 | C | T | 14 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-4094G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430336 | |||||||
| chr3:179430378 | C | T | 1 | a0001c0002t0065g0315 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42-4136G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430378 | |||||||
| chr3:179430544 | C | G | 2 | a0001c0002t0001g0069 a0001c0002t0001g0094 |
2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-42-4302G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430544 | |||||||
| chr3:179430620 | A | AT | 25 | a0001c0001t0001g0212 a0001c0001t0008g0185 a0001c0001t0010g0004 others(22): Show |
30 | HG00544.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-42-4379dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430620 | |||||||
| chr3:179430620 | AT | A | 69 | a0001c0001t0002g0053 a0001c0001t0002g0124 a0001c0001t0002g0136 others(66): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.-42-4379delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430620 | |||||||
| chr3:179430622 | T | A | 1 | a0001c0002t0022g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-42-4380A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430622 | |||||||
| chr3:179430937 | T | G | 14 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-4695A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430937 | |||||||
| chr3:179430960 | G | A | 5 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 others(2): Show |
7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42-4718C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430960 | |||||||
| chr3:179430960 | G | C | 2 | a0001c0002t0001g0110 a0001c0002t0001g0112 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-42-4718C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179430960 | |||||||
| chr3:179431012 | T | G | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-42-4770A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431012 | |||||||
| chr3:179431159 | T | G | 3 | a0001c0001t0010g0330 a0001c0001t0010g0331 a0001c0001t0010g0332 |
3 | HG02486.hp2 HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-42-4917A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431159 | |||||||
| chr3:179431224 | C | T | 4 | a0001c0002t0004g0036 a0001c0002t0004g0243 a0001c0002t0007g0242 others(1): Show |
5 | HG01261.hp1 HG02886.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-4982G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431224 | |||||||
| chr3:179431261 | G | A | 7 | a0001c0001t0002g0006 a0001c0001t0002g0121 a0001c0001t0002g0136 others(4): Show |
9 | HG01070.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-5019C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431261 | |||||||
| chr3:179431289 | G | T | 3 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0064g0291 |
3 | HG02647.hp1 HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-42-5047C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431289 | |||||||
| chr3:179431388 | C | G | 7 | a0001c0001t0010g0330 a0001c0001t0010g0331 a0001c0001t0010g0332 others(4): Show |
7 | HG02132.hp2 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42-5146G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431388 | |||||||
| chr3:179431401 | A | G | 12 | a0001c0001t0002g0114 a0001c0001t0002g0122 a0001c0001t0002g0123 others(9): Show |
13 | HG01081.hp1 HG01106.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.-42-5159T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431401 | |||||||
| chr3:179431450 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-42-5208A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431450 | |||||||
| chr3:179431510 | G | A | 1 | a0001c0002t0006g0093 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-42-5268C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431510 | |||||||
| chr3:179431515 | C | T | 1 | a0001c0002t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-42-5273G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431515 | |||||||
| chr3:179431557 | C | CA | 146 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(143): Show |
171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-42-5316dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | |||||||
| chr3:179431557 | C | CAA | 6 | a0001c0001t0003g0299 a0001c0001t0017g0150 a0001c0001t0070g0337 others(3): Show |
6 | HG00408.hp2 HG01515.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-5317_-42-5316d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | |||||||
| chr3:179431557 | C | CAAA | 75 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(72): Show |
86 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-42-5318_-42-5316d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | |||||||
| chr3:179431557 | C | CAAAA | 6 | a0001c0002t0001g0094 a0001c0002t0001g0095 a0001c0002t0001g0096 others(3): Show |
6 | HG01074.hp1 HG01978.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-42-5319_-42-5316d others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431557 | |||||||
| chr3:179431821 | A | C | 1 | a0001c0001t0011g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-5579T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179431821 | |||||||
| chr3:179432590 | T | C | 1 | a0001c0001t0010g0004 | 4 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-6348A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432590 | |||||||
| chr3:179432614 | A | C | 14 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-6372T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432614 | |||||||
| chr3:179432726 | A | G | 1 | a0001c0002t0004g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-42-6484T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179432726 | |||||||
| chr3:179433068 | C | A | 81 | a0001c0001t0012g0024 a0001c0001t0072g0329 a0001c0002t0001g0002 others(78): Show |
