Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55188 |
| ensemblid | ENSG00000111785.21 |
| hgncid | 25555 |
| symbol | RIC8B |
| name | RIC8 guanine nucleotide exchange factor B |
| refseq_nuc | NM_001330145.2 |
| refseq_prot | NP_001317074.1 |
| ensembl_nuc | ENST00000392837.9 |
| ensembl_prot | ENSP00000376582.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 106774682 |
| end | 106889316 |
| strand | + |
| ver | v1.2 |
| region | chr12:106774682-106889316 |
| region5000 | chr12:106769682-106894316 |
| regionname0 | RIC8B_chr12_106774682_106889316 |
| regionname5000 | RIC8B_chr12_106769682_106894316 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 560 | 312 | 77 | 75 | 108 | 16 | 34 | 78 | RIC8B_chr12_106769682_106894316 | RIC8B | MDEER others(555): Show |
chr12 | 106769682 | 106894316 |
| a0002 | 0/0 | 560 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | MDEER others(555): Show |
chr12 | 106769682 | 106894316 |
| a0003 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | MDEER others(555): Show |
chr12 | 106769682 | 106894316 |
| a0004 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | MDEER others(555): Show |
chr12 | 106769682 | 106894316 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1680 | 302 | 72 | 74 | 105 | 16 | 33 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 | ||
| a0001c0002 | 0/0 | 1680 | 8 | 5 | 1 | 1 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 | ||
| a0001c0004 | 0/0 | 1680 | 2 | 0 | 0 | 2 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 | ||
| a0002c0003 | 0/0 | 1680 | 4 | 3 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 | ||
| a0003c0006 | 0/0 | 1680 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 | ||
| a0004c0005 | 0/0 | 1680 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | ATGGA others(1675): Show |
chr12 | 106769682 | 106894316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5048 | 131 | 8 | 42 | 57 | 9 | 13 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0002 | 0/0 | 5048 | 81 | 21 | 19 | 34 | 2 | 5 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0003 | 0/0 | 5048 | 22 | 4 | 5 | 0 | 3 | 10 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0004 | 0/0 | 5048 | 21 | 21 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0005 | 0/0 | 5048 | 13 | 6 | 3 | 0 | 2 | 2 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0006 | 0/0 | 5048 | 7 | 0 | 0 | 7 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0007 | 0/0 | 5048 | 5 | 3 | 2 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0008 | 0/0 | 5048 | 3 | 1 | 2 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0010 | 0/0 | 5048 | 3 | 3 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0011 | 0/0 | 5048 | 3 | 3 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0012 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0013 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0015 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0016 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0017 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0018 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0019 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0020 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0021 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0022 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5057): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0024 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0026 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0001t0027 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0004 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0009 | 0/0 | 5048 | 3 | 1 | 1 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0014 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0023 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0025 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0002t0028 | 0/0 | 5048 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0001c0004t0001 | 0/0 | 5048 | 2 | 0 | 0 | 2 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0002c0003t0001 | 0/0 | 5048 | 4 | 3 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0003c0006t0002 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| a0004c0005t0001 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | GCGTT others(5043): Show |
chr12 | 106769682 | 106894316 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0242 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0008g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0011g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0011g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0012g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0015g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0016g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0017g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0018g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0019g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0020g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0021g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0022g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0024g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0026g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0001t0027g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0009g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0009g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0014g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0023g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0025g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0002t0028g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0002c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0002c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0003c0006t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| a0004c0005t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | GBR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0019 | EUR | GBR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0106 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00408 | hp2 | a0001 | c0001 | t0019 | g0170 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00544 | hp2 | a0001 | c0001 | t0021 | g0232 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01071 | hp1 | a0001 | c0001 | t0022 | g0020 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0290 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0114 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01168 | hp2 | a0001 | c0001 | t0008 | g0302 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0303 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01175 | hp1 | a0001 | c0002 | t0009 | g0308 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0309 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0268 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0285 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0196 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0284 | EUR | IBS | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01884 | hp2 | a0002 | c0003 | t0001 | g0083 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0040 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0305 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0225 | EAS | CDX | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0306 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0011 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0012 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02683 | hp1 | a0001 | c0002 | t0009 | g0307 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02717 | hp1 | a0001 | c0001 | t0020 | g0178 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02738 | hp1 | a0001 | c0001 | t0012 | g0257 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0082 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0315 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | ESN | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0304 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03654 | hp1 | a0001 | c0001 | t0026 | g0198 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0287 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0286 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0316 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03834 | hp1 | a0003 | c0006 | t0002 | g0139 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | BEB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG04228 | hp2 | a0004 | c0005 | t0001 | g0221 | SAS | STU | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18522 | hp2 | a0001 | c0002 | t0028 | g0006 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18747 | hp2 | a0001 | c0001 | t0027 | g0219 | EAS | CHB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0233 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18951 | hp2 | a0001 | c0004 | t0001 | g0038 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18956 | hp2 | a0001 | c0001 | t0018 | g0200 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19030 | hp1 | a0001 | c0002 | t0014 | g0317 | AFR | LWK | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0079 | AFR | LWK | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19058 | hp1 | a0001 | c0001 | t0017 | g0160 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0094 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19085 | hp1 | a0001 | c0001 | t0016 | g0193 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | YRI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ASW | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20129 | hp2 | a0001 | c0002 | t0025 | g0297 | AFR | ASW | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA20905 | hp2 | a0001 | c0001 | t0013 | g0063 | SAS | GIH | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| HG06807 | hp2 | a0001 | c0002 | t0023 | g0300 | AFR | USA | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | LWK | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0137 | AFR | LWK | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0173 | REF | REF | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0242 | REF | REF | RIC8B_chr12_106769682_106894316 | RIC8B | chr12 | 106769682 | 106894316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106815012 | A | G | 1 | a0002 | 4 | HG01167.hp2 HG01884.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.449A>G | p.Lys150Arg | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/10 | 513/5048 | 449/1683 | 150/560 | chr12 | 106815012 | |||
| chr12:106815141 | C | T | 1 | a0003 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.578C>T | p.Thr193Met | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/10 | 642/5048 | 578/1683 | 193/560 | chr12 | 106815141 | |||
| chr12:106843921 | A | C | 1 | a0004 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1135A>C | p.Asn379His | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/10 | 1199/5048 | 1135/1683 | 379/560 | chr12 | 106843921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106825794 | T | G | 1 | a0001c0004 | 2 | HG02135.hp1 NA18951.hp2 |
synonymous_variant | LOW | c.810T>G | p.Thr270Thr | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/10 | 874/5048 | 810/1683 | 270/560 | chr12 | 106825794 | |||
| chr12:106842619 | A | G | 1 | a0001c0002 | 8 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
synonymous_variant | LOW | c.867A>G | p.Pro289Pro | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/10 | 931/5048 | 867/1683 | 289/560 | chr12 | 106842619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106774712 | G | C | 1 | a0001c0001t0012 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/10 | 34 | chr12 | 106774712 | ||||||
| chr12:106774725 | G | C | 1 | a0001c0001t0013 | 1 | NA20905.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/10 | 21 | chr12 | 106774725 | ||||||
| chr12:106886026 | T | C | 1 | a0001c0001t0006 | 7 | HG00408.hp1 HG02155.hp1 NA18948.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 11 | chr12 | 106886026 | ||||||
| chr12:106886155 | A | G | 1 | a0001c0002t0028 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 140 | chr12 | 106886155 | ||||||
| chr12:106886316 | A | G | 1 | a0001c0001t0011 | 3 | HG02257.hp2 HG02622.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*301A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 301 | chr12 | 106886316 | ||||||
| chr12:106886524 | A | C | 1 | a0001c0001t0027 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*509A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 509 | chr12 | 106886524 | ||||||
| chr12:106886751 | A | T | 1 | a0001c0001t0010 | 3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*736A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 736 | chr12 | 106886751 | ||||||
| chr12:106886917 | A | G | 1 | a0001c0001t0026 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*902A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 902 | chr12 | 106886917 | ||||||
| chr12:106886978 | T | C | 1 | a0001c0002t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*963T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 963 | chr12 | 106886978 | ||||||
| chr12:106887092 | G | A | 1 | a0001c0002t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1077 | chr12 | 106887092 | ||||||
| chr12:106887215 | T | A | 1 | a0001c0001t0015 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1200 | chr12 | 106887215 | ||||||
| chr12:106887229 | G | A | 1 | a0001c0001t0016 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1214G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1214 | chr12 | 106887229 | ||||||
| chr12:106887322 | G | C | 1 | a0001c0001t0017 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1307 | chr12 | 106887322 | ||||||
| chr12:106887323 | C | T | 1 | a0001c0001t0017 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1308C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1308 | chr12 | 106887323 | ||||||
| chr12:106887324 | T | A | 1 | a0001c0001t0017 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1309T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1309 | chr12 | 106887324 | ||||||
| chr12:106887428 | C | G | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(12): Show |
80 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1413C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1413 | chr12 | 106887428 | ||||||
| chr12:106887654 | A | G | 1 | a0001c0001t0021 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1639A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1639 | chr12 | 106887654 | ||||||
| chr12:106887674 | G | A | 2 | a0001c0001t0003 a0001c0001t0022 |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1659G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1659 | chr12 | 106887674 | ||||||
| chr12:106887896 | A | G | 1 | a0001c0001t0020 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1881A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 1881 | chr12 | 106887896 | ||||||
| chr12:106888237 | T | C | 1 | a0001c0001t0008 | 3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2222T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2222 | chr12 | 106888237 | ||||||
| chr12:106888403 | A | G | 8 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0017 others(5): Show |
88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2388A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2388 | chr12 | 106888403 | ||||||
| chr12:106888441 | T | A | 1 | a0001c0002t0023 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2426T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2426 | chr12 | 106888441 | ||||||
| chr12:106888452 | C | A | 1 | a0001c0001t0007 | 5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2437C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2437 | chr12 | 106888452 | ||||||
| chr12:106888540 | C | A | 1 | a0001c0001t0018 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2525C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2525 | chr12 | 106888540 | ||||||
| chr12:106888721 | A | G | 1 | a0001c0002t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2706 | chr12 | 106888721 | ||||||
| chr12:106888813 | C | T | 1 | a0001c0001t0019 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2798C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2798 | chr12 | 106888813 | ||||||
| chr12:106888819 | C | T | 1 | a0001c0002t0025 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2804C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2804 | chr12 | 106888819 | ||||||
| chr12:106888845 | G | A | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0010 others(2): Show |
40 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2830G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 2830 | chr12 | 106888845 | ||||||
| chr12:106889023 | G | GACTAGGT others(7): Show |
1 | a0001c0001t0022 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3009_*3022dupACTA others(10): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 3023 | INFO_REALIGN_3_PRIME | chr12 | 106889023 | |||||
| chr12:106889043 | G | C | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3028G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 3028 | chr12 | 106889043 | ||||||
| chr12:106889126 | C | T | 1 | a0001c0002t0009 | 3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3111C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 10/10 | 3111 | chr12 | 106889126 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:106774920 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.84+91C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106774920 | |||||||
| chr12:106774931 | A | T | 2 | a0001c0001t0003g0315 a0001c0001t0003g0316 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.84+102A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106774931 | |||||||
| chr12:106774962 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.84+133G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106774962 | |||||||
| chr12:106775097 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.84+268C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775097 | |||||||
| chr12:106775164 | G | C | 1 | a0001c0001t0005g0003 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84+335G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775164 | |||||||
| chr12:106775303 | A | G | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG00639.hp2 HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.84+474A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775303 | |||||||
| chr12:106775481 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84+652C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775481 | |||||||
| chr12:106775711 | T | G | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.84+882T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775711 | |||||||
| chr12:106775793 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.84+964A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106775793 | |||||||
| chr12:106776148 | T | C | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.84+1319T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776148 | |||||||
| chr12:106776344 | G | A | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84+1515G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776344 | |||||||
| chr12:106776350 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.84+1521T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776350 | |||||||
| chr12:106776567 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.84+1738C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776567 | |||||||
| chr12:106776606 | C | T | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.84+1777C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776606 | |||||||
| chr12:106776622 | C | G | 3 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 |
3 | HG02630.hp2 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.84+1793C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776622 | |||||||
| chr12:106776894 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.84+2065A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106776894 | |||||||
| chr12:106777325 | G | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.84+2496G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106777325 | |||||||
| chr12:106777482 | G | A | 6 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 others(3): Show |
6 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2653G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106777482 | |||||||
| chr12:106777547 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | NA18964.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.84+2718G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106777547 | |||||||
| chr12:106778021 | A | G | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+3192A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778021 | |||||||
| chr12:106778030 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.84+3201A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778030 | |||||||
| chr12:106778052 | G | A | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.84+3223G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778052 | |||||||
| chr12:106778134 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.84+3305C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778134 | |||||||
| chr12:106778244 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.84+3415C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778244 | |||||||
| chr12:106778247 | G | A | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+3418G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778247 | |||||||
| chr12:106778470 | T | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG01106.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.84+3641T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778470 | |||||||
| chr12:106778746 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.84+3917A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778746 | |||||||
| chr12:106778884 | A | T | 7 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(4): Show |
7 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+4055A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778884 | |||||||
| chr12:106778982 | C | G | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.84+4153C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106778982 | |||||||
| chr12:106779193 | G | A | 30 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.84+4364G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779193 | |||||||
| chr12:106779233 | A | AT | 7 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
7 | HG00280.hp1 HG01175.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+4420dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779233 | ||||||
| chr12:106779233 | AT | A | 36 | a0001c0001t0001g0036 a0001c0001t0001g0131 a0001c0001t0001g0132 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.84+4420delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779233 | ||||||
| chr12:106779443 | G | A | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-4554G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779443 | |||||||
| chr12:106779519 | A | T | 7 | a0001c0001t0001g0289 a0001c0001t0002g0284 a0001c0001t0005g0285 others(4): Show |
7 | HG00738.hp1 HG01099.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-4478A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779519 | |||||||
| chr12:106779570 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.85-4427G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779570 | |||||||
| chr12:106779660 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85-4337C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779660 | |||||||
| chr12:106779681 | A | AT | 17 | a0001c0001t0001g0132 a0001c0001t0001g0280 a0001c0001t0002g0279 others(14): Show |
17 | HG01099.hp2 HG01167.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.85-4299dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779681 | ||||||
| chr12:106779681 | A | ATT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(73): Show |
77 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.85-4300_85-4299dup others(2): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779681 | ||||||
| chr12:106779681 | A | ATTT | 11 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
11 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.85-4301_85-4299dup others(3): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779681 | ||||||
| chr12:106779681 | A | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0004g0110 |
3 | HG03209.hp2 NA19057.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.85-4316A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779681 | |||||||
| chr12:106779681 | AT | A | 17 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0002g0134 others(14): Show |
17 | HG01069.hp1 HG01069.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.85-4299delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779681 | ||||||
| chr12:106779683 | T | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-4314T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779683 | |||||||
| chr12:106779702 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.85-4295A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779702 | |||||||
| chr12:106779742 | A | C | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.85-4255A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779742 | |||||||
| chr12:106779856 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.85-4141C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779856 | |||||||
| chr12:106779856 | CGG | C | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-4137_85-4136del others(2): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779856 | ||||||
| chr12:106779868 | C | CT | 7 | a0001c0001t0001g0131 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-4108dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779868 | ||||||
| chr12:106779868 | CT | C | 13 | a0001c0001t0001g0121 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
