Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51463 |
| ensemblid | ENSG00000188092.15 |
| hgncid | 13840 |
| symbol | GPR89B |
| name | G protein-coupled receptor 89B |
| refseq_nuc | NM_016334.5 |
| refseq_prot | NP_057418.1 |
| ensembl_nuc | ENST00000314163.12 |
| ensembl_prot | ENSP00000358233.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 147928420 |
| end | 147993592 |
| strand | + |
| ver | v1.2 |
| region | chr1:147928420-147993592 |
| region5000 | chr1:147923420-147998592 |
| regionname0 | GPR89B_chr1_147928420_147993592 |
| regionname5000 | GPR89B_chr1_147923420_147998592 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 455 | 268 | 68 | 48 | 113 | 10 | 27 | 83 | GPR89B_chr1_147923420_147998592 | GPR89B | MSFLI others(450): Show |
chr1 | 147923420 | 147998592 |
| a0002 | 0/0 | 455 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | MSFLI others(450): Show |
chr1 | 147923420 | 147998592 |
| a0003 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | MSFLI others(450): Show |
chr1 | 147923420 | 147998592 |
| a0004 | 0/0 | 127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | MSFLI others(122): Show |
chr1 | 147923420 | 147998592 |
| a0005 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | MSFLI others(450): Show |
chr1 | 147923420 | 147998592 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1365 | 217 | 54 | 43 | 90 | 9 | 19 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0001c0002 | 0/0 | 1365 | 29 | 6 | 2 | 12 | 1 | 8 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0001c0003 | 0/0 | 1365 | 21 | 7 | 3 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0001c0006 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0002c0004 | 0/0 | 1365 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0003c0005 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0004c0008 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 | ||
| a0005c0007 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | ATGAG others(1360): Show |
chr1 | 147923420 | 147998592 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2160 | 208 | 48 | 41 | 89 | 9 | 19 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0001t0004 | 0/0 | 2161 | 6 | 5 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2156): Show |
chr1 | 147923420 | 147998592 |
| a0001c0001t0005 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0001t0006 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0001t0008 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0002t0001 | 0/0 | 2160 | 29 | 6 | 2 | 12 | 1 | 8 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0003t0002 | 0/0 | 2160 | 11 | 0 | 0 | 11 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0003t0003 | 0/0 | 2160 | 10 | 7 | 3 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0001c0006t0007 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0002c0004t0002 | 0/0 | 2160 | 3 | 3 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0003c0005t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0004c0008t0001 | 0/0 | 2160 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| a0005c0007t0001 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | GCAGT others(2155): Show |
chr1 | 147923420 | 147998592 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0003t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0001c0006t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0002c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0003c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0004c0008t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| a0005c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | GBR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00423 | hp2 | a0001 | c0003 | t0002 | g0230 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0223 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | CHS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0237 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0236 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01934 | hp2 | a0001 | c0003 | t0003 | g0235 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0224 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02055 | hp1 | a0001 | c0006 | t0007 | g0253 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0239 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0243 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0097 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0240 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0238 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02735 | hp2 | a0004 | c0008 | t0001 | g0088 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02818 | hp2 | a0001 | c0003 | t0003 | g0242 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02886 | hp2 | a0002 | c0004 | t0002 | g0233 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03453 | hp2 | a0001 | c0003 | t0003 | g0241 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03486 | hp1 | a0002 | c0004 | t0002 | g0227 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | MSL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0189 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | STU | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0229 | EAS | CHB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18906 | hp1 | a0002 | c0004 | t0002 | g0226 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18944 | hp1 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0225 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18974 | hp2 | a0005 | c0007 | t0001 | g0091 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18982 | hp1 | a0001 | c0003 | t0002 | g0220 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0221 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19006 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0214 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ASW | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0234 | AFR | ASW | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | GIH | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02109 | hp2 | a0003 | c0005 | t0001 | g0114 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0135 | REF | REF | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0078 | REF | REF | GPR89B_chr1_147923420_147998592 | GPR89B | chr1 | 147923420 | 147998592 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147944065 | G | T | 1 | a0004 | 1 | HG02735.hp2 | stop_gained | HIGH | c.382G>T | p.Gly128* | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/14 | 499/2160 | 382/1368 | 128/455 | chr1 | 147944065 | |||
| chr1:147954366 | T | C | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.581T>C | p.Leu194Pro | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/14 | 698/2160 | 581/1368 | 194/455 | chr1 | 147954366 | |||
| chr1:147966594 | G | A | 1 | a0002 | 3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.658G>A | p.Val220Met | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/14 | 775/2160 | 658/1368 | 220/455 | chr1 | 147966594 | |||
| chr1:147969869 | G | T | 1 | a0005 | 1 | NA18974.hp2 | missense_variant&splice_region_variant | MODERATE | c.819G>T | p.Glu273Asp | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/14 | 936/2160 | 819/1368 | 273/455 | chr1 | 147969869 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147943471 | T | C | 2 | a0001c0003 a0002c0004 |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.240T>C | p.Cys80Cys | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/14 | 357/2160 | 240/1368 | 80/455 | chr1 | 147943471 | |||
| chr1:147954337 | G | A | 2 | a0001c0003 a0002c0004 |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.552G>A | p.Thr184Thr | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/14 | 669/2160 | 552/1368 | 184/455 | chr1 | 147954337 | |||
| chr1:147988461 | C | T | 2 | a0001c0003 a0002c0004 |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
synonymous_variant | LOW | c.1035C>T | p.Phe345Phe | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/14 | 1152/2160 | 1035/1368 | 345/455 | chr1 | 147988461 | |||
| chr1:147992555 | A | G | 3 | a0001c0002 a0003c0005 a0005c0007 |
31 | HG00140.hp2 HG00597.hp2 HG00673.hp2 others(28): Show |
synonymous_variant | LOW | c.1149A>G | p.Leu383Leu | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 13/14 | 1266/2160 | 1149/1368 | 383/455 | chr1 | 147992555 | |||
| chr1:147992848 | C | T | 1 | a0001c0006 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1299C>T | p.Ser433Ser | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 1416/2160 | 1299/1368 | 433/455 | chr1 | 147992848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147928427 | C | G | 1 | a0001c0001t0008 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/14 | 110 | chr1 | 147928427 | ||||||
| chr1:147992979 | G | GA | 1 | a0001c0001t0004 | 6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*67dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 68 | INFO_REALIGN_3_PRIME | chr1 | 147992979 | |||||
| chr1:147993201 | G | T | 1 | a0001c0006t0007 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*284G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 284 | chr1 | 147993201 | ||||||
| chr1:147993259 | G | A | 1 | a0001c0001t0005 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 342 | chr1 | 147993259 | ||||||
| chr1:147993414 | C | T | 3 | a0001c0003t0002 a0001c0003t0003 a0002c0004t0002 |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*497C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 497 | chr1 | 147993414 | ||||||
| chr1:147993478 | C | T | 3 | a0001c0001t0006 a0001c0003t0002 a0002c0004t0002 |
15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*561C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 561 | chr1 | 147993478 | ||||||
| chr1:147993532 | T | G | 3 | a0001c0003t0002 a0001c0003t0003 a0002c0004t0002 |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*615T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 14/14 | 615 | chr1 | 147993532 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:147928621 | C | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.42+43C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928621 | |||||||
| chr1:147928646 | C | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42+68C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928646 | |||||||
| chr1:147928667 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.42+89G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928667 | |||||||
| chr1:147928671 | C | G | 1 | a0001c0002t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.42+93C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928671 | |||||||
| chr1:147928711 | A | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0244 a0001c0001t0001g0245 others(39): Show |
43 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.42+133A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928711 | |||||||
| chr1:147928833 | G | T | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+255G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928833 | |||||||
| chr1:147928941 | C | T | 9 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.42+363C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928941 | |||||||
| chr1:147928960 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+382G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928960 | |||||||
| chr1:147928974 | G | T | 1 | a0001c0002t0001g0219 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.42+396G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147928974 | |||||||
| chr1:147929088 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG00140.hp1 HG00673.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+510A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929088 | |||||||
| chr1:147929157 | C | T | 1 | a0001c0001t0008g0214 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.42+579C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929157 | |||||||
| chr1:147929356 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.42+778C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929356 | |||||||
| chr1:147929420 | C | G | 1 | a0001c0002t0001g0212 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.42+842C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929420 | |||||||
| chr1:147929790 | G | GT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(119): Show |
128 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.42+1217dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147929790 | ||||||
| chr1:147929820 | C | G | 1 | a0001c0001t0008g0214 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.42+1242C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929820 | |||||||
| chr1:147929838 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1260T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929838 | |||||||
| chr1:147929853 | G | T | 10 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(7): Show |
10 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+1275G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929853 | |||||||
| chr1:147929934 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.42+1356C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147929934 | |||||||
| chr1:147930107 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0128 others(5): Show |
8 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+1529A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930107 | |||||||
| chr1:147930192 | A | T | 1 | a0001c0002t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.42+1614A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930192 | |||||||
| chr1:147930287 | T | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+1709T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930287 | |||||||
| chr1:147930421 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+1843T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930421 | |||||||
| chr1:147930724 | T | TGCCTTTT others(15): Show |
4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2146_42+2147ins others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930724 | |||||||
| chr1:147930996 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.42+2418A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147930996 | |||||||
| chr1:147931044 | T | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(35): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.42+2466T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931044 | |||||||
| chr1:147931063 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+2485C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931063 | |||||||
| chr1:147931234 | GC | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+2657delC | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931234 | |||||||
| chr1:147931324 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+2746A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931324 | |||||||
| chr1:147931341 | A | G | 15 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(12): Show |
15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.42+2763A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931341 | |||||||
| chr1:147931413 | A | G | 1 | a0001c0001t0004g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2835A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931413 | |||||||
| chr1:147931440 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.42+2862G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931440 | |||||||
| chr1:147931585 | CT | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+3019delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147931585 | ||||||
| chr1:147931623 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.42+3045G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931623 | |||||||
| chr1:147931692 | G | A | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.42+3114G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931692 | |||||||
| chr1:147931846 | C | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+3268C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931846 | |||||||
| chr1:147931876 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3298G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931876 | |||||||
| chr1:147931893 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.42+3315G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147931893 | |||||||
| chr1:147932078 | A | AT | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+3511dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147932078 | ||||||
| chr1:147932215 | C | T | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+3637C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932215 | |||||||
| chr1:147932216 | G | A | 17 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(14): Show |
17 | HG00408.hp1 HG00609.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.42+3638G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932216 | |||||||
| chr1:147932281 | T | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+3703T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932281 | |||||||
| chr1:147932337 | G | A | 1 | a0001c0002t0001g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.42+3759G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932337 | |||||||
| chr1:147932355 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.42+3777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932355 | |||||||
| chr1:147932553 | C | G | 1 | a0002c0004t0002g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.42+3975C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932553 | |||||||
| chr1:147932592 | T | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42+4014T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932592 | |||||||
| chr1:147932612 | G | A | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-4015G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932612 | |||||||
| chr1:147932739 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.43-3888G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932739 | |||||||
| chr1:147932847 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-3780G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932847 | |||||||
| chr1:147932882 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.43-3745T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147932882 | |||||||
| chr1:147933160 | G | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
182 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.43-3467G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933160 | |||||||
| chr1:147933242 | T | C | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-3385T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933242 | |||||||
| chr1:147933250 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-3377C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933250 | |||||||
| chr1:147933435 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.43-3192G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933435 | |||||||
| chr1:147933617 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-3010A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933617 | |||||||
| chr1:147933845 | C | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-2782C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933845 | |||||||
| chr1:147933981 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2646A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933981 | |||||||
| chr1:147933998 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43-2629A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147933998 | |||||||
| chr1:147934210 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-2417T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934210 | |||||||