92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-42-6826G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433068 | |||||||
| chr3:179433181 | G | A | 5 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 others(2): Show |
7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-42-6939C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433181 | |||||||
| chr3:179433192 | C | T | 1 | a0001c0002t0021g0311 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-42-6950G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433192 | |||||||
| chr3:179433312 | A | G | 1 | a0001c0001t0054g0277 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-42-7070T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433312 | |||||||
| chr3:179433601 | C | T | 13 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(10): Show |
16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-7359G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433601 | |||||||
| chr3:179433618 | G | GA | 20 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(17): Show |
26 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.-42-7377dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433618 | |||||||
| chr3:179433763 | T | C | 1 | a0001c0001t0002g0025 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-42-7521A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433763 | |||||||
| chr3:179433776 | A | G | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-7534T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179433776 | |||||||
| chr3:179434083 | G | A | 1 | a0001c0001t0003g0293 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-42-7841C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434083 | |||||||
| chr3:179434175 | A | C | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-42-7933T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434175 | |||||||
| chr3:179434685 | C | G | 13 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(10): Show |
16 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-42-8443G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434685 | |||||||
| chr3:179434786 | C | T | 1 | a0001c0002t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-42-8544G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434786 | |||||||
| chr3:179434892 | C | T | 14 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(11): Show |
17 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-42-8650G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179434892 | |||||||
| chr3:179435053 | G | A | 38 | a0001c0002t0004g0010 a0001c0002t0004g0032 a0001c0002t0004g0033 others(35): Show |
44 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.-42-8811C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435053 | |||||||
| chr3:179435061 | TAAAAATA others(4): Show |
T | 1 | a0001c0002t0001g0073 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-42-8830_-42-8820d others(13): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435061 | |||||||
| chr3:179435275 | C | G | 1 | a0001c0002t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-42-9033G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435275 | |||||||
| chr3:179435470 | C | CA | 36 | a0001c0001t0001g0212 a0001c0001t0002g0054 a0001c0001t0002g0059 others(33): Show |
37 | HG01167.hp1 HG01192.hp2 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.-42-9229dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | |||||||
| chr3:179435470 | C | CAA | 101 | a0001c0001t0002g0077 a0001c0001t0003g0042 a0001c0001t0003g0274 others(98): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-42-9230_-42-9229d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | |||||||
| chr3:179435470 | C | CAAA | 23 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0019 others(20): Show |
28 | HG00438.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42-9231_-42-9229d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | |||||||
| chr3:179435470 | CAAAAA | C | 9 | a0001c0002t0001g0017 a0001c0002t0001g0063 a0001c0002t0001g0068 others(6): Show |
10 | HG00408.hp1 HG01978.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42-9233_-42-9229d others(7): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435470 | |||||||
| chr3:179435532 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-42-9290A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435532 | |||||||
| chr3:179435775 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-42-9533C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435775 | |||||||
| chr3:179435879 | T | G | 1 | a0001c0001t0005g0144 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-42-9637A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179435879 | |||||||
| chr3:179436214 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-42-9972G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436214 | |||||||
| chr3:179436258 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-10016G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436258 | |||||||
| chr3:179436330 | C | T | 1 | a0001c0001t0011g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-10088G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436330 | |||||||
| chr3:179436361 | G | A | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-42-10119C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436361 | |||||||
| chr3:179436385 | C | T | 5 | a0001c0002t0007g0198 a0001c0002t0007g0199 a0001c0002t0007g0201 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42-10143G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436385 | |||||||
| chr3:179436724 | T | C | 2 | a0001c0002t0001g0102 a0001c0002t0001g0192 |
2 | HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-42-10482A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436724 | |||||||
| chr3:179436866 | T | C | 1 | a0001c0002t0001g0103 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-42-10624A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179436866 | |||||||