13 | HG00741.hp2 HG01255.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.85-4108delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779868 | ||||||
| chr12:106779868 | CTT | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0138 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.85-4109_85-4108del others(2): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779868 | ||||||
| chr12:106779868 | CTTTT | C | 43 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(40): Show |
43 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.85-4111_85-4108del others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779868 | ||||||
| chr12:106779886 | TTTTG | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(72): Show |
76 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.85-4109_85-4106del others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779886 | ||||||
| chr12:106779888 | T | G | 9 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0133 others(6): Show |
9 | HG01943.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-4109T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779888 | |||||||
| chr12:106779888 | TTGTG | T | 73 | a0001c0001t0001g0180 a0001c0001t0001g0241 a0001c0001t0002g0135 others(70): Show |
73 | HG00673.hp2 HG01074.hp1 HG01081.hp1 others(70): Show |
intron_variant | MODIFIER | c.85-4093_85-4090del others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106779888 | ||||||
| chr12:106779892 | G | T | 3 | a0001c0002t0004g0305 a0001c0002t0009g0308 a0001c0002t0014g0317 |
3 | HG01175.hp1 HG02027.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.85-4105G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106779892 | |||||||
| chr12:106780010 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.85-3987T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780010 | |||||||
| chr12:106780560 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0149 |
2 | NA19056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.85-3437T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780560 | |||||||
| chr12:106780575 | A | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.85-3422A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780575 | |||||||
| chr12:106780760 | G | A | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.85-3237G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780760 | |||||||
| chr12:106780778 | A | G | 1 | a0001c0001t0004g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.85-3219A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780778 | |||||||
| chr12:106780868 | A | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(90): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.85-3129A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106780868 | |||||||
| chr12:106780915 | ATAGG | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.85-3078_85-3075del others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106780915 | ||||||
| chr12:106781760 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.85-2237G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106781760 | |||||||
| chr12:106781959 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.85-2038G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106781959 | |||||||
| chr12:106782039 | TATCTATT others(159): Show |
T | 1 | a0001c0001t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.85-1957_85-1792del | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782039 | |||||||
| chr12:106782048 | A | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.85-1949A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782048 | |||||||
| chr12:106782206 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.85-1791T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782206 | |||||||
| chr12:106782208 | T | A | 1 | a0001c0001t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.85-1789T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782208 | |||||||
| chr12:106782303 | C | CTTTTGTT others(159): Show |
1 | a0001c0001t0002g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.85-1693_85-1692ins others(166): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr12 | 106782303 | ||||||
| chr12:106782607 | G | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
6 | HG00673.hp1 HG02135.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-1390G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782607 | |||||||
| chr12:106782615 | T | C | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.85-1382T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782615 | |||||||
| chr12:106782674 | TC | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-1322delC | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106782674 | |||||||
| chr12:106783202 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.85-795A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106783202 | |||||||
| chr12:106783239 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG01346.hp1 HG01361.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.85-758T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106783239 | |||||||
| chr12:106783587 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.85-410G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106783587 | |||||||
| chr12:106783712 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.85-285G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106783712 | |||||||
| chr12:106783886 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.85-111C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 1/9 | chr12 | 106783886 | |||||||
| chr12:106784370 | T | G | 4 | a0001c0001t0002g0134 a0001c0001t0002g0158 a0001c0001t0002g0159 others(1): Show |
4 | NA18950.hp1 NA18951.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+326T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784370 | |||||||
| chr12:106784497 | A | T | 1 | a0001c0001t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.132+453A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784497 | |||||||
| chr12:106784552 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.132+508G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784552 | |||||||
| chr12:106784579 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0015g0094 |
2 | NA19062.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.132+535A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784579 | |||||||
| chr12:106784875 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(73): Show |
77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.132+831A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784875 | |||||||
| chr12:106784911 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+867C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106784911 | |||||||
| chr12:106785069 | A | G | 1 | a0001c0001t0004g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.132+1025A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785069 | |||||||
| chr12:106785263 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.132+1219C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785263 | |||||||
| chr12:106785439 | T | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1395T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785439 | |||||||
| chr12:106785563 | A | AT | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132+1520dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785563 | ||||||
| chr12:106785753 | T | TGGGAGGT others(73): Show |
1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+1770_132+1771i others(82): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785753 | ||||||
| chr12:106785785 | G | GTC | 3 | a0001c0001t0004g0111 a0001c0001t0004g0161 a0001c0001t0004g0162 |
3 | HG02145.hp1 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.132+1769_132+1770d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTC | 4 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0011g0011 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1767_132+1770d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTC | 5 | a0001c0001t0001g0091 a0001c0001t0001g0108 a0001c0001t0004g0110 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1765_132+1770d others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(3): Show |
13 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0086 others(10): Show |
14 | HG00280.hp2 HG01168.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.132+1761_132+1770d others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(5): Show |
16 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0080 others(13): Show |
16 | HG01167.hp2 HG01175.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+1759_132+1770d others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(7): Show |
19 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.132+1757_132+1770d others(16): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(9): Show |
16 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0046 others(13): Show |
16 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+1755_132+1770d others(18): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(11): Show |
11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
11 | HG01243.hp1 HG02074.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.132+1753_132+1770d others(20): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(13): Show |
10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0066 others(7): Show |
10 | HG00733.hp1 HG01070.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+1751_132+1770d others(22): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(35): Show |
1 | a0001c0002t0009g0306 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.132+1761_132+1762i others(44): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(41): Show |
1 | a0001c0002t0009g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.132+1761_132+1762i others(50): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(15): Show |
7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0095 others(4): Show |
7 | HG02486.hp1 HG02818.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+1749_132+1770d others(24): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(17): Show |
3 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0013g0063 |
3 | HG00099.hp1 HG02922.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.132+1747_132+1770d others(26): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(19): Show |
2 | a0001c0001t0001g0062 a0001c0001t0003g0013 |
2 | HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.132+1745_132+1770d others(28): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(21): Show |
5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(2): Show |
5 | HG00140.hp1 HG00642.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+1743_132+1770d others(30): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(23): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0003g0008 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.132+1770_132+1771i others(32): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(25): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0014 |
2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.132+1770_132+1771i others(34): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785785 | G | GTCTCTCT others(29): Show |
1 | a0001c0002t0009g0307 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.132+1770_132+1771i others(38): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785785 | ||||||
| chr12:106785809 | CTCTCTG | C | 5 | a0001c0001t0001g0130 a0001c0001t0002g0262 a0001c0001t0002g0263 others(2): Show |
5 | HG00673.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+1767_132+1772d others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785809 | ||||||
| chr12:106785813 | CTG | C | 136 | a0001c0001t0001g0121 a0001c0001t0001g0129 a0001c0001t0001g0131 others(133): Show |
136 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.132+1803_132+1804d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785813 | ||||||
| chr12:106785813 | CTGTG | C | 4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0006g0109 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1801_132+1804d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785813 | ||||||
| chr12:106785813 | CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+1795_132+1804d others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785813 | ||||||
| chr12:106785813 | CTGTGTGT others(5): Show |
C | 2 | a0001c0001t0001g0276 a0001c0001t0002g0217 |
2 | HG00741.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.132+1793_132+1804d others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106785813 | ||||||
| chr12:106785815 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(131): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.132+1771G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785815 | |||||||
| chr12:106785817 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(143): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.132+1773G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785817 | |||||||
| chr12:106785819 | G | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.132+1775G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785819 | |||||||
| chr12:106785821 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.132+1777G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785821 | |||||||
| chr12:106785823 | G | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(17): Show |
21 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.132+1779G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785823 | |||||||
| chr12:106785825 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0004g0128 a0001c0002t0004g0305 |
3 | HG02027.hp1 HG02109.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.132+1781G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785825 | |||||||
| chr12:106785827 | G | C | 2 | a0001c0001t0001g0108 a0001c0002t0004g0305 |
2 | HG02027.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.132+1783G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785827 | |||||||
| chr12:106785829 | G | C | 2 | a0001c0001t0001g0108 a0001c0002t0004g0305 |
2 | HG02027.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.132+1785G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785829 | |||||||
| chr12:106785831 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.132+1787G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785831 | |||||||
| chr12:106785862 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.132+1818A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106785862 | |||||||
| chr12:106786005 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0022g0020 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.132+1961C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786005 | |||||||
| chr12:106786007 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.132+1963C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786007 | |||||||
| chr12:106786007 | C | T | 1 | a0001c0001t0002g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.132+1963C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786007 | |||||||
| chr12:106786026 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+1982T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786026 | |||||||
| chr12:106786027 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0071 |
2 | NA18959.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.132+1983T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786027 | |||||||
| chr12:106786035 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+1991C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786035 | |||||||
| chr12:106786141 | A | AT | 66 | a0001c0001t0001g0036 a0001c0001t0001g0056 a0001c0001t0001g0057 others(63): Show |
66 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.132+2123dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106786141 | ||||||
| chr12:106786141 | AT | A | 18 | a0001c0001t0001g0041 a0001c0001t0001g0075 a0001c0001t0001g0175 others(15): Show |
18 | HG01070.hp1 HG01070.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.132+2123delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106786141 | ||||||
| chr12:106786291 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.132+2247A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786291 | |||||||
| chr12:106786439 | G | A | 8 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.132+2395G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786439 | |||||||
| chr12:106786921 | T | C | 3 | a0001c0001t0004g0179 a0001c0001t0004g0252 a0001c0001t0020g0178 |
3 | HG02572.hp1 HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.132+2877T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106786921 | |||||||
| chr12:106787031 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+2987A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787031 | |||||||
| chr12:106787058 | G | A | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+3014G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787058 | |||||||
| chr12:106787326 | T | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+3282T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787326 | |||||||
| chr12:106787518 | T | G | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+3474T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787518 | |||||||
| chr12:106787728 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0081 others(7): Show |
11 | HG00280.hp2 HG02523.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.132+3684C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787728 | |||||||
| chr12:106787788 | C | T | 2 | a0001c0001t0001g0157 a0001c0002t0014g0317 |
2 | HG01346.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.132+3744C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787788 | |||||||
| chr12:106787921 | C | A | 1 | a0001c0001t0005g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.132+3877C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787921 | |||||||
| chr12:106787930 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.132+3886T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106787930 | |||||||
| chr12:106788241 | T | C | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+4197T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788241 | |||||||
| chr12:106788253 | C | A | 2 | a0001c0001t0011g0011 a0001c0001t0011g0012 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.132+4209C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788253 | |||||||
| chr12:106788256 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.132+4212C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788256 | |||||||
| chr12:106788307 | G | C | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+4263G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788307 | |||||||
| chr12:106788357 | A | G | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+4313A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788357 | |||||||
| chr12:106788458 | C | T | 7 | a0001c0001t0002g0145 a0001c0001t0002g0246 a0001c0001t0002g0247 others(4): Show |
7 | HG01123.hp1 HG01433.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.132+4414C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788458 | |||||||
| chr12:106788474 | T | C | 1 | a0001c0001t0002g0292 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.132+4430T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788474 | |||||||
| chr12:106788500 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+4456G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106788500 | |||||||
| chr12:106789064 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+5020C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789064 | |||||||
| chr12:106789077 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.132+5033C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789077 | |||||||
| chr12:106789187 | C | G | 1 | a0001c0001t0001g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.132+5143C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789187 | |||||||
| chr12:106789200 | C | T | 2 | a0001c0001t0003g0315 a0001c0001t0003g0316 |
2 | HG03017.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.132+5156C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789200 | |||||||
| chr12:106789437 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+5393A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789437 | |||||||
| chr12:106789446 | C | T | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+5402C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789446 | |||||||
| chr12:106789451 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(46): Show |
50 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.132+5407A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789451 | |||||||
| chr12:106789487 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG01123.hp2 HG01516.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+5443T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789487 | |||||||
| chr12:106789523 | C | T | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.132+5479C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789523 | |||||||
| chr12:106789651 | A | G | 3 | a0001c0001t0004g0179 a0001c0001t0004g0252 a0001c0001t0020g0178 |
3 | HG02572.hp1 HG02717.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.132+5607A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789651 | |||||||
| chr12:106789811 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.132+5767G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789811 | |||||||
| chr12:106789819 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+5775G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789819 | |||||||
| chr12:106789929 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(93): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.132+5898dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106789929 | ||||||
| chr12:106789929 | C | CAA | 32 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(29): Show |
32 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+5897_132+5898d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106789929 | ||||||
| chr12:106789929 | C | CG | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+5885_132+5886i others(3): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106789929 | |||||||
| chr12:106790171 | A | C | 4 | a0001c0001t0006g0104 a0001c0001t0006g0105 a0001c0001t0006g0106 others(1): Show |
4 | HG00408.hp1 NA18967.hp2 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+6127A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790171 | |||||||
| chr12:106790249 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.132+6205A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790249 | |||||||
| chr12:106790261 | G | C | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.132+6217G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790261 | |||||||
| chr12:106790322 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+6278G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790322 | |||||||
| chr12:106790450 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.132+6406T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790450 | |||||||
| chr12:106790584 | G | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+6540G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790584 | |||||||
| chr12:106790585 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.132+6541T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106790585 | |||||||
| chr12:106791009 | T | C | 1 | a0003c0006t0002g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.132+6965T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791009 | |||||||
| chr12:106791060 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+7016C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791060 | |||||||
| chr12:106791163 | A | G | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+7119A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791163 | |||||||
| chr12:106791198 | C | T | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.132+7154C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791198 | |||||||
| chr12:106791322 | A | G | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+7278A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791322 | |||||||
| chr12:106791347 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.132+7303G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791347 | |||||||
| chr12:106791406 | A | T | 1 | a0001c0001t0002g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.132+7362A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791406 | |||||||
| chr12:106791409 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(79): Show |
83 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.132+7365G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791409 | |||||||
| chr12:106791440 | T | G | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+7396T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791440 | |||||||
| chr12:106791486 | G | A | 4 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 others(1): Show |
4 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+7442G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791486 | |||||||
| chr12:106791534 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+7490C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791534 | |||||||
| chr12:106791540 | A | G | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132+7496A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791540 | |||||||
| chr12:106791545 | G | A | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132+7501G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791545 | |||||||
| chr12:106791631 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.132+7587A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791631 | |||||||
| chr12:106791705 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.132+7661C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791705 | |||||||