| chr1:147934378 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.43-2249C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934378 | |||||||
| chr1:147934382 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.43-2245G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934382 | |||||||
| chr1:147934449 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.43-2178C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934449 | |||||||
| chr1:147934470 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-2157C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934470 | |||||||
| chr1:147934526 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.43-2101C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934526 | |||||||
| chr1:147934566 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.43-2061A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934566 | |||||||
| chr1:147934700 | T | C | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.43-1927T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934700 | |||||||
| chr1:147934747 | ATTATG | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-1875_43-1871del others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147934747 | ||||||
| chr1:147934953 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.43-1674G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147934953 | |||||||
| chr1:147935180 | G | A | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-1447G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935180 | |||||||
| chr1:147935238 | C | T | 1 | a0001c0001t0004g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.43-1389C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935238 | |||||||
| chr1:147935297 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1330G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935297 | |||||||
| chr1:147935516 | G | A | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1111G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935516 | |||||||
| chr1:147935595 | T | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-1032T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935595 | |||||||
| chr1:147935814 | A | C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.43-813A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935814 | |||||||
| chr1:147935901 | A | G | 2 | a0001c0001t0001g0217 a0001c0002t0001g0120 |
2 | HG00140.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.43-726A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147935901 | |||||||
| chr1:147936178 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.43-449A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936178 | |||||||
| chr1:147936200 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-427C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936200 | |||||||
| chr1:147936264 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG01169.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.43-363G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936264 | |||||||
| chr1:147936313 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.43-314C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | chr1 | 147936313 | |||||||
| chr1:147936560 | AAG | A | 4 | a0001c0003t0002g0229 a0001c0003t0002g0230 a0001c0003t0002g0231 others(1): Show |
4 | HG00423.hp2 HG00621.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-64_43-63delAG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr1 | 147936560 | ||||||
| chr1:147936945 | A | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+259A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147936945 | |||||||
| chr1:147937028 | CTTATA | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+348_102+352del others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 147937028 | ||||||
| chr1:147937163 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.102+477A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937163 | |||||||
| chr1:147937196 | A | G | 18 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(15): Show |
19 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+510A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937196 | |||||||
| chr1:147937223 | C | T | 1 | a0001c0003t0002g0228 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.102+537C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937223 | |||||||
| chr1:147937239 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.102+553C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937239 | |||||||
| chr1:147937278 | T | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.102+592T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937278 | |||||||
| chr1:147937557 | G | A | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.102+871G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937557 | |||||||
| chr1:147937689 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.102+1003T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937689 | |||||||
| chr1:147937720 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-994C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937720 | |||||||
| chr1:147937820 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103-894G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937820 | |||||||
| chr1:147937872 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.103-842C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147937872 | |||||||
| chr1:147938061 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-653T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938061 | |||||||
| chr1:147938090 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-624G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938090 | |||||||
| chr1:147938403 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.103-311G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938403 | |||||||
| chr1:147938430 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.103-284A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938430 | |||||||
| chr1:147938518 | A | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-196A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938518 | |||||||
| chr1:147938548 | A | G | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.103-166A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938548 | |||||||
| chr1:147938636 | C | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.103-78C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 2/13 | chr1 | 147938636 | |||||||
| chr1:147938900 | GA | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0081 others(9): Show |
13 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.206+96delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147938900 | ||||||
| chr1:147938900 | GAA | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+95_206+96delAA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147938900 | ||||||
| chr1:147938912 | A | C | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+95A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147938912 | |||||||
| chr1:147939058 | A | G | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+241A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939058 | |||||||
| chr1:147939133 | G | T | 1 | a0001c0001t0004g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+316G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939133 | |||||||
| chr1:147939429 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.206+612C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939429 | |||||||
| chr1:147939494 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.206+677C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939494 | |||||||
| chr1:147939638 | G | A | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+821G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939638 | |||||||
| chr1:147939852 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.206+1035C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939852 | |||||||
| chr1:147939871 | A | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206+1054A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939871 | |||||||
| chr1:147939872 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.206+1055C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939872 | |||||||
| chr1:147939943 | G | A | 26 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0003t0002g0220 others(23): Show |
26 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.206+1126G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147939943 | |||||||
| chr1:147940130 | G | A | 5 | a0001c0001t0001g0024 a0001c0003t0003g0234 a0001c0003t0003g0235 others(2): Show |
5 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+1313G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940130 | |||||||
| chr1:147940132 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA19063.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.206+1315G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940132 | |||||||
| chr1:147940200 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.206+1383A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940200 | |||||||
| chr1:147940214 | T | C | 2 | a0001c0003t0003g0234 a0001c0003t0003g0235 |
2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.206+1397T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940214 | |||||||
| chr1:147940230 | C | T | 1 | a0001c0003t0002g0232 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.206+1413C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940230 | |||||||
| chr1:147940264 | A | G | 7 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(4): Show |
7 | HG01934.hp2 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206+1447A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940264 | |||||||
| chr1:147940298 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+1481G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940298 | |||||||
| chr1:147940320 | C | G | 5 | a0001c0002t0001g0009 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
6 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.206+1503C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940320 | |||||||
| chr1:147940328 | A | G | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.206+1511A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940328 | |||||||
| chr1:147940353 | A | G | 1 | a0001c0002t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.206+1536A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940353 | |||||||
| chr1:147940357 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0263 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.206+1540T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940357 | |||||||
| chr1:147940359 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0263 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.206+1542T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940359 | |||||||
| chr1:147940565 | T | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.206+1748T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940565 | |||||||
| chr1:147940588 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.206+1771T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940588 | |||||||
| chr1:147940658 | C | A | 1 | a0001c0003t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206+1841C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940658 | |||||||
| chr1:147940663 | G | A | 1 | a0001c0003t0003g0234 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.206+1846G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940663 | |||||||
| chr1:147940664 | C | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.206+1847C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940664 | |||||||
| chr1:147940880 | T | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206+2063T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940880 | |||||||
| chr1:147940901 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.206+2084C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147940901 | |||||||
| chr1:147941099 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.206+2282G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941099 | |||||||
| chr1:147941354 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.207-2084A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941354 | |||||||
| chr1:147941430 | C | CA | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.207-2004dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147941430 | ||||||
| chr1:147941879 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.207-1559T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147941879 | |||||||
| chr1:147942110 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.207-1328C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147942110 | |||||||
| chr1:147942293 | C | CA | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.207-1135dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr1 | 147942293 | ||||||
| chr1:147942780 | CAG | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.207-657_207-656del others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147942780 | |||||||
| chr1:147943028 | A | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG00438.hp1 NA18947.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.207-410A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943028 | |||||||
| chr1:147943149 | A | G | 1 | a0001c0003t0002g0231 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.207-289A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943149 | |||||||
| chr1:147943281 | C | T | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-157C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 3/13 | chr1 | 147943281 | |||||||
| chr1:147943571 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.313+27G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943571 | |||||||
| chr1:147943644 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.313+100T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943644 | |||||||
| chr1:147943786 | A | G | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.314-211A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943786 | |||||||
| chr1:147943836 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.314-161C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943836 | |||||||
| chr1:147943959 | A | G | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.314-38A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 4/13 | chr1 | 147943959 | |||||||
| chr1:147944137 | A | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG00408.hp2 NA18957.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+39A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944137 | |||||||
| chr1:147944361 | A | G | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.415+263A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944361 | |||||||
| chr1:147944502 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
6 | HG01256.hp1 HG01346.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+404A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944502 | |||||||
| chr1:147944545 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+447A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944545 | |||||||
| chr1:147944714 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+616C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944714 | |||||||
| chr1:147944715 | AG | A | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+618delG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944715 | |||||||
| chr1:147944798 | TGAATCTA others(15): Show |
T | 12 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+725_415+746del others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147944798 | ||||||
| chr1:147944813 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.415+715A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944813 | |||||||
| chr1:147944872 | T | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+774T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944872 | |||||||
| chr1:147944973 | A | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+875A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944973 | |||||||
| chr1:147944991 | C | G | 4 | a0001c0003t0002g0229 a0001c0003t0002g0230 a0001c0003t0002g0231 others(1): Show |
4 | HG00423.hp2 HG00621.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+893C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147944991 | |||||||
| chr1:147945031 | CT | C | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+936delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147945031 | ||||||
| chr1:147945067 | A | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+969A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945067 | |||||||
| chr1:147945251 | T | C | 1 | a0004c0008t0001g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.415+1153T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945251 | |||||||
| chr1:147945701 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+1603C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945701 | |||||||
| chr1:147945724 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.415+1626T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945724 | |||||||
| chr1:147945844 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.415+1746C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945844 | |||||||
| chr1:147945887 | G | T | 5 | a0001c0001t0001g0217 a0001c0002t0001g0009 a0001c0002t0001g0115 others(2): Show |
6 | HG00140.hp1 HG00741.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1789G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945887 | |||||||
| chr1:147945927 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.415+1829C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147945927 | |||||||
| chr1:147946183 | A | G | 4 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.415+2085A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946183 | |||||||
| chr1:147946273 | G | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+2175G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946273 | |||||||
| chr1:147946279 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01255.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.415+2181T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946279 | |||||||
| chr1:147946564 | T | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(25): Show |
29 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.415+2466T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946564 | |||||||
| chr1:147946964 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+2866C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147946964 | |||||||
| chr1:147947135 | G | A | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.415+3037G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947135 | |||||||
| chr1:147947333 | C | CA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0190 a0001c0001t0001g0247 others(17): Show |
21 | HG00738.hp1 HG02055.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.415+3252dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147947333 | ||||||
| chr1:147947333 | C | CAAA | 11 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(8): Show |
11 | HG00423.hp2 HG00597.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+3250_415+3252d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147947333 | ||||||
| chr1:147947352 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+3254A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947352 | |||||||
| chr1:147947359 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.415+3261C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947359 | |||||||