| chr3:179437089 | T | TAC | 2 | a0001c0001t0002g0026 a0001c0002t0018g0153 |
3 | HG01358.hp2 HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-42-10849_-42-1084 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437089 | |||||||
| chr3:179437117 | C | T | 2 | a0001c0001t0070g0337 a0001c0001t0071g0256 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-42-10875G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437117 | |||||||
| chr3:179437137 | T | C | 1 | a0001c0002t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-42-10895A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437137 | |||||||
| chr3:179437306 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-11064A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437306 | |||||||
| chr3:179437464 | C | G | 1 | a0001c0002t0001g0071 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-42-11222G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437464 | |||||||
| chr3:179437512 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-42-11270G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437512 | |||||||
| chr3:179437514 | G | C | 1 | a0001c0001t0005g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-42-11272C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437514 | |||||||
| chr3:179437562 | C | CA | 92 | a0001c0001t0002g0077 a0001c0001t0002g0140 a0001c0001t0002g0141 others(89): Show |
105 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-42-11321dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437562 | |||||||
| chr3:179437634 | T | C | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-42-11392A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437634 | |||||||
| chr3:179437659 | C | A | 1 | a0001c0001t0003g0287 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-42-11417G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437659 | |||||||
| chr3:179437845 | T | A | 1 | a0001c0002t0051g0210 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-42-11603A>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179437845 | |||||||
| chr3:179438022 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-11780G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438022 | |||||||
| chr3:179438071 | C | CA | 138 | a0001c0001t0002g0077 a0001c0001t0003g0042 a0001c0001t0003g0333 others(135): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-42-11830dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438071 | |||||||
| chr3:179438071 | C | T | 2 | a0001c0001t0070g0337 a0001c0001t0071g0256 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-42-11829G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438071 | |||||||
| chr3:179438161 | C | T | 1 | a0001c0001t0003g0276 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-42-11919G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438161 | |||||||
| chr3:179438232 | T | C | 8 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(5): Show |
9 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-42-11990A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438232 | |||||||
| chr3:179438237 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42-11995T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438237 | |||||||
| chr3:179438238 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42-11996G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438238 | |||||||
| chr3:179438286 | T | C | 1 | a0001c0001t0011g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-42-12044A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438286 | |||||||
| chr3:179438339 | C | T | 1 | a0001c0003t0009g0320 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-42-12097G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438339 | |||||||
| chr3:179438349 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-42-12107G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438349 | |||||||
| chr3:179438491 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-42-12249C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438491 | |||||||
| chr3:179438799 | G | C | 1 | a0001c0002t0007g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-43+12547C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438799 | |||||||
| chr3:179438859 | C | T | 43 | a0001c0001t0002g0121 a0001c0002t0004g0010 a0001c0002t0004g0032 others(40): Show |
50 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.-43+12487G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179438859 | |||||||
| chr3:179439330 | C | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+12016G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439330 | |||||||
| chr3:179439445 | G | T | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+11901C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439445 | |||||||
| chr3:179439520 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43+11826C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439520 | |||||||
| chr3:179439531 | C | G | 1 | a0001c0002t0001g0046 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-43+11815G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439531 | |||||||
| chr3:179439579 | T | G | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11767A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439579 | |||||||
| chr3:179439693 | TAA | T | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11651_-43+1165 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439693 | |||||||
| chr3:179439712 | A | C | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+11634T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439712 | |||||||
| chr3:179439893 | T | C | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+11453A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179439893 | |||||||
| chr3:179440114 | C | T | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+11232G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440114 | |||||||