| chr12:106791799 | T | C | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.132+7755T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106791799 | |||||||
| chr12:106792027 | C | G | 2 | a0001c0001t0004g0126 a0001c0001t0004g0127 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.132+7983C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792027 | |||||||
| chr12:106792116 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.132+8072C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792116 | |||||||
| chr12:106792203 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(311): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.132+8159G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792203 | |||||||
| chr12:106792237 | T | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+8193T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792237 | |||||||
| chr12:106792470 | A | G | 2 | a0001c0001t0002g0138 a0001c0002t0025g0297 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.132+8426A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792470 | |||||||
| chr12:106792671 | C | G | 1 | a0002c0003t0001g0039 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.132+8627C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792671 | |||||||
| chr12:106792760 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.132+8716C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792760 | |||||||
| chr12:106792893 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.132+8849T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792893 | |||||||
| chr12:106792969 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(79): Show |
83 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.132+8925G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106792969 | |||||||
| chr12:106793011 | C | G | 1 | a0001c0001t0004g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132+8967C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793011 | |||||||
| chr12:106793051 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0253 |
2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.132+9007G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793051 | |||||||
| chr12:106793152 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.132+9108C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793152 | |||||||
| chr12:106793206 | A | G | 1 | a0001c0001t0005g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.132+9162A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793206 | |||||||
| chr12:106793347 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.132+9303A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793347 | |||||||
| chr12:106793563 | C | G | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.132+9519C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793563 | |||||||
| chr12:106793634 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00639.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+9590A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793634 | |||||||
| chr12:106793682 | AAGTC | A | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132+9641_132+9644d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106793682 | ||||||
| chr12:106793768 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.132+9724G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793768 | |||||||
| chr12:106793968 | G | A | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.132+9924G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106793968 | |||||||
| chr12:106794002 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(217): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.132+9958G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794002 | |||||||
| chr12:106794066 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.132+10022A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794066 | |||||||
| chr12:106794472 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.132+10428A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794472 | |||||||
| chr12:106794610 | G | A | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+10566G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794610 | |||||||
| chr12:106794677 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+10633A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794677 | |||||||
| chr12:106794936 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+10892C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794936 | |||||||
| chr12:106794937 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0253 |
2 | NA18975.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.132+10893G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794937 | |||||||
| chr12:106794963 | C | A | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.132+10919C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106794963 | |||||||
| chr12:106795133 | A | G | 32 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.132+11089A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106795133 | |||||||
| chr12:106795166 | A | G | 1 | a0001c0001t0002g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.132+11122A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106795166 | |||||||
| chr12:106795581 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.132+11537A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106795581 | |||||||
| chr12:106795746 | A | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0290 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.132+11702A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106795746 | |||||||
| chr12:106796060 | T | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.132+12016T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796060 | |||||||
| chr12:106796099 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+12055C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796099 | |||||||
| chr12:106796152 | T | G | 29 | a0001c0001t0001g0141 a0001c0001t0002g0140 a0001c0001t0002g0163 others(26): Show |
29 | HG00741.hp2 HG01074.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.132+12108T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796152 | |||||||
| chr12:106796292 | C | T | 1 | a0001c0001t0002g0251 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.132+12248C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796292 | |||||||
| chr12:106796335 | C | T | 3 | a0001c0001t0002g0251 a0001c0002t0023g0300 a0001c0002t0028g0006 |
3 | HG00544.hp1 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+12291C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796335 | |||||||
| chr12:106796369 | C | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.132+12325C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796369 | |||||||
| chr12:106796401 | T | C | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.132+12357T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796401 | |||||||
| chr12:106796821 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+12777A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106796821 | |||||||
| chr12:106797040 | C | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+12996C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797040 | |||||||
| chr12:106797371 | A | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.132+13327A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797371 | |||||||
| chr12:106797527 | T | C | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+13483T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797527 | |||||||
| chr12:106797536 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(44): Show |
48 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.132+13492T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797536 | |||||||
| chr12:106797557 | G | A | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.132+13513G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797557 | |||||||
| chr12:106797589 | A | T | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.132+13545A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797589 | |||||||
| chr12:106797724 | G | A | 23 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.132+13680G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797724 | |||||||
| chr12:106797787 | A | G | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+13743A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797787 | |||||||
| chr12:106797829 | G | A | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.132+13785G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797829 | |||||||
| chr12:106797880 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.132+13836C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797880 | |||||||
| chr12:106797888 | C | T | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.132+13844C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797888 | |||||||
| chr12:106797901 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.132+13857G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797901 | |||||||
| chr12:106797952 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+13908G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106797952 | |||||||
| chr12:106798093 | A | G | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.132+14049A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798093 | |||||||
| chr12:106798237 | T | C | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.132+14193T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798237 | |||||||
| chr12:106798304 | G | A | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.132+14260G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798304 | |||||||
| chr12:106798317 | T | A | 4 | a0001c0001t0002g0199 a0001c0001t0002g0281 a0001c0001t0002g0282 others(1): Show |
4 | NA18956.hp2 NA18989.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+14273T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798317 | |||||||
| chr12:106798330 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.132+14286C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798330 | |||||||
| chr12:106798824 | A | C | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+14780A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798824 | |||||||
| chr12:106798965 | C | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0058 |
2 | HG00639.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.132+14921C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106798965 | |||||||
| chr12:106799087 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.132+15043A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799087 | |||||||
| chr12:106799089 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.132+15045A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799089 | |||||||
| chr12:106799322 | C | A | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.132+15278C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799322 | |||||||
| chr12:106799459 | T | TCAAGTGA | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-15237_133-1523 others(11): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799459 | |||||||
| chr12:106799460 | G | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-15236G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799460 | |||||||
| chr12:106799461 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-15235C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799461 | |||||||
| chr12:106799462 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-15234C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799462 | |||||||
| chr12:106799532 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-15164A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799532 | |||||||
| chr12:106799745 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.133-14951C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799745 | |||||||
| chr12:106799852 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.133-14844C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799852 | |||||||
| chr12:106799886 | C | T | 1 | a0001c0001t0002g0271 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.133-14810C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106799886 | |||||||
| chr12:106800058 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.133-14638T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800058 | |||||||
| chr12:106800277 | C | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-14419C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800277 | |||||||
| chr12:106800354 | GAA | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(79): Show |
83 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.133-14341_133-1434 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800354 | |||||||
| chr12:106800474 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.133-14222C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800474 | |||||||
| chr12:106800683 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.133-14013G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800683 | |||||||
| chr12:106800744 | G | C | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.133-13952G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800744 | |||||||
| chr12:106800802 | G | A | 32 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(29): Show |
32 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.133-13894G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800802 | |||||||
| chr12:106800808 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-13888A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800808 | |||||||
| chr12:106800998 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.133-13698T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106800998 | |||||||
| chr12:106801044 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-13652C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801044 | |||||||
| chr12:106801392 | A | G | 7 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(4): Show |
7 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-13304A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801392 | |||||||
| chr12:106801510 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133-13186A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801510 | |||||||
| chr12:106801572 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-13124T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801572 | |||||||
| chr12:106801786 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-12910G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801786 | |||||||
| chr12:106801913 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.133-12783T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106801913 | |||||||
| chr12:106802025 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.133-12671T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802025 | |||||||
| chr12:106802054 | T | C | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.133-12642T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802054 | |||||||
| chr12:106802151 | C | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.133-12545C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802151 | |||||||
| chr12:106802490 | G | A | 1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.133-12206G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802490 | |||||||
| chr12:106802534 | A | AT | 12 | a0001c0001t0001g0260 a0001c0001t0001g0280 a0001c0001t0001g0289 others(9): Show |
12 | HG00597.hp2 HG01255.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-12135dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106802534 | ||||||
| chr12:106802534 | A | T | 1 | a0001c0001t0007g0117 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.133-12162A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802534 | |||||||
| chr12:106802534 | AT | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(59): Show |
63 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.133-12135delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106802534 | ||||||
| chr12:106802534 | ATT | A | 71 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(68): Show |
71 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-12136_133-1213 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106802534 | ||||||
| chr12:106802534 | ATTTTTTT others(3): Show |
A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-12144_133-1213 others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106802534 | ||||||
| chr12:106802651 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | NA18964.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.133-12045C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106802651 | |||||||
| chr12:106803047 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.133-11649T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803047 | |||||||
| chr12:106803061 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.133-11635A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803061 | |||||||
| chr12:106803118 | A | G | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.133-11578A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803118 | |||||||
| chr12:106803137 | C | T | 34 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.133-11559C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803137 | |||||||
| chr12:106803214 | T | TA | 3 | a0001c0001t0003g0029 a0001c0001t0010g0033 a0001c0001t0010g0034 |
3 | HG02896.hp1 HG02897.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.133-11482_133-1148 others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAA | 22 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAAA | 6 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0030 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(7): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAAAAA | 10 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0001g0095 others(7): Show |
10 | HG00280.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(9): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAAAAAA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0046 others(52): Show |
56 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(10): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAAAAAAA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0041 others(17): Show |
20 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(11): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | T | TAAAAAAA others(1): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | HG00733.hp1 HG00735.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-11482_133-1148 others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803214 | TCAAAAAA | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-11481_133-1147 others(11): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803214 | |||||||
| chr12:106803215 | C | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(118): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.133-11481C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803215 | |||||||
| chr12:106803215 | C | CA | 11 | a0001c0001t0001g0153 a0001c0001t0001g0240 a0001c0001t0001g0272 others(8): Show |
11 | HG00673.hp1 HG01109.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-11458dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106803215 | ||||||
| chr12:106803215 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.133-11468_133-1145 others(15): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106803215 | ||||||
| chr12:106803215 | C | CAAAAAAA others(8): Show |
2 | a0001c0002t0009g0306 a0001c0002t0009g0307 |
2 | HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.133-11472_133-1145 others(19): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106803215 | ||||||
| chr12:106803215 | C | CAAAAAAA others(9): Show |
1 | a0001c0002t0009g0308 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.133-11473_133-1145 others(20): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106803215 | ||||||
| chr12:106803215 | CA | C | 6 | a0001c0001t0002g0195 a0001c0001t0002g0197 a0001c0001t0002g0238 others(3): Show |
6 | HG02273.hp1 HG02615.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-11458delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106803215 | ||||||
| chr12:106803441 | G | A | 3 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0007g0040 |
3 | HG01943.hp2 HG03017.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.133-11255G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803441 | |||||||
| chr12:106803656 | C | T | 1 | a0001c0001t0002g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.133-11040C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803656 | |||||||
| chr12:106803724 | C | G | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-10972C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803724 | |||||||
| chr12:106803888 | C | T | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-10808C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106803888 | |||||||
| chr12:106804085 | A | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133-10611A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804085 | |||||||
| chr12:106804219 | C | CT | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(125): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.133-10464dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106804219 | ||||||
| chr12:106804254 | G | A | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-10442G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804254 | |||||||
| chr12:106804256 | C | T | 7 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(4): Show |
7 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.133-10440C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804256 | |||||||
| chr12:106804402 | A | G | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-10294A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804402 | |||||||
| chr12:106804458 | C | T | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.133-10238C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804458 | |||||||
| chr12:106804459 | G | A | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.133-10237G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804459 | |||||||
| chr12:106804511 | A | G | 1 | a0001c0002t0009g0306 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.133-10185A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804511 | |||||||
| chr12:106804564 | G | A | 4 | a0001c0001t0002g0150 a0001c0001t0002g0167 a0001c0001t0002g0168 others(1): Show |
4 | HG00597.hp2 HG02074.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-10132G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804564 | |||||||
| chr12:106804589 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133-10107G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804589 | |||||||
| chr12:106804657 | T | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(298): Show |
302 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.133-10039T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804657 | |||||||
| chr12:106804725 | A | G | 1 | a0001c0001t0006g0233 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.133-9971A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804725 | |||||||
| chr12:106804833 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(146): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.133-9863G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804833 | |||||||
| chr12:106804870 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-9826G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804870 | |||||||
| chr12:106804892 | G | A | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133-9804G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106804892 | |||||||
| chr12:106805149 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.133-9547G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106805149 | |||||||
| chr12:106805364 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(96): Show |
100 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.133-9332G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106805364 | |||||||
| chr12:106805506 | C | A | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.133-9190C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106805506 | |||||||
| chr12:106805758 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.133-8938C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106805758 | |||||||
| chr12:106805848 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.133-8848A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106805848 | |||||||
| chr12:106806003 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.133-8693G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806003 | |||||||
| chr12:106806012 | C | T | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-8684C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806012 | |||||||
| chr12:106806110 | C | T | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.133-8586C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806110 | |||||||
| chr12:106806175 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.133-8521G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806175 | |||||||
| chr12:106806278 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(130): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.133-8418C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806278 | |||||||
| chr12:106806290 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(74): Show |
78 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.133-8406C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806290 | |||||||
| chr12:106806346 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(2): Show |
5 | HG01346.hp1 HG01361.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-8350A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806346 | |||||||
| chr12:106806567 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.133-8129C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806567 | |||||||