| chr1:147947389 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415+3291C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947389 | |||||||
| chr1:147947410 | T | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+3312T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947410 | |||||||
| chr1:147947523 | C | T | 1 | a0001c0002t0001g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.415+3425C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947523 | |||||||
| chr1:147947649 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+3551T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947649 | |||||||
| chr1:147947748 | A | G | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+3650A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947748 | |||||||
| chr1:147947997 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.415+3899C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147947997 | |||||||
| chr1:147948038 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.415+3940T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948038 | |||||||
| chr1:147948154 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+4056G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948154 | |||||||
| chr1:147948756 | AT | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(51): Show |
56 | HG00323.hp2 HG00597.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.416-4567delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | ||||||
| chr1:147948756 | ATT | A | 20 | a0001c0001t0004g0256 a0001c0001t0004g0257 a0001c0001t0004g0258 others(17): Show |
20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-4568_416-4567d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | ||||||
| chr1:147948756 | ATTT | A | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-4569_416-4567d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147948756 | ||||||
| chr1:147948783 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416-4562G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948783 | |||||||
| chr1:147948849 | G | T | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-4496G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948849 | |||||||
| chr1:147948905 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.416-4440C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147948905 | |||||||
| chr1:147949005 | A | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18955.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-4340A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949005 | |||||||
| chr1:147949036 | G | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG02083.hp1 NA18952.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-4309G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949036 | |||||||
| chr1:147949047 | G | A | 28 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(25): Show |
28 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.416-4298G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949047 | |||||||
| chr1:147949109 | G | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.416-4236G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949109 | |||||||
| chr1:147949112 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-4233G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949112 | |||||||
| chr1:147949123 | A | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.416-4222A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949123 | |||||||
| chr1:147949290 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-4055A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949290 | |||||||
| chr1:147949297 | TGGCTGGG others(116): Show |
T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-4041_416-3919d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949297 | ||||||
| chr1:147949332 | G | A | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-4013G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949332 | |||||||
| chr1:147949335 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-4010G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949335 | |||||||
| chr1:147949348 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(35): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.416-3997T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949348 | |||||||
| chr1:147949363 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3982A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949363 | |||||||
| chr1:147949367 | C | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3978C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949367 | |||||||
| chr1:147949371 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3974T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949371 | |||||||
| chr1:147949379 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3966T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949379 | |||||||
| chr1:147949384 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3961G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949384 | |||||||
| chr1:147949385 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3960G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949385 | |||||||
| chr1:147949393 | AC | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3945delC | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949393 | ||||||
| chr1:147949412 | G | A | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3933G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949412 | |||||||
| chr1:147949426 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3919G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949426 | |||||||
| chr1:147949428 | C | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3917C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949428 | |||||||
| chr1:147949432 | T | C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3913T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949432 | |||||||
| chr1:147949447 | C | CCCACCTC others(412): Show |
1 | a0001c0003t0003g0236 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.416-3897_416-3896i others(421): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(413): Show |
1 | a0001c0003t0003g0237 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.416-3897_416-3896i others(422): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(111): Show |
20 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(17): Show |
20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.416-3897_416-3896i others(120): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(412): Show |
2 | a0001c0003t0003g0234 a0001c0003t0003g0235 |
2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-3897_416-3896i others(421): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(111): Show |
229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
238 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.416-3897_416-3896i others(120): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(112): Show |
1 | a0001c0001t0001g0012 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.416-3897_416-3896i others(121): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949447 | C | CCCACCTC others(110): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
3 | HG03491.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.416-3897_416-3896i others(119): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949447 | ||||||
| chr1:147949464 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3881C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949464 | |||||||
| chr1:147949472 | C | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3873C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949472 | |||||||
| chr1:147949485 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3860C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949485 | |||||||
| chr1:147949497 | C | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3848C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949497 | |||||||
| chr1:147949534 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3811C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949534 | |||||||
| chr1:147949550 | C | T | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3795C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949550 | |||||||
| chr1:147949551 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-3794G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949551 | |||||||
| chr1:147949552 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3793G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949552 | |||||||
| chr1:147949554 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3791G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949554 | |||||||
| chr1:147949555 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3790C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949555 | |||||||
| chr1:147949568 | G | A | 2 | a0001c0003t0003g0238 a0001c0006t0007g0253 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.416-3777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949568 | |||||||
| chr1:147949568 | G | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3777G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949568 | |||||||
| chr1:147949569 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3776G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949569 | |||||||
| chr1:147949577 | ACCCCCCC others(345): Show |
A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3761_416-3410d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949577 | ||||||
| chr1:147949589 | C | CCCTCCCG others(71): Show |
1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3751_416-3750i others(80): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949589 | ||||||
| chr1:147949594 | CAGGACCG others(91): Show |
C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3750_416-3653d others(100): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949594 | |||||||
| chr1:147949595 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3750A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949595 | |||||||
| chr1:147949595 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3750A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949595 | |||||||
| chr1:147949600 | C | G | 39 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0247 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-3745C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949600 | |||||||
| chr1:147949605 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3740A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949605 | |||||||
| chr1:147949610 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3735A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949610 | |||||||
| chr1:147949611 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3734C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949611 | |||||||
| chr1:147949612 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.416-3733G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949612 | |||||||
| chr1:147949616 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.416-3729C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949616 | |||||||
| chr1:147949694 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3651G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949694 | |||||||
| chr1:147949707 | G | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3638G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949707 | |||||||
| chr1:147949722 | A | C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3623A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949722 | |||||||
| chr1:147949744 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3601A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949744 | |||||||
| chr1:147949771 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.416-3574C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949771 | |||||||
| chr1:147949776 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3569A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949776 | |||||||
| chr1:147949778 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3567A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949778 | |||||||
| chr1:147949787 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3558C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949787 | |||||||
| chr1:147949792 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3553A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949792 | |||||||
| chr1:147949808 | G | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-3537G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949808 | |||||||
| chr1:147949813 | CCCTCCCG others(71): Show |
C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3516_416-3439d others(80): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949813 | ||||||
| chr1:147949829 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3516A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949829 | |||||||
| chr1:147949836 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.416-3509C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949836 | |||||||
| chr1:147949837 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.416-3508G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949837 | |||||||
| chr1:147949884 | G | A | 5 | a0001c0001t0001g0062 a0001c0002t0001g0082 a0001c0002t0001g0083 others(2): Show |
5 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.416-3461G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949884 | |||||||
| chr1:147949906 | C | CGGCTGGC others(42): Show |
10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949906 | ||||||
| chr1:147949906 | C | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-3439C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949906 | |||||||
| chr1:147949919 | G | GGGGGGCT others(42): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG02965.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949919 | ||||||
| chr1:147949919 | G | GGGGGGCT others(43): Show |
1 | a0001c0001t0001g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.416-3410_416-3409i others(52): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949919 | ||||||
| chr1:147949929 | CCCCCCCA others(140): Show |
C | 1 | a0001c0001t0001g0003 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.416-3392_416-3246d others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949929 | ||||||
| chr1:147949946 | C | CGGACGGG others(42): Show |
1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-3393_416-3392i others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949946 | ||||||
| chr1:147949953 | T | G | 27 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(24): Show |
27 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.416-3392T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949953 | |||||||
| chr1:147949955 | C | T | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3390C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949955 | |||||||
| chr1:147949967 | T | C | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3378T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949967 | |||||||
| chr1:147949969 | T | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3376T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949969 | |||||||
| chr1:147949980 | CCCCCACC others(42): Show |
C | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.416-3331_416-3283d others(51): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147949980 | ||||||
| chr1:147949996 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-3349G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147949996 | |||||||
| chr1:147950002 | G | T | 18 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(15): Show |
18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.416-3343G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950002 | |||||||
| chr1:147950004 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-3341C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950004 | |||||||
| chr1:147950016 | C | T | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.416-3329C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950016 | |||||||
| chr1:147950029 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3316T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950029 | |||||||
| chr1:147950054 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3291G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950054 | |||||||
| chr1:147950063 | T | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3282T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950063 | |||||||
| chr1:147950076 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-3269T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950076 | |||||||
| chr1:147950082 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.416-3263C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950082 | |||||||
| chr1:147950113 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3232C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950113 | |||||||
| chr1:147950115 | G | C | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.416-3230G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950115 | |||||||
| chr1:147950126 | C | G | 1 | a0003c0005t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.416-3219C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950126 | |||||||
| chr1:147950190 | A | G | 3 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 |
3 | HG00423.hp2 HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.416-3155A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950190 | |||||||
| chr1:147950194 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.416-3151G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950194 | |||||||
| chr1:147950196 | A | G | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.416-3149A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950196 | |||||||
| chr1:147950293 | A | ACGGGGCG others(1): Show |
14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3045_416-3038d others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950293 | ||||||
| chr1:147950294 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-3051C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950294 | |||||||
| chr1:147950311 | G | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-3034G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950311 | |||||||
| chr1:147950338 | C | T | 1 | a0001c0003t0002g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.416-3007C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950338 | |||||||
| chr1:147950352 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.416-2993C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950352 | |||||||
| chr1:147950421 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.416-2924C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950421 | |||||||
| chr1:147950526 | C | CG | 4 | a0001c0001t0001g0155 a0001c0001t0001g0169 a0001c0001t0001g0218 others(1): Show |
4 | HG00673.hp1 HG01109.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-2815dupG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950526 | ||||||
| chr1:147950572 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2773C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950572 | |||||||
| chr1:147950581 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
80 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.416-2764C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950581 | |||||||
| chr1:147950621 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.416-2724G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950621 | |||||||
| chr1:147950688 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2657C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950688 | |||||||