| chr3:179440158 | T | TA | 6 | a0001c0001t0019g0214 a0001c0002t0015g0215 a0001c0002t0015g0216 others(3): Show |
7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+11187dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440158 | |||||||
| chr3:179440346 | T | C | 3 | a0001c0002t0022g0186 a0001c0002t0022g0187 a0001c0002t0022g0191 |
3 | HG01433.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-43+11000A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440346 | |||||||
| chr3:179440534 | T | C | 2 | a0001c0001t0010g0330 a0001c0001t0010g0332 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-43+10812A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440534 | |||||||
| chr3:179440730 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-43+10616A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440730 | |||||||
| chr3:179440842 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0118 others(3): Show |
9 | HG00438.hp1 HG02083.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43+10504G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440842 | |||||||
| chr3:179440843 | G | A | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+10503C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440843 | |||||||
| chr3:179440874 | G | T | 2 | a0001c0001t0010g0330 a0001c0001t0010g0332 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-43+10472C>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440874 | |||||||
| chr3:179440876 | T | TAGAGAGA others(7): Show |
1 | a0001c0001t0010g0319 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43+10469_-43+1047 others(18): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440876 | |||||||
| chr3:179440880 | T | G | 3 | a0001c0001t0010g0319 a0001c0002t0007g0198 a0001c0002t0050g0197 |
3 | HG02572.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-43+10466A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAG | 138 | a0001c0001t0002g0077 a0001c0001t0003g0042 a0001c0001t0003g0333 others(135): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-43+10464_-43+1046 others(6): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAG | 8 | a0001c0001t0067g0306 a0001c0002t0007g0009 a0001c0002t0007g0199 others(5): Show |
10 | HG01167.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43+10460_-43+1046 others(10): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(3): Show |
7 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 others(4): Show |
9 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43+10456_-43+1046 others(14): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(5): Show |
6 | a0001c0001t0009g0257 a0001c0001t0072g0329 a0001c0002t0014g0259 others(3): Show |
7 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+10454_-43+1046 others(16): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(7): Show |
3 | a0001c0001t0010g0004 a0001c0002t0015g0196 a0001c0002t0068g0258 |
6 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+10452_-43+1046 others(18): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(9): Show |
6 | a0001c0001t0010g0330 a0001c0001t0010g0331 a0001c0001t0010g0332 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+10450_-43+1046 others(20): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(11): Show |
1 | a0001c0001t0019g0225 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43+10448_-43+1046 others(22): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | T | TAGAGAGA others(13): Show |
3 | a0001c0001t0019g0226 a0001c0001t0070g0337 a0001c0001t0071g0256 |
3 | HG02109.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+10446_-43+1046 others(24): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440880 | TAGAGAGA others(1): Show |
T | 13 | a0001c0001t0001g0212 a0001c0001t0003g0313 a0001c0001t0005g0193 others(10): Show |
13 | HG01346.hp2 HG01496.hp2 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43+10458_-43+1046 others(12): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440880 | |||||||
| chr3:179440909 | T | C | 4 | a0001c0002t0021g0307 a0001c0002t0021g0308 a0001c0002t0021g0311 others(1): Show |
4 | HG03540.hp1 HG03669.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+10437A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179440909 | |||||||
| chr3:179441174 | A | G | 1 | a0001c0001t0002g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-43+10172T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441174 | |||||||
| chr3:179441324 | A | T | 1 | a0001c0002t0013g0309 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43+10022T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441324 | |||||||
| chr3:179441371 | T | C | 65 | a0001c0001t0001g0212 a0001c0001t0003g0011 a0001c0001t0003g0012 others(62): Show |
76 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-43+9975A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441371 | |||||||
| chr3:179441470 | A | T | 9 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(6): Show |
10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+9876T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441470 | |||||||
| chr3:179441595 | A | G | 1 | a0001c0002t0004g0032 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-43+9751T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441595 | |||||||
| chr3:179441625 | G | A | 7 | a0001c0002t0013g0268 a0001c0002t0013g0288 a0001c0002t0013g0309 others(4): Show |
7 | HG02257.hp1 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43+9721C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441625 | |||||||
| chr3:179441693 | A | C | 1 | a0001c0002t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-43+9653T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441693 | |||||||
| chr3:179441733 | T | C | 144 | a0001c0001t0002g0077 a0001c0001t0003g0042 a0001c0001t0003g0333 others(141): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-43+9613A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441733 | |||||||