| chr12:106806704 | C | G | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-7992C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806704 | |||||||
| chr12:106806761 | C | T | 1 | a0001c0001t0021g0232 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.133-7935C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106806761 | |||||||
| chr12:106807119 | C | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.133-7577C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106807119 | |||||||
| chr12:106807214 | A | G | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.133-7482A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106807214 | |||||||
| chr12:106807271 | C | A | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-7425C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106807271 | |||||||
| chr12:106807711 | C | T | 47 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0145 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.133-6985C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106807711 | |||||||
| chr12:106807735 | TA | T | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.133-6960delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106807735 | |||||||
| chr12:106808072 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-6624G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808072 | |||||||
| chr12:106808084 | CA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(126): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.133-6595delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106808084 | ||||||
| chr12:106808095 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-6601A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808095 | |||||||
| chr12:106808335 | T | C | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.133-6361T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808335 | |||||||
| chr12:106808460 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133-6236G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808460 | |||||||
| chr12:106808465 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133-6231G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808465 | |||||||
| chr12:106808484 | A | G | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.133-6212A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808484 | |||||||
| chr12:106808564 | T | G | 1 | a0001c0001t0003g0023 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.133-6132T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808564 | |||||||
| chr12:106808793 | A | G | 2 | a0001c0001t0003g0019 a0001c0002t0004g0305 |
2 | HG00140.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.133-5903A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808793 | |||||||
| chr12:106808880 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133-5816A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106808880 | |||||||
| chr12:106809049 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133-5647G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809049 | |||||||
| chr12:106809106 | G | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-5590G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809106 | |||||||
| chr12:106809168 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-5528T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809168 | |||||||
| chr12:106809197 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.133-5499A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809197 | |||||||
| chr12:106809221 | G | A | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.133-5475G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809221 | |||||||
| chr12:106809476 | T | C | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.133-5220T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809476 | |||||||
| chr12:106809522 | C | CA | 15 | a0001c0001t0001g0142 a0001c0001t0001g0241 a0001c0001t0002g0140 others(12): Show |
15 | HG00738.hp1 HG01099.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-5151dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106809522 | ||||||
| chr12:106809522 | CA | C | 11 | a0001c0001t0001g0092 a0001c0001t0001g0133 a0001c0001t0001g0276 others(8): Show |
11 | HG01168.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.133-5151delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106809522 | ||||||
| chr12:106809522 | CAAAAAAA others(3): Show |
C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.133-5160_133-5151d others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106809522 | ||||||
| chr12:106809682 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.133-5014T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809682 | |||||||
| chr12:106809687 | C | CA | 35 | a0001c0001t0002g0138 a0001c0001t0003g0007 a0001c0001t0003g0008 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.133-4999dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106809687 | ||||||
| chr12:106809905 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.133-4791G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809905 | |||||||
| chr12:106809912 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.133-4784T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106809912 | |||||||
| chr12:106810024 | ATATTTAT | A | 12 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(9): Show |
12 | HG01109.hp2 HG02027.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-4649_133-4643d others(9): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106810024 | ||||||
| chr12:106810089 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-4607T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810089 | |||||||
| chr12:106810114 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.133-4582C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810114 | |||||||
| chr12:106810156 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.133-4526dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106810156 | ||||||
| chr12:106810290 | T | TA | 48 | a0001c0001t0001g0146 a0001c0001t0001g0215 a0001c0001t0001g0216 others(45): Show |
48 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.133-4391dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106810290 | ||||||
| chr12:106810352 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.133-4344G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810352 | |||||||
| chr12:106810355 | C | G | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.133-4341C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810355 | |||||||
| chr12:106810466 | C | T | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.133-4230C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810466 | |||||||
| chr12:106810510 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-4186G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810510 | |||||||
| chr12:106810560 | T | A | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.133-4136T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810560 | |||||||
| chr12:106810653 | A | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.133-4043A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810653 | |||||||
| chr12:106810744 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.133-3952A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810744 | |||||||
| chr12:106810762 | A | G | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.133-3934A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106810762 | |||||||
| chr12:106811169 | T | G | 5 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.133-3527T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811169 | |||||||
| chr12:106811291 | G | A | 1 | a0001c0001t0024g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.133-3405G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811291 | |||||||
| chr12:106811612 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(81): Show |
85 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.133-3084A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811612 | |||||||
| chr12:106811635 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.133-3061T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811635 | |||||||
| chr12:106811678 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | HG01256.hp1 HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.133-3018G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811678 | |||||||
| chr12:106811699 | A | T | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.133-2997A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811699 | |||||||
| chr12:106811738 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.133-2958G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811738 | |||||||
| chr12:106811790 | GGAGAGCA others(16): Show |
G | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.133-2902_133-2880d others(25): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106811790 | ||||||
| chr12:106811975 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(123): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.133-2721A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106811975 | |||||||
| chr12:106812044 | TA | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(120): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.133-2651delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106812044 | |||||||
| chr12:106812092 | G | A | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.133-2604G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106812092 | |||||||
| chr12:106812445 | G | GT | 7 | a0001c0001t0001g0154 a0001c0001t0004g0123 a0001c0001t0004g0124 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-2238dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106812445 | ||||||
| chr12:106812445 | GT | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0037 others(80): Show |
84 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.133-2238delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106812445 | ||||||
| chr12:106812458 | T | TA | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.133-2236dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106812458 | ||||||
| chr12:106812774 | A | G | 1 | a0001c0001t0003g0315 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.133-1922A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106812774 | |||||||
| chr12:106812801 | A | C | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.133-1895A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106812801 | |||||||
| chr12:106813033 | A | G | 3 | a0001c0001t0002g0262 a0001c0001t0002g0263 a0001c0001t0002g0265 |
3 | HG02572.hp2 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.133-1663A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813033 | |||||||
| chr12:106813187 | C | CT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(119): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.133-1487dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106813187 | ||||||
| chr12:106813187 | C | CTT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0049 others(7): Show |
10 | HG01952.hp2 HG02056.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.133-1488_133-1487d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106813187 | ||||||
| chr12:106813187 | C | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-1509C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813187 | |||||||
| chr12:106813187 | CT | C | 9 | a0001c0001t0001g0132 a0001c0001t0004g0123 a0001c0001t0004g0124 others(6): Show |
9 | HG01169.hp2 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.133-1487delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr12 | 106813187 | ||||||
| chr12:106813337 | C | T | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133-1359C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813337 | |||||||
| chr12:106813432 | C | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0018g0200 |
3 | NA18956.hp2 NA19057.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.133-1264C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813432 | |||||||
| chr12:106813469 | C | T | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.133-1227C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813469 | |||||||
| chr12:106813534 | A | G | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.133-1162A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813534 | |||||||
| chr12:106813579 | G | A | 12 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(9): Show |
12 | HG01109.hp2 HG01943.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-1117G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813579 | |||||||
| chr12:106813801 | GTT | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.133-894_133-893del others(2): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813801 | |||||||
| chr12:106813811 | C | A | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.133-885C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813811 | |||||||
| chr12:106813989 | T | G | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0195 |
3 | NA18942.hp2 NA18970.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.133-707T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106813989 | |||||||
| chr12:106814050 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133-646A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814050 | |||||||
| chr12:106814058 | A | G | 1 | a0001c0001t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.133-638A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814058 | |||||||
| chr12:106814354 | A | G | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.133-342A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814354 | |||||||
| chr12:106814469 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133-227C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814469 | |||||||
| chr12:106814517 | G | C | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0195 |
3 | NA18942.hp2 NA18970.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.133-179G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814517 | |||||||
| chr12:106814525 | T | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.133-171T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 2/9 | chr12 | 106814525 | |||||||
| chr12:106815556 | G | C | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.741+252G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106815556 | |||||||
| chr12:106815691 | T | A | 2 | a0001c0001t0002g0284 a0001c0001t0005g0285 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.741+387T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106815691 | |||||||
| chr12:106816179 | AT | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(98): Show |
102 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.741+880delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106816179 | ||||||
| chr12:106816284 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.741+980A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816284 | |||||||
| chr12:106816322 | G | C | 1 | a0001c0001t0004g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741+1018G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816322 | |||||||
| chr12:106816451 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.741+1147A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816451 | |||||||
| chr12:106816463 | G | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.741+1159G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816463 | |||||||
| chr12:106816480 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.741+1176C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816480 | |||||||
| chr12:106816608 | C | A | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+1304C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816608 | |||||||
| chr12:106816616 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+1312C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816616 | |||||||
| chr12:106816675 | A | G | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.741+1371A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816675 | |||||||
| chr12:106816903 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.741+1599T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106816903 | |||||||
| chr12:106817128 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.741+1824C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106817128 | |||||||
| chr12:106817416 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.741+2112G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106817416 | |||||||
| chr12:106817537 | C | T | 1 | a0001c0001t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.741+2233C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106817537 | |||||||
| chr12:106817547 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.741+2243T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106817547 | |||||||
| chr12:106817824 | C | CA | 101 | a0001c0001t0001g0146 a0001c0001t0001g0154 a0001c0001t0001g0216 others(98): Show |
101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.741+2539dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106817824 | ||||||
| chr12:106817824 | C | CAA | 20 | a0001c0001t0002g0150 a0001c0001t0002g0164 a0001c0001t0002g0201 others(17): Show |
20 | HG00597.hp2 HG01109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.741+2538_741+2539d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106817824 | ||||||
| chr12:106817824 | C | CAAA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.741+2537_741+2539d others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106817824 | ||||||
| chr12:106817824 | C | CAAAA | 11 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0090 others(8): Show |
11 | HG00408.hp1 HG00438.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.741+2536_741+2539d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106817824 | ||||||
| chr12:106817849 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.741+2545C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106817849 | |||||||
| chr12:106818086 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.741+2782T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818086 | |||||||
| chr12:106818227 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.741+2923C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818227 | |||||||
| chr12:106818312 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.741+3008G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818312 | |||||||
| chr12:106818439 | C | T | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+3135C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818439 | |||||||
| chr12:106818455 | C | T | 32 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(29): Show |
32 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.741+3151C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818455 | |||||||
| chr12:106818459 | C | T | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.741+3155C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818459 | |||||||
| chr12:106818766 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.741+3462T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818766 | |||||||
| chr12:106818949 | A | G | 12 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(9): Show |
12 | HG01109.hp2 HG01943.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.741+3645A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106818949 | |||||||
| chr12:106819008 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.741+3704G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819008 | |||||||
| chr12:106819416 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.741+4112G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819416 | |||||||
| chr12:106819552 | G | A | 1 | a0001c0001t0027g0219 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.741+4248G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819552 | |||||||
| chr12:106819736 | GA | G | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.741+4449delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106819736 | ||||||
| chr12:106819759 | G | T | 1 | a0001c0001t0005g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.741+4455G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819759 | |||||||
| chr12:106819823 | A | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(245): Show |
249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.741+4519A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819823 | |||||||
| chr12:106819952 | C | G | 1 | a0001c0001t0005g0287 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.741+4648C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819952 | |||||||
| chr12:106819961 | T | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.741+4657T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106819961 | |||||||
| chr12:106820178 | C | T | 2 | a0001c0001t0001g0073 a0001c0002t0004g0305 |
2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.741+4874C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106820178 | |||||||
| chr12:106820345 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.741+5041C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106820345 | |||||||
| chr12:106820686 | A | G | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742-5040A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106820686 | |||||||
| chr12:106820752 | CAA | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.742-4971_742-4970d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106820752 | ||||||
| chr12:106820906 | T | C | 1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.742-4820T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106820906 | |||||||
| chr12:106821148 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.742-4578C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106821148 | |||||||
| chr12:106821526 | T | C | 8 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(5): Show |
8 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-4200T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106821526 | |||||||
| chr12:106821654 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.742-4072A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106821654 | |||||||
| chr12:106821980 | A | C | 12 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(9): Show |
12 | HG01109.hp2 HG01943.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-3746A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106821980 | |||||||
| chr12:106822002 | C | T | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.742-3724C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822002 | |||||||
| chr12:106822033 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(90): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.742-3693G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822033 | |||||||
| chr12:106822033 | G | C | 6 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(3): Show |
6 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-3693G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822033 | |||||||
| chr12:106822077 | C | CA | 16 | a0001c0001t0001g0220 a0001c0001t0001g0272 a0001c0001t0001g0289 others(13): Show |
16 | HG01358.hp1 HG01981.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.742-3625dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106822077 | ||||||
| chr12:106822077 | CA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.742-3625delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106822077 | ||||||
| chr12:106822077 | CAA | C | 12 | a0001c0001t0001g0054 a0001c0001t0001g0058 a0001c0001t0001g0059 others(9): Show |
12 | HG00639.hp1 HG01169.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-3626_742-3625d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr12 | 106822077 | ||||||
| chr12:106822092 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.742-3634A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822092 | |||||||
| chr12:106822099 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | NA18942.hp1 NA18974.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.742-3627A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822099 | |||||||
| chr12:106822105 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.742-3621G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822105 | |||||||
| chr12:106822246 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.742-3480G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822246 | |||||||
| chr12:106822504 | A | T | 7 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(4): Show |
7 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-3222A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822504 | |||||||
| chr12:106822520 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.742-3206A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822520 | |||||||
| chr12:106822581 | C | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(101): Show |
105 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.742-3145C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822581 | |||||||
| chr12:106822690 | C | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.742-3036C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106822690 | |||||||
| chr12:106823489 | A | G | 5 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-2237A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106823489 | |||||||
| chr12:106823762 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.742-1964G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106823762 | |||||||
| chr12:106823938 | G | A | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.742-1788G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106823938 | |||||||
| chr12:106824110 | CT | C | 3 | a0001c0001t0004g0298 a0001c0001t0004g0299 a0001c0002t0014g0317 |
3 | HG02723.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.742-1615delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824110 | |||||||
| chr12:106824198 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.742-1528T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824198 | |||||||