| chr1:147950714 | C | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-2631C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950714 | |||||||
| chr1:147950724 | AGCTGGAG others(5): Show |
A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2620_416-2609d others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950724 | |||||||
| chr1:147950751 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
121 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.416-2594T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950751 | |||||||
| chr1:147950760 | G | C | 1 | a0001c0002t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-2585G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950760 | |||||||
| chr1:147950768 | CA | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2570delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950768 | ||||||
| chr1:147950801 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-2544C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950801 | |||||||
| chr1:147950825 | C | T | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-2520C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950825 | |||||||
| chr1:147950861 | G | T | 2 | a0001c0003t0003g0234 a0001c0003t0003g0235 |
2 | HG01934.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.416-2484G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147950861 | |||||||
| chr1:147950926 | A | AGAGAGG | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2408_416-2403d others(8): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147950926 | ||||||
| chr1:147951283 | T | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.416-2062T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951283 | |||||||
| chr1:147951381 | A | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.416-1964A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951381 | |||||||
| chr1:147951436 | G | C | 1 | a0001c0002t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-1909G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951436 | |||||||
| chr1:147951446 | A | G | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1899A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951446 | |||||||
| chr1:147951482 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1863T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951482 | |||||||
| chr1:147951496 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1849A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951496 | |||||||
| chr1:147951554 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.416-1791G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951554 | |||||||
| chr1:147951628 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1717A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951628 | |||||||
| chr1:147951690 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1655T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951690 | |||||||
| chr1:147951710 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.416-1635G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951710 | |||||||
| chr1:147951778 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.416-1567C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951778 | |||||||
| chr1:147951859 | T | C | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1486T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951859 | |||||||
| chr1:147951977 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.416-1368C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147951977 | |||||||
| chr1:147952000 | TGTAGAGT others(14): Show |
T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0260 a0001c0001t0004g0255 |
3 | HG02809.hp1 HG02896.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.416-1326_416-1306d others(23): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147952000 | ||||||
| chr1:147952112 | G | A | 1 | a0005c0007t0001g0091 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.416-1233G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952112 | |||||||
| chr1:147952121 | A | G | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.416-1224A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952121 | |||||||
| chr1:147952125 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1220G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952125 | |||||||
| chr1:147952193 | T | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1152T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952193 | |||||||
| chr1:147952232 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-1113T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952232 | |||||||
| chr1:147952244 | A | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-1101A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952244 | |||||||
| chr1:147952283 | G | T | 1 | a0001c0002t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.416-1062G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952283 | |||||||
| chr1:147952455 | G | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-890G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952455 | |||||||
| chr1:147952619 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.416-726A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952619 | |||||||
| chr1:147952668 | A | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.416-677A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952668 | |||||||
| chr1:147952928 | A | G | 1 | a0001c0002t0001g0100 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.416-417A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147952928 | |||||||
| chr1:147952997 | G | GT | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0111 others(6): Show |
9 | HG01175.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.416-333dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr1 | 147952997 | ||||||
| chr1:147953029 | A | G | 9 | a0001c0001t0001g0254 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-316A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953029 | |||||||
| chr1:147953078 | A | G | 1 | a0001c0002t0001g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.416-267A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953078 | |||||||
| chr1:147953200 | A | C | 1 | a0001c0002t0001g0009 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416-145A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953200 | |||||||
| chr1:147953207 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.416-138A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 5/13 | chr1 | 147953207 | |||||||
| chr1:147953672 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.536+207A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953672 | |||||||
| chr1:147953749 | C | T | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.536+284C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953749 | |||||||
| chr1:147953909 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.537-413C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147953909 | |||||||
| chr1:147954080 | T | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.537-242T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147954080 | |||||||
| chr1:147954229 | A | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(8): Show |
11 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-93A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 6/13 | chr1 | 147954229 | |||||||
| chr1:147954513 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+111G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954513 | |||||||
| chr1:147954589 | G | A | 1 | a0001c0001t0004g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.617+187G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954589 | |||||||
| chr1:147954686 | T | A | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.617+284T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954686 | |||||||
| chr1:147954825 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+423A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954825 | |||||||
| chr1:147954873 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+471G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954873 | |||||||
| chr1:147954877 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.617+475G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954877 | |||||||
| chr1:147954966 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+564C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147954966 | |||||||
| chr1:147955013 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+611C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955013 | |||||||
| chr1:147955209 | T | C | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+807T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955209 | |||||||
| chr1:147955267 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+865G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955267 | |||||||
| chr1:147955284 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+882T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955284 | |||||||
| chr1:147955287 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+885C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955287 | |||||||
| chr1:147955339 | G | A | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+937G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955339 | |||||||
| chr1:147955471 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+1069G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955471 | |||||||
| chr1:147955497 | G | A | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+1095G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955497 | |||||||
| chr1:147955521 | A | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(13): Show |
17 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+1119A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955521 | |||||||
| chr1:147955568 | T | C | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+1166T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955568 | |||||||
| chr1:147955636 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | NA18957.hp2 NA18963.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+1234T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955636 | |||||||
| chr1:147955700 | C | G | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+1298C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955700 | |||||||
| chr1:147955822 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0161 |
2 | NA18942.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.617+1420T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955822 | |||||||
| chr1:147955975 | T | C | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+1573T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147955975 | |||||||
| chr1:147956207 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+1805A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956207 | |||||||
| chr1:147956226 | G | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.617+1824G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956226 | |||||||
| chr1:147956435 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617+2033G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956435 | |||||||
| chr1:147956452 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2050G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956452 | |||||||
| chr1:147956467 | A | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+2065A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956467 | |||||||
| chr1:147956581 | G | C | 1 | a0001c0001t0001g0039 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.617+2179G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956581 | |||||||
| chr1:147956655 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.617+2253A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956655 | |||||||
| chr1:147956657 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2255G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956657 | |||||||
| chr1:147956686 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+2284T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956686 | |||||||
| chr1:147956741 | A | AT | 11 | a0001c0001t0001g0020 a0001c0001t0001g0254 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.617+2353dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147956741 | ||||||
| chr1:147956741 | AT | A | 24 | a0001c0001t0001g0145 a0001c0003t0002g0220 a0001c0003t0002g0221 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+2353delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147956741 | ||||||
| chr1:147956770 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.617+2368C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956770 | |||||||
| chr1:147956833 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+2431A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956833 | |||||||
| chr1:147956836 | C | A | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.617+2434C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956836 | |||||||
| chr1:147956836 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+2434C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956836 | |||||||
| chr1:147956953 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617+2551G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956953 | |||||||
| chr1:147956965 | T | C | 11 | a0001c0001t0001g0260 a0001c0001t0004g0255 a0001c0001t0004g0256 others(8): Show |
11 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+2563T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956965 | |||||||
| chr1:147956981 | T | C | 2 | a0001c0002t0001g0116 a0001c0002t0001g0117 |
2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.617+2579T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956981 | |||||||
| chr1:147956986 | A | C | 9 | a0001c0001t0001g0254 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2584A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147956986 | |||||||
| chr1:147957004 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.617+2602G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957004 | |||||||
| chr1:147957085 | A | C | 1 | a0002c0004t0002g0233 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.617+2683A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957085 | |||||||
| chr1:147957160 | T | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2758T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957160 | |||||||
| chr1:147957162 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2760T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957162 | |||||||
| chr1:147957192 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.617+2790G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957192 | |||||||
| chr1:147957238 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.617+2836A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957238 | |||||||
| chr1:147957259 | G | T | 1 | a0001c0003t0003g0242 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.617+2857G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957259 | |||||||
| chr1:147957285 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.617+2883T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957285 | |||||||
| chr1:147957309 | G | A | 9 | a0001c0001t0001g0254 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+2907G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957309 | |||||||
| chr1:147957331 | G | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+2929G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957331 | |||||||
| chr1:147957392 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0163 a0001c0001t0001g0165 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+2990G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957392 | |||||||
| chr1:147957540 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+3138C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957540 | |||||||
| chr1:147957546 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3144A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957546 | |||||||
| chr1:147957559 | T | C | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+3157T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957559 | |||||||
| chr1:147957706 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.617+3304T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957706 | |||||||
| chr1:147957715 | C | G | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+3313C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957715 | |||||||
| chr1:147957722 | A | G | 2 | a0001c0001t0001g0260 a0001c0003t0003g0243 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.617+3320A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957722 | |||||||
| chr1:147957755 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.617+3353T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957755 | |||||||
| chr1:147957790 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3388C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957790 | |||||||
| chr1:147957798 | C | G | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.617+3396C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957798 | |||||||
| chr1:147957835 | C | T | 12 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+3433C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957835 | |||||||
| chr1:147957880 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0001g0164 others(2): Show |
6 | HG00323.hp2 HG01243.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+3478C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957880 | |||||||
| chr1:147957962 | A | G | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3560A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957962 | |||||||
| chr1:147957969 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.617+3567C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957969 | |||||||
| chr1:147957977 | C | T | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3575C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147957977 | |||||||
| chr1:147958015 | C | G | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+3613C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958015 | |||||||
| chr1:147958021 | G | A | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+3619G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958021 | |||||||
| chr1:147958070 | G | GA | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+3679dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958070 | ||||||
| chr1:147958140 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3738A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958140 | |||||||
| chr1:147958141 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3739G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958141 | |||||||
| chr1:147958142 | TAAAGACA others(10): Show |
T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3742_617+3758d others(19): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958142 | ||||||
| chr1:147958253 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3851A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958253 | |||||||
| chr1:147958271 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+3869A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958271 | |||||||
| chr1:147958287 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+3885A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958287 | |||||||
| chr1:147958385 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.617+3983G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958385 | |||||||