| chr3:179441751 | C | CA | 16 | a0001c0001t0002g0146 a0001c0001t0005g0193 a0001c0001t0005g0195 others(13): Show |
19 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43+9594dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441751 | |||||||
| chr3:179441751 | CA | C | 153 | a0001c0001t0002g0077 a0001c0001t0002g0115 a0001c0001t0002g0155 others(150): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-43+9594delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441751 | |||||||
| chr3:179441827 | C | T | 1 | a0001c0002t0016g0241 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43+9519G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179441827 | |||||||
| chr3:179442087 | G | A | 80 | a0001c0001t0002g0077 a0001c0002t0001g0002 a0001c0002t0001g0005 others(77): Show |
90 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-43+9259C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442087 | |||||||
| chr3:179442147 | T | C | 3 | a0001c0002t0001g0113 a0001c0002t0001g0164 a0001c0002t0047g0107 |
3 | HG02698.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-43+9199A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442147 | |||||||
| chr3:179442189 | C | T | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+9157G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442189 | |||||||
| chr3:179442300 | C | T | 2 | a0001c0002t0007g0242 a0001c0002t0034g0294 |
2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-43+9046G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442300 | |||||||
| chr3:179442367 | G | A | 12 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0001t0010g0330 others(9): Show |
15 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43+8979C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442367 | |||||||
| chr3:179442737 | C | T | 1 | a0001c0002t0066g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-43+8609G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442737 | |||||||
| chr3:179442915 | C | A | 1 | a0001c0001t0003g0273 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-43+8431G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442915 | |||||||
| chr3:179442923 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+8423G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442923 | |||||||
| chr3:179442925 | C | T | 9 | a0001c0002t0007g0009 a0001c0002t0007g0198 a0001c0002t0007g0199 others(6): Show |
11 | HG01433.hp1 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43+8421G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442925 | |||||||
| chr3:179442926 | G | A | 1 | a0001c0002t0016g0241 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43+8420C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179442926 | |||||||
| chr3:179443026 | T | C | 9 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(6): Show |
10 | HG01069.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43+8320A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443026 | |||||||
| chr3:179443152 | C | G | 1 | a0001c0001t0009g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43+8194G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443152 | |||||||
| chr3:179443187 | T | C | 1 | a0001c0002t0001g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43+8159A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443187 | |||||||
| chr3:179443235 | T | C | 1 | a0001c0001t0070g0337 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-43+8111A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443235 | |||||||
| chr3:179443433 | C | A | 144 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0019g0214 others(141): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-43+7913G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443433 | |||||||
| chr3:179443477 | T | C | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+7869A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443477 | |||||||
| chr3:179443488 | G | A | 4 | a0001c0002t0021g0307 a0001c0002t0021g0308 a0001c0002t0021g0311 others(1): Show |
4 | HG03540.hp1 HG03669.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7858C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443488 | |||||||
| chr3:179443510 | G | C | 3 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 |
4 | HG02622.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+7836C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443510 | |||||||
| chr3:179443572 | G | C | 1 | a0001c0002t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-43+7774C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443572 | |||||||
| chr3:179443832 | C | A | 3 | a0001c0001t0020g0043 a0001c0001t0020g0338 a0001c0001t0020g0339 |
4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7514G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443832 | |||||||
| chr3:179443851 | C | T | 3 | a0001c0001t0020g0043 a0001c0001t0020g0338 a0001c0001t0020g0339 |
4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+7495G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443851 | |||||||
| chr3:179443911 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-43+7435C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443911 | |||||||
| chr3:179443956 | G | A | 81 | a0001c0001t0002g0077 a0001c0002t0001g0002 a0001c0002t0001g0005 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-43+7390C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443956 | |||||||
| chr3:179443991 | C | T | 1 | a0001c0002t0001g0066 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43+7355G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179443991 | |||||||
| chr3:179444016 | C | T | 2 | a0001c0002t0032g0316 a0001c0002t0032g0317 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-43+7330G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444016 | |||||||
| chr3:179444182 | T | C | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+7164A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444182 | |||||||