| chr12:106824381 | C | G | 1 | a0001c0001t0002g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.742-1345C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824381 | |||||||
| chr12:106824537 | A | G | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742-1189A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824537 | |||||||
| chr12:106824542 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.742-1184A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824542 | |||||||
| chr12:106824801 | G | T | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.742-925G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824801 | |||||||
| chr12:106824822 | G | A | 1 | a0001c0001t0005g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.742-904G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824822 | |||||||
| chr12:106824855 | C | T | 5 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-871C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824855 | |||||||
| chr12:106824904 | T | C | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.742-822T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824904 | |||||||
| chr12:106824926 | G | T | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.742-800G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824926 | |||||||
| chr12:106824941 | A | C | 1 | a0001c0001t0016g0193 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.742-785A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824941 | |||||||
| chr12:106824998 | C | T | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.742-728C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106824998 | |||||||
| chr12:106825002 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.742-724A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106825002 | |||||||
| chr12:106825082 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(41): Show |
45 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.742-644G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106825082 | |||||||
| chr12:106825310 | T | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.742-416T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106825310 | |||||||
| chr12:106825397 | C | A | 1 | a0001c0001t0002g0199 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.742-329C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106825397 | |||||||
| chr12:106825530 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(156): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.742-196A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 3/9 | chr12 | 106825530 | |||||||
| chr12:106826194 | A | G | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.836+374A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826194 | |||||||
| chr12:106826200 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.836+380A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826200 | |||||||
| chr12:106826284 | C | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0207 |
2 | NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.836+464C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826284 | |||||||
| chr12:106826367 | A | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0090 others(2): Show |
5 | HG02135.hp1 NA18747.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.836+547A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826367 | |||||||
| chr12:106826374 | C | G | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.836+554C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826374 | |||||||
| chr12:106826447 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0002g0211 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.836+627G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826447 | |||||||
| chr12:106826562 | T | TGGCCAAC others(57): Show |
1 | a0001c0001t0002g0243 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.836+743_836+806dup others(64): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106826562 | ||||||
| chr12:106826604 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.836+784A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826604 | |||||||
| chr12:106826617 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.836+797A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826617 | |||||||
| chr12:106826649 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.836+829G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826649 | |||||||
| chr12:106826709 | C | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.836+889C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826709 | |||||||
| chr12:106826710 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.836+890G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826710 | |||||||
| chr12:106826747 | T | TC | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.836+929dupC | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106826747 | ||||||
| chr12:106826758 | AAATT | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0060 others(38): Show |
42 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.836+951_836+954del others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106826758 | ||||||
| chr12:106826886 | C | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.836+1066C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826886 | |||||||
| chr12:106826943 | G | A | 4 | a0001c0001t0001g0256 a0001c0002t0009g0306 a0001c0002t0009g0307 others(1): Show |
4 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.836+1123G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106826943 | |||||||
| chr12:106827149 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.836+1329T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827149 | |||||||
| chr12:106827157 | T | C | 1 | a0001c0001t0002g0292 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.836+1337T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827157 | |||||||
| chr12:106827400 | A | G | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.836+1580A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827400 | |||||||
| chr12:106827511 | A | G | 2 | a0001c0002t0009g0306 a0001c0002t0009g0308 |
2 | HG01175.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.836+1691A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827511 | |||||||
| chr12:106827857 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.836+2037G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827857 | |||||||
| chr12:106827877 | T | C | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.836+2057T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827877 | |||||||
| chr12:106827956 | C | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.836+2136C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827956 | |||||||
| chr12:106827985 | G | A | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.836+2165G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106827985 | |||||||
| chr12:106828072 | T | G | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.836+2252T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828072 | |||||||
| chr12:106828160 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.836+2340C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828160 | |||||||
| chr12:106828441 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.836+2621A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828441 | |||||||
| chr12:106828568 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.836+2748C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828568 | |||||||
| chr12:106828737 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(91): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.836+2917G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828737 | |||||||
| chr12:106828907 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.836+3087G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828907 | |||||||
| chr12:106828912 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.836+3092A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828912 | |||||||
| chr12:106828996 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.836+3176C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106828996 | |||||||
| chr12:106829019 | G | A | 5 | a0001c0002t0004g0305 a0001c0002t0014g0317 a0001c0002t0023g0300 others(2): Show |
5 | HG02027.hp1 HG06807.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.836+3199G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829019 | |||||||
| chr12:106829076 | A | G | 1 | a0001c0001t0011g0012 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.836+3256A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829076 | |||||||
| chr12:106829211 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(127): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.836+3391C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829211 | |||||||
| chr12:106829274 | A | G | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.836+3454A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829274 | |||||||
| chr12:106829383 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0061 others(27): Show |
31 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.836+3563A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829383 | |||||||
| chr12:106829482 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.836+3662G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829482 | |||||||
| chr12:106829662 | A | G | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.836+3842A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829662 | |||||||
| chr12:106829691 | A | C | 1 | a0001c0001t0002g0211 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.836+3871A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829691 | |||||||
| chr12:106829877 | G | A | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.836+4057G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106829877 | |||||||
| chr12:106830191 | G | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(121): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.836+4371G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106830191 | |||||||
| chr12:106830489 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.836+4669C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106830489 | |||||||
| chr12:106830651 | C | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.836+4831C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106830651 | |||||||
| chr12:106830652 | T | G | 1 | a0001c0001t0002g0251 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.836+4832T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106830652 | |||||||
| chr12:106830840 | T | G | 1 | a0001c0001t0002g0167 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.836+5020T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106830840 | |||||||
| chr12:106831184 | A | G | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.836+5364A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831184 | |||||||
| chr12:106831390 | T | C | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.836+5570T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831390 | |||||||
| chr12:106831553 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(90): Show |
94 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.836+5733A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831553 | |||||||
| chr12:106831775 | A | G | 48 | a0001c0001t0001g0289 a0001c0001t0003g0007 a0001c0001t0003g0008 others(45): Show |
48 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.836+5955A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831775 | |||||||
| chr12:106831854 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.836+6034C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831854 | |||||||
| chr12:106831988 | T | C | 8 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.836+6168T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106831988 | |||||||
| chr12:106832049 | C | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.836+6229C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832049 | |||||||
| chr12:106832159 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.836+6339C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832159 | |||||||
| chr12:106832240 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.836+6420A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832240 | |||||||
| chr12:106832378 | G | C | 1 | a0001c0001t0002g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.836+6558G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832378 | |||||||
| chr12:106832382 | A | T | 1 | a0001c0001t0002g0265 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.836+6562A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832382 | |||||||
| chr12:106832435 | T | C | 17 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(14): Show |
17 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.836+6615T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832435 | |||||||
| chr12:106832566 | G | GA | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.836+6761dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106832566 | ||||||
| chr12:106832566 | G | GAA | 6 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(3): Show |
6 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.836+6760_836+6761d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106832566 | ||||||
| chr12:106832580 | A | G | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.836+6760A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832580 | |||||||
| chr12:106832942 | G | A | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(290): Show |
294 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.836+7122G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106832942 | |||||||
| chr12:106833216 | C | G | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.836+7396C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833216 | |||||||
| chr12:106833289 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0005g0196 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.836+7469A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833289 | |||||||
| chr12:106833327 | C | T | 87 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0140 others(84): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.836+7507C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833327 | |||||||
| chr12:106833409 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.836+7589C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833409 | |||||||
| chr12:106833470 | G | A | 6 | a0001c0001t0004g0298 a0001c0001t0004g0299 a0001c0002t0004g0305 others(3): Show |
6 | HG02027.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.836+7650G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833470 | |||||||
| chr12:106833654 | A | C | 1 | a0001c0001t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.836+7834A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833654 | |||||||
| chr12:106833779 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.836+7959G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833779 | |||||||
| chr12:106833867 | T | A | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.836+8047T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833867 | |||||||
| chr12:106833898 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.836+8078G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833898 | |||||||
| chr12:106833915 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | NA18969.hp2 NA19011.hp2 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.836+8095A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833915 | |||||||
| chr12:106833950 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.836+8130C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833950 | |||||||
| chr12:106833984 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.836+8164G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106833984 | |||||||
| chr12:106834079 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.836+8259A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834079 | |||||||
| chr12:106834120 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.836+8300T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834120 | |||||||
| chr12:106834191 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.836+8371A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834191 | |||||||
| chr12:106834230 | G | A | 2 | a0001c0002t0014g0317 a0001c0002t0025g0297 |
2 | NA19030.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837-8359G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834230 | |||||||
| chr12:106834321 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.837-8268T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834321 | |||||||
| chr12:106834440 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.837-8149A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834440 | |||||||
| chr12:106834774 | G | T | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.837-7815G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834774 | |||||||
| chr12:106834898 | G | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(73): Show |
77 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.837-7691G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834898 | |||||||
| chr12:106834900 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.837-7689C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834900 | |||||||
| chr12:106834939 | G | A | 3 | a0001c0001t0005g0003 a0001c0001t0005g0213 a0001c0001t0005g0214 |
3 | HG03139.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.837-7650G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834939 | |||||||
| chr12:106834947 | G | A | 23 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.837-7642G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834947 | |||||||
| chr12:106834949 | A | G | 3 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0030 |
3 | HG03017.hp1 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.837-7640A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106834949 | |||||||
| chr12:106834983 | C | CA | 38 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0068 others(35): Show |
38 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.837-7580dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106834983 | ||||||
| chr12:106834983 | C | CAAA | 27 | a0001c0001t0001g0289 a0001c0001t0002g0138 a0001c0001t0003g0007 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.837-7582_837-7580d others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106834983 | ||||||
| chr12:106834983 | C | CAAAA | 12 | a0001c0001t0002g0284 a0001c0001t0003g0015 a0001c0001t0003g0016 others(9): Show |
12 | HG00738.hp1 HG01099.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.837-7583_837-7580d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106834983 | ||||||
| chr12:106834983 | CA | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0088 a0001c0001t0001g0220 others(5): Show |
8 | HG01167.hp2 HG01168.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.837-7580delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106834983 | ||||||
| chr12:106835191 | A | G | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.837-7398A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835191 | |||||||
| chr12:106835230 | T | C | 1 | a0001c0001t0004g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.837-7359T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835230 | |||||||
| chr12:106835618 | T | A | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.837-6971T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835618 | |||||||
| chr12:106835693 | A | G | 1 | a0001c0001t0006g0225 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.837-6896A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835693 | |||||||
| chr12:106835707 | G | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837-6882G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835707 | |||||||
| chr12:106835881 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.837-6708T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835881 | |||||||
| chr12:106835927 | C | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(78): Show |
82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.837-6662C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106835927 | |||||||
| chr12:106836201 | T | C | 6 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(3): Show |
6 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-6388T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106836201 | |||||||
| chr12:106836406 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | NA18969.hp2 NA19011.hp2 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-6183A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106836406 | |||||||
| chr12:106836582 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.837-6007G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106836582 | |||||||
| chr12:106836649 | A | G | 1 | a0001c0001t0006g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.837-5940A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106836649 | |||||||
| chr12:106836978 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00639.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.837-5611G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106836978 | |||||||
| chr12:106837008 | T | G | 1 | a0001c0001t0017g0160 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.837-5581T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837008 | |||||||
| chr12:106837072 | C | T | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.837-5517C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837072 | |||||||
| chr12:106837081 | C | T | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.837-5508C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837081 | |||||||
| chr12:106837146 | G | A | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.837-5443G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837146 | |||||||
| chr12:106837230 | C | T | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.837-5359C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837230 | |||||||
| chr12:106837323 | T | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837-5266T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837323 | |||||||
| chr12:106837399 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.837-5190C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837399 | |||||||
| chr12:106837410 | A | C | 17 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(14): Show |
17 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.837-5179A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837410 | |||||||
| chr12:106837634 | C | CTT | 5 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(2): Show |
5 | HG02615.hp2 HG02683.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.837-4952_837-4951d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106837634 | ||||||
| chr12:106837639 | G | GT | 41 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(38): Show |
41 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.837-4930dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106837639 | ||||||
| chr12:106837639 | G | GTT | 24 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.837-4931_837-4930d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106837639 | ||||||
| chr12:106837639 | G | T | 7 | a0001c0001t0001g0289 a0001c0001t0002g0187 a0001c0001t0005g0286 others(4): Show |
7 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.837-4950G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837639 | |||||||
| chr12:106837642 | T | G | 1 | a0001c0001t0002g0279 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.837-4947T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837642 | |||||||
| chr12:106837668 | G | A | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.837-4921G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837668 | |||||||
| chr12:106837789 | G | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0004t0001g0038 others(1): Show |
4 | HG02135.hp1 NA18951.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-4800G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837789 | |||||||
| chr12:106837843 | C | T | 4 | a0002c0003t0001g0039 a0002c0003t0001g0079 a0002c0003t0001g0082 others(1): Show |
4 | HG01167.hp2 HG01884.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-4746C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106837843 | |||||||
| chr12:106838068 | G | C | 1 | a0001c0001t0001g0235 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.837-4521G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838068 | |||||||
| chr12:106838071 | G | A | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.837-4518G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838071 | |||||||
| chr12:106838148 | A | C | 17 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(14): Show |
17 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.837-4441A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838148 | |||||||
| chr12:106838151 | A | G | 27 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.837-4438A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838151 | |||||||
| chr12:106838276 | C | T | 31 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(28): Show |
31 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.837-4313C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838276 | |||||||
| chr12:106838535 | C | CA | 61 | a0001c0001t0001g0047 a0001c0001t0002g0140 a0001c0001t0002g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.837-4038dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106838535 | ||||||
| chr12:106838658 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0215 a0001c0001t0001g0224 |
3 | HG01256.hp2 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.837-3931A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838658 | |||||||