| chr1:147958410 | G | A | 12 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.617+4008G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958410 | |||||||
| chr1:147958529 | CT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
238 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.617+4130delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958529 | ||||||
| chr1:147958604 | C | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+4202C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958604 | |||||||
| chr1:147958638 | C | CA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0247 others(2): Show |
6 | HG00673.hp1 HG02258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+4250dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958638 | ||||||
| chr1:147958638 | CA | C | 25 | a0001c0001t0001g0260 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.617+4250delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958638 | ||||||
| chr1:147958660 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+4258C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958660 | |||||||
| chr1:147958668 | A | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4266A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958668 | |||||||
| chr1:147958736 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4334G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958736 | |||||||
| chr1:147958745 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.617+4343A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958745 | |||||||
| chr1:147958782 | A | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.617+4380A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958782 | |||||||
| chr1:147958834 | C | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.617+4432C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958834 | |||||||
| chr1:147958853 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4451G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958853 | |||||||
| chr1:147958855 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0260 |
2 | HG01099.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.617+4453A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958855 | |||||||
| chr1:147958863 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4461A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958863 | |||||||
| chr1:147958867 | CCA | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+4468_617+4469d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147958867 | ||||||
| chr1:147958923 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.617+4521A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958923 | |||||||
| chr1:147958974 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4572A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147958974 | |||||||
| chr1:147959016 | A | AT | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.617+4622dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147959016 | ||||||
| chr1:147959207 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.617+4805T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959207 | |||||||
| chr1:147959222 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4820G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959222 | |||||||
| chr1:147959283 | A | G | 3 | a0002c0004t0002g0226 a0002c0004t0002g0227 a0002c0004t0002g0233 |
3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.617+4881A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959283 | |||||||
| chr1:147959292 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.617+4890G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959292 | |||||||
| chr1:147959325 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+4923C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959325 | |||||||
| chr1:147959418 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5016A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959418 | |||||||
| chr1:147959548 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5146A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959548 | |||||||
| chr1:147959553 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5151C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959553 | |||||||
| chr1:147959563 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0008g0214 |
2 | NA19058.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.617+5161A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959563 | |||||||
| chr1:147959656 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5254G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959656 | |||||||
| chr1:147959739 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5337T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959739 | |||||||
| chr1:147959752 | G | T | 1 | a0002c0004t0002g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.617+5350G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959752 | |||||||
| chr1:147959762 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5360A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959762 | |||||||
| chr1:147959871 | G | T | 1 | a0001c0001t0001g0017 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.617+5469G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959871 | |||||||
| chr1:147959874 | T | G | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.617+5472T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959874 | |||||||
| chr1:147959961 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+5559A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147959961 | |||||||
| chr1:147960046 | G | A | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+5644G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960046 | |||||||
| chr1:147960179 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5777G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960179 | |||||||
| chr1:147960189 | T | A | 1 | a0001c0003t0002g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.617+5787T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960189 | |||||||
| chr1:147960280 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+5878C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960280 | |||||||
| chr1:147960497 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.618-6057G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960497 | |||||||
| chr1:147960618 | C | T | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618-5936C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960618 | |||||||
| chr1:147960882 | T | G | 1 | a0001c0003t0003g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.618-5672T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960882 | |||||||
| chr1:147960993 | C | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-5561C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147960993 | |||||||
| chr1:147961042 | G | A | 7 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0100 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-5512G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961042 | |||||||
| chr1:147961161 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.618-5393A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961161 | |||||||
| chr1:147961258 | A | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-5296A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961258 | |||||||
| chr1:147961275 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.618-5279A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961275 | |||||||
| chr1:147961537 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0263 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.618-5017T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961537 | |||||||
| chr1:147961622 | C | A | 7 | a0001c0001t0001g0158 a0001c0001t0004g0255 a0001c0001t0004g0256 others(4): Show |
7 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-4932C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961622 | |||||||
| chr1:147961646 | T | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.618-4908T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961646 | |||||||
| chr1:147961657 | T | A | 1 | a0001c0002t0001g0116 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.618-4897T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961657 | |||||||
| chr1:147961775 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-4779G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961775 | |||||||
| chr1:147961917 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.618-4637A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147961917 | |||||||
| chr1:147962081 | T | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4473T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962081 | |||||||
| chr1:147962178 | C | G | 1 | a0001c0002t0001g0067 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.618-4376C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962178 | |||||||
| chr1:147962313 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.618-4241A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962313 | |||||||
| chr1:147962421 | CT | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4132delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962421 | |||||||
| chr1:147962423 | C | CA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(14): Show |
20 | HG00735.hp1 HG01243.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.618-4115dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962423 | ||||||
| chr1:147962423 | CA | C | 27 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(24): Show |
27 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.618-4115delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962423 | ||||||
| chr1:147962424 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4130A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962424 | |||||||
| chr1:147962553 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-4001C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962553 | |||||||
| chr1:147962567 | A | C | 1 | a0001c0003t0002g0225 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.618-3987A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962567 | |||||||
| chr1:147962595 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618-3959C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962595 | |||||||
| chr1:147962668 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.618-3886G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962668 | |||||||
| chr1:147962743 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-3811A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962743 | |||||||
| chr1:147962755 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.618-3799C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962755 | |||||||
| chr1:147962792 | G | A | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3762G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962792 | |||||||
| chr1:147962820 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3734C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962820 | |||||||
| chr1:147962890 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.618-3664C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962890 | |||||||
| chr1:147962891 | G | A | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-3663G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962891 | |||||||
| chr1:147962896 | A | G | 1 | a0001c0002t0001g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618-3658A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962896 | |||||||
| chr1:147962900 | A | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.618-3654A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962900 | |||||||
| chr1:147962941 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0163 a0001c0001t0001g0165 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-3613A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147962941 | |||||||
| chr1:147962953 | GA | G | 31 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(28): Show |
31 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.618-3589delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147962953 | ||||||
| chr1:147963174 | A | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-3380A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963174 | |||||||
| chr1:147963205 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01109.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.618-3349G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963205 | |||||||
| chr1:147963256 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.618-3298A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963256 | |||||||
| chr1:147963359 | G | A | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-3195G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963359 | |||||||
| chr1:147963375 | TA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.618-3161delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147963375 | ||||||
| chr1:147963375 | TAA | T | 10 | a0001c0001t0001g0249 a0001c0003t0003g0234 a0001c0003t0003g0235 others(7): Show |
10 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-3162_618-3161d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147963375 | ||||||
| chr1:147963377 | A | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-3177A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963377 | |||||||
| chr1:147963548 | T | C | 1 | a0001c0002t0001g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.618-3006T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963548 | |||||||
| chr1:147963575 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.618-2979T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963575 | |||||||
| chr1:147963587 | A | G | 1 | a0003c0005t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.618-2967A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963587 | |||||||
| chr1:147963880 | A | C | 1 | a0001c0001t0001g0200 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.618-2674A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963880 | |||||||
| chr1:147963943 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.618-2611G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147963943 | |||||||
| chr1:147964025 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.618-2529A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964025 | |||||||
| chr1:147964032 | G | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618-2522G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964032 | |||||||
| chr1:147964194 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-2360T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964194 | |||||||
| chr1:147964215 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0208 |
2 | NA18986.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.618-2339T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964215 | |||||||
| chr1:147964323 | T | C | 3 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0003c0005t0001g0114 |
3 | HG02109.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.618-2231T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964323 | |||||||
| chr1:147964364 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-2190C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964364 | |||||||
| chr1:147964437 | T | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0173 a0001c0001t0001g0209 others(1): Show |
4 | NA18944.hp2 NA18952.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-2117T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964437 | |||||||
| chr1:147964580 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.618-1974A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147964580 | |||||||
| chr1:147965032 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-1522A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965032 | |||||||
| chr1:147965307 | C | G | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.618-1247C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965307 | |||||||
| chr1:147965506 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-1048A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965506 | |||||||
| chr1:147965787 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-767G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965787 | |||||||
| chr1:147965792 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(35): Show |
39 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.618-762A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147965792 | |||||||
| chr1:147966037 | G | C | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-517G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966037 | |||||||
| chr1:147966055 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.618-499C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966055 | |||||||
| chr1:147966207 | A | AG | 7 | a0001c0001t0001g0056 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-346dupG | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147966207 | ||||||
| chr1:147966237 | A | G | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0003t0002g0220 others(13): Show |
16 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.618-317A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966237 | |||||||
| chr1:147966312 | TAGC | T | 19 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(16): Show |
19 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-239_618-237del others(3): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 147966312 | ||||||
| chr1:147966440 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.618-114C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966440 | |||||||
| chr1:147966521 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0071 others(1): Show |
4 | NA18939.hp2 NA18955.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-33C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 7/13 | chr1 | 147966521 | |||||||
| chr1:147966689 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.727+26C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147966689 | |||||||
| chr1:147967001 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.727+338A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967001 | |||||||
| chr1:147967069 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0001g0164 others(2): Show |
6 | HG00323.hp2 HG01243.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.727+406T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967069 | |||||||
| chr1:147967173 | T | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.727+510T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967173 | |||||||
| chr1:147967465 | A | G | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+802A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967465 | |||||||
| chr1:147967478 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.727+815T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967478 | |||||||
| chr1:147967743 | G | A | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.727+1080G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967743 | |||||||
| chr1:147967797 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.728-1078T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967797 | |||||||
| chr1:147967849 | A | G | 4 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0241 others(1): Show |
4 | HG02055.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.728-1026A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967849 | |||||||
| chr1:147967921 | G | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.728-954G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147967921 | |||||||
| chr1:147968040 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-835G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968040 | |||||||