| chr3:179444227 | T | C | 1 | a0001c0002t0004g0220 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-43+7119A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444227 | |||||||
| chr3:179444235 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-43+7111G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444235 | |||||||
| chr3:179444423 | G | GT | 58 | a0001c0001t0003g0039 a0001c0001t0003g0269 a0001c0001t0003g0270 others(55): Show |
66 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-43+6922dupA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444423 | |||||||
| chr3:179444423 | GT | G | 8 | a0001c0001t0002g0147 a0001c0002t0001g0046 a0001c0002t0001g0110 others(5): Show |
8 | HG01433.hp1 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+6922delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444423 | |||||||
| chr3:179444429 | T | G | 4 | a0001c0001t0005g0027 a0001c0001t0005g0148 a0001c0001t0005g0149 others(1): Show |
5 | HG02486.hp1 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+6917A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444429 | |||||||
| chr3:179444528 | C | A | 174 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0003g0042 others(171): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-43+6818G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444528 | |||||||
| chr3:179444562 | G | A | 176 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0003g0042 others(173): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-43+6784C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444562 | |||||||
| chr3:179444569 | C | T | 2 | a0001c0001t0027g0253 a0001c0001t0027g0254 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-43+6777G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444569 | |||||||
| chr3:179444705 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 |
4 | HG02622.hp1 HG02970.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6641G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444705 | |||||||
| chr3:179444716 | A | G | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+6630T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444716 | |||||||
| chr3:179444811 | A | C | 1 | a0001c0002t0001g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43+6535T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444811 | |||||||
| chr3:179444840 | C | T | 1 | a0001c0001t0069g0318 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-43+6506G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444840 | |||||||
| chr3:179444841 | G | A | 1 | a0001c0003t0009g0328 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-43+6505C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444841 | |||||||
| chr3:179444932 | T | C | 16 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(13): Show |
20 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-43+6414A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179444932 | |||||||
| chr3:179445003 | A | C | 336 | a0001c0001t0001g0212 a0001c0001t0002g0001 a0001c0001t0002g0003 others(333): Show |
396 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.-43+6343T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445003 | |||||||
| chr3:179445023 | G | A | 4 | a0001c0002t0018g0151 a0001c0002t0018g0152 a0001c0002t0018g0153 others(1): Show |
4 | HG03688.hp2 HG03704.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43+6323C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445023 | |||||||
| chr3:179445047 | A | T | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+6299T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445047 | |||||||
| chr3:179445104 | C | T | 5 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+6242G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445104 | |||||||
| chr3:179445157 | A | G | 1 | a0001c0001t0003g0039 | 2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-43+6189T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445157 | |||||||
| chr3:179445158 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-43+6188A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445158 | |||||||
| chr3:179445374 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-43+5972A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445374 | |||||||
| chr3:179445627 | T | C | 1 | a0001c0002t0004g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-43+5719A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445627 | |||||||
| chr3:179445635 | C | T | 1 | a0001c0002t0004g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-43+5711G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445635 | |||||||
| chr3:179445732 | G | A | 162 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0003g0292 others(159): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.-43+5614C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445732 | |||||||
| chr3:179445755 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-43+5591C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445755 | |||||||
| chr3:179445863 | T | C | 183 | a0001c0001t0002g0077 a0001c0001t0002g0190 a0001c0001t0003g0042 others(180): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-43+5483A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179445863 | |||||||
| chr3:179446249 | C | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0165 |
2 | NA19065.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-43+5097G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446249 | |||||||
| chr3:179446392 | A | C | 3 | a0001c0001t0010g0004 a0001c0001t0010g0319 a0001c0002t0068g0258 |
6 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+4954T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446392 | |||||||
| chr3:179446598 | G | A | 1 | a0001c0001t0003g0298 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-43+4748C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446598 | |||||||