| chr12:106838703 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.837-3886T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838703 | |||||||
| chr12:106838813 | A | AATT | 3 | a0001c0001t0004g0179 a0001c0001t0004g0252 a0001c0001t0004g0266 |
3 | HG02572.hp1 HG02717.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.837-3775_837-3774i others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106838813 | ||||||
| chr12:106838827 | C | CA | 16 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(13): Show |
16 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.837-3752dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106838827 | ||||||
| chr12:106838900 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.837-3689A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838900 | |||||||
| chr12:106838903 | A | G | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.837-3686A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106838903 | |||||||
| chr12:106838986 | CA | C | 48 | a0001c0001t0001g0223 a0001c0001t0001g0289 a0001c0001t0002g0195 others(45): Show |
48 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.837-3587delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr12 | 106838986 | ||||||
| chr12:106839071 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.837-3518G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839071 | |||||||
| chr12:106839394 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.837-3195C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839394 | |||||||
| chr12:106839408 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.837-3181G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839408 | |||||||
| chr12:106839410 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.837-3179G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839410 | |||||||
| chr12:106839569 | A | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0258 |
3 | NA18954.hp2 NA18965.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.837-3020A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839569 | |||||||
| chr12:106839714 | C | G | 1 | a0001c0001t0002g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.837-2875C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839714 | |||||||
| chr12:106839733 | G | T | 2 | a0001c0001t0011g0011 a0001c0001t0011g0012 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.837-2856G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839733 | |||||||
| chr12:106839886 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.837-2703C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106839886 | |||||||
| chr12:106840115 | G | A | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.837-2474G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106840115 | |||||||
| chr12:106840370 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.837-2219C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106840370 | |||||||
| chr12:106840412 | A | G | 1 | a0001c0001t0001g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.837-2177A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106840412 | |||||||
| chr12:106840858 | G | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0090 |
2 | NA18956.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.837-1731G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106840858 | |||||||
| chr12:106840902 | T | A | 1 | a0001c0001t0001g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.837-1687T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106840902 | |||||||
| chr12:106841289 | T | G | 1 | a0001c0001t0002g0169 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.837-1300T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106841289 | |||||||
| chr12:106841307 | C | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.837-1282C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106841307 | |||||||
| chr12:106841775 | T | C | 2 | a0001c0001t0004g0298 a0001c0001t0004g0299 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.837-814T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106841775 | |||||||
| chr12:106841831 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.837-758A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106841831 | |||||||
| chr12:106842173 | T | C | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.837-416T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106842173 | |||||||
| chr12:106842188 | A | C | 4 | a0001c0001t0001g0220 a0001c0001t0001g0222 a0001c0001t0001g0258 others(1): Show |
4 | NA18954.hp2 NA18965.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.837-401A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106842188 | |||||||
| chr12:106842294 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | NA18969.hp2 NA19011.hp2 NA19089.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-295G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106842294 | |||||||
| chr12:106842530 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.837-59G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106842530 | |||||||
| chr12:106842565 | T | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.837-24T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 4/9 | chr12 | 106842565 | |||||||
| chr12:106842992 | G | T | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065+175G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106842992 | |||||||
| chr12:106843228 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1065+411G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843228 | |||||||
| chr12:106843298 | A | C | 1 | a0001c0001t0001g0314 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1065+481A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843298 | |||||||
| chr12:106843647 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1066-205G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843647 | |||||||
| chr12:106843671 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1066-181G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843671 | |||||||
| chr12:106843699 | G | A | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1066-153G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843699 | |||||||
| chr12:106843723 | C | CA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(91): Show |
95 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.1066-108dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr12 | 106843723 | ||||||
| chr12:106843847 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.1066-5T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 5/9 | chr12 | 106843847 | |||||||
| chr12:106844099 | T | G | 15 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1161+152T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844099 | |||||||
| chr12:106844266 | T | G | 1 | a0001c0001t0002g0309 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1161+319T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844266 | |||||||
| chr12:106844309 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1161+362G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844309 | |||||||
| chr12:106844414 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1161+467A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844414 | |||||||
| chr12:106844465 | G | A | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+518G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844465 | |||||||
| chr12:106844614 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1161+667G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844614 | |||||||
| chr12:106844924 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1161+977A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844924 | |||||||
| chr12:106844962 | A | G | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1161+1015A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106844962 | |||||||
| chr12:106845070 | A | G | 1 | a0001c0001t0002g0230 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1161+1123A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845070 | |||||||
| chr12:106845111 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | HG03710.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1161+1164C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845111 | |||||||
| chr12:106845116 | C | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1161+1169C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845116 | |||||||
| chr12:106845146 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1161+1199G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845146 | |||||||
| chr12:106845156 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1161+1209G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845156 | |||||||
| chr12:106845224 | A | G | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1161+1277A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845224 | |||||||
| chr12:106845328 | C | CTTCT | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(156): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1161+1383_1161+138 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106845328 | ||||||
| chr12:106845657 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1161+1710A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845657 | |||||||
| chr12:106845814 | C | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1161+1867C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845814 | |||||||
| chr12:106845852 | A | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1161+1905A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845852 | |||||||
| chr12:106845890 | T | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1161+1943T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106845890 | |||||||
| chr12:106846169 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(137): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1161+2222G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846169 | |||||||
| chr12:106846286 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1161+2339C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846286 | |||||||
| chr12:106846462 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | NA18969.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1161+2515A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846462 | |||||||
| chr12:106846536 | G | A | 11 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(8): Show |
11 | HG02027.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1161+2589G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846536 | |||||||
| chr12:106846654 | C | T | 9 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1161+2707C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846654 | |||||||
| chr12:106846711 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1161+2764A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846711 | |||||||
| chr12:106846716 | G | C | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1161+2769G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846716 | |||||||
| chr12:106846723 | C | CA | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(124): Show |
128 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1161+2792dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106846723 | ||||||
| chr12:106846723 | C | CAAAA | 23 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1161+2789_1161+279 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106846723 | ||||||
| chr12:106846738 | A | C | 1 | a0001c0001t0001g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1161+2791A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846738 | |||||||
| chr12:106846745 | T | C | 1 | a0001c0001t0020g0178 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1161+2798T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106846745 | |||||||
| chr12:106847201 | G | A | 2 | a0001c0001t0002g0281 a0001c0001t0002g0282 |
2 | NA19057.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1161+3254G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106847201 | |||||||
| chr12:106847367 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1161+3420A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106847367 | |||||||
| chr12:106848023 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0223 a0001c0001t0001g0227 |
3 | HG00609.hp2 HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1162-3427T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848023 | |||||||
| chr12:106848029 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(249): Show |
253 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1162-3421A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848029 | |||||||
| chr12:106848054 | G | A | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1162-3396G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848054 | |||||||
| chr12:106848489 | A | C | 1 | a0001c0001t0002g0190 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1162-2961A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848489 | |||||||
| chr12:106848511 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0026 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1162-2939A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848511 | |||||||
| chr12:106848774 | C | T | 24 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1162-2676C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848774 | |||||||
| chr12:106848802 | TG | T | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1162-2646delG | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106848802 | ||||||
| chr12:106848804 | G | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1162-2646G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848804 | |||||||
| chr12:106848805 | A | T | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1162-2645A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848805 | |||||||
| chr12:106848807 | G | A | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1162-2643G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848807 | |||||||
| chr12:106848808 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1162-2642T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106848808 | |||||||
| chr12:106849248 | T | C | 1 | a0001c0001t0002g0147 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1162-2202T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849248 | |||||||
| chr12:106849287 | G | GTTTA | 11 | a0001c0001t0002g0209 a0001c0001t0002g0269 a0001c0001t0004g0123 others(8): Show |
11 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162-2129_1162-212 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106849287 | ||||||
| chr12:106849287 | GTTTA | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0046 others(132): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1162-2129_1162-212 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106849287 | ||||||
| chr12:106849287 | GTTTATTT others(1): Show |
G | 5 | a0001c0001t0005g0003 a0001c0001t0005g0213 a0001c0001t0005g0288 others(2): Show |
5 | HG00738.hp1 HG01099.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-2133_1162-212 others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106849287 | ||||||
| chr12:106849353 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
6 | HG00280.hp2 NA18954.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1162-2097A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849353 | |||||||
| chr12:106849390 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1162-2060C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849390 | |||||||
| chr12:106849466 | T | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162-1984T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849466 | |||||||
| chr12:106849535 | A | T | 2 | a0001c0001t0001g0244 a0001c0001t0027g0219 |
2 | HG00597.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1162-1915A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849535 | |||||||
| chr12:106849673 | A | G | 10 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(7): Show |
10 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1162-1777A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106849673 | |||||||
| chr12:106850022 | G | A | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1162-1428G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850022 | |||||||
| chr12:106850042 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162-1408C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850042 | |||||||
| chr12:106850227 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0314 |
2 | HG01168.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1162-1223A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850227 | |||||||
| chr12:106850231 | A | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162-1219A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850231 | |||||||
| chr12:106850238 | C | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162-1212C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850238 | |||||||
| chr12:106850278 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0293 a0001c0001t0012g0257 |
3 | HG00280.hp1 HG00733.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1162-1172G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850278 | |||||||
| chr12:106850526 | A | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1162-924A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850526 | |||||||
| chr12:106850663 | G | A | 1 | a0002c0003t0001g0079 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162-787G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106850663 | |||||||
| chr12:106851015 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1162-435G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106851015 | |||||||
| chr12:106851061 | A | G | 1 | a0001c0001t0006g0233 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1162-389A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106851061 | |||||||
| chr12:106851267 | A | G | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-183A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | chr12 | 106851267 | |||||||
| chr12:106851315 | C | CT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1162-114dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106851315 | ||||||
| chr12:106851315 | C | CTT | 45 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0042 others(42): Show |
45 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1162-115_1162-114d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106851315 | ||||||
| chr12:106851315 | C | CTTT | 7 | a0001c0001t0004g0123 a0001c0001t0004g0125 a0001c0001t0004g0126 others(4): Show |
7 | HG02027.hp1 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1162-116_1162-114d others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr12 | 106851315 | ||||||
| chr12:106852110 | G | C | 1 | a0001c0001t0005g0286 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1306+516G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852110 | |||||||
| chr12:106852331 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1306+737C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852331 | |||||||
| chr12:106852436 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0295 |
3 | NA18967.hp1 NA18974.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1306+842G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852436 | |||||||
| chr12:106852472 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1306+878A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852472 | |||||||
| chr12:106852691 | G | A | 1 | a0001c0001t0017g0160 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1306+1097G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852691 | |||||||
| chr12:106852958 | T | A | 17 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(14): Show |
17 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1306+1364T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106852958 | |||||||
| chr12:106853205 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1306+1611A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853205 | |||||||
| chr12:106853230 | T | C | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1306+1636T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853230 | |||||||
| chr12:106853453 | C | CT | 60 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0129 others(57): Show |
60 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1306+1892dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTT | 10 | a0001c0001t0001g0092 a0001c0001t0001g0132 a0001c0001t0001g0142 others(7): Show |
10 | HG01258.hp1 HG02523.hp2 HG04228.hp2 others(7): Show |
intron_variant | MODIFIER | c.1306+1891_1306+189 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTT | 8 | a0001c0001t0001g0223 a0001c0001t0001g0256 a0001c0001t0001g0261 others(5): Show |
8 | HG00609.hp2 HG02683.hp2 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306+1890_1306+189 others(7): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTT | 7 | a0001c0001t0001g0133 a0001c0001t0001g0146 a0001c0001t0001g0259 others(4): Show |
7 | HG02056.hp1 HG02451.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1306+1889_1306+189 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0081 others(5): Show |
8 | HG01256.hp2 HG01516.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306+1885_1306+189 others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(2): Show |
26 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0046 others(23): Show |
26 | HG01070.hp2 HG01074.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1306+1884_1306+189 others(13): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0051 others(17): Show |
20 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1306+1883_1306+189 others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(4): Show |
12 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
13 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306+1882_1306+189 others(15): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0060 others(8): Show |
11 | HG00408.hp1 HG00609.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+1881_1306+189 others(16): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0066 a0001c0001t0004g0098 a0001c0001t0006g0105 |
3 | HG02280.hp2 NA18967.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1306+1880_1306+189 others(17): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1306+1879_1306+189 others(18): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1306+1877_1306+189 others(20): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1306+1876_1306+189 others(21): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0010g0033 a0001c0001t0010g0034 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1306+1875_1306+189 others(22): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0010g0035 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1306+1874_1306+189 others(23): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | CT | C | 23 | a0001c0001t0002g0134 a0001c0001t0002g0166 a0001c0001t0002g0174 others(20): Show |
23 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1306+1892delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0003g0014 a0001c0001t0003g0016 a0001c0001t0003g0017 others(1): Show |
4 | HG02145.hp2 HG03831.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+1883_1306+189 others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | CTTTTTTT others(4): Show |
C | 18 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(15): Show |
18 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1306+1882_1306+189 others(15): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853453 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1306+1881_1306+189 others(16): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106853453 | ||||||
| chr12:106853488 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+1894A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853488 | |||||||
| chr12:106853572 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1306+1978G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853572 | |||||||
| chr12:106853590 | G | A | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1306+1996G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853590 | |||||||
| chr12:106853689 | G | A | 32 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(29): Show |
32 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1306+2095G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853689 | |||||||
| chr12:106853720 | G | T | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1306+2126G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853720 | |||||||
| chr12:106853721 | C | T | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1306+2127C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853721 | |||||||
| chr12:106853829 | A | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0154 a0001c0001t0001g0291 others(1): Show |
4 | HG02135.hp2 NA18967.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+2235A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106853829 | |||||||
| chr12:106854041 | G | A | 2 | a0001c0002t0023g0300 a0001c0002t0028g0006 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1306+2447G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854041 | |||||||
| chr12:106854275 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1306+2681T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854275 | |||||||
| chr12:106854312 | TTAAAA | T | 9 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1306+2743_1306+274 others(9): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106854312 | ||||||
| chr12:106854319 | A | G | 1 | a0001c0001t0003g0316 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1306+2725A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854319 | |||||||
| chr12:106854405 | T | G | 6 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(3): Show |
6 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+2811T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854405 | |||||||