| chr1:147968240 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0133 |
2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.728-635G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968240 | |||||||
| chr1:147968539 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.728-336A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968539 | |||||||
| chr1:147968707 | A | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.728-168A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968707 | |||||||
| chr1:147968744 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.728-131A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 8/13 | chr1 | 147968744 | |||||||
| chr1:147969015 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.816+52G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969015 | |||||||
| chr1:147969024 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.816+61T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969024 | |||||||
| chr1:147969151 | T | G | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.816+188T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969151 | |||||||
| chr1:147969354 | A | G | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+391A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969354 | |||||||
| chr1:147969413 | A | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.816+450A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969413 | |||||||
| chr1:147969462 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-405T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969462 | |||||||
| chr1:147969751 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.817-116G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 9/13 | chr1 | 147969751 | |||||||
| chr1:147970003 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+44C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970003 | |||||||
| chr1:147970026 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.909+67A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970026 | |||||||
| chr1:147970115 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.909+156A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970115 | |||||||
| chr1:147970162 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.909+203C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970162 | |||||||
| chr1:147970271 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.909+312A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970271 | |||||||
| chr1:147970453 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909+494C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970453 | |||||||
| chr1:147970482 | T | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+523T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970482 | |||||||
| chr1:147970491 | A | ATC | 52 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(49): Show |
53 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.909+574_909+575dup others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTC | 16 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(13): Show |
16 | HG00323.hp1 HG00438.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.909+572_909+575dup others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTC | 29 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0026 others(26): Show |
33 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.909+570_909+575dup others(6): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(1): Show |
10 | a0001c0001t0001g0134 a0001c0001t0001g0140 a0001c0001t0001g0143 others(7): Show |
10 | HG00140.hp1 HG01928.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+568_909+575dup others(8): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(3): Show |
12 | a0001c0001t0001g0029 a0001c0001t0001g0056 a0001c0001t0001g0099 others(9): Show |
12 | HG00408.hp1 HG00438.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+566_909+575dup others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(5): Show |
4 | a0001c0001t0001g0038 a0001c0001t0001g0136 a0001c0001t0001g0181 others(1): Show |
4 | HG01243.hp2 HG02027.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+564_909+575dup others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(7): Show |
1 | a0001c0001t0001g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.909+562_909+575dup others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(11): Show |
1 | a0001c0001t0001g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.909+558_909+575dup others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | A | ATCTCTCT others(13): Show |
1 | a0001c0001t0001g0202 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.909+556_909+575dup others(20): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | ATC | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00741.hp2 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.909+574_909+575del others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | ATCTC | A | 14 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0077 others(11): Show |
14 | HG01074.hp2 HG02015.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.909+572_909+575del others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | ATCTCTCT others(3): Show |
A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+566_909+575del others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970491 | ATCTCTCT others(7): Show |
A | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.909+562_909+575del others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970491 | ||||||
| chr1:147970521 | C | A | 1 | a0001c0001t0004g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+562C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970521 | |||||||
| chr1:147970525 | CTCTCTCT others(3): Show |
C | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+572_909+581del others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970525 | ||||||
| chr1:147970527 | C | A | 1 | a0001c0001t0004g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+568C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970527 | |||||||
| chr1:147970535 | A | C | 20 | a0001c0001t0001g0176 a0001c0001t0004g0257 a0001c0003t0002g0220 others(17): Show |
20 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+576A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970535 | |||||||
| chr1:147970541 | A | C | 15 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(12): Show |
15 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.909+582A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970541 | |||||||
| chr1:147970543 | CTCTCTCT others(5): Show |
C | 1 | a0001c0001t0004g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.909+596_909+607del others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970543 | ||||||
| chr1:147970545 | C | A | 8 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(5): Show |
8 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+586C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970545 | |||||||
| chr1:147970547 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.909+588C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970547 | |||||||
| chr1:147970549 | C | A | 14 | a0001c0003t0002g0221 a0001c0003t0002g0224 a0001c0003t0003g0234 others(11): Show |
14 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.909+590C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970549 | |||||||
| chr1:147970549 | C | CTA | 3 | a0001c0003t0002g0220 a0001c0003t0002g0222 a0002c0004t0002g0226 |
3 | NA18906.hp1 NA18982.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.909+591_909+592ins others(2): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | ||||||
| chr1:147970549 | C | CTCTCTCT others(3): Show |
1 | a0001c0003t0002g0230 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+595_909+596ins others(10): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | ||||||
| chr1:147970549 | C | CTCTCTCT others(9): Show |
1 | a0001c0003t0002g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.909+595_909+596ins others(16): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | ||||||
| chr1:147970549 | C | CTCTCTCT others(11): Show |
1 | a0001c0003t0002g0228 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.909+595_909+596ins others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147970549 | ||||||
| chr1:147970549 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0064 |
2 | HG02155.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.909+590C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970549 | |||||||
| chr1:147970555 | A | C | 1 | a0001c0001t0001g0002 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.909+596A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970555 | |||||||
| chr1:147970567 | C | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0260 a0001c0001t0001g0261 others(4): Show |
8 | HG01099.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+608C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970567 | |||||||
| chr1:147970569 | C | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0024 others(51): Show |
56 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.909+610C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970569 | |||||||
| chr1:147970571 | A | C | 17 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0155 others(14): Show |
17 | HG00673.hp1 HG00673.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.909+612A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970571 | |||||||
| chr1:147970584 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.909+625A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970584 | |||||||
| chr1:147970599 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02083.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.909+640A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970599 | |||||||
| chr1:147970617 | T | C | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+658T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970617 | |||||||
| chr1:147970706 | C | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.909+747C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970706 | |||||||
| chr1:147970841 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.909+882T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970841 | |||||||
| chr1:147970931 | C | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+972C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147970931 | |||||||
| chr1:147971141 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.909+1182G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971141 | |||||||
| chr1:147971157 | C | CTT | 37 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(34): Show |
38 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.909+1208_909+1209d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971157 | ||||||
| chr1:147971182 | C | T | 1 | a0001c0003t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+1223C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971182 | |||||||
| chr1:147971230 | A | C | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1271A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971230 | |||||||
| chr1:147971230 | A | G | 1 | a0001c0002t0001g0115 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.909+1271A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971230 | |||||||
| chr1:147971256 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.909+1297T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971256 | |||||||
| chr1:147971300 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.909+1341C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971300 | |||||||
| chr1:147971302 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+1343G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971302 | |||||||
| chr1:147971314 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.909+1355T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971314 | |||||||
| chr1:147971464 | C | CT | 39 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0027 others(36): Show |
39 | HG00323.hp1 HG00673.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.909+1530dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | ||||||
| chr1:147971464 | C | CTTT | 9 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0224 others(6): Show |
9 | HG02040.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+1528_909+1530d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | ||||||
| chr1:147971464 | C | CTTTT | 8 | a0001c0003t0002g0222 a0001c0003t0002g0230 a0001c0003t0002g0231 others(5): Show |
8 | HG00423.hp2 HG00621.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1527_909+1530d others(6): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | ||||||
| chr1:147971464 | C | CTTTTT | 10 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(7): Show |
11 | HG00597.hp1 HG01109.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+1526_909+1530d others(7): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147971464 | ||||||
| chr1:147971562 | C | T | 1 | a0001c0003t0002g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.909+1603C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971562 | |||||||
| chr1:147971678 | C | T | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+1719C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971678 | |||||||
| chr1:147971766 | C | T | 3 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0002t0001g0100 |
3 | NA18965.hp2 NA18971.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.909+1807C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147971766 | |||||||
| chr1:147972079 | A | G | 23 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.909+2120A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972079 | |||||||
| chr1:147972176 | G | T | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2217G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972176 | |||||||
| chr1:147972302 | T | G | 18 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(15): Show |
18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.909+2343T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972302 | |||||||
| chr1:147972371 | A | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0131 a0001c0003t0003g0243 |
3 | HG01175.hp1 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.909+2412A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972371 | |||||||
| chr1:147972375 | A | G | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2416A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972375 | |||||||
| chr1:147972437 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.909+2478C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972437 | |||||||
| chr1:147972528 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+2569G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972528 | |||||||
| chr1:147972665 | A | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0027 others(5): Show |
8 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+2706A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972665 | |||||||
| chr1:147972739 | G | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
6 | HG00735.hp2 HG01074.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+2780G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972739 | |||||||
| chr1:147972748 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+2789G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972748 | |||||||
| chr1:147972790 | A | AT | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+2834dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147972790 | ||||||
| chr1:147972804 | C | T | 4 | a0001c0002t0001g0082 a0001c0002t0001g0083 a0001c0002t0001g0084 others(1): Show |
4 | HG03688.hp2 HG03710.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+2845C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972804 | |||||||
| chr1:147972887 | A | G | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+2928A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147972887 | |||||||
| chr1:147973129 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.909+3170A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973129 | |||||||
| chr1:147973538 | G | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0174 a0001c0001t0001g0179 others(3): Show |
6 | HG00438.hp2 HG02027.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+3579G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973538 | |||||||
| chr1:147973766 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.909+3807G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973766 | |||||||
| chr1:147973781 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+3822T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147973781 | |||||||
| chr1:147974149 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.909+4190C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974149 | |||||||
| chr1:147974305 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.909+4346A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974305 | |||||||
| chr1:147974654 | A | G | 1 | a0001c0003t0002g0224 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.909+4695A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974654 | |||||||
| chr1:147974713 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.909+4754A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974713 | |||||||
| chr1:147974737 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.909+4778C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974737 | |||||||
| chr1:147974943 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+4984C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147974943 | |||||||
| chr1:147975102 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.909+5143T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975102 | |||||||
| chr1:147975186 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.909+5227A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975186 | |||||||
| chr1:147975844 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.909+5885C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147975844 | |||||||
| chr1:147976064 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.909+6105A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976064 | |||||||
| chr1:147976104 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+6145G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976104 | |||||||
| chr1:147976155 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0208 |
2 | NA18986.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.909+6196A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976155 | |||||||
| chr1:147976238 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.909+6279C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976238 | |||||||
| chr1:147976268 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0163 a0001c0001t0001g0165 others(2): Show |
6 | HG01891.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.909+6309T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976268 | |||||||
| chr1:147976660 | G | T | 1 | a0001c0002t0001g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.909+6701G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976660 | |||||||
| chr1:147976922 | T | G | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.909+6963T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976922 | |||||||
| chr1:147976927 | G | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+6968G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147976927 | |||||||
| chr1:147977111 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.909+7152A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977111 | |||||||