| chr3:179446738 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-43+4608T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446738 | |||||||
| chr3:179446764 | A | G | 93 | a0001c0001t0002g0051 a0001c0001t0002g0057 a0001c0001t0002g0059 others(90): Show |
104 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-43+4582T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446764 | |||||||
| chr3:179446942 | T | C | 2 | a0001c0002t0013g0309 a0001c0002t0066g0310 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43+4404A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179446942 | |||||||
| chr3:179447101 | G | A | 1 | a0001c0002t0004g0177 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-43+4245C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447101 | |||||||
| chr3:179447135 | C | T | 6 | a0001c0002t0007g0198 a0001c0002t0007g0199 a0001c0002t0007g0200 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+4211G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447135 | |||||||
| chr3:179447253 | G | A | 1 | a0001c0001t0012g0028 | 2 | HG02027.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-43+4093C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447253 | |||||||
| chr3:179447346 | T | TA | 278 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0006 others(275): Show |
331 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.-43+3999dupT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447346 | |||||||
| chr3:179447346 | T | TAA | 30 | a0001c0001t0001g0212 a0001c0001t0002g0008 a0001c0001t0002g0168 others(27): Show |
35 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-43+3998_-43+3999d others(4): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447346 | |||||||
| chr3:179447397 | C | A | 1 | a0001c0001t0008g0030 | 2 | NA18951.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.-43+3949G>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447397 | |||||||
| chr3:179447397 | C | G | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+3949G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447397 | |||||||
| chr3:179447553 | G | A | 1 | a0001c0002t0040g0178 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43+3793C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447553 | |||||||
| chr3:179447717 | T | C | 2 | a0001c0001t0070g0337 a0001c0001t0071g0256 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+3629A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447717 | |||||||
| chr3:179447769 | T | C | 2 | a0001c0002t0001g0179 a0001c0002t0001g0180 |
2 | NA18959.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-43+3577A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447769 | |||||||
| chr3:179447820 | G | A | 1 | a0001c0002t0022g0191 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43+3526C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447820 | |||||||
| chr3:179447962 | C | T | 1 | a0001c0001t0011g0266 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-43+3384G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179447962 | |||||||
| chr3:179448044 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-43+3302C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448044 | |||||||
| chr3:179448099 | G | A | 4 | a0001c0001t0069g0318 a0001c0002t0032g0316 a0001c0002t0032g0317 others(1): Show |
4 | HG02559.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+3247C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448099 | |||||||
| chr3:179448184 | T | C | 1 | a0001c0002t0007g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-43+3162A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448184 | |||||||
| chr3:179448295 | G | A | 166 | a0001c0001t0001g0212 a0001c0001t0002g0223 a0001c0001t0003g0011 others(163): Show |
192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-43+3051C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448295 | |||||||
| chr3:179448296 | T | C | 9 | a0001c0002t0004g0010 a0001c0002t0004g0037 a0001c0002t0004g0246 others(6): Show |
12 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43+3050A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448296 | |||||||
| chr3:179448353 | T | C | 6 | a0001c0001t0019g0214 a0001c0002t0015g0215 a0001c0002t0015g0216 others(3): Show |
7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2993A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448353 | |||||||
| chr3:179448406 | T | C | 22 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(19): Show |
26 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-43+2940A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448406 | |||||||
| chr3:179448474 | GT | G | 7 | a0001c0001t0002g0181 a0001c0001t0009g0257 a0001c0001t0069g0318 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2871delA | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448474 | |||||||
| chr3:179448521 | C | T | 1 | a0001c0001t0061g0335 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-43+2825G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448521 | |||||||
| chr3:179448537 | T | G | 23 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(20): Show |
29 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+2809A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448537 | |||||||
| chr3:179448539 | T | G | 23 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(20): Show |
29 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.-43+2807A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448539 | |||||||
| chr3:179448636 | G | A | 5 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43+2710C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448636 | |||||||
| chr3:179448763 | C | T | 1 | a0001c0001t0003g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43+2583G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448763 | |||||||
| chr3:179448783 | G | A | 3 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0002g0184 |