| chr12:106854473 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18961.hp2 NA18970.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+2879A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854473 | |||||||
| chr12:106854519 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1306+2925G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854519 | |||||||
| chr12:106854526 | C | G | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1306+2932C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854526 | |||||||
| chr12:106854589 | G | A | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1306+2995G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854589 | |||||||
| chr12:106854704 | A | G | 21 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(18): Show |
21 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1306+3110A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854704 | |||||||
| chr12:106854745 | C | T | 23 | a0001c0001t0002g0138 a0001c0001t0002g0140 a0001c0001t0002g0163 others(20): Show |
23 | HG00741.hp1 HG01074.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.1306+3151C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854745 | |||||||
| chr12:106854852 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1306+3258A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854852 | |||||||
| chr12:106854957 | A | G | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1306+3363A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106854957 | |||||||
| chr12:106855109 | T | G | 6 | a0001c0001t0001g0289 a0001c0001t0005g0286 a0001c0001t0005g0287 others(3): Show |
6 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1306+3515T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855109 | |||||||
| chr12:106855337 | A | G | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1306+3743A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855337 | |||||||
| chr12:106855365 | G | A | 1 | a0001c0001t0005g0004 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1306+3771G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855365 | |||||||
| chr12:106855436 | C | CT | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(306): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1306+3843dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106855436 | ||||||
| chr12:106855799 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1306+4205G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855799 | |||||||
| chr12:106855832 | A | G | 4 | a0001c0002t0004g0305 a0001c0002t0023g0300 a0001c0002t0025g0297 others(1): Show |
4 | HG02027.hp1 HG06807.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4238A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855832 | |||||||
| chr12:106855856 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1306+4262T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106855856 | |||||||
| chr12:106856083 | C | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1307-4185C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856083 | |||||||
| chr12:106856184 | A | C | 1 | a0001c0001t0003g0018 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1307-4084A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856184 | |||||||
| chr12:106856344 | C | G | 23 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1307-3924C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856344 | |||||||
| chr12:106856366 | C | T | 1 | a0001c0002t0023g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1307-3902C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856366 | |||||||
| chr12:106856474 | A | G | 30 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1307-3794A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856474 | |||||||
| chr12:106856607 | T | C | 1 | a0001c0001t0002g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1307-3661T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106856607 | |||||||
| chr12:106857204 | A | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1307-3064A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106857204 | |||||||
| chr12:106857547 | T | C | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1307-2721T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106857547 | |||||||
| chr12:106857925 | C | T | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-2343C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106857925 | |||||||
| chr12:106858341 | C | T | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-1927C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858341 | |||||||
| chr12:106858402 | C | G | 3 | a0001c0001t0002g0163 a0001c0001t0002g0185 a0003c0006t0002g0139 |
3 | HG03834.hp1 HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1307-1866C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858402 | |||||||
| chr12:106858428 | G | T | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0002g0192 |
3 | HG01496.hp1 HG01943.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1307-1840G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858428 | |||||||
| chr12:106858703 | T | G | 27 | a0001c0001t0002g0183 a0001c0001t0003g0007 a0001c0001t0003g0008 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1307-1565T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858703 | |||||||
| chr12:106858828 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1307-1440G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858828 | |||||||
| chr12:106858906 | T | C | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1307-1362T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858906 | |||||||
| chr12:106858933 | G | A | 8 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0120 others(5): Show |
8 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1307-1335G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858933 | |||||||
| chr12:106858991 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1307-1277C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106858991 | |||||||
| chr12:106859019 | C | A | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1307-1249C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859019 | |||||||
| chr12:106859191 | A | G | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-1077A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859191 | |||||||
| chr12:106859326 | G | T | 3 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 |
3 | HG03041.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1307-942G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859326 | |||||||
| chr12:106859568 | G | GGT | 14 | a0001c0001t0001g0289 a0001c0001t0004g0123 a0001c0001t0004g0124 others(11): Show |
14 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1307-699_1307-698d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr12 | 106859568 | ||||||
| chr12:106859574 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1307-694T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859574 | |||||||
| chr12:106859595 | A | G | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1307-673A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859595 | |||||||
| chr12:106859705 | C | T | 9 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1307-563C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859705 | |||||||
| chr12:106859775 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1307-493A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859775 | |||||||
| chr12:106859809 | T | A | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1307-459T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859809 | |||||||
| chr12:106859870 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1307-398G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859870 | |||||||
| chr12:106859900 | T | C | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-368T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106859900 | |||||||
| chr12:106860011 | G | T | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-257G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 7/9 | chr12 | 106860011 | |||||||
| chr12:106860534 | G | C | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1451+122G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106860534 | |||||||
| chr12:106860779 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(113): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1451+367T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106860779 | |||||||
| chr12:106860843 | T | A | 4 | a0001c0001t0004g0123 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02258.hp2 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1451+431T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106860843 | |||||||
| chr12:106860924 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0314 |
2 | HG01168.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1451+512A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106860924 | |||||||
| chr12:106860962 | GTAGGCAA others(23): Show |
G | 12 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(9): Show |
12 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1451+552_1451+581d others(32): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106860962 | ||||||
| chr12:106861076 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1451+664C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861076 | |||||||
| chr12:106861164 | T | C | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1451+752T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861164 | |||||||
| chr12:106861189 | A | G | 1 | a0001c0001t0003g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1451+777A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861189 | |||||||
| chr12:106861300 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1451+888G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861300 | |||||||
| chr12:106861542 | T | G | 15 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(12): Show |
15 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1451+1130T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861542 | |||||||
| chr12:106861552 | C | G | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1451+1140C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861552 | |||||||
| chr12:106861769 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(237): Show |
241 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1451+1357T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861769 | |||||||
| chr12:106861848 | G | A | 26 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(23): Show |
26 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1451+1436G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861848 | |||||||
| chr12:106861985 | C | T | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1451+1573C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106861985 | |||||||
| chr12:106862150 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1451+1738T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862150 | |||||||
| chr12:106862196 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1451+1784A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862196 | |||||||
| chr12:106862208 | T | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(236): Show |
240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1451+1796T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862208 | |||||||
| chr12:106862435 | A | C | 12 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(9): Show |
12 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1451+2023A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862435 | |||||||
| chr12:106862628 | T | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1451+2216T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862628 | |||||||
| chr12:106862647 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1451+2235T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862647 | |||||||
| chr12:106862839 | A | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0085 others(2): Show |
6 | HG00280.hp2 NA18954.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1451+2427A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862839 | |||||||
| chr12:106862911 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1451+2499A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862911 | |||||||
| chr12:106862982 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1451+2570A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106862982 | |||||||
| chr12:106863358 | T | C | 5 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451+2946T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106863358 | |||||||
| chr12:106863461 | C | G | 1 | a0001c0001t0001g0113 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1451+3049C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106863461 | |||||||
| chr12:106863624 | A | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1451+3212A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106863624 | |||||||
| chr12:106863811 | G | A | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451+3399G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106863811 | |||||||
| chr12:106863868 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1451+3456T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106863868 | |||||||
| chr12:106864206 | A | G | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451+3794A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864206 | |||||||
| chr12:106864243 | C | G | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1451+3831C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864243 | |||||||
| chr12:106864280 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1451+3868C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864280 | |||||||
| chr12:106864350 | G | T | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1451+3938G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864350 | |||||||
| chr12:106864419 | A | C | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1451+4007A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864419 | |||||||
| chr12:106864430 | G | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1451+4018G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864430 | |||||||
| chr12:106864443 | A | T | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1451+4031A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864443 | |||||||
| chr12:106864445 | C | A | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1451+4033C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864445 | |||||||
| chr12:106864468 | CACA | C | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0195 |
3 | NA18942.hp2 NA18970.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1451+4061_1451+406 others(7): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106864468 | ||||||
| chr12:106864493 | A | G | 1 | a0001c0001t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1451+4081A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864493 | |||||||
| chr12:106864526 | A | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1451+4114A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864526 | |||||||
| chr12:106864533 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1451+4121G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864533 | |||||||
| chr12:106864833 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0022 |
2 | HG00099.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.1451+4421C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864833 | |||||||
| chr12:106864929 | T | C | 15 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(12): Show |
15 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1451+4517T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106864929 | |||||||
| chr12:106864986 | CAA | C | 5 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0179 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1451+4576_1451+457 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106864986 | ||||||
| chr12:106865177 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1451+4765C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865177 | |||||||
| chr12:106865578 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1451+5166A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865578 | |||||||
| chr12:106865692 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(148): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1452-5131T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865692 | |||||||
| chr12:106865751 | T | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | HG01256.hp1 HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1452-5072T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865751 | |||||||
| chr12:106865791 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1452-5032G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865791 | |||||||
| chr12:106865796 | C | T | 6 | a0001c0001t0004g0096 a0001c0001t0004g0098 a0001c0001t0004g0099 others(3): Show |
6 | HG01175.hp1 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1452-5027C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865796 | |||||||
| chr12:106865951 | C | T | 2 | a0001c0001t0004g0161 a0001c0001t0004g0162 |
2 | HG02145.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1452-4872C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865951 | |||||||
| chr12:106865952 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1452-4871G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106865952 | |||||||
| chr12:106866170 | TTTTG | T | 13 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(10): Show |
13 | HG01175.hp1 HG02027.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1452-4649_1452-464 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106866170 | ||||||
| chr12:106866209 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-4614G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866209 | |||||||
| chr12:106866236 | C | T | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1452-4587C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866236 | |||||||
| chr12:106866360 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-4463G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866360 | |||||||
| chr12:106866462 | TC | T | 14 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(11): Show |
14 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1452-4356delC | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106866462 | ||||||
| chr12:106866463 | C | T | 3 | a0001c0001t0010g0033 a0001c0001t0010g0034 a0001c0001t0010g0035 |
3 | HG02559.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1452-4360C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866463 | |||||||
| chr12:106866524 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1452-4299C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866524 | |||||||
| chr12:106866688 | G | GC | 20 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1452-4135_1452-413 others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866688 | |||||||
| chr12:106866697 | A | ATAAT | 3 | a0001c0001t0008g0302 a0001c0001t0008g0303 a0001c0001t0008g0304 |
3 | HG01168.hp2 HG01169.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1452-4124_1452-412 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106866697 | ||||||
| chr12:106866697 | ATAATT | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | NA18961.hp2 NA18970.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452-4120_1452-411 others(9): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106866697 | ||||||
| chr12:106866858 | T | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(246): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1452-3965T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866858 | |||||||
| chr12:106866963 | C | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-3860C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866963 | |||||||
| chr12:106866969 | T | C | 4 | a0001c0001t0004g0123 a0001c0001t0004g0125 a0001c0001t0004g0126 others(1): Show |
4 | HG02258.hp2 HG02280.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452-3854T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866969 | |||||||
| chr12:106866992 | G | A | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1452-3831G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106866992 | |||||||
| chr12:106867194 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1452-3629A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867194 | |||||||
| chr12:106867367 | C | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-3456C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867367 | |||||||
| chr12:106867382 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1452-3441G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867382 | |||||||
| chr12:106867427 | A | T | 1 | a0001c0001t0002g0238 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1452-3396A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867427 | |||||||
| chr12:106867428 | T | A | 1 | a0001c0001t0002g0238 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1452-3395T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867428 | |||||||
| chr12:106867636 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(250): Show |
254 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1452-3187A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867636 | |||||||
| chr12:106867920 | T | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1452-2903T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106867920 | |||||||
| chr12:106868064 | C | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1452-2759C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868064 | |||||||
| chr12:106868122 | A | C | 5 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1452-2701A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868122 | |||||||
| chr12:106868252 | T | C | 5 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1452-2571T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868252 | |||||||
| chr12:106868381 | T | C | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-2442T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868381 | |||||||
| chr12:106868625 | T | C | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-2198T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868625 | |||||||
| chr12:106868766 | G | GAC | 10 | a0001c0001t0001g0152 a0001c0001t0001g0280 a0001c0001t0002g0164 others(7): Show |
10 | HG00438.hp2 HG01243.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1452-2009_1452-200 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACAC | 7 | a0001c0001t0001g0216 a0001c0001t0001g0236 a0001c0001t0001g0283 others(4): Show |
7 | HG00140.hp2 HG00738.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-2011_1452-200 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(1): Show |
3 | a0001c0001t0004g0126 a0001c0001t0004g0128 a0001c0001t0004g0162 |
3 | HG02109.hp2 HG02145.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1452-2015_1452-200 others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(3): Show |
1 | a0001c0001t0004g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1452-2017_1452-200 others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(9): Show |
1 | a0001c0001t0004g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1452-2023_1452-200 others(20): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(11): Show |
1 | a0001c0001t0004g0127 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1452-2025_1452-200 others(22): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(13): Show |
1 | a0001c0001t0004g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1452-2027_1452-200 others(24): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | G | GACACACA others(15): Show |
1 | a0001c0001t0004g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1452-2029_1452-200 others(26): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GAC | G | 51 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0001g0132 others(48): Show |
51 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1452-2009_1452-200 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACAC | G | 70 | a0001c0001t0001g0121 a0001c0001t0001g0130 a0001c0001t0001g0131 others(67): Show |
70 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1452-2011_1452-200 others(8): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACAC | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0076 others(34): Show |
37 | HG00099.hp1 HG00639.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452-2013_1452-200 others(10): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(1): Show |
G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(65): Show |
69 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.1452-2015_1452-200 others(12): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(3): Show |
G | 8 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0077 others(5): Show |
8 | HG01168.hp1 HG03654.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1452-2017_1452-200 others(14): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(5): Show |
G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0093 a0001c0001t0001g0101 others(3): Show |
6 | HG02074.hp2 HG02723.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1452-2019_1452-200 others(16): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(7): Show |
G | 11 | a0001c0001t0002g0267 a0001c0001t0004g0118 a0001c0001t0004g0119 others(8): Show |
11 | HG01081.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1452-2021_1452-200 others(18): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(9): Show |
G | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1452-2023_1452-200 others(20): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(13): Show |
G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452-2027_1452-200 others(24): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868766 | GACACACA others(15): Show |
G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0224 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1452-2029_1452-200 others(26): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868766 | ||||||