| chr1:147977166 | G | A | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+7207G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977166 | |||||||
| chr1:147977192 | C | A | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+7233C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977192 | |||||||
| chr1:147977233 | C | CA | 17 | a0001c0001t0001g0028 a0001c0001t0001g0062 a0001c0001t0001g0068 others(14): Show |
17 | HG01109.hp2 HG01175.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.909+7303dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | ||||||
| chr1:147977233 | CA | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
170 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.909+7303delA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | ||||||
| chr1:147977233 | CAA | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0168 a0001c0001t0001g0177 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.909+7302_909+7303d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147977233 | ||||||
| chr1:147977252 | A | C | 1 | a0001c0001t0001g0199 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.909+7293A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977252 | |||||||
| chr1:147977253 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.909+7294A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977253 | |||||||
| chr1:147977262 | A | C | 2 | a0001c0001t0004g0259 a0001c0003t0003g0243 |
2 | HG00738.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.909+7303A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977262 | |||||||
| chr1:147977448 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | NA18939.hp1 NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.909+7489G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977448 | |||||||
| chr1:147977523 | G | A | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.909+7564G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977523 | |||||||
| chr1:147977563 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.909+7604C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977563 | |||||||
| chr1:147977589 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0022 |
2 | NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.909+7630C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977589 | |||||||
| chr1:147977596 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+7637G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977596 | |||||||
| chr1:147977631 | G | A | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+7672G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977631 | |||||||
| chr1:147977672 | T | C | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.909+7713T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977672 | |||||||
| chr1:147977744 | A | G | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.909+7785A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977744 | |||||||
| chr1:147977747 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0027 others(5): Show |
8 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+7788T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147977747 | |||||||
| chr1:147978135 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-8064C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978135 | |||||||
| chr1:147978146 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.910-8053G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978146 | |||||||
| chr1:147978437 | T | TGGG | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-7761_910-7759d others(5): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147978437 | ||||||
| chr1:147978513 | T | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-7686T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978513 | |||||||
| chr1:147978568 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.910-7631C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978568 | |||||||
| chr1:147978628 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0160 a0001c0001t0001g0167 others(6): Show |
12 | HG00738.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.910-7571G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978628 | |||||||
| chr1:147978631 | C | T | 2 | a0002c0004t0002g0226 a0002c0004t0002g0233 |
2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.910-7568C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978631 | |||||||
| chr1:147978858 | T | TTTGCCTC | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7341_910-7340i others(9): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978858 | |||||||
| chr1:147978859 | G | C | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7340G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978859 | |||||||
| chr1:147978860 | A | C | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7339A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978860 | |||||||
| chr1:147978860 | A | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-7339A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978860 | |||||||
| chr1:147978861 | T | G | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-7338T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978861 | |||||||
| chr1:147978869 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-7330A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978869 | |||||||
| chr1:147978886 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.910-7313G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147978886 | |||||||
| chr1:147979171 | T | G | 1 | a0001c0003t0003g0241 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.910-7028T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979171 | |||||||
| chr1:147979307 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.910-6892C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979307 | |||||||
| chr1:147979310 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-6889C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979310 | |||||||
| chr1:147979407 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
79 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.910-6792C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979407 | |||||||
| chr1:147979458 | T | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-6741T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979458 | |||||||
| chr1:147979459 | T | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0211 |
2 | HG00738.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.910-6740T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979459 | |||||||
| chr1:147979677 | T | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0195 a0001c0001t0001g0247 others(37): Show |
41 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-6522T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979677 | |||||||
| chr1:147979699 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.910-6500A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979699 | |||||||
| chr1:147979788 | C | T | 6 | a0001c0001t0001g0166 a0001c0001t0001g0190 a0001c0002t0001g0082 others(3): Show |
6 | HG02129.hp1 HG02280.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-6411C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979788 | |||||||
| chr1:147979827 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.910-6372A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979827 | |||||||
| chr1:147979843 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-6356C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979843 | |||||||
| chr1:147979886 | C | T | 3 | a0001c0001t0001g0051 a0001c0002t0001g0089 a0001c0006t0007g0253 |
3 | HG02015.hp1 HG02055.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.910-6313C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979886 | |||||||
| chr1:147979906 | T | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0102 a0001c0001t0001g0247 others(14): Show |
18 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.910-6293T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147979906 | |||||||
| chr1:147980007 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.910-6192G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980007 | |||||||
| chr1:147980043 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0005g0090 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.910-6156G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980043 | |||||||
| chr1:147980085 | C | CA | 22 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(19): Show |
22 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-6100dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980085 | ||||||
| chr1:147980151 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0149 |
3 | NA18943.hp1 NA18975.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.910-6048G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980151 | |||||||
| chr1:147980274 | C | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.910-5925C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980274 | |||||||
| chr1:147980302 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.910-5897A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980302 | |||||||
| chr1:147980358 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.910-5841T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980358 | |||||||
| chr1:147980462 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.910-5737A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980462 | |||||||
| chr1:147980515 | C | A | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-5684C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980515 | |||||||
| chr1:147980633 | A | T | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0183 |
3 | HG00438.hp2 HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.910-5566A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980633 | |||||||
| chr1:147980768 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0134 |
2 | HG02602.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.910-5431G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980768 | |||||||
| chr1:147980776 | G | A | 4 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(1): Show |
4 | NA18974.hp1 NA18982.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-5423G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980776 | |||||||
| chr1:147980788 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0104 |
3 | HG02809.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.910-5411C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147980788 | |||||||
| chr1:147980818 | C | CA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.910-5353dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | ||||||
| chr1:147980818 | C | CAA | 17 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0001g0140 others(14): Show |
17 | HG00323.hp2 HG01169.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.910-5354_910-5353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | ||||||
| chr1:147980818 | CAA | C | 13 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(10): Show |
13 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.910-5354_910-5353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | ||||||
| chr1:147980818 | CAAAAAAA others(4): Show |
C | 3 | a0001c0003t0003g0239 a0001c0003t0003g0240 a0001c0003t0003g0242 |
3 | HG02055.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.910-5363_910-5353d others(13): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147980818 | ||||||
| chr1:147981023 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-5176A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981023 | |||||||
| chr1:147981028 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.910-5171G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981028 | |||||||
| chr1:147981037 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.910-5162G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981037 | |||||||
| chr1:147981078 | A | G | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-5121A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981078 | |||||||
| chr1:147981295 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01891.hp1 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.910-4904C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981295 | |||||||
| chr1:147981318 | G | GAC | 7 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
8 | HG02258.hp2 HG02572.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-4871_910-4870d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(3): Show |
3 | a0001c0003t0003g0239 a0001c0003t0003g0241 a0001c0003t0003g0242 |
3 | HG02055.hp2 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.910-4879_910-4870d others(12): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(5): Show |
2 | a0001c0003t0003g0238 a0001c0003t0003g0240 |
2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.910-4870_910-4869i others(14): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(7): Show |
1 | a0001c0003t0002g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.910-4870_910-4869i others(16): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(9): Show |
4 | a0001c0003t0003g0234 a0001c0003t0003g0236 a0001c0003t0003g0237 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-4870_910-4869i others(18): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(11): Show |
10 | a0001c0003t0002g0221 a0001c0003t0002g0222 a0001c0003t0002g0223 others(7): Show |
10 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-4870_910-4869i others(20): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981318 | G | GACACACA others(13): Show |
3 | a0002c0004t0002g0226 a0002c0004t0002g0227 a0002c0004t0002g0233 |
3 | HG02886.hp2 HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.910-4870_910-4869i others(22): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147981318 | ||||||
| chr1:147981330 | T | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(37): Show |
41 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.910-4869T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981330 | |||||||
| chr1:147981349 | A | ACACACAC others(10): Show |
1 | a0001c0003t0003g0235 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.910-4850_910-4849i others(19): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981349 | |||||||
| chr1:147981453 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.910-4746G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981453 | |||||||
| chr1:147981469 | A | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981469 | |||||||
| chr1:147981500 | A | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0098 |
2 | HG02895.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.910-4699A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981500 | |||||||
| chr1:147981611 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4588T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981611 | |||||||
| chr1:147981631 | T | C | 3 | a0001c0003t0002g0223 a0001c0003t0002g0224 a0001c0003t0002g0228 |
3 | HG00597.hp1 HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.910-4568T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981631 | |||||||
| chr1:147981731 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.910-4468C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981731 | |||||||
| chr1:147981827 | A | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-4372A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147981827 | |||||||
| chr1:147982090 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-4109C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982090 | |||||||
| chr1:147982099 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.910-4100G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982099 | |||||||
| chr1:147982145 | C | T | 9 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 others(6): Show |
9 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-4054C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982145 | |||||||
| chr1:147982193 | C | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-4006C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982193 | |||||||
| chr1:147982221 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-3978G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982221 | |||||||
| chr1:147982302 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0133 |
2 | HG01175.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.910-3897T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982302 | |||||||
| chr1:147982306 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.910-3893C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982306 | |||||||
| chr1:147982349 | T | G | 11 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(8): Show |
11 | HG00738.hp1 HG02055.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-3850T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982349 | |||||||
| chr1:147982427 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.910-3772G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982427 | |||||||
| chr1:147982437 | C | T | 2 | a0001c0001t0005g0090 a0001c0001t0008g0214 |
2 | HG03139.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.910-3762C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982437 | |||||||
| chr1:147982469 | A | C | 1 | a0001c0002t0001g0093 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.910-3730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982469 | |||||||
| chr1:147982861 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.910-3338C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982861 | |||||||
| chr1:147982863 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.910-3336T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982863 | |||||||
| chr1:147982987 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-3212C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982987 | |||||||
| chr1:147982988 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.910-3211A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147982988 | |||||||
| chr1:147983019 | G | A | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-3180G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983019 | |||||||
| chr1:147983229 | AACCTAGG others(4): Show |
A | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2966_910-2956d others(13): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147983229 | ||||||
| chr1:147983237 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.910-2962C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983237 | |||||||
| chr1:147983262 | G | A | 1 | a0002c0004t0002g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.910-2937G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983262 | |||||||
| chr1:147983336 | T | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2863T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983336 | |||||||
| chr1:147983434 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-2765G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983434 | |||||||
| chr1:147983496 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2703C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983496 | |||||||
| chr1:147983512 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.910-2687C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983512 | |||||||
| chr1:147983555 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0205 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.910-2644C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983555 | |||||||
| chr1:147983695 | G | A | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-2504G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983695 | |||||||