3 | NA18947.hp1 NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-43+2563C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448783 | |||||||
| chr3:179448807 | C | T | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+2539G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448807 | |||||||
| chr3:179448900 | G | A | 1 | a0001c0001t0003g0303 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-43+2446C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179448900 | |||||||
| chr3:179449008 | CA | C | 6 | a0001c0001t0019g0214 a0001c0002t0015g0215 a0001c0002t0015g0216 others(3): Show |
7 | HG00735.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43+2337delT | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449008 | |||||||
| chr3:179449178 | A | G | 6 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+2168T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449178 | |||||||
| chr3:179449422 | C | T | 1 | a0001c0001t0003g0264 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-43+1924G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449422 | |||||||
| chr3:179449500 | A | G | 1 | a0001c0002t0001g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43+1846T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449500 | |||||||
| chr3:179449690 | C | G | 1 | a0001c0002t0005g0049 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-43+1656G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449690 | |||||||
| chr3:179449866 | T | G | 1 | a0001c0001t0008g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-43+1480A>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179449866 | |||||||
| chr3:179450037 | T | C | 1 | a0001c0001t0003g0304 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-43+1309A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450037 | |||||||
| chr3:179450099 | AGAT | A | 6 | a0001c0001t0002g0190 a0001c0001t0046g0189 a0001c0001t0048g0188 others(3): Show |
6 | HG01433.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+1244_-43+1246d others(5): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450099 | |||||||
| chr3:179450111 | A | G | 2 | a0001c0001t0067g0306 a0001c0002t0063g0305 |
2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-43+1235T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450111 | |||||||
| chr3:179450121 | ATTTCAG | A | 5 | a0001c0001t0003g0042 a0001c0001t0003g0333 a0001c0001t0003g0334 others(2): Show |
6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+1219_-43+1224d others(8): Show |
GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450121 | |||||||
| chr3:179450166 | A | T | 1 | a0001c0001t0011g0263 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43+1180T>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450166 | |||||||
| chr3:179450318 | G | A | 3 | a0001c0001t0014g0013 a0001c0001t0014g0336 a0001c0001t0061g0335 |
5 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43+1028C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450318 | |||||||
| chr3:179450364 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-43+982C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450364 | |||||||
| chr3:179450434 | C | T | 1 | a0001c0002t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-43+912G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450434 | |||||||
| chr3:179450619 | A | C | 1 | a0001c0001t0009g0257 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43+727T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450619 | |||||||
| chr3:179450673 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-43+673T>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450673 | |||||||
| chr3:179450674 | C | T | 52 | a0001c0001t0003g0011 a0001c0001t0003g0012 a0001c0001t0003g0039 others(49): Show |
61 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-43+672G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450674 | |||||||
| chr3:179450810 | T | C | 1 | a0001c0001t0005g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-43+536A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450810 | |||||||
| chr3:179450811 | C | T | 1 | a0001c0001t0005g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-43+535G>A | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450811 | |||||||
| chr3:179450875 | A | C | 6 | a0001c0001t0009g0257 a0001c0002t0014g0259 a0001c0002t0014g0261 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43+471T>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450875 | |||||||
| chr3:179450896 | C | G | 2 | a0001c0001t0070g0337 a0001c0001t0071g0256 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-43+450G>C | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450896 | |||||||
| chr3:179450977 | G | C | 1 | a0001c0001t0070g0337 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-43+369C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179450977 | |||||||
| chr3:179451032 | G | C | 3 | a0001c0001t0020g0043 a0001c0001t0020g0338 a0001c0001t0020g0339 |
4 | NA18961.hp2 NA19012.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+314C>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451032 | |||||||
| chr3:179451170 | T | C | 166 | a0001c0001t0001g0212 a0001c0001t0002g0223 a0001c0001t0003g0011 others(163): Show |
192 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.-43+176A>G | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451170 | |||||||
| chr3:179451249 | G | A | 47 | a0001c0001t0002g0223 a0001c0001t0019g0214 a0001c0001t0019g0224 others(44): Show |
56 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-43+97C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451249 | |||||||
| chr3:179451317 | G | A | 2 | a0001c0001t0027g0253 a0001c0001t0027g0254 |
2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-43+29C>T | GNB4 | ENSG00000114450.11 | transcript | ENST00000232564.8 | protein_coding | 1/9 | chr3 | 179451317 |