| chr12:106868848 | C | CT | 31 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0061 others(28): Show |
31 | HG00140.hp1 HG00673.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1452-1951dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868848 | ||||||
| chr12:106868848 | CT | C | 15 | a0001c0001t0001g0041 a0001c0001t0001g0132 a0001c0001t0001g0220 others(12): Show |
15 | HG01070.hp2 HG01516.hp1 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.1452-1951delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106868848 | ||||||
| chr12:106868868 | T | G | 1 | a0001c0001t0002g0206 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1452-1955T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868868 | |||||||
| chr12:106868878 | G | A | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452-1945G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106868878 | |||||||
| chr12:106869044 | T | G | 2 | a0001c0001t0005g0288 a0001c0001t0005g0290 |
2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1452-1779T>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106869044 | |||||||
| chr12:106869187 | G | GT | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1452-1632dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106869187 | ||||||
| chr12:106869446 | C | CT | 7 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0006g0104 others(4): Show |
7 | HG00408.hp1 NA18939.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.1452-1364dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106869446 | ||||||
| chr12:106869446 | CT | C | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-1364delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106869446 | ||||||
| chr12:106869572 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1452-1251G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106869572 | |||||||
| chr12:106869737 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-1086G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106869737 | |||||||
| chr12:106869933 | C | T | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1452-890C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106869933 | |||||||
| chr12:106869984 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1452-839A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106869984 | |||||||
| chr12:106870077 | C | CA | 6 | a0001c0001t0003g0017 a0001c0001t0004g0179 a0001c0001t0004g0298 others(3): Show |
6 | HG02109.hp1 HG02723.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452-730dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106870077 | ||||||
| chr12:106870077 | CA | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0001c0001t0001g0133 others(3): Show |
6 | HG01256.hp1 HG01943.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1452-730delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106870077 | ||||||
| chr12:106870390 | CCTCT | C | 5 | a0001c0001t0002g0184 a0001c0001t0002g0253 a0001c0001t0010g0033 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452-430_1452-427d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr12 | 106870390 | ||||||
| chr12:106870520 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1452-303G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106870520 | |||||||
| chr12:106870707 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1452-116T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 8/9 | chr12 | 106870707 | |||||||
| chr12:106871397 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1571+455A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871397 | |||||||
| chr12:106871471 | T | TA | 54 | a0001c0001t0001g0065 a0001c0001t0001g0071 a0001c0001t0001g0090 others(51): Show |
54 | HG00544.hp2 HG00597.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.1571+556dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106871471 | ||||||
| chr12:106871471 | T | TAA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0037 others(43): Show |
47 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1571+555_1571+556d others(4): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106871471 | ||||||
| chr12:106871471 | T | TAAA | 34 | a0001c0001t0001g0036 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
34 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1571+554_1571+556d others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106871471 | ||||||
| chr12:106871488 | A | C | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1571+546A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871488 | |||||||
| chr12:106871491 | A | C | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1571+549A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871491 | |||||||
| chr12:106871492 | A | C | 2 | a0001c0001t0005g0005 a0001c0002t0025g0297 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1571+550A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871492 | |||||||
| chr12:106871492 | AAAAAAAC others(1): Show |
A | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1571+558_1571+565d others(10): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106871492 | ||||||
| chr12:106871493 | A | C | 22 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1571+551A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871493 | |||||||
| chr12:106871494 | A | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0316 |
2 | HG03710.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1571+552A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871494 | |||||||
| chr12:106871498 | AC | A | 39 | a0001c0001t0001g0256 a0001c0001t0001g0274 a0001c0001t0001g0289 others(36): Show |
39 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1571+558delC | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106871498 | ||||||
| chr12:106871499 | C | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(262): Show |
266 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1571+557C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871499 | |||||||
| chr12:106871500 | C | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01256.hp1 HG01516.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1571+558C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871500 | |||||||
| chr12:106871670 | A | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1571+728A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106871670 | |||||||
| chr12:106872051 | T | C | 8 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(5): Show |
8 | HG02027.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1571+1109T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872051 | |||||||
| chr12:106872165 | A | G | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571+1223A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872165 | |||||||
| chr12:106872352 | G | C | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1571+1410G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872352 | |||||||
| chr12:106872502 | C | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0217 a0001c0001t0002g0279 |
3 | HG00741.hp1 HG01074.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1571+1560C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872502 | |||||||
| chr12:106872629 | T | C | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1571+1687T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872629 | |||||||
| chr12:106872669 | C | CA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(118): Show |
122 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1571+1744dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106872669 | ||||||
| chr12:106872669 | C | CAA | 18 | a0001c0001t0001g0057 a0001c0001t0001g0076 a0001c0001t0001g0095 others(15): Show |
18 | HG02027.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1571+1743_1571+174 others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106872669 | ||||||
| chr12:106872687 | C | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1571+1745C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872687 | |||||||
| chr12:106872941 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0311 a0001c0001t0001g0312 others(1): Show |
4 | HG00639.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571+1999G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106872941 | |||||||
| chr12:106873145 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571+2203C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106873145 | |||||||
| chr12:106873504 | CT | C | 8 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(5): Show |
8 | HG02027.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1571+2563delT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106873504 | |||||||
| chr12:106873682 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1571+2740G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106873682 | |||||||
| chr12:106873995 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1571+3053G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106873995 | |||||||
| chr12:106874011 | T | C | 5 | a0001c0001t0005g0286 a0001c0001t0005g0287 a0001c0002t0009g0306 others(2): Show |
5 | HG01175.hp1 HG02615.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571+3069T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106874011 | |||||||
| chr12:106874183 | G | C | 1 | a0001c0001t0002g0229 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1571+3241G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106874183 | |||||||
| chr12:106874533 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1571+3591G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106874533 | |||||||
| chr12:106874924 | T | C | 1 | a0001c0001t0003g0315 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1571+3982T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106874924 | |||||||
| chr12:106875074 | C | T | 1 | a0001c0001t0011g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1571+4132C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875074 | |||||||
| chr12:106875199 | AATG | A | 33 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0041 others(30): Show |
33 | HG00408.hp1 HG00609.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1571+4260_1571+426 others(7): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106875199 | ||||||
| chr12:106875209 | G | C | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1571+4267G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875209 | |||||||
| chr12:106875261 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1571+4319A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875261 | |||||||
| chr12:106875293 | G | A | 9 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1571+4351G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875293 | |||||||
| chr12:106875305 | C | T | 3 | a0001c0001t0004g0179 a0001c0001t0004g0252 a0001c0001t0004g0266 |
3 | HG02572.hp1 HG02717.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1571+4363C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875305 | |||||||
| chr12:106875307 | G | A | 2 | a0001c0001t0005g0196 a0001c0001t0005g0285 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1571+4365G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875307 | |||||||
| chr12:106875368 | C | T | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1571+4426C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875368 | |||||||
| chr12:106875606 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(2): Show |
5 | HG01123.hp2 HG01516.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571+4664C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875606 | |||||||
| chr12:106875694 | A | G | 3 | a0001c0001t0001g0311 a0001c0001t0001g0312 a0001c0001t0001g0313 |
3 | HG00639.hp2 HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1571+4752A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875694 | |||||||
| chr12:106875824 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1571+4882C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875824 | |||||||
| chr12:106875921 | A | G | 1 | a0001c0001t0004g0266 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1571+4979A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875921 | |||||||
| chr12:106875994 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1571+5052C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106875994 | |||||||
| chr12:106876742 | A | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0227 |
2 | HG00609.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1571+5800A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106876742 | |||||||
| chr12:106877135 | T | TA | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571+6201dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106877135 | ||||||
| chr12:106877170 | A | T | 20 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(17): Show |
20 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.1571+6228A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106877170 | |||||||
| chr12:106877180 | C | T | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1571+6238C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106877180 | |||||||
| chr12:106877793 | T | C | 1 | a0001c0001t0004g0099 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1571+6851T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106877793 | |||||||
| chr12:106877998 | A | G | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1571+7056A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106877998 | |||||||
| chr12:106878100 | C | A | 1 | a0001c0001t0002g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1571+7158C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878100 | |||||||
| chr12:106878120 | G | C | 1 | a0001c0001t0024g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1571+7178G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878120 | |||||||
| chr12:106878161 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0113 |
2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1571+7219C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878161 | |||||||
| chr12:106878259 | C | G | 2 | a0001c0001t0011g0011 a0001c0001t0011g0012 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1571+7317C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878259 | |||||||
| chr12:106878404 | A | AG | 18 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(15): Show |
18 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1571+7462_1571+746 others(5): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878404 | |||||||
| chr12:106878670 | G | A | 68 | a0001c0001t0002g0135 a0001c0001t0002g0138 a0001c0001t0002g0140 others(65): Show |
68 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.1572-7234G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878670 | |||||||
| chr12:106878812 | A | G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572-7092A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878812 | |||||||
| chr12:106878824 | T | C | 14 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(11): Show |
14 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1572-7080T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878824 | |||||||
| chr12:106878824 | T | TC | 117 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0037 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1572-7071dupC | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106878824 | ||||||
| chr12:106878831 | C | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572-7073C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878831 | |||||||
| chr12:106878832 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0149 |
2 | NA19056.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1572-7072C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106878832 | |||||||
| chr12:106879152 | T | C | 2 | a0001c0001t0003g0030 a0001c0001t0003g0315 |
2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1572-6752T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106879152 | |||||||
| chr12:106879429 | C | A | 1 | a0001c0001t0003g0315 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1572-6475C>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106879429 | |||||||
| chr12:106879544 | A | C | 2 | a0001c0001t0008g0302 a0001c0001t0008g0303 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1572-6360A>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106879544 | |||||||
| chr12:106880106 | TGGCCTGT others(8): Show |
T | 10 | a0001c0001t0005g0003 a0001c0001t0005g0196 a0001c0001t0005g0213 others(7): Show |
10 | HG00738.hp1 HG01099.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1572-5793_1572-577 others(19): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106880106 | ||||||
| chr12:106880308 | G | A | 24 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(21): Show |
24 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1572-5596G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106880308 | |||||||
| chr12:106880325 | T | C | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1572-5579T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106880325 | |||||||
| chr12:106880466 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1572-5438C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106880466 | |||||||
| chr12:106880676 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1572-5228A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106880676 | |||||||
| chr12:106881107 | T | C | 1 | a0001c0001t0005g0005 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1572-4797T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881107 | |||||||
| chr12:106881212 | G | A | 20 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(17): Show |
20 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1572-4692G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881212 | |||||||
| chr12:106881339 | G | GT | 9 | a0001c0001t0002g0204 a0001c0001t0003g0007 a0001c0001t0004g0162 others(6): Show |
9 | HG01099.hp1 HG01175.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572-4552dupT | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106881339 | ||||||
| chr12:106881579 | C | T | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572-4325C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881579 | |||||||
| chr12:106881812 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572-4092G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881812 | |||||||
| chr12:106881822 | G | A | 10 | a0001c0001t0005g0003 a0001c0001t0005g0196 a0001c0001t0005g0213 others(7): Show |
10 | HG00738.hp1 HG01099.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1572-4082G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881822 | |||||||
| chr12:106881950 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1572-3954T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106881950 | |||||||
| chr12:106882140 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0004g0096 others(2): Show |
5 | HG02280.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572-3764C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106882140 | |||||||
| chr12:106882340 | G | A | 3 | a0001c0001t0004g0096 a0001c0001t0004g0098 a0001c0001t0004g0099 |
3 | HG02280.hp2 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1572-3564G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106882340 | |||||||
| chr12:106882389 | C | G | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572-3515C>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106882389 | |||||||
| chr12:106882475 | C | CTTA | 3 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0002t0023g0300 |
3 | HG02145.hp1 HG02451.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1572-3410_1572-340 others(7): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106882475 | ||||||
| chr12:106882712 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1572-3192T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106882712 | |||||||
| chr12:106883032 | T | C | 3 | a0001c0001t0002g0269 a0001c0001t0002g0270 a0001c0001t0002g0271 |
3 | HG02257.hp1 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1572-2872T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883032 | |||||||
| chr12:106883035 | G | A | 7 | a0001c0001t0002g0138 a0001c0001t0002g0140 a0001c0001t0002g0174 others(4): Show |
7 | HG00741.hp1 HG01074.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1572-2869G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883035 | |||||||
| chr12:106883052 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1572-2852C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883052 | |||||||
| chr12:106883072 | C | T | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572-2832C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883072 | |||||||
| chr12:106883393 | T | C | 5 | a0001c0001t0007g0040 a0001c0001t0007g0114 a0001c0001t0007g0115 others(2): Show |
5 | HG01109.hp2 HG01943.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1572-2511T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883393 | |||||||
| chr12:106883479 | T | C | 4 | a0001c0001t0007g0114 a0001c0001t0007g0115 a0001c0001t0007g0116 others(1): Show |
4 | HG01109.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572-2425T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883479 | |||||||
| chr12:106883709 | T | TA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(91): Show |
95 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1572-2194dupA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106883709 | ||||||
| chr12:106883747 | A | G | 5 | a0001c0002t0004g0305 a0001c0002t0009g0306 a0001c0002t0009g0307 others(2): Show |
5 | HG01175.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1572-2157A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883747 | |||||||
| chr12:106883848 | A | G | 1 | a0001c0002t0014g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1572-2056A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883848 | |||||||
| chr12:106883904 | C | T | 7 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1572-2000C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106883904 | |||||||
| chr12:106884177 | C | T | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1572-1727C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884177 | |||||||
| chr12:106884255 | G | A | 1 | a0001c0002t0025g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1572-1649G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884255 | |||||||
| chr12:106884386 | A | T | 9 | a0001c0001t0004g0111 a0001c0001t0004g0118 a0001c0001t0004g0119 others(6): Show |
9 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1572-1518A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884386 | |||||||
| chr12:106884409 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1572-1495C>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884409 | |||||||
| chr12:106884436 | G | A | 1 | a0001c0001t0002g0230 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1572-1468G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884436 | |||||||
| chr12:106884768 | A | G | 18 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(15): Show |
18 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1572-1136A>G | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884768 | |||||||
| chr12:106884806 | G | C | 3 | a0001c0002t0009g0306 a0001c0002t0009g0307 a0001c0002t0009g0308 |
3 | HG01175.hp1 HG02615.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1572-1098G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884806 | |||||||
| chr12:106884972 | A | T | 6 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1572-932A>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106884972 | |||||||
| chr12:106885224 | G | A | 2 | a0001c0001t0002g0268 a0001c0001t0002g0284 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1572-680G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885224 | |||||||
| chr12:106885269 | T | C | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572-635T>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885269 | |||||||
| chr12:106885370 | G | C | 18 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(15): Show |
18 | HG01109.hp2 HG01175.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1572-534G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885370 | |||||||
| chr12:106885376 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1572-528G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885376 | |||||||
| chr12:106885453 | G | A | 9 | a0001c0001t0004g0123 a0001c0001t0004g0124 a0001c0001t0004g0125 others(6): Show |
9 | HG02027.hp1 HG02109.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1572-451G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885453 | |||||||
| chr12:106885468 | T | A | 1 | a0001c0002t0028g0006 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1572-436T>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885468 | |||||||
| chr12:106885576 | CA | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(128): Show |
132 | HG00408.hp1 HG00438.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1572-313delA | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106885576 | ||||||
| chr12:106885593 | G | A | 1 | a0001c0002t0004g0305 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1572-311G>A | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885593 | |||||||
| chr12:106885723 | TTTTC | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0195 |
3 | NA18942.hp2 NA18970.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1572-176_1572-173d others(6): Show |
RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr12 | 106885723 | ||||||
| chr12:106885836 | G | C | 1 | a0001c0001t0026g0198 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1572-68G>C | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885836 | |||||||
| chr12:106885837 | G | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | HG01256.hp1 HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1572-67G>T | RIC8B | ENSG00000111785.21 | transcript | ENST00000392837.9 | protein_coding | 9/9 | chr12 | 106885837 |