| chr1:147983763 | G | T | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-2436G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983763 | |||||||
| chr1:147983799 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2400C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983799 | |||||||
| chr1:147983811 | G | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2388G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983811 | |||||||
| chr1:147983855 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.910-2344T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983855 | |||||||
| chr1:147983882 | G | A | 3 | a0001c0003t0002g0223 a0001c0003t0002g0224 a0001c0003t0002g0228 |
3 | HG00597.hp1 HG02040.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.910-2317G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983882 | |||||||
| chr1:147983955 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-2244C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147983955 | |||||||
| chr1:147984071 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.910-2128G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984071 | |||||||
| chr1:147984107 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2092C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984107 | |||||||
| chr1:147984176 | G | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-2023G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984176 | |||||||
| chr1:147984178 | G | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02559.hp2 HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.910-2021G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984178 | |||||||
| chr1:147984237 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.910-1962T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984237 | |||||||
| chr1:147984243 | G | T | 1 | a0001c0001t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.910-1956G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984243 | |||||||
| chr1:147984244 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.910-1955G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984244 | |||||||
| chr1:147984257 | G | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0113 a0001c0001t0001g0157 others(10): Show |
13 | HG00438.hp2 HG01978.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.910-1942G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984257 | |||||||
| chr1:147984262 | T | G | 1 | a0001c0002t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.910-1937T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984262 | |||||||
| chr1:147984301 | C | A | 5 | a0001c0002t0001g0025 a0001c0002t0001g0089 a0001c0002t0001g0096 others(2): Show |
5 | HG00673.hp2 HG02015.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-1898C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984301 | |||||||
| chr1:147984306 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.910-1893A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984306 | |||||||
| chr1:147984397 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.910-1802G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984397 | |||||||
| chr1:147984456 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.910-1743T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984456 | |||||||
| chr1:147984542 | C | G | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-1657C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984542 | |||||||
| chr1:147984578 | A | G | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-1621A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984578 | |||||||
| chr1:147984838 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.910-1361T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984838 | |||||||
| chr1:147984854 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-1345G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984854 | |||||||
| chr1:147984890 | T | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-1309T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147984890 | |||||||
| chr1:147985120 | T | C | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-1079T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985120 | |||||||
| chr1:147985125 | A | G | 3 | a0001c0003t0002g0230 a0001c0003t0002g0231 a0001c0003t0002g0232 |
3 | HG00423.hp2 HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.910-1074A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985125 | |||||||
| chr1:147985138 | G | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1061G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985138 | |||||||
| chr1:147985385 | A | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0183 |
2 | HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.910-814A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985385 | |||||||
| chr1:147985412 | T | G | 1 | a0001c0001t0001g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.910-787T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985412 | |||||||
| chr1:147985475 | G | C | 25 | a0001c0001t0001g0066 a0001c0003t0002g0220 a0001c0003t0002g0221 others(22): Show |
25 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.910-724G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985475 | |||||||
| chr1:147985581 | G | C | 1 | a0004c0008t0001g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.910-618G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985581 | |||||||
| chr1:147985595 | A | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.910-604A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985595 | |||||||
| chr1:147985614 | T | G | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-585T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985614 | |||||||
| chr1:147985636 | G | GT | 22 | a0001c0001t0001g0254 a0001c0001t0001g0261 a0001c0001t0004g0255 others(19): Show |
22 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-552dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 147985636 | ||||||
| chr1:147985783 | G | A | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.910-416G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985783 | |||||||
| chr1:147985953 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.910-246C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147985953 | |||||||
| chr1:147986034 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.910-165C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147986034 | |||||||
| chr1:147986185 | C | T | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.910-14C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 10/13 | chr1 | 147986185 | |||||||
| chr1:147986545 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1005+251C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986545 | |||||||
| chr1:147986826 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1005+532A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986826 | |||||||
| chr1:147986842 | G | A | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1005+548G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986842 | |||||||
| chr1:147986959 | C | T | 1 | a0001c0002t0001g0219 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1005+665C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147986959 | |||||||
| chr1:147987018 | G | T | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1005+724G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987018 | |||||||
| chr1:147987173 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 |
3 | HG00741.hp2 HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1005+879T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987173 | |||||||
| chr1:147987519 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1006-913T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987519 | |||||||
| chr1:147987711 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0079 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1006-721G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987711 | |||||||
| chr1:147987743 | T | G | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1006-689T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987743 | |||||||
| chr1:147987754 | G | T | 1 | a0001c0002t0001g0101 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1006-678G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987754 | |||||||
| chr1:147987809 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1006-623A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987809 | |||||||
| chr1:147987896 | A | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006-536A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147987896 | |||||||
| chr1:147988042 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-390C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988042 | |||||||
| chr1:147988062 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-370G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988062 | |||||||
| chr1:147988098 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1006-334G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988098 | |||||||
| chr1:147988107 | C | T | 5 | a0001c0003t0003g0238 a0001c0003t0003g0239 a0001c0003t0003g0240 others(2): Show |
5 | HG02055.hp2 HG02615.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-325C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988107 | |||||||
| chr1:147988122 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18957.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1006-310G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988122 | |||||||
| chr1:147988410 | T | A | 1 | a0001c0003t0003g0238 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1006-22T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 11/13 | chr1 | 147988410 | |||||||
| chr1:147988588 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+67G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988588 | |||||||
| chr1:147988589 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+68G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988589 | |||||||
| chr1:147988666 | C | T | 1 | a0001c0003t0003g0243 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1095+145C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147988666 | |||||||
| chr1:147988861 | C | CA | 37 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0122 others(34): Show |
37 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1095+353dupA | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147988861 | ||||||
| chr1:147988861 | C | CAA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+352_1095+353d others(4): Show |
GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147988861 | ||||||
| chr1:147989127 | G | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+606G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989127 | |||||||
| chr1:147989234 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+713A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989234 | |||||||
| chr1:147989251 | A | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0203 |
2 | HG00408.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1095+730A>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989251 | |||||||
| chr1:147989322 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1095+801C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989322 | |||||||
| chr1:147989427 | C | CT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0051 others(3): Show |
6 | HG02258.hp1 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1095+921dupT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147989427 | ||||||
| chr1:147989427 | CT | C | 26 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0200 others(23): Show |
26 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.1095+921delT | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 147989427 | ||||||
| chr1:147989443 | A | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
2 | HG02080.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1095+922A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989443 | |||||||
| chr1:147989686 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1095+1165G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989686 | |||||||
| chr1:147989754 | C | A | 1 | a0001c0001t0001g0087 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1095+1233C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989754 | |||||||
| chr1:147989845 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1324G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989845 | |||||||
| chr1:147989963 | C | G | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1095+1442C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147989963 | |||||||
| chr1:147990004 | T | G | 10 | a0001c0001t0001g0254 a0001c0001t0001g0260 a0001c0001t0001g0261 others(7): Show |
10 | HG00738.hp1 HG02572.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1095+1483T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990004 | |||||||
| chr1:147990033 | C | T | 1 | a0001c0001t0005g0090 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1095+1512C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990033 | |||||||
| chr1:147990044 | C | G | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1095+1523C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990044 | |||||||
| chr1:147990064 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1095+1543G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990064 | |||||||
| chr1:147990099 | A | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1578A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990099 | |||||||
| chr1:147990168 | T | A | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1647T>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990168 | |||||||
| chr1:147990177 | C | G | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1095+1656C>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990177 | |||||||
| chr1:147990333 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1095+1812A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990333 | |||||||
| chr1:147990362 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0131 |
2 | HG01175.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1095+1841A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990362 | |||||||
| chr1:147990403 | G | A | 1 | a0003c0005t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1095+1882G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990403 | |||||||
| chr1:147990451 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0131 |
2 | HG01175.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1095+1930C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990451 | |||||||
| chr1:147990496 | T | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1095+1975T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990496 | |||||||
| chr1:147990591 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1096-1911T>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990591 | |||||||
| chr1:147990736 | T | C | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-1766T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990736 | |||||||
| chr1:147990806 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1696G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990806 | |||||||
| chr1:147990880 | C | T | 4 | a0001c0003t0003g0234 a0001c0003t0003g0235 a0001c0003t0003g0236 others(1): Show |
4 | HG01099.hp1 HG01109.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1096-1622C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990880 | |||||||
| chr1:147990959 | G | A | 1 | a0001c0006t0007g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1096-1543G>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147990959 | |||||||
| chr1:147991024 | T | C | 13 | a0001c0001t0001g0045 a0001c0001t0001g0105 a0001c0001t0001g0106 others(10): Show |
13 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1478T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991024 | |||||||
| chr1:147991031 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1096-1471C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991031 | |||||||
| chr1:147991057 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1096-1445A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991057 | |||||||
| chr1:147991080 | A | G | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1422A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991080 | |||||||
| chr1:147991101 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1096-1401G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991101 | |||||||
| chr1:147991120 | G | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-1382G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991120 | |||||||
| chr1:147991166 | C | T | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-1336C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991166 | |||||||
| chr1:147991183 | C | A | 12 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0001g0191 others(9): Show |
12 | HG00673.hp1 HG02080.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096-1319C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991183 | |||||||
| chr1:147991208 | C | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(36): Show |
40 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1096-1294C>A | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991208 | |||||||
| chr1:147991413 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1096-1089C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991413 | |||||||
| chr1:147991461 | C | T | 14 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(11): Show |
14 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1096-1041C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991461 | |||||||
| chr1:147991493 | A | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0099 others(10): Show |
13 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1009A>G | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991493 | |||||||
| chr1:147991494 | G | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0099 others(10): Show |
13 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1096-1008G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991494 | |||||||
| chr1:147991665 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1096-837G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991665 | |||||||
| chr1:147991666 | A | T | 1 | a0001c0001t0001g0118 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1096-836A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991666 | |||||||
| chr1:147991751 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-751A>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991751 | |||||||
| chr1:147991832 | C | T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0263 |
3 | HG02572.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1096-670C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991832 | |||||||
| chr1:147991878 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG02258.hp2 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-624T>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147991878 | |||||||
| chr1:147992390 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1096-112G>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147992390 | |||||||
| chr1:147992467 | G | C | 24 | a0001c0003t0002g0220 a0001c0003t0002g0221 a0001c0003t0002g0222 others(21): Show |
24 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.1096-35G>C | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 12/13 | chr1 | 147992467 | |||||||
| chr1:147992585 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1161+18C>T | GPR89B | ENSG00000188092.15 | transcript | ENST00000314163.12 | protein_coding | 13/13 | chr1 | 147992585